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Publications - Developmental Studies

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A Modified golgi staining protocol for use in the human brain stem and cerebellum. Friedland, D., Los, J. and Ryugo, D. J. Neurosci. Methods 150:90-95, 2006. [paper] 

A common polymorphism decreases low-density lipoprotein receptor exon 12 splicing efficiency and associates with increased cholesterol. Zhu, H., Tucker, M., Grear, K., Simpson, J., Manning, A., Cupples. L. and Estus, S. Human Molecular Genetics 16: 1765-1772, 2007 [paper] 

A distinct familial Ssndrome of combined multiple pituitary hormone deficiency with structural abnormality: implications for uncontrolled pituitary apoptosis. Sanchez, J., Schiavi, A., Perera, E., Falcone, S., Brown, M., Parks, J., Cleveland, W. and Baumbach, L. 46th Annual Amer. Society of Human Genetics Meeting, 1996. [abstract] 

A novel nuclear localization of the G protein - coupled receptor for apelin in human brain and cultured cells. Lee, D.K., Lanca, A.J., Cheng, R., Gobeil, F., Chemtob, S., George, S., andO'Dowd, B.F. Society for Neuroscience, 2002. [abstract] 

A putative imprinting control region in 11p15.5 and its loss of methylation in Beckwith-Wiedemann syndrome. Smilinich, N.J., Day, C.D., Fitzpatraick, G.V., Diaz-Meyer, N., Titus, R.L., G.M., Lossie, A.C., Samllwood, A.C., Joyce, J.A., Schofield, P.N., Reik, W., Nicholls, R.D., Weksberg, R., Driscoll, D.J., Mahler, E.R., Shows, T.B., and Higgins, J.J. American Soc. of Human Genetics Meeting,Oct. 19-23, 1999. [abstract] 

A putative imprinting control region in 11p15.5 and its loss of methylation in Beckwith-Wiedemann syndrome. Smilinich, N.J., Day, C.D., Fitzpatraick, G.V., Diaz-Meyer, N., Titus, R.L., G.M., Lossie, A.C., Samllwood, A.C., Joyce, J.A., Schofield, P.N., Reik, W., Nicholls, R.D., Weksberg, R., Driscoll, D.J., Mahler, E.R., Shows, T.B., and Higgins, J.J. International Genomic Imprinting Meeting, August 24-26, 1999. [abstract] 

A secreted DNA-Binding protein that is translated through an internal ribosome entry site (IRES) and distributed in a discrete pattern in the central nervous system. Kim, J.G., Armstrong, R.C., Berndt, J.A., Kim, N.W. and Hudson, L.D. Mol. Cell. Neurosci. 12:119-140, 1998. [paper] 

A set of differentially expressed miRNAs, inclluding miR-30a-5p, act a s post-transcriptional inhibitors of BDNF in prefrontal cortex. Mellios, N., Huang, H., Grigorenko, A., Rogaev, E. and Akbarian, S. HMG 17: 3030-3042, 2008. [paper] 

A stop codon mutation in SCN9A causes lack of pain sensation. Ahmad, S., Dahllund, L., Eriksson, A.B., Hellgren, D., Karlsson, U., Lund, P.E., Meijer, I.A., Meury, L., Mills, T., Moody, A., Morinville, A., Morten, A., O'Donnell, D., Raynoschek, C., Salter, H., Rouleau, G.A. and Krupp, J. Hum. Mol. Gen. 16(17): 2114-2121, 2007. [paper] 

Abundant quantitative trait loci exist for DNA methylation and gene expression in human brain. Gibbs, R., van der Brug, M., Hernandez, D, Traynor, B., Nalls, M., Lai, S., Arepalli, S., Dillman, A., Rafferty, I., Troncoso, J., Johnson, R., Zielke, H.R., Ferrucci, L., Longo, D., Cookson, M. and Singleton, A. PLOS Genetics, 2010, 6(5): e1000952. [paper] 

Activation of a TRPC3-dependent cation current through the neurotrophin BDNF. Li, H.-S., Xu, X.-Z.,S. and Montell, C. Neuron 24:261-273, 1999. [paper] 

Affinity purification and characterization of the zonulin/zonula occudens toxin (Zot) receptor from human brain. Lu, R., Wang, W., Uzzau, S., Vigorito, R., Zielke, H.R. and Fasano, A. J. Neurochem. 74:320-326, 2000. [paper] 

Age-dependent changes in the structure, composition and biophysical properties of a human basement membrane. Candiello, J., Cole, G.J., Halfter, W. Matrix Biology, 29(5):402-10, 2010. [paper] 

Age-dependent telomere attrition as a potential indicator of racial differences in renal growth patterns. Tchakmakjian, L, Gardner, J., Wilson, P., Kimura, M., Skurnick, J., Zielke, H.R. and Aviv. A. Nephron Exp Nephrol 98: e82-e88, 2004. [paper] 

Agonist-independent nuclear localization of the apelin, angiotensin AT, and bradykinin B2 receptors. Lee, D., Lanca, J., Cheng, R., Nguyen, T., Ji, X.,, Gobeil, F., Chemtob, S., George, S and O'Dowd. J. Biol. Chem. 279: 7901-7908, 2004. [paper] 

Allelic expression of serotonin transporter (SERT) mRNA in human pons: lack of correlation with the polymorphism SERTLPR. Lim, J., Papp, A., Pinsonneault, J., Sad#e, W. and Saffen, D. Molecular Psychiatry, 1-14, 2006. [paper] 

Alternative processing events in human FMO genes. Lattard, V., Zhand, J. and Cashman, J. Mol. Pharmacol. 65: 1517-1525, 2004. [paper] 

Alternative splicing of G6PC2, the gene coding for the islet-specific glucose-6-phosphatase catalytic subunit-related protein (IGRP), results in differential expression in human thymus and spleen compared with pancreas. Dogra, R., Vaidyanatham, P., Prabakar, K., Marshall, K., Hutton, J. and Pugliese, A. Diabetologia, 49: 953-957, 2006. [paper] 

Analysis of DNA methylation in brain-derived neurotrophic factor (BDNF) promoter 4 in developing human prefrontal cortex. Salimi, K., Hamer, R., Vadlamudi, S., Barros, S., Offenbacher, S., Gilmore, J and Jarskog, L. Presented 2008. [abstract] 

Analysis of human and rodent beta 3-adrenergic receptor messenger ribonucleic acids. Granneman, J.G. and Lahners, K.N. Endocrinology 135:1025-1031, 1994. [paper] 

Analysis of the PIT-1 gene locus in a jamaican family with combined pituitary hormone deficiency. Sanchez, J., Schiavi, A., Perera, E., Falcone, S. and Baumbach, L. 10th International Congress of Endocrinology, San Francisco, CA., 1996. [abstract] 

Analysis of the imprinted status of the genes andmethylation of cpG islands around mouse Murr1/U2af1-rs1 and in the human syntenic region. Zhang, Z., Yatsuki, H., Wang, W., Joh, K., Soejima, H., Arai, Y., Matsuhashi, S., Iwasaka, T. and Mukai, T. Molecular Biology Society of Japan, Kobe, Japan, 2003. [abstract] 

Anatomical characterization of human fetal brain development with diffusion tensor magnetic resonance imaging. Huang, H., Xue, R., Zhang, J., Ren, T., Richards, L.J., Yarowsky, P., Miller, M.I. and Mori, S. J. Neuroscience 29(13): 4263-4273, 2009. [paper] 

Ancient DNA analysis. Baumback, L. Southeastern Regional Genetics Group, Atlanta, GA., 1995. [abstract] 

Apelin, a new enteric peptide: Localization in the gastrointesinal tract, ontogeny, and stimulation of gastric cell proliferation and of cholecystokinin secretion. Wang, G., Anini, Y., Wei, W., Qi, X., O'Carroll, A., Mochizuki, T., Wnag, H., Hellmich, M., Englanders, E. and Greeley, G. Endocrinology 145: 1342-1348, 2004. [paper] 

Apotosis, neuronal maturation, and neurotrophin expression within medulloblastoma nodules. Eberhart, C.G., Kaufmann, W.E., Tihan, T. and Burger, P.C. J. Neuropath. Exp. Neurol. 60: 462-469, 2001. [paper] 

Application of pharmacogenomic strategies to the study of drug-induced birth defects. Leeder, J. and Mitchell, A. Clinical Pharmacology & Therapeutics 81: 595-599. 2007. [paper] 

Axonal development in the cerebral white matter of the human fetus and infant. Haynes, R., Borenstein, N., Desilva, T., Folkerth, R., Liu, L., Volpe, J. and Kinney, H. J. Comparative Neurology 484: 156-167, 2005. [paper] 

BMP expression in the developing human brain: implications for CNS axis formation. Fu L, Abu-Khalil, A. and Geschwind D.H. Soc. of Neurosci. Abstracts 27: 25.4, 2001. [abstract] 

Binding of antipsychotic drugs to human brain receptors. Focus on newer generation compounds. Richelson and Souder, T. Life Sci. 68:29-39, 2000. [paper] 

Binding studies with some new neuroleptics at human brain receptors. Richelson, E. Souder, T., Acuna, J. and Chou, T., Biol. Psychiatry. 41:67S, 1997. [abstract] 

Biotransformation of fluticasone: in vitro characterization. Pearce, R., Leeder, J. and Kearns, G. Drug Metab. Disp. 34: 1035-1040, 2006. [paper] 

CYP2D6*36 gene arrangements within the CYP2D6 locus: association of CYP2D6*36 with poor metabolizer status. Gaedigk, A., Bradford, L., Alander, S. and Leeder, J. Drug Metab Disp 34: m563-569, 2006. [paper] 

CYP2D7 splice variants in human liver and brain: does CYP2D7 encode functional protein? Gaedigk, A., Gaedigk, R. and Leeder, J. Biochem. Biophys. Res. Commun. 336: 1241-1250, 2005. [paper] 

Carbamazepine bioactivation in children: characterization of carbamazepine 2- and 3-hydroxylase pathways in vitro. Pearce, R and Leeder, J.S. Drug. Metab. Rev. 36: 196, 2004. [abstract] 

Carbonic anhydrase II in the developing and adult human brain. Kida, E., Palminiello, S., Golabeck, A., Walus, M., Wierzba-Bobrowicz, T., Rabe, A., Albertini, G. and Wisniewski, K. J. Neuropathol. Exp. Neurol. 65: 664-674, 2006. [paper] 

Cartilage-selective genes identified in genome-scale analysis of non-cartilage and cartilage gene expression. Chen, Z., Nelson, S. and Cohn, D. BMC Genomics 8:165-178, 2007. [paper] 

Celsius: a community resource for Affymetrix microarray data. Day, A., Carlson, M., Dong, J., O'Connor, B and Nelson, S. Genome Biology 8:R112, 2007. [paper] 

Central and peripheral autoantigen presentation in immune tolerance. Pugliese, A. Immunology, 111:138-146 [paper] 

Changes in GABAergic inhibitory mechanisms in human cortex throughout the life span. Boley, P., Jones, D., Pinto, J. and Murphy, K. SFN, 2005 [abstract] 

Changes in inhibitory mechanisms in human visual cortex throughout the lifespan. Pinto, J., Beston, B., Jones, D. and Murphy, K. Vision Science Society, 2007. [abstract] 

Characterization of Foxp2 and Foxp1 mRNA and protein in the developing and mature brain. Ferland, R.J., Cherry, T.J., Preware, P.O., Morrisey, E.E. and Walsh, C.A. J. Comp. Neurol. 460: 266-279, 2003. [paper] 

Characterization of interindividual variability in CYPP3A7 expression of fetal liver. Leeder, J.S., Marcucci, K., Gaedigk, R., Gaedigk, A. and Pearce, R. Conference on Pharmacogenomics, Hinxton, UK, Sept, 2003. [abstract] 

Characterization of new transcripts of the human PLP1gene. Vaurs-Barriere, C. and Boespflug-Tanguy, O. First EA Research Foundation Meeting, Paris, 2006. [abstract] 

Characterization of new transcripts of the human PLP1gene. Vaurs-Barriere, C. and Boespflug-Tanguy, O. Gordon Research Conference on Myelin, Ventura Beach, CA, 2006. [abstract] 

Characterization of new transcripts of the human PLP1gene. Vaurs-Barriere, C., Sarret, C., Combes, P., Micheau, P. and Boespflug-Tanguy, O. Glial Cells in Health and Disease, Villth European meeting, London, 2007. [abstract] 

Chondroitinase ABC improves basic and skilled locomotion in spinal cord injured cats. Tester, N. and Howland, D. Experimental Neurology 209: 483-496, 2008. [paper] 

Chromosomal rearrangements and the genomic distribution of gene-expression devergence in humans and chimpanzees. Marques-Bonet, T., Caceres, M., Bertranpetit, J., Preuss, T. Thomas, J. and Navarro, A. Trends in Genetics: 20: 524-528, 2004. [paper] 

Comparative analyses of genomic imprinting and CpG island-methylation in mouse Murr1 and human MURR1 loci revealed a putative imprinting control region in mice. Zang, Z., Joh K., Yatsuki, H., Wang, W., Arai, Y., Soejima, H., Higashimoto, K. Iwasaka, T. and Mukai, T. Gene 366: 77-86, 2006. [paper] 

Conservation of the developmentally regulated dendritic localization of a purkinje cell-specific mRNA that encodes a G-protein modulator: comparison of rodent and human Pcp(L7) gene structure and expression. Zhang, X, Zhang, H. and Oberdick, J. Molecular Brain Research 105:1-10, 2002. [paper] 

Constitutional aneuploidy in the normal human brain. Rehen, S., Yung, Y., McCreight, M., Kaushal, D., Yang, A., Almeida, B., Kingsbury, M., Cabral, K., McConnell, M., Anliker, B., Fontanoz, M. and Chun, J. J. Neuroscience 25: 1-5, 2005. [paper] 

Cyclic dimers of c-terminal g2-MSH analogs as selective antagonists of the human sensory nerve-specific receptor (SNSR-4). Schmidt, R., Butterworth, J., O'Donnell, D., Santhakumar, V., Tomaszewski, M. 20th American peptide Symposium, Montreal, 2007 [abstract] 

Cyclin D1 in exitatory neurons of the adult brain enhances kainate-induced neurotoxicity. Koeller, H., Ross, E. and Glickstein, S. Neurobiology of Disease 31: 230-241, 2008. [paper] 

DNA methylation in the human cerebral coretx is dynamically regulated throughout the life span and involves differentiated neurons. Siegmund, K., Connor, C., Campag, M., Long, T., Weisenberger, D., Biniszkiewicz, D., Jaenisch, R., Laird, P. and Akbarian, S. PLoS One, Sept. 2007, issue 9, e895. [paper] 

DTI Contrast reveals the organization and shape of cortical structures during fetal development. Zhang, J., Xue, R., Yarowsky, P. and Mori, S. Society for Neuroscience, 2004. [abstract] 

DYX1C1 functions in neuronal migration in developing neocortex. Wan, Y., Paramasivam, M., Thoams, A., Bai, J., Kaminen-Hhola, N., Kere, J., Voskuil, J., Rosen, G., Galaburda, A. and Loturco, J. Neuroscience 143: 515-522, 2006. [paper] 

Database of mRNA gene expression profiles of multiple human organs. Son, C.G., Bilke, S., Davis, S., Greer, B.T., Wei, J.S., Whiteford, C.C., Chen, Q.-R., Cenacchi, N. and Khan, J. Genome Research 15:443-450, 2005. [paper] 

Dendritic anomalies in disorders associated with mental retardation. Kaufman, W.E. and Moser, H.W. Cerebral Cortex 10:981-991, 2000. [paper] 

Dendritic architecture of the von Economo neurons. Watson, K.K., Jones, T.K. and Allman, J.M. Neuroscience, 141(3):1107-12, 2006. [paper] 

Development of human hepatic CYP2E1: implications for pediatric therapeutics. Johnsrud, E., Koukouritaki, S., Hines, R. and McCarver, D. Pediatric Research 51:463A (Abstr. 2700), 2002. [abstract] 

Development of human visual cortex: a balance between excitatory and inhibitory plasticity mechanisms. Murphy, K., Beston, B., Boley, P. and Jones, D. Developmental Psychobiology, 46: 209-221, 2005. [paper] 

Developmental anatomy of prefrontal cortex. Huttenlocher, P.R. and Dabholkar, A.S. "Development of the Prefrontal Cortex: Evolution, Neurobiol" book, 1997. [paper] 

Developmental and tissue-specific splicing of CYP2D6 mRNA. Gaedigk, A., Gaedigk, R and Leeder, J.S. Proceedings of the 15th Intl Symp on Microsomes and Drug Oxidations [abstract] 

Developmental expression AHR, ARNT, AHRR and CYP1A1 in humans Bhathena, A., Gaedigk, R and Leeder, J.S. Drug. Metab. Rev. 36: 319, 2004. [abstract] 

Developmental expression of CYP3J2 in prenatal tissues. Baker, D., Gaedigk, A, Gaedigk, R and Leeder, J.S. Drug. Metab. Rev. 36: 321, 2004. [abstract] 

Developmental expression of cytochrome P450, 3A4, 3A5, 3A and 3A43 and characterization of CYP3A5 splice variants. Gaedigk, R., Gaedigk, A., Marcucci, K., Pearce, R., Rogan, P. and Leeder, J. Conference on Pharmacogenomics, Hinxton, UK, Sept, 2003. [abstract] 

Developmental expression of human hepatic CYP2C9 and YCP2C19. Koukouritaki, S., Stevens, J., Rettie, A., McCarver, D. and Hines, R. Drug Metab. Revs. 35 (Supplement 2): 131 (Abstr. 261), 2003. [abstract] 

Developmental expression of human hepatic CYP3A and 2B enzymes. Stevens, J., Marsh, S., Zaya, M. Manro, J. Koukouritaki, S. and Hines, R. Toxicol. Sci. 72 (Supplement 1): 226 (Abstr. 1097), 2003. [abstract] 

Developmental expression of the major human hepatic CYP3A enzymes. Stevens, J., Hines, R., Gu, C., Koukouritaki, B. , Manro, J. Tandler, P., and Zaya, M. J. Pharmacol. Expt. Ther. 307: 573-582, 2003. [paper] 

Developmental lag in superoxide dismutases relative to other antioxidant enzymes in premyelinated human telencephalic white matter. Folkerth, R., Haynes, R., Borenstein, N., Belliveau, R., Trachtenberg, F., Rosenberg, P., Volpe, J. and Kinney, H. J. Neuropath.Experim. Neurology 63: 990-999, 2004. [paper] 

Developmental regulation and individual differences of neuronal H3K4me3 epigenomes in the prefrontal cortex. Cheung, I., Shulha, H.P., Jiang, Y., Matevossian, A., Wang, J., Weng, Z., and Akbarian, S. PNAS Early Edition, 2010. [paper] 

Developmental regulation of a-amino-3-hydroxy-5-methyl-4-isoxazole-propionic acid receptor subunit expression in forebrain and relationship to regional susceptibility to hypoxic/ischemic injury. II. Human cerebral white matter and cortex. Talos, D., Follett, P., Folkerth, R., Fishman, R., Trachtenbert, F., Volpe. J. and Jensen, F. J. Comparative Neurology 497:61-77, 2006. [paper] 

Developmental-specific expression of human hepatic flavin-containing monooxygenases 1 (FM01) and 3 (FM03). Hines, R., Koukouritaki, S., Hoop, K. and Luo, Z. Drug Metab. Revs. 34 (Supplement 1): 15 (Abstr. 29), 2002. [abstract] 

Differences in the expression of delta opeioid receptors between rodent and primate spinal cord and dorsal root ganglia. Mennicken, F., Zhang, J., Hoffert, C., Ahmad, S., Beaudet, A. and O'Donnell, D. Society For Neuroscience, New Orleans, LA, USA, 2003. [abstract] 

Differences in the expression of delta opioid receptors between rodent and primate spinal cord and dorsal root ganglia. Beaudet, A., Mennicken, F., Zhang, J., Hoffert, C., Ahmand, S. and O'Donnell, D National Narcotics Research Conference, Perpignan, FRANCE, 2003. [abstract] 

Differential gene expression in the hypothalamus of obese and humans: a preliminary report. Beach, D.A., Page, T., Allison, G., Tataranni, D. and Antonio, P. 85th Annual Endocrine Society Meeting, Philadelphia, PA, June 2003. [abstract] 

Differential splicing of the IA-2 mRNA in pancreas and lymphoid organs as a permissive genetic mechanism for autoimmunity against the IA-2 Type 1 diabetes autoantigen. Diez, J., Park, Y., Zeller, M., Brown, D., Garza, D., Ricordi, C., Hutton, J., Eisenbarth, G. and Pugliese, A. Diabetes 50: 895-900, 2001. [paper] 

Discovery of novel flavin-containing monooygenase 3 (FMO3) single nucleotide polymorphisms and functional analysis of upstream haplotype variants. Koukouritaki, SB, Poch, MT, Cabacungen, ET, McCarver, DG and Hines, RN. Molecular Pharmacology 68(2):383-392, 2005. [paper] 

Distribution of class I, III and IV alcohol dehydrogenase mRNAs in the adult rat, mouse and human brain. Galter, D., Carmine, A., Beurvenich, S., Duester, G. and Olson, L. Eur. J. Biochem. 270: 1316-1326, 2003. [paper] 

Distribution of glutamate transporter subtypes during human brain development. Bar-Peled, O., Ben-Hur, H. Biegon, A., Groner, Y., Dewhurst, S., Furuta, A. and Rothstein, J.D. J. Neurochem. 69:2571-2580, 1997. [paper] 

Distribution of the voltage-sensitive Ca2+ channel a2o subunit subtypes 1 and 2 in rat, monkey and human brains. Li, A., Benoit, C., Staimmer, A, Dumont, Y., Su, T., Dooley, D. and Quirion, R. SFN, 2007. [abstract] 

Divergently transcribed overlapping genes expressed in liver and kidney and located in the 11p15,5 imprinted domain. Cooper, P.R., Smilinich, N.J., Day, C.D., Nowak, N.J., Reid, L.H., Pearsall, R.S., Reece, M., Prawitt, D., Landers, J., Housman, D.E., Winterpacht, A., Zabel, B.U., Pelletier, J., Weisman, B.E., Shows, T.B. and Higgins, M.J. Genomics 48:38-51, 1998. [paper] 

Do disappearing synapeses underlie cortical maturation. Weickert, C., Rakic, P., Benes, F., Webster, M. Kleinman, J. and Weinberger, D. ACNP meeting, 2003. [abstract] 

Does microwaving enhance the Golgi methods? A quantitative analysis of disparate staining patterns in the cerebral cortex. Weng, S., Zhang, H. and Hutsler, J. J. Neurosci. Methods, 124: 145-155, 2003. [paper] 

Dopamine D1 and D1 receptors traffic together and co-localize in neurons. So, C.H., Varghese, G., Lanca, A.J., Cheng, R., Lee, S.P., Fan, T., O'Dowd, B.F. and George, S.R. Society for Neuroscience, 2002. [abstract] 

Dopamine D1 and D1 receptors traffic together in cells and CO-localize in human and rodent striatal neurons. So, C.H., Rashid, A.J., Varghese, G., Lanca, A.J., Cheng, R., Lee, S.L., O'Dowd, B.F. and George, S.R. Society for Neuroscience, 2003. [abstract] 

Early asymmetry of gene transcription in embryonic human left and right cerebral cortex. Sun, T., Patoine, C., Abu-Khalil, A., Visvader, J., Sum, E., Cherry, T., Orkin, S., Geschwind, D. and Walsh, C. Science 308: 1794-1798, 2005. [paper] 

Early rapid rise in EAAT2 expression follows the period of maximal seizure susceptibility in human brain. Lauriat, T., Schmeidler, J. and McInnes, L. Neurosci. Lett. 22: 412(1) 89-94, 2007. [paper] 

Ectopic mRNA expression of IDDM autoantigens and monoallelic expression of the insulin message (imprinting?) in the human thymus. Pugliese, A., Fernandez, A., Zeller, M., Pietropaolo, M., Eisenbarth, G., Ricordi, C. and Patel, D. American Diabetes Association Meeting, San Francisco, 1996. [abstract] 

Elevated gene expression levels distinguish human from non-human primate brains. Caceres, M., Lachuer, J., Zapala, M., Redmond, J., Kudo, L., Geschwind, D., Lockhart, D., Preuss, T. and Barlow, C. PNAS, 100: 13030-13035, 2003. [paper] 

Embryonic synthesis of the inner limiting membrane and vitreous body. Halfter, W., Dong, S., Schurer, B., Ring, C., Cole, G. and Eller A. Investigative Ophthalmology & Visual Science, 46: 2202-2208, 2005. [paper] 

Ethylmalonic encephalopathy with seizures and normal MRI. Schwartz, P., Fowler, G., Sweetman, L., Roe, C. and Stein, S. Society for Inherited Metabolic Disorders, Georgia, 35, 1999. [abstract] 

Expressing what's on your mind: DNA arrays and the brain. Lockhart, D.J. and Barlow, C. Nature Reviews 2:63-68, 2001. [paper] 

Expression HNF4a variants in fetal and pediatric liver. Vyhlidal, C. Gaedigk, R and Leeder, J.S. Drug. Metab. Rev. 36: 301, 2004. [abstract] 

Expression of estvogen receptor alpha exon-deleted MRNA variants in the human and non-human primate frontal cortex. Perlman, W., Matsumoto, M., Beltaifa, S., Hyde, T., Saunders, R., Webster, M., Rubinow, D., Kleinman, J. and Weickert, C. Neuroscience, 134: 81-95, 2005. [paper] 

Expression patterns of epidermal growth factor receptor and fibroblast growth factor receptor 1 mRNA in fetal human brain. Fu, L., Abu-Khalil, A., Morrison, R.S., Geschwind, D.H. and Kornblum, H.I. J. Compar. Neurology 462: 265-273, 2003. [paper] 

Finding the differences between the developing cerebral hemispheres using RDA and DNA microarray technology. Geschwind, D.H., Loginov, M., Karrim, J. and Nelson, S.F. Soc. for Neurosci. Abstracts 24(1): 398.3, 1998. [abstract] 

Fluoro jade stains early and reactive Aatroglia in the primate cerebral cortex. Colombo, J. and Puissant, V. J. Histochem. Cytochem. 50(8): 1135-1137, 2002. [paper] 

Gender influences monoallelic expression of ATP10A in human brain. Hogart, A., Patzel, K. and LaSalle, J. Hum. Genet. 124: 235-242, 2008. [paper] 

Gene expression changes in the course of normal brain aging are sexually dimorphic. Berchtold, N.C., Cribbs, D.H., Coleman, P.D., Rogers, J., Head, E., Beach, T., Miller, C., Troncoso, J., Trojanowski, J., Zielke, H.R.. and Cotman, C.W. PNAS 105(40): 15605-15610, 2008. [paper] 

Gene expression in the human cortex. Allen Insitute for Brain Science - Computer data base http://humancortex.alleninstitute.org/has/ (acknowledgements) [abstract] 

Gene expression of Na+/Ca2+ exchanger during development in human heart. Qu, Y., Ghatpande, A., El-Sherif, N. and Boutjdir, M. Cardiovasc. Res. 45:866-873, 2000. [paper] 

Gene expression of Na/Ca exchanger during development in human fetal heart. Qu, Y., Ghatpande, A., El-Sherif, N. and Boutjdir, M. Cardiov. Res., 2000. [abstract] 

Gene expression profiles in microdissected neurons from human hippocampal subregions. Torres-Munoz, J., Waveren, C., Keegan, M., Bookman, R. and Petito, C. Molecular Brain Research 127: 105-114, 2004. [paper] 

Gene regulation and DNA damage in the ageing human brain. Lu, T., Pan, Y., Kao, S., Li, C., Kohane, I., Chan, J. and Yankner, B. Nature 429: 883-891, 2004. [paper] 

Gene stucture and alternative splicing of glycogen synthase kinase-3 beta (GSK-3B) in neural and non-neural tissue. Schaffer, B., Wiedau-Pazos, M., and Geschwind, D. Gene 302: 73-81, 2003. [paper] 

Genetic control of DNA methylation and expression in the human brain. Hernandez, G., Gibbs, R., van der Brug, M., Traynor, B., Nalls, M., Shiao-Lin, L., Arepalli, S., Zonozi, R., Dillman, A., Tronocos, J., Johnson, R., Zielke, H., Ferrrucci, L., Longo, D., Cookson, M. and Singleton, A. Human Genetics, 2009. [abstract] 

Genetic variability at the human FMO1 locus: significance of basal promoter yin yang 1 element polymorphism (FMO1*6). Hines, R.N., Luo, Z., Hopp, K.A., Cabacungan, E.T., Koukouritaki, S.B. and McCarver, D.G. J. Pharmacol. Exp. Therap. 306(3):1210-1218, 2003. [paper] 

Gephyrin levels over the course of human cortical development. Hills-Carpenter, K., Jarskog, L., Glimore, J and Grobin, A. Presented 2007. [abstract] 

Global analysis of alternative splicing differences between humans and chimpanzees. Calarco, J., Xing, Y., Caceres, M., Clarco, J., Xiao, X., Pan, Q., Lee, C., Preuss, T. and Blencowe, B. Genes & Dev 21: 2963-2975, 2007. [paper] 

Global scope of the NICHD Brain and Tissue Bank for Developmental Disorders Zielke, H.R., Currey, K.M., Khaitovich, P., Nickel, B., Kleinman, J.E., Hyde, T.M., Lipska, B.K. Biospecimen Research Network Symposium, 2010. [abstract] 

Glycobiology-based therapeutic development for glioblastoma multiforme. Kroes, R., Schmidt, M., Dawson, G. and Moskal, J. SFN, 2007. [abstract] 

Golgi staining in the human auditory brain stem. Friedland, D.R. and Ryugo, D.K. Association for Research in Otolaryngology, 2003. [abstract] 

HIV-1 selectively depresses neuronal cytoskeletal antigen expression in cultures of differentiating human neuroepithelial precursor cells. McCarthy, M. and Vidaurre, I. Journal of Neurovirology 9: 44-45, 2003. [abstract] 

High thoughput analysis of gene expression in the human brain. Contantuoni, C., Purcell, A.E., Bouton, C.M.L. and Pevsner, J. J. Neurosci. Res. 59:1-10, 2000. [paper] 

High throughput imaging of brain gene expression. Brown, V.M., Ossadtchi, A., Khan,A.H., Cherry, S.R., Leahy, R.M. and Smith, D.J. Genome Research 12:244-254 2002. [paper] 

High-resolution anatomical study of human fetal brain development based on diffusion tensor imaging. Mori, S., Xue, R., Zhang, J., van Zijl, P. and Yarowsky, P. ISMRM, Honolulu, HI, 2002. [abstract] 

High-resolution voxelation mapping of human and rodent brain gene expression. Singh, R., Brown, V., Chaudhari, A., Khan, A., Ossadtchi, A., Sforza, D., Meadors, A., Cherry, S., Leahy, R. and Smith, D. J. Neuroscience Methods 125: 93-101, 2003. [paper] 

Human ARX gene: genomic characterization and expression. Ohira, R., Zhang, Y.H., Guo, W., Dipple, K., Shih, S.L., Doerr, B.L., Huang, B.L., Fu, L.J., Abu-Khalil, A., Geschwind, D. and McCabe, E.R.B. Mol. Gen. Met. 77: 179-188, 2002. [paper] 

Human brain derived neurotrophic factor (BDNF) genes, splicing patterns and assessments of associations with substance abuse and Parkinson's disease. Liu, Q., Walther, D., Grgon, T., Polesskaya, o, Lesnick, T., Strain K, deAndrade, M., Bower, J., Maraganore, D. and Uhl, G. Am. J. Med. Genet. B Neuropsychaiatr. Genet. 134B:93-103, 2005. [paper] 

Human brain evolution: insights from microarrays. Preuss, T., Caceres, M., Oldham, M. and Geshwind, D. Nature: 5: 850-860, 2004. [paper] 

Human cannabinoid receptor 1:5' exons, candidate regulatory regions, polymorphisms, haplotypes and association with polysubstance abuse. Zhang, P., Ishiguro, H., Ohtsuki, T., Hess, J., Carillo-London, F., Walther, D., Onaivi, E., Arinami, T and Uhl, G. Mol. Psychiatry. 9(10):916-3, 2004. [abstract] 

Human flavin-containing monooxygenase 1 and 3 developmental expression. Koukouritaki, S.B., Yeung, C.K., Retie, A.E., Williams, D.E. and Hines, R.N. FASEB J. 15(4):A549 (Abstr#447.8), 2001. [abstract] 

Human gamma-aminobutyric acid-type A receptor a5 subunit gene (GABRA5): characterization and structural organization of the 5' flanking region. Kim, Y., Glatt, H., Xie, W., Sinnett, D. and Lalande, M. Genomics 42: 378-387, 1997. [paper] 

Human hepatic CYP2E1 expression during development. Johnsrud, E., Koukouritaki, S., Divakaran, K., Brunengraber, L., Hines, R. and McCarver, D. J. Pharmacol. Expt. Ther. 307:402-407, 2003. [paper] 

Human hepatic flavin-containing monooxygenases 1 (FMO1) and 3 (FMO3) developmental expression. Sevasti B. Koukouritaki, Pippa Simpson, Catherine K. Yeung, Allan E. Rettie, and Ronald N. Hines Pediatric Research 51:236-243, 2002. [paper] 

IKAP/hELP1 deficiency in the cerebrum of familial dysautonomia patients results in down regulation of genes involved in oligodendrocyte differentiation and in myelination. Cheishvili, D., Maayan, C., Smith, Y., Ast, G. and Razin, A. Human Molecular Genetics 16: 2097-2104, 2007. [paper] 

IKAP/hELP1 deficiency in the cerebrum of familial dysautonomia patients results in down regulation of genes involved in oligodendrocyte differentiation and in myelination. Cheishvilli, D., Maayan, C., Smith, Y., Ast, G. and Razin, A. HMG 16: 2097-2104, 2007. [paper] 

Identification and characterization of novel sequence variations in the cytochrome P4502D6 (CYP2D6) gene in African Americans. Gaedigk, A., Bhathena, A., Ndjountche, L., Pearce, R., Abdel-Rahman, S., Alander, S., Bradford, L. and Leeder, S. Pharacogenomics J. 5: 173-182, 2005. [paper] 

Imaging, anatomical, and molecular analysis of callosal formation in the developing human fetal brain. Ren, T., Anderson, A., Shen, W., Huang, H., Plachez, C., Zhang, J., Mori, S., Kinsman, S. and Richards, L. Anat. Rec. A. Discov. Mol. Cell Evol. Biol. 288A: 191-204, 2006. [paper] 

Immuno-characterization of neonatal and fetal myoblast cultures. Gonzalez, I., Secore, S. and Bartlett, R. University of Miami School of Medicine, 1996. [abstract] 

Immunoblotting patterns of cytoskeletal dendritic protein expression in human neocortex. Kaufmann, W.E., Taylor, C.V. and Lishaa, N.A., Mol. Chem. Neuropathol. 31:235-244, 1997. [paper] 

Immunohistochemical localization of human sensory neuron specific g-protein coupled receptor in primate pain pathway. Mennicken, F., N-Merandi, S., Hoffert, C., Ahmad, S., O'Donnell, D. SFN, 2006. [abstract] 

Immunostaining of oxytocin receptors in human female amygdala area, hypothalamus, nucleus accumbens and cingulate gyrus. Boccia, M.., Petrusz, P., Suzuki, K., Razoli and M.Pedersen, C.A. Society for Neuroscience, 2003. [abstract] 

In vitro characterizaiton of 6-[18F] fluoro-A-85380, a high-affinity ligand for a4B2* nicotinic acetylcholine receptors. Gundisch, D., Koren, A., Horti, A., Pavlova, O., Kimes, A., Mukhin, A. and London, E. Synapse 55: 89-97, 2004. [paper] 

Increased expression of 72-kd type IV collagenase (MMP-2) in human aortic atherosclerotic lesions. Li, Z., Li, L., Zielke, H.R., Cheng, L., Xiao, R.,Crow, M.T., Stetler-Stevenson, W.G., Froehlich , J. and Lakatta, E.G. Amer. J. Path. 148:121-128, 1996. [paper] 

Increased sensitivity to human immunodeficiency virus Type I of maturing human central nervous system neurons in differentiating neuroepithelial precursor cell cultures. McCarthy, M., Galey, D., Vidaurre, I., Nath, A. and Whittemore, S. American Academy of Neurology Annual Meeting, 2002. [abstract] 

Indentification of the transciptional targets of FOXP2, a gene linked to speech and language, in developing human brain. Spiteri, E., Konopka, G., Coppola G., Bomar, J., Oldham, M., Ou, J., Vernes, S., Fisher, S., Ren, B., Geschwind, D. The American Journal of Human Genetics 81: 1144-1157, 2007. [paper] 

Infantile hypertrophic cardiomyopathy of glycogenosis type IX: isolated cardiac phosphorylase kinase Ddficiency. Regalado, J., Rodriguez, M. and Ferrer, P. Pediatric Cardiol. 20: 304-307, 1999. [paper] 

Influence of Genomic Variance on the Transcripome in Human Brain Tissues. Gibbs, J., Brug, M., Hernandez, D., Lai, S., Traynor, B., Cookson, M. and Singleton, A. ASHG, 2008. [abstract] 

Insulin gene transcription in the human thymus correlates with allelic variation at the IDDM2 susceptibility locus. Pugliese, A., Zeller, M., Bartlett, R., Eisenbarth, G., Ricordi, C., Bennett, S. and Patel, D. Immunology of Diabetes Society Meeting, Australia, 1996. [abstract] 

Interindividual variability in acetaminophen sulfation by human fetal liver: implications for pharmacogenetic investigations of drug-induced birth defects. Adjei, A., Gaedigk, A., Simon, S., Weishilbourm, R. and Leeder, S. Birth Defects Research (part A): Clin. & Mol. Teratology 82:155-165, 2008. [paper] 

International scope of the NICHD Brain and Tissue Bank for Developmental Disorders. Currey, K., Zielke, H., Paabo, S., Khaitovich, P., Nickel, B., Kleiman, J., Hyde, T. and Lipska, B. J of Neural Transm 115: 1728, 2008. [abstract] 

Interneuron neuropeptide expression in the human prefrontal cortex during development. Fung, S.J., Sivagnanasundaram, S., Duncan, C.E., Webster, M.J. and Weickert, C.S. SFN, 2008: 557.14/CC28 [abstract] 

Intraventricular enzyme replacement improves disease phenotypes in a mouse model of late infantile neuronal ceroid lipofuscinosis. Chang, M., Cooper, J., Sleat, D., Cheng, S., Dodge, J., Passini, M., Lobel, P., and Davidson, B. Molecular Therapy, 16:649-656, 2008. [paper] 

Investigation of different transcript quantitation tools for high-throughput mapping of brain gene expression using voxelation. Singh, R., Liu, D., Chaudhari, A., Cherry, S., Leahy, R. and Smith, D. J. Mol. Histol. 35: 397-402, 2004. [paper] 

Isolation and characterization of neural progenitor cells from post-mortem human cortex. Schwartz, P., Bryant, P., Fuja, T., Su, H., O'Dowd, D. and Klassen, H. J. Neuroscience Res. 74:838-851, 2003. [paper] 

Isolation and culture of primary Schwann cells from human fetal peripheral nerve. Lopez, T.J. and DeVries, G.H. Experim. Neurol. 158:1-8, 1999. [paper] 

Isolation and partial purification of the zonula occludens toxin (ZOT) human receptor. Lu, R., Vigorito, R., Wisniewski, S., Zielke, H.R., Wang, W. and Fasano, A. J. Pediatr. Gastroenterol. Nutr. 26:555S, 1998. [abstract] 

Isolation of Ca2+ channel a1A, a2 and beta subunit segments from human spinal cord RNA. Hajela, R.K. and Atchison, W.D. 9th Intern. Conf. on Myasthenia Gravis & Related Disorders, 1997. [abstract] 

Isolation of Ca2+ channel a1A, a2, and beta subunit segments from human spinal cord RNA. Hajela, R.K. and Atchison, W.D. Annals NY Acad. Sci., 841: 115-118, 1998. [paper] 

KCNE4 Can co-associate with the Lks (KCNQ1/KCNE1) channel complex. Manderfield, L., and George, A. Presented 2007. [abstract] 

KCNE4 can co-associate with the Iks (KCNQ1-KCNE1) channel complex. Manderfield, L. and George, A. FEBS 275: 1336-1349, 2008. [paper] 

Lamin A-dependent nuclear defrects in human aging. Scaffidi, P. and Misteli, T. Science 312: 1059-1063, 2006. [paper] 

Laser-capture microdissection (LCM): defining the quantity and cellular distribution of latent HSV DNA. Wang, K., Mont, E., Williams, R., Grosvenor, T. and Straus, S. Int. HSV Workshop, 2001. [abstract] 

Late developmental changes in synaptophysin and spinophilin in the human prefrontal cortex are associated with changes in calpain but not caspase-3. Glantz, L., Gilmore, J., Lieberman, J. and Jarskog, L. Society of Neuroscience Meeting, 2005. [abstract] 

Localization of ADP-ribosylation factor domain protein 1 (ARD1) in lysosomes and golgi apparatus. Vitale, N., Horiba, K., Ferrans, V., Moss, J. and Vaughan, M. Proc. Natl. Acad. Sci., 95: 8613-8618, 1998. [paper] 

Localization of N-methyl-norsalsolinol within rodent and human brain. Zhou, Q., Kalabokis, V., Hao, R., Stuart, J., Schroeder, D., Kalyuzhny, A., Tsang, M. and LeDoux, M. SFN, 2001. [abstract] 

Loss of imprinting of IGF2 and a novel CpG-island in a BWS fetus with an inversion chromosome 11. Higgins, M.J., Cooper, P.R., Nowak, N.J., Reid, L.H., Crider-Miller, S.J., Davies, C., Gabriel, J.M., Nicholls, R.D., deJong, P., Evans, G., Weissmann, B.E. and Shows T.B. Gordon Conference, Epigenetics, August 1997. [abstract] 

Lymphocytic infiltrates in eosinophilic gastroantaropathy. McGeady, S. J. Allergy Clin. Immunol. February 2006. [abstract] 

Macrophage impairment underlies airway occlusions in primary respiratory syncytial virus bronchiolitis. Reed, J., Brewah, Y., Delaney, T., Williver, T., Burwell, T., Benjamin, E., Kuta, E., Kozhich, A., McKinney, L., Suzich, J., Kiener, P., Avendano, L, Velozo, L., Hubles, A., Welliver, R. and Coyle, A. JID 198: 1783-1793, 2008. [paper] 

Measurement of the dynamic bulk and shear response of soft human tissues. Saraf, H., Ramesh, K., Lennon, A., Merkle, A. and Roberts, J. Experimental Mechanics 47:439-449, 2007. [paper] 

Mechanical properties of soft human tissues under dynamic loading. Saraf, H., Ramesh, K., Lennon, A., Merkle, A. and Roberts, J. SEM, St. Louis, 2006. [abstract] 

Mechanical properties of soft human tissues under dynamic loading. Saraf, H., Ramesh, K., Lennon, A., Merkle, A. and Roberts, J. J. Biomechanics 40: 1960-1967, 2007. [paper] 

Methylation of the UBE3A CpG island does not mediate transcriptional repression of the paternal allele in brain. Han, M.K., Butler, M.G. and Sutcliffe, J.S. AJHG 65:A273, 1999. [abstract] 

Mitochondrial DNA point mutations in patients with MNGIE. Niahigaki, Y., Marti, R., Lin, M. and Hirano, M. American Journal of Human Genetics 71:165, 2002. [abstract] 

Molecular mechanisms regulating FMO temporal-specific expression. Hines, R., Koukouritaki, S., Hoop, K. and Lou, Z. Toxicol. Sci. 72 (Supplement 1): 225 (Abstr. 1095), 2003. [abstract] 

Molecular targets of Lambert Myasthenic syndrome antibodies. Hajela, R.K. and Atchinson, W.D.. FASEB Meeting, March 28 - April 1, 1993. [abstract] 

Monallelic expression of the insulin gene message in the human thymus provides additional evidence for parental imprinting. Pugliese, A., Fernandez, A., Bartlett, R., Eisenbarth, G., Ricordi, C., Haynes, B. and Patel, D. Immunology of Diabetes Society Meeting, Orvieto, Italy, 1995. [abstract] 

Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesis. Jen, Chan, Bosley, Wan, Carr, Rub, Shattuck, Salamon, Kudo, Ou, Lin, Salih, Kansu, Dhalaan, Zayed, MacDonald, Stigsby, Plaitakis, Dretakis, Gottlob, Pieh, Traboulsi, Wang, Wang, Andrews, Yamada, Demer, Karim, Alger, Geschwind, Deller, Sicote, Nelson. Science 304: 1509-1513, 2004. [paper] 

Mutations in a human ROBO gene disrupt hindbrain axon pathway crossing and morphogenesis. Jen, J., Chan, W., Bosley, T., Wan, J., Carr, J., Rub, U., Shattuck, D., Salamon, G., Kudo, L., Ou, J., Lin, D., Salih, M., Kansu, T., Dhalaan, H., Zayed, Z., MacDonald, D., Stigsby, B., Plaitakis, A., Dretakis, E.... Geschwind, D., et al. Science 304: 1509-1513, 2004. [paper] 

Myometrial hyperplasia in "unnecessary hysterectomies" - a histopathologic review. Cramer, S.F., Hernandez, C., Khan, A., Newcomb, P. and Marchett, C. Advances in Uterine Leiomyoma Research Mtg, October 7-8, 1999. [abstract] 

NKCC1 transporter facilitates seizures in the developing brain. Dzhala, V., Talos, D., Sdrulla, D., Brumback, A., Mathews, G., Benke, T., Delpire, E., Jensen, F and Staley, K. Nature Medicine 11:1205-1213, 2005. [paper] 

NKCC1 transporter facilitates seizures in the developing brain. Dzhala, V., Talos, D., Sdrulla, D., Brumback, A., Mathews, G., Benke, T., Delpire, E., Jensen, F. and Staley, K. Nature Medicine 11: 1205-1213, 2005. [paper] 

Neocortical RELN promoter methylation increases significantly after puberty. Lintas, C. and Persico, A.M. NeuroReport 21:114-118, 2010. [paper] 

Neuregulins in primary fetal human Schwann cells. Lopez, T.J. and DeVries, G.H. J. Neurochem. Suppl. 69:S197, 1997. [abstract] 

Neurexin 3 polymorphisms are associated with alcohol dependence and altered expression of specific isoforms. Hishimoto, A., Liu, Q, Drgon, T., Pletnikova, O., Walther, D., Zhu, X., Troncoso, J and Uhl, G. Hum. Mol. Genet. 16: 2880-2891, 2007. [paper] 

Neurogulins and erbB receptors in fetal human Schwann cells and DRGs. Lopez, T.J. and De Vries, G.H. Exp. Neurol., 1998. [abstract] 

Neuronal cell cultures from cryopreserved fetal tissue with neurogenetic disease. Schwartz, P., Petite, D., Privat, A., Petito, C., Calvet, M., and Stein, S. AAN Meeting, 1999. [abstract] 

Neurotransmitter receptor expression in the spindle cells: a class of neurons unique to humans and apes. Watson, K., Tetreault, N., Teegarden, S. and Allman, J. Society for Neuroscience, 2004. [abstract] 

New insights into inherited disorders of growth: molecular biology and biochemical investigations. Baumbach, L. Dept. of Biochemistry and Molecular Biology Seminar Series, 1995. [abstract] 

Notch-1 signalling is activated in brain arterivenous malformations in humans. ZhuGe, Q., Zhong, M., Zheng, W., Yang, G., Mao, X., Xie, L., Chen, G., Chen, Y., Lawton, M.T., Young, W.L., Greenberg, D.A. and Jin, K. Brain - A Journal of Neurology 132: 3231-3241. [paper] 

Novel neuronal proteolipid protein isoforms encoded by the human myelin proteolipid protein 1 gene. Sarret, C., Combes, P., Micheau, P., Gelot, A., Boespflug-Tanguy, O. and Vaurs-Barriere, C. Neuroscience 166: 522-538, 2010. [paper] 

Novel non-peptide ligands for human sensory neuron specific receptor 4 (MRGX1). Payza, K., Butterworth, J., Godbout, C., Gosselin, M., Fleurent M., Buon, C., Santhakumar, V., O'Donnell, D., Mennicken, F., and Tomaszewski, M. SFN, 2007. [abstract] 

NrCAM in addiction vulnerability: positional cloning, drug-regulation, haplotype-specific expression and altered drug reward in knockout mice. Ishiguro, H., Liu, Q., Gong, J., Hall, F., Ujike, H., Morales, M., Sakurai, T., Grumet, M. and Uhl, G. Neuropsychopharmacology 31(3):572-84, 2006. [paper] 

Nuclear localization of the MRN proteins in large neurons of the human brain. Ahn, J., Marietta, C. and Brooks, P.J. Meeting of the Environmantal Mutagen Society, 2003. [abstract] 

Nuclear localization of the apelin, bradykinin b2 and angiotensin at1 receptors. Lee, D.K., Lanca, A.J., Cheng, R., Nguyen, T., Ji, X.D., George, S.R. and O'Dowd, B.F. Society for Neuroscience, 2003. [abstract] 

Nuclear receptor expression in fetal and pediatric liver: correlation with CYP3A expression. Vyhlidal, C., Gaedigk, R. and Leeder, J. Drug Metab Disp 34: 131-137, 2006 [paper] 

Ocular motor anatomy in a case of interrupted saccades. Rucker, J., Leigh, R., Opitican, L., Keller, E., Buettner-Ennever, J. Prog. Brain Res. 171:563-566, 2008. [paper] 

Ocular motor anatomy in a case of interrupted saccades. Rucker, J., Leigh, R., Opitican, L., Keller, E., Buettner-Ennever, J. Presented 2007. [abstract] 

Ontogeny of pregnane X receptor in fetal and peditric liver. Vyhlidal, C., Gaedigk, R. and Leeder, J.S. Drug Metab Rev 35(Suppl 2): 145 (abstract 290), 2003. [abstract] 

Origin and turnover of ECM proteins from the inner limiting membrane and vitreous body. Halfter, W., Dong, S., Dong, A., Eller, A. and Nischt, R. Eye 1-7, 2008. [paper] 

PCR amplification and DNA sequence analysis of ancient DNA from 400 year old human skeletal specimens. Perera, E., Schiavi, A., Gonzales, R., Day, J., Moraes, C. and Baumbach, L. ASHG, 1995. [abstract] 

PCR amplification and cloning of human genomic and cDNA sequences similar to a P-type Ca2+ channel segment from SCLC cell lines. Hajela, R.K. and Atchison, W.D. Soc. for Neuroscience, 21:1574, 1995. [abstract] 

PET quantitation of nicotinic acetylcholine receptors in the human brain. Kimes, A., Chefer, S., Matochik, J., Pavlova, O., Contoreggi, C., Horti, A., Kurian, V., Vaupel, D., Koren, A., Ernst, M., London, E. and Mukhin, A. NeuroImage 22 Suppl. 2 (2204) T61-T200, 2004. [abstract] 

Parallel FoxP1 and FoxP2 expression in songbird and human brain predicts functional interaction. Teramitsu, I., Kudo, L.C., London, S.E., Geschwind, D.H. and White, S.A. J. Neuroscience 24: 3152-3163, 2004. [paper] 

Pathogen specificity and autoimmunity are distinct features of antigen-driven immune responses in neuroborreliosis. Kuenzle, S., Budingen, H., Meier, M., Harrer, M., Urich, E., Becher, B. and Goebels, N. Infection and Immunity 75: 3842-3847, 2007. [paper] 

Peripheral antigen-expressing Cells in Type 1 Diabetes. Prabakar, K. and Pugliese, A. Current Diabetes Reports, 4:101-107, 2004. [paper] 

Peripheral antigen-expressing cells and autoimmunity. Pugliese, A. Endocrinology and Metabolism Clinics in North America, 31:411-430, 2002. [paper] 

Pharmacogenetics of CYP#A7 variability in fetal liver. Leeder, J., Marcucci, K., Gaedigk, R., Gaedigk, A. and Pearce, R. Clin. Pharmacol. Ther. 75: P51, 2004. [abstract] 

Phylogenetic changes in the expression of delta opioid receptors in spinal cord and dorsal root ganglia. Mennicken, F., Zhang, J., Hoffert, C., Ahmad, S., Beaudet, A., and O'Donnell, D. J. Compar. Neurology 465: 349-360, 2003. [paper] 

Postnatal development of interlaminar astroglia in human cerebral cortex. Colombo, J.A., Jones, M., Puissant, V. and Reisin, H. Socity of Neuroscience, 2001. [abstract] 

Postnatal development of the human cortex. Webster, M. and Weickert, S. SFN, 2004. [abstract] 

Progenitor cells from human brain after death. Palmer, D., Schwartz, P., Taupin, P., Kaspar, B., Stein, S. and Gage, F. Nature, 411:42-43, 2001. [paper] 

Purification and functional analysis of primary fetal human Schwann cells. Lopez, T.J., Dauzvardis, M.F. and DeVries, G.H. SFN, 22: 1724, 1996. [abstract] 

Quantitative expression analysis of GLT1/EAAT2 glutamate transporter isoforms suggests a role for GLT1 in reward circuitry. Lauriat, T., Richler, E. and McInnes, L. SFN, 2005. [abstract] 

Quantitative expression profiling of EAAT2/GLT1 glutamate transporter splice variants supports a role for GLT1 in reward circuitry. Lauriat, T., Richler, E. and McInnes, L. Society of Biological Psychiatry, 2005. [abstract] 

Regional concentrations of (R) salsolinol, (S) salsolinol and their methyl derivatives in mammalian brain. Decuypere, M.G., Rakov, I., MIller, D.D. and Ledoux, M.S. SFN, 2007. [abstract] 

Regional differences in synaptogenesis in human cerebral cortex. Huttenlocher, P.R. and Dabholkar, A.S. J. Compar. Neurol. 387:167-178, 1997. [paper] 

Registries and data collection: NICHD Brain and Tissue Bank. Baumbach, L. AmerColl.Med.Gen., 3rd Joint Clin.Gen. and Ann.March of Dimes, TX. 1996. [abstract] 

Regulation of Complexin 1 and complexin 2 in the Developing Human Prefrontal Cortex. Salimi, K., Glantz, L., Hamer, R., German, T., Gilmore, J. and Jarskog, L. Synapse 62:273-282, 2008. [paper] 

Regulation of brain-derived neurotrophic factor (BNDF) and BNDF alternative splicing transcript 4 expression during development in human prefrontal cortex. Salimi, K., Vadlamudi, S., Gilmore, J., Jarskog, L. and Hamer, R. Presented 2007. [abstract] 

Respiratory syncytial virus (RSV) bronchiolitis is a result of unrestricted virus growth not immunologic hypersensitivity. Welliver R., Reed, J., Welliver, T., Hintz, K., Garogalo, R., Avendano, L., Velozo, L. Amer. Thoracic Society International Meeting, 2006. [abstract] 

Retroviral transformation of primary human fetal Schwann cells. Lopez, T.J. and De Vries, G.H. Soc. for Neuroscience, 1998. [abstract] 

SCN5A Allelic expression imbalance in African-American heterozygous for the common variant S1103Y. Killen S., Kunic, J., WAng, L., Lewis, A., Levy, B., Ackerman, M. and George, A. Congenit Heart Dis 4:398-420, 2009. [abstract] 

Selective vulnerability of preterm white matter of oxidative damage defined by F2-isoprostanes. Back, S., Luo, N., Mallinson, R., O'Malley, J., Wallen, L., Frei, B., Morrow, J, Petito, C., Roberts, C., Murdock, G. and Montine, T. Ann. Neurol. 58: 108-120, 2005. [paper] 

Self-antigen-presenting cells expressing diabetes-associated autoantigens exist in both thymus and peripheral lymphoid organs. Pugliese, A., Brown, D., Garza, D., Murchison, D., Zeller, M., Redondo, M, Diez, J., Eisenbarth, G., Patel, D. and Ricordi, C. J. Clin. Invest. 107: 555-564, 2001. [paper] 

Severe human Lower respiratory tract illness caused by respiratory syncytial virus and influenza virus is characterized by the absence of pulmonary cytotoxic lymphocyte responses. Welliver, T., Garafalo, R., Hosakote, Y., Hintz, K., Avendana, L., Sanchez, K., Velozo, L., Jafri, H., Chavez-Bueno, S., Ogra, P., McKinney, L., Reed, J. and Welliver, R. JID 195: 1126-1136, 2007. [paper] 

Sex-specific effects of scavenger receptor class B type 1 (SR-BI) gene variants on serum lipid levels and hepatic gene expression. Chiba-Falek, O., Nichols, M., Suchindran, S., Guyton, J., Ginsburg, G., Barrett-Connor, E. and McCarthy, J. BMC Med Gene 11:9, 2010. [paper] 

Simultaneous quantitation of CYP3A4 and 3A7 in human liver microsomes using dehydroepiandrosterone (DHEA). Zaya, M., Gu, C., White, M., Tandler, P., Hines, R. and Stevens, J. Drug Metab. Revs. 34 (Supplement 1): 108 (Abstr. 215), 2002. [abstract] 

Sodium valproate inhibits glucose transport and exacerbates Glut1-deficiency in vitro. Wong, H., Chu, T., Lai, J., Fung, K., Y., Fok, Fujii, T. and Ho, Y. J. Cellular Biochemistry 96:7775-785, 2005. [paper] 

Specific developmental reductions in subventricalar zone ErbB1 and ErbB4 mRNA in the human brain. Chong, V., Webster, M., Rothmond, D and Weickert, C. Int. J. Dev. Neurosci. 26:791-803, 2008 . [paper] 

Stem cells grown from postmortem human brain. Palmer, T., Schwartz, P., Taupin, P., Kaspar, B., Stein, S. and Gage, F. Nature, 1222, 1999. [abstract] 

Subunit composition and novel localization of K+ channels in spinal cord. Rasband, M.N. and Trimmer, J.S. J. Comp. Neurol. 429:166-176, 2001. [paper] 

Sulfonylurea recoptor 1 upregulation predisposes the premature infant brain to intraventricular hemorrhage. Castellani, R., ivanova, S., Bhatta, S., Gerzanich, V and Simard, J. SFN, 2007. [abstract] 

Synaptogenesis in human cerebral cortex. Huttenlocher, P.R. "Human Behavior and the Developing Brain," Ch 4, p.137, [paper] 

Synaptophysin and postsynaptic density protein 95 in the human prefrontal cortex from mid-gestation into early adulthood. Glantz, L., Gilmore, J., Hamer, R., Lieberman, J and Jarskog, L. Neuroscience 149: 582-591, 2007. [paper] 

Synaptophysin and postsynaptic density protein 95 in the human prefrontal cortex from mid-gestation into early adulthood. Glantz, L., Gilmore, J., Hamer, R., Lieberman, J. and Jarskog, L. Neuroscience 149: 582-591, 2007. [paper] 

Synchronized overproduction of AMPA, Kainate, and NMDA glutamate receptors during human spinal cord development. Kalb, R.G. and Fox, A.J. J. Compar. Neurol. 384:200-210, 1997. [paper] 

The MEL1a melatonin receptor gene is expressed in human suprachiasmatic nuclei. Weaver, D.R. and Reppert, S.M. NeuroReport 8:109-112, 1996. [paper] 

The effects of phenytoin and its metabolite 5-(4-hydroxyphenyl)-5-phenylydantoin on cellular glucose transport. Wong, H., Chu, T., Chan, Y., Fok, T., Fung, L., Fung, K. and Ho, Y. Life Sciences 76:1859-1872, 2005. [paper] 

The insulin gene in diabetes. Pugliese, A. and Miceli, D. Diabetes Metabolism Research and Reviews, 18:13-25, 2002. [paper] 

The insulin gene is transcribed in the human thymus and transcription levels correlated with allelic variation at the INS VNTR-IDDM2 susceptibility locus for type 1 diabetes. Pugliese, A., Zeller, M., Fernandez, A., Zalcberg, L., Bartlett, R., Ricordi, C., Pietropaolo, M. Eisenbarth, G., Bennett, S. and Patel, D. Nature Genet. 15: 293-297, 1997. [paper] 

The liver is an important organ in cholesterol homeostasis. Grear, K., Tucker, H., Zhu, H., Manning, A., Cupples, L. and Estus, S. Amer. Soc. Human Genetics, 2006. [abstract] 

The proteins synaptotagmin and syntaxin are not general targets of Lambert-Eaton Myasthenic syndrome autoantibody. Hajela, R.K. and Atchison, W.D. J. Neurochem. 64:1245-1251, 1995. [paper] 

The role of neonatal carnitine palmitoyl transferase deficiency type II on proloferation of neuronal progenitor cells and layering of the cerebral cortex in the developing brain. Chang, H., and Faust, P. Columbia Undergrad Science Journal, Spring 2007, vol 2, issue 1. [paper] 

The role of testisin in sperm biology: generation of testisin knockout mice. Netzel-Arnet, S., Bugge, T., Hess, R. and Antalis, T. 4th Gen Mtg of Intl Proteolysis Society, 2005. [abstract] 

The spindle neurons of frontoinsular cortex (Area FI) are unique to humans and African apres. Allman, J., Hakeem, A., Tetreault, N. and Semendeferi, K. Society for Neuroscience Meeting, 2003. [abstract] 

Tissue-specific reduction in splicing efficiency of IKBKAP due to the major mutation associated with familial dysautonomia. Cuajungco, M., Leyne, M., Mull, J., Gill, S., Lu, W., Zagzag, D., Axelrod, F., Maayan, C., Gusella, J. and Slaugenhaupt, S. Am. J. Hum. Genet., 72: 749-758, 2003. [paper] 

Towards a human model of branched chain amino acid (BCAA) metabolism. Suryawan, A., Bedsoe, R., Shimomura, Y. and Hutson, S. Experimental Biology 1996. [abstract] 

Towards the molecular dissection of the imprinted domains in human chromosome band 11p15.5 and mouse distal chromosome 7. Cooper, P.R., Reid, L.H., Crider-Miller, S.J., Pelletier, J., Pearsall, R.S., Zabel, B.U., Weissmann, B.E., Shows, T.B. and Higgins, M.J. Great Lakes Mammalian Development Meeting, Toronto, April 19, 1998. [abstract] 

Transcriptional suppression of the adrenal cortical peripheral-type benzodiazepine receptor gene and inhibition of steroid synthesis by ginkgolide B. Amri, H., Drieu, K. and Papadopoulos, V. Biochemical Pharmacology 65: 717-729, 2003. [paper] 

Traumatic brain injury increases  -Amyloid peptide 1-42 in cerbrospinal fluid. Raby, C., Morganti-Kossmann, M., Kossmann, T, Stahel, P., Watson, M., Evans, L., Mehta, P., Spiegel, K., Kuo, Y, Roher, A. and Emmerling, M. J. Neurochem. 71: 2505-2509, 1998. [paper] 

Tryptophan hydroxylase 2 (TPH2) haplotypes predict levels of TPH2 mRNA expression in human pons. Lim, J., Pinsonneault, J., Sadee, W. and Saffen, D. Molecular Psychiatry 1-11, 2006. [paper] 

Ultrastructural features of the developing and adult human striatum. Roberts, R.C., Strain-Saloum, C.E., Gaither, L.A., Perretti, F.J. and Vigorito, R.D. Soc. For Neuroscience Meeting, 20:785, 1994. [abstract] 

Unique ichthyosis/MR syndrome with seizures, severe developmental delay, failure to thrive, mild dysmorphology and eye findings. Benke, P., Lallouz, M., Franco, B., Hannanian, J., Munoz, M. and Lam, B. ASHG, Genetics in Medicine 1:52, 1999. [abstract] 

Use of mitochondrial D-loop polymorphisms to determine genetic relationships between ancient remains and a contemporary population over a four hundred year period. Perera, E., Schiavi, A., Day, J., Moraes, C., Wallace, D. and Baumbach, L. 46th Annual Amer. Society of Human Genetics Meeting, 1996. [abstract] 

Variability in expression of PXR and CAR in human fetal liver. Vyhlidal, C., Gaedigk, R. and Leeder, J. S. Conference on Pharmacogenomics, Hinxton, UK, Sept, 2003. [abstract] 

Variability of CYP2J2 expression in human fetal tissues. Gaedigk, A., Baker, D., Total, R., Gaedigk, R., Pearce, R., Vyhlidal, C., Zeldin, D. and Leeder, S. JPET 319: 523-532, 2006. [paper] 

Variability of CYP3A7 expression in human fetal liver. Leeder, J., Gaedigk, R., Marcucci, K., Gaedigk, A., Vyhlidal, C., Schindel, B. and Pearce, R. J. Pharmacol. Exp. Ther. 314: 626-635, 2005. [paper] 

Visualization of chemokine binding sites on human brain microvessels. Pachter, J.S. International Society of Neuroimmunology, 1998. [abstract] 

Visualization of chemokine binding sites on human brain microvessels. Andjelkovic, A., Spencer, D. and Pachter, J. J. Cell Biol. 145: 403-412, 1999. [paper] 

WNT genes define sharp boundaries in the developing human brain. Fu, L., Abu-Khalil, A., Grove, E.A., and Geschwind, D.H. Soc. for Neurosci. Abstracts 26(1): 116.3, 2000. [abstract] 

Why do adipocytes make the beta 3-adrenergic receptor? Granneman, J.G. Cellular Signaling 7:9-15, 1995. [paper] 

Wnt genes define distinct boundaries in the developing human brain: implications for human forebrain patterning. Abu-Khalil, Ful, L, Grove, E., Zecevic, N. and Geschwind, D. J. Comparative Neurology 474: 276-288, 2004. [paper] 

X chromosome gene expression in human tissues: male and female comparisons. Talebizadeh, Z., Simon, S and Butler, M. Genomics 88: 675-681, 2006. [paper] 

X-linked gene expression in fibroblasts and brain tissue from patients with supernumerary X chromosomes. Heling, T., Jie., C., Zhang, L and Wang, T. Human Genetics Meeting, 2007. [abstract] 

cDNA cloning, chromosomal localization, and expression analysis of human BEHAB/brevicam, a brain specific proteoglycan regulated during cortical development and in glioma. Gary, S.C., Zerillo, C.A., Chiang, V.L., Gaw, J.U., Gray, G., and Hockfield, S. Gene 256:139-147, 2000. [paper]