CENTER PUBLICATIONS

Publications prepared during the past four years since the onset of the current grant cycle in 1996 are listed next in alphabetical order. Publications are listed in the Progress Report for individual MRRC investigators (see Section B), according to the author's primary affiliation in one of the four MRRC programs, i.e., Genetics, Developmental Biology, Basic Neuroscience, and Clinical Neuroscience/Behavior.

Abe Y, Chen W, Huang W, Li Y-P, CNBP regulates forebrain formation at organogenesis stage in chick embryos, Dev Biol , 2006, 295(1), 116-27 pubmed

Aboody-Guterman, K.S.; Pechan, P.A.; Rainov, N.G.; Sena-Esteves, M.; Jacobs, A.; Snyder, E.Y.; Wild, P.; Schraner, E.; Tobler, K.; Breakefield, X. O.; Fraefel, C., Green fluorescent protein as a reporter for retrovirus and helper virus-free HSV-1 amplicon vector-mediated gene transfer into neural cells in culture and in vivo, 8 , 1997, 8, 3801-8 pubmed

Abraham, H. D.; Duffy, F. H., Stable quantitative EEG difference in post-LSD visual disorder by split-half analysis: evidence for disinhibition, Psychiatr. Res. , 1996, 67, 173-87

Abraira V, Hyun N, Tucker A, Coling D, Lu C, Hoffman G, Brown M, Goodrich L, Sef regulation of FGF signaling influences auditory brainstem development and function, J Neurosci , 2007, In Press, pubmed

Abraira VE, Hyun N, Tucker AF, Coling DE, Brown MC, Lu C, Hoffman GR, Goodrich LV, Changes in Sef levels influence auditory brainstem development and function, J Neurosci , 2007, 27(16), 4273-82 pubmed

Abu-Jawdeh, G.; Comella, N.; Tomita, Y.; Brown, L.F.; Tognazzi, K.; Sokol, S.Y.; Kocher, O., Differential expression of frpHE: a novel human stromal protein of the secreted frizzled gene family during the endometrial cycle and malignancy, Lab. Invest. , 1999, 79, 439-447

Abzhanov A, Rodda SJ, McMahon AP, Tabin CJ, Regulation of skeletogenic differentiation in cranial dermal bone, Development , 2007, 134(17), 3133-44 pubmed

Ackerman K, Wang J, Luo L, Fujiwara Y, Orkin S, Beier D, Gata4 is Necessary for Normal Pulmonary Lobar Development, Am J Respir Cell Mol Biol , 2007, 39, 391-7 pubmed

Ackerman, M.J.; Splawski, I.; Makielski, J.C.; Tester, D.J.; Will, M.L.; Timothy, K.W.; Keating, M.T.; Jones, G.; Chadha, M.; Burrow, C.R.; Stephens, J.C.; Xu, C.; Judson, R.; and Curran, M.E., Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic testing., Heart Rhythm. , 2004 , 1(5), 600-7 pubmed

Adam, R.M.; Eaton, S.H.; Estrada, C.; Nimgaonkar, A.; Shih, S.C.; Smith, L.E.; Kohane, I.S.; Bagli, D.; Freeman M.R., Mechanical stretch is a highly selective regulator of gene expression in human bladder smooth muscle cells., Physiol. Genomics , 2004 , 20(1), 36-44 pubmed

Affar eB, Gay F, Shi Y, Liu H, Huarte M, Wu S, Collins T, Li E, Shi Y, Essential dosage-dependent functions of the transcription factor yin yang 1 in the late embryonic development and cell cycle progression, Mol Cell Biol , 2006, 26, 3565-81

Afshari, M.; Afshari, N.; Fulton, A.B., Cortical visual impairment in infants and children, Int. Ophthalmol. Clin. , 2001, 41(1), 159-169 pubmed

Agarwal P, Greenleaf R, Tomczak K, Lehtokari V-L, Wallgren-Pettersson C, Wallefeld W, Laing N, Darras BT, Maciver S, Dormitzer P, Beggs A, Nemaline myopathy with minicores caused by mutation of the CFL2 gene encoding the skeletal muscle actin-binding protein, cofilin-2, Am J Hum Genet , 2007, 80, 162-7

Ahn, A.H.; Freener, C.A.; Gussoni, E.; Yoshida, M.; Ozawa, E.; Kunkel, L.M., The three human syntrophin genes are expressed in diverse tissues, have distinct chromosomal locations, and each bind to dystrophin and its relatives, J. Biol. Chem. , 1996, 271, 2724-30

Aiello, L.P.; Bursell, S.; Clermont, A.; Duh, E.; Ishii, H.; Takagi, C.; Mori, F.; Ciulla, T.A.; Ways, K.; Jirousek, M.; Smith, L.E.H.; King, G.L., Vascular endothelial growth factor-induced retinal permeability is mediated by protein kinase C in vivo and suppressed by an orally effective beta isoform-selective inhibitor, Diabetes , 1997, 46, 1473-1480

Aizenman, E.; Brimecombe, J.C.; Potthoff, W.K.; Rosenberg, P.A., Why is the role of nitric oxide in NMDA receptor function and dysfunction so controversial?, Prg. Brain Res. , 1998, 118, 53-71

Aksoy, I.A.; Ramsey, M.J.; Fruman, D.A.; Aksoy, S.; Cantley, L.C.; Tucker, J.D.; Roberts, T.M., Mouse phosphinositide 3-kinase p110a gene: Cloning structural organization and localization to chromosome 3 Band B, B.B.R.C. , 1999, 262 (2), 438-442

Al-Baradie, R.; Yamada, K.; St Hilaire, C.; Chan, W.M.; Andrews, C.; McIntosh, N.; Nakano, M.; Martonyi, E.J.; Raymond, W.R.; Okumura, S.; Okihiro, M.M.; Engle, E. C., Duane radial ray syndrome (Okihiro syndrome) maps to 20q13 and results from mutations in SALL4, a new member of the SAL family, Am. J. Hum. Genet. , 2002, 71, 1195-9 pubmed

Al-Khunaizi, M.; Luke, C.J.; Askew, Y.S.; Pak, S.C.O.; Askew, D.J.; Cataltepe, S.; Miller, D.; Bromme, D.; Silverman, G.A., The serpin SQN5 is a dual-class inhibitor of serine and cysteine proteinases, Biochemistry , 2002, 41, 3189-3199

Alayon S, Robertson R, Warfield SK, Ruiz-Alzola J, A fuzzy system for helping medical diagnosis of malformations of cortical development, J Biomed Inform , 2007, 40(3), 221-35 pubmed