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.

Gagnon ML, Bielenberg DR, Gechtman Z, Miao HQ, Takashima S, Soker S, Klagsbrun M., Identification of a natural soluble neuropilin-1 that binds vascular endothelial growth factor: In vivo expression and antitumor activity., Proc Natl Acad Sci U S A , 2000 , 97(6), 2573-8 pubmed

Galaburda, A., More evidence for a neurophysiologic basis for dyslexia, Journal Watch Neurology , 2000, 2, 3

Galaburda, A. M., Toxicity of plasticity. Lesson from a model of developmental learning disorder, Normal and Abnormal Development of Cortex , 1997, , 135-144

Galaburda, A. M.;Bellugi, U., V. Multi-level analysis of cortical neuroanatomy in Williams syndrome, J Cogn Neurosci , 2000, 12 Suppl 1, 74-88 pubmed

Galaburda, A. M.;Cestnick, L., [Developmental dyslexia], Rev Neurol , 2003, 36 Suppl 1, S3-9 pubmed

Galaburda, A. M.;Holinger, D. P.;Bellugi, U.;Sherman, G. F., Williams syndrome: neuronal size and neuronal-packing density in primary visual cortex, Arch Neurol , 2002, 59, 1461-7 pubmed

Galaburda, A. M.;Holinger, D.;Mills, D.;Reiss, A.;Korenberg, J. R.;Bellugi, U., Williams syndrome. A summary of cognitive, electrophysiological, anatomofunctional, microanatomical and genetic findings, Rev Neurol , 2003, 36 Suppl 1, S132-7 pubmed

Galaburda, A. M.;Rosen, G. D., Dyslexia, Encyclopedia of Neuroscience , 1999, , 585-586

Galaburda, A. M.;Schmitt, J. E.;Atlas, S. W.;Eliez, S.;Bellugi, U.;Reiss, A. L., Dorsal forebrain anomaly in Williams syndrome, Arch Neurol , 2001, 58, 1865-9 pubmed

Galaburda, A. M.;Schrott, L. S.;Sherman, G. F.;Rosen, G. D.;Denenberg, V. H., Animal models of developmental dyslexia, Developmental Dyslexia: Neural, Cognitive, and Genetic Mechanisms , 1996, , 14-Jan

Galaburda, A., Duchaine, B., Developmental Disorders of Vision, Neurologic Clinics of North America , 2001, , 687-707

Galaburda, A., Holinger, D., Bellugi, U., Sherman, G., Neuronal size and Neuronal Packing Density in Primar Visual Cortex, Achives of Neurology , 2002, 59, 1461-7

Galaburda, A., Rosen, G.D., Denenberg, V.H., Fitch, R.H., LoTurco, J.J., Sherman, G.F., Models of temporal processing and language development, Clin Neurosci Res , 2001, ,

Gallo, R. L.;Dorschner, R. A.;Takashima, S.;Klagsbrun, M.;Eriksson, E.;Bernfield, M., Endothelial cell surface alkaline phosphatase activity is induced by IL-6 released during wound repair, J. Invest. Dermatol. , 1997, 109, 597-603

Gallo, R. L.;Kainulainen, V.;Bernfield, M., Syndecan biology in wound repair, Scarless Wound Healing , 1999, ,

Gallo, R. L.;Kim, K. J.;Bernfield, M.;Kozak, C. A.;Zanetti, M.;Merluzzi, L.;Gennaro, R., Identification of CRAMP, a cathelin-related antimicrobial peptide expressed in the embryonic and adult mouse, J. Biol. Chem. , 1997, 272, 13088-93

Gallo, R.;Kim, K.;Kokenyesi, R.;Adzick, N. S.;Bernfield, M., Syndecans-1 and -4 are induced during wound repair of neonatal but not fetal skin, J. Invest. Dermatol , 1996, 107, 676-683

Gao, Y.;Sun, Y.;Frank, K. M.;Dikkes, P.;Fujiwara, Y.;Seidl, K. J.;Sekiguchi, J. M.;Rathbun, G. A.;Swat, W.;Wang, J.;Bronson, R. T.;Malynn, B. A.;Bryans, M.;Zhu, C.;Chaudhuri, J.;Davidson, L.;Ferrini, R.;Stamato, T.;Orkin, S. H.;Greenberg, M. E.;Alt, F. W., A critical role for DNA end-joining proteins in both lymphogenesis and neurogenesis, Cell , 1998, 95, 891-902

Gardner, H.;Kreidberg, J.;Koteliansky, V.;Jaenisch, R., Deletion of integrin alpha 1 by homologous recombination permits normal murine development but gives rise to a specific deficit in cell adhesion, Dev Biol , 1996, 175, 301-13 pubmed

Gariboldi, M.;Peissel, B.;Fabbri, A.;Saran, A.;Zaffroni, D.;Falvella, P. S.;Spinola, M.;Tanuma, J.;Pazzaglia, S.;Mancusco, M. T.;Maurichi, A.;Bartoli, C.;Cataltepe, S.;Silverman, G. A.;Pilotti, S.;Hayashizaki, Y.;Okazaki, Y.;Dragani, T. A., SCCA2-like serpins mediate genetic predisposition to skin tumors, Cancer Res , 2003, 63, 1871-1875

Gates, M. A.;Fricker-Gates, R. A.;Macklis, J. D., Reconstruction of cortical circuitry (comprehensive review), Functional Neural Transplantation , 2000, , pubmed

Gates, M. A.;Fricker-Gates, R. A.;Macklis, J. D., Reconstruction of cortical circuitry, Prog Bran Res , 2000, 127, 115-156 pubmed

Gates, M. A.;Fricker-Gates, R. A.;Magavi, S. S.;Macklis, J. D., Cellular repair of complex cortical circuitry, The Neuroscientist , 2000, 6, 326-337

Gates, M. A.;Tai, C. C. S.;Macklis, J. D., Neocortical neurons lacking the TrkB receptor display abnormal differentiation and process elongation in vitro and in vivo, Neuroscience , 2000, 98, 437-447 pubmed

Gazda HT, Grabowska A, Merida-Long L, Latawiec E, Schneider H, Lipton J, Vlachos A, Atsidaftos E, Ball SO, KA, Niewiadomska E, Da Costa L, Tchernia G, Niemeyer C, Meerpohl J, Stahl J, Schratt GM, Glader B, Backer K, Wong C, Nathan D, Beggs AH, Sieff CA, Ribosomal protein S24 is mutated in Diamond-Blackfan anemia, Am J Hum Genet , 2006, 79:, 1110-8 pubmed

Gazda, H.;Lipton, J. M.;Willig, T. N.;Ball, S.;Niemeyer, C. M.;Tchernia, G.;Mohandas, N.;Daly, M. J.;Ploszynska, A.;Orfali, K. A.;Vlachos, A.;Glader, B. E.;Rokicka-Milewska, R.;Ohara, A.;Baker, D.;Pospisilova, D.;Weber, A.;Viskochil, D. H.;Nathan, D. G.;Beggs, A. H.;Sieff, C. A., Evidence for linkage of familial Diamond-Blackfan anemia to chromosome 8p23.3-p22 and for non-19q non-8p disease, Blood , 2001, 97, 2145-2150 pubmed

Gazda, H.T.; Kho, A.T.; Sanoudou, D.; Zaucha, J.M.; Kohane, I.S.; Sieff, C.A.; Beggs, A.H., Defective ribosomal protein gene expression alters transcription, translation, apoptosis, and oncogenic pathways in Diamond-Blackfan anemia, Stem Cells , 2006, 24, 2034-2044 pubmed

Ge W, He F, Kim KJ, Blanchi B, Coskun V, Nguyen L, Wu X, Zhao J, Heng JI, Martinowich K, Tao J, Wu H, Castro D, Sobeih MM, Corfas G, Gleeson JG, Greenberg ME, Guillemot G, Sun YE, Coupling of cell migration with neurogenesis by proneural bHLH factors, Proc Natl Acad Sci U S A , 2006, 5, 1319-24 pubmed

Geller, A. I.;Yu, L.;Wang, Y.;Fraefel, C., Virus-free HSV-1 plasmid vectors for gene therapy of Parkinson's disease and other neurological disorders, Exper. Neurol. , 1997, 144, 98-102

Gelman, R., Martinez-Perez, M.E., Vanderveen, D., Moskowitz, A., Fulton, A., Diagnosis of plus disease in retinopathy of prematurity using retinal image multiscale analysis, Invest Ophthalmol Vis Sci , 2005, 46, 4724-8

Gemmel, A.; Tavares, M.; Alperin, S.; Soncini, J.; Daniel, D.; Dunn, J.; Crawford, S.; Braveman, N.; Clarkson, T.; McKinley, S.; Bellinger, D., Blood lead level and dental caries in school- aged children, Environmental Health Perspectives , 2002, 110, A265-A630

Gentles, T. L.;Gauvreau, K.;Mayer, J. E., Jr.;Fishberger, S. B.;Burnett, J.;Colan, S. C.;Newburger, J. W.;Wernovsky, G., Functional outcome after the Fontan operation: factors influencing late morbidity, J. Thorac Cardiovasc Surg , 1997, 114, 392-403

Gentles, T. L.;Mayer, J. E., Jr.;Gauvreau, K.;Newburger, J. W.;Lock, J. E.;Kupferschmid, J. P.;Burnett, J.;Jonas, Ra;Castaneda, A. R.;Wernovsky, G., Fontan operation in 500 consecutive patients: factors influencing early and late outcome, J Thorac Cardiovasc Surg , 1997, 114, 376-391

Geretti E, Shimizu A, Klagsbrun M, Neuropilin structure governs VEGF and semaphorin binding and regulates angiogenesis, Angiogenesis , 2008, 11(1), 31-9 pubmed

Geretti, E., Shimizu, A., Kurschat, P., Klagsbrun, M., Site-directed mutagenesis in the B-neuropilin-2 domain selectively enhances its affinity to VEGF165, but not to SEMA3F, Journal of Biological Chemistry , 2007, PrePub,

Gering, D. T.;Nabavi, A.;Kikinis, R.;Hata, N.;O\'Donnell, L. J.;Grimson, W. E.;Jolesz, F. A.;Black, P. M.;Wells, W. M., 3rd, An integrated visualization system for surgical planning and guidance using image fusion and an open MR, J Magn Reson Imaging , 2001, 13, 967-975 pubmed

Gerstner B, DeSilva TM, Genz K, Armstrong A, Brehmer F, Neve RL, Felderhoff-Mueser U, Volpe JJ, Rosenberg PA, Hyperoxia causes maturation-dependent cell death in the developing white matter, J Neurosci , 2008, 28(5), 1236-45 pubmed

Gerstner B, Sifringer M, Dzietko M, Schuller A, Lee J, Simons S, Obladen M, Volpe JJ, Rosenberg PA, Felderhoff-Mueser U, Estradiol attenuates hyperoxia-induced cell death in the developing white matter, Ann Neurol , 2007, 61(6), 562-73 pubmed

Geula, C.;Wu, C. K.;Saroff, D.;Lorenzo, A.;Yuan, M.;Yankner, B. A., Aging renders the brain vulnerable to amyloid b-protein neurotoxicity, Nature Med. , 1998, 4, 827-831

Ghaffari S, Kitidis C, Zhao W, Marinkovic D, Fleming M, Luo B, Marszalek J, Lodish H, AKT induces erythroid cell maturation of JAK2-deficient fetal liver progenitor cells and is required for epo regulation of erythroid cell differentiation, Blood , 2006, 107(5), 1888-91 pubmed

Ghavami, M.;Levy, H. L.;Erbe, R. W., Prevention of fetal damage through dietary control of maternal hyperphenylalaninemia, Clin Obstet Gynecol , 1986, 29, 580-5 pubmed

Ghose AaVV, D, Regulating Receptor PTP Activity, Handbook of Cell Signalling, Second Edition , 2008, ,

Gilles, F. H.;Leviton, A.;Golden, J. A.;Paneth, N.;Rudelli, R. D., Groups of histopathologic abnormalities in brains of very low birthweight infants, J Neuropathol Exper Neurol , 1998, 57, 1026-1034

Gilles, F. H.;Leviton, A.;Tavare, C. J.;Adelman, L.;Rorke, L. B.;Sobel, E. L.;Hedley-Whyte, E. T.;Davis, R. L. for the Childhood Brain Tumor Consortium, Definitive classes of childhood supratentorial neuroglial tumors, Pediatr. Dev. Pathol. , 2000, 3, 126-139 pubmed

Gilles, F. H.;Leviton, A.;Tavare, J. C.;Adelman, L.;Rorke, L. B.;Sobel, E. L.;Hedley-Whyte, E. T.;Davis, R. L., Clinical and survival covariates of eight classes of childhood supratentorial neuroglial tumors, Cancer , 2002, 95, 1302-1310 pubmed

Gilles, F. H.;Sobel, E. L.;Leviton, A.;Tavare, C. J., Clusters of histologic characteristics in children with infratentorial neuroglial tumors. The Childhood Brain Tumor Consortium, J. Neuro-Oncol , 1998, 39, 51-63

Gilles, F. H.;Sobel, E. L.;Leviton, A.;Tavare, C. J.;Hedley-Whyte, E. T.;Rorke, L.;Adelman, L.;Sobel, R., Quantitative histologic factors for grouping childhood infratentorial neuroglial tumors, Pediatr Pathol Lab Med , 1997, 17, 729-754

Gilmore, D. S.;Schalock, R. L.;Kiernan, W. E.;Butterworth, J., National comparisons and critical findings in integrated employment, Integrated Employment: Current Status and Future Directors , 1997, , 49-66

Glatt, K.;Glatt, H.;Lalande, M., Structure and organization of GABRB3 and GABRA5, Genomics , 1997, 41, 63-9

Gleeson, J. G.;Allen, K. M.;Fox, J. W.;Lamperti, E. D.;Berkovic, S.;Scheffer, I.;Cooper, E. C.;Dobyns, W. B.;Minnerath, S. R.;Ross, M. E.;Walsh, C. A., Doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein, Cell , 1998, 92, 63-72

Gleeson, J. G.;du Plessis, A. J.;Barnes, P. D.;Riviello, J. J., Cyclosporin A acute encephalopathy and seizure syndrome in childhood: clinical features and risk of seizure recurrence, J. Child Neurol. , 1998, 13, 336-344

Gleeson, J. G.;Lin, P. T.;Flanagan, L. A.;Walsh, C. A., Doublecortin is a microtubule-associated protein and is expressed widely by migrating neurons, Neuron , 1999, 23, 257-271

Gleeson, J. G.;Luo, R. F.;Grant, P. E.;Guerrini, R.;Huttenlocher, P. R.;Berg, M. J.;Ricci, S.;Cusmai, R.;Wheless, J. W.;Berkovic, S.;Scheffer, I.;Dobyns, W. B.;Walsh, C. A., Genetic and neuroradiological heterogeneity of double cortex syndrome, Ann Neurol , 2000, 47, 265-9 pubmed

Gleeson, J. G.;Minnerath, S. R.;Fox, J. W.;Allen, K. M.;Luo, R. F.;Hong, S. E.;Berg, M. J.;Kuzniecky, R.;Reitnauer, P. J.;Borgatti, R.;Mira, A. P.;Guerrini, R.;Holmes, G. L.;Rooney, C. M.;Berkovic, S.;Scheffer, I.;Cooper, E. C.;Ricci, S.;Cusmai, R.;Crawford, T. O.;Leory, R.;Andermann, E.;Wheless, J. W.;Dobyns, W. B.;Ross, M. E.;Walsh, C. A., Characterization of mutations in the gene doublecortin in patients with double cortex syndrome, Ann. Neurol. , 1999, 45, 146-153

Gleeson, J. G.;Minnerath, S.;Kuzniecky, R. I.;Dobyns, W. B.;Young, I. D.;Ross, M. E.;Walsh, C. A., Somatic and germline mosaic mutations in the doublecortin gene are associated with variable phenotypes, Am J Hum Genet , 2000, 67, 574-81 pubmed

Gleeson, J. G.;Walsh, C. A., New genetic insights into cerebral cortical development, Normal and Abnormal Development of the Cerebral Cortex , 1997, , 145-163

Gleeson, J. G.;Walsh, C. A., Neuronal migration disorders: from genetic diseases to developmental mechanisms, Trends Neurosci , 2000, 23, 352-9 pubmed

Gloy, J.;Hikasa, H.;Sokol, S. Y., Frodo interacts with dishevelled to transduce Wnt signals, Nat Cell Biol , 2002, 9, 9

Goddard C, Butts D, Shatz C, Regulation of CNS synapses by neuronal MHC Class I, PNAS , 2006, , Manuscript in press pubmed

Goh K.L., Cai L., Cepko C.L., Gertler F.B., Ena/VASP proteins regulate cortical neuronal positioning., Curr. Biol. , 2002, 12, 565-9 pubmed

Goishi K, Klagsbrun M., Vascular endothelial growth factor and its receptors in embryonic zebrafish blood vessel development., Curr Top Dev Biol. , 2004, 62, 127-52 pubmed

Goishi K, Lee P, Davidson AJ, Nishi E, Zon LI, Klagsbrun M., Inhibition of zebrafish epidermal growth factor receptor activity results in cardiovascular defects., Mech Dev. , 2003 , 120(7), 811-22 pubmed

Goishi K, Shimizu A, Najarro G, Watanabe S, Rogers R, Zon L, Klagsbrun M, αA-crystallin expression prevents γ-crystallin insolubility and cataract formation in the zebrafish cloche mutant lens, Development , 2006, 133, 2585-93 pubmed

Golden, J. A.;Gilles, F. H.;Rudelli, R.;Leviton, A., Frequency of neuropathological abnormalities in very low birth weight infants, J Neuropathol Exper Neurol , 1997, 56, 472-478

Goldfield E, Newborn Behavior, Encyclopedia of Infant and Early Childhood Development , 2008, , 438-449

Goldfield, E. C., Commentary: Towards a developmental ecological psychology, Monograph Soc. Res. Child Dev. , 1997, , 221-231

Goldfield, E. C., Prosody during disyllable production of full term and preterm infants, Ecological Psychol. , 1999, 11, 81-102

Goldfield, E. C.;Schmidt, R. C.;Fitzpatrick, P., Coordination dynamics of abdomen and chest during infant breathing: A comparison of full term and preterm infants at 38 weeks postconceptional age, Ecol. Psychol. , 1999, 11, 209-232

Goldfield, E. C.;Wolff, P. H., Attractor dynamics in early infant sucking and respiration, Infant Behav. Dev. , 1996, 19, 94

Goldfield, E. C.;Wolff, P. H., Motor development in Infancy, Introduction to Infant Development , 2001, , 77-97

Goldfield, E. C.;Wolff, P. H.;Schmidt, R. C., Dynamics of oral-respiratory coordination in full term and preterm infants: I. Comparisons at 38 to 40 weeks postconceptional age, Dev. Sci. , 1999, 2(3), 248-258

Goldfield, E. C.;Wolff, P. H.;Schmidt, R. C., Dynamics of oral-respiratory coordination in full term and preterm infants: II. Continuing effects at 3 months post term, Dev. Sci. , 1999, 2, 259-68

Goldfield, E.C., A dynamical systems approach to infant oral feeding and dysphagia: From model system to theraputic medical device, , 2005, ,

Goldfield, E.C., Goodkin, H., Bellinger, D., Jonas, R., Roth, S.J., Rappaport, L., Wypij, D., Bartlett, J., McGrath, E., Newburger, J., Oral-respiratory coordination of infants following surgery to correct congenital heart defects, Dev Med Child Neurology , 2004, ,

Goldfield, E.C.; Richardosn, M.J.; Saltzman, E.; Margetts, S.; Lee, K.G., Effect of swallowing on oxygen saturation and on coordination of sucking and breathing during infant breastfeeding and bottle feeding, , 2005, , (submitted)

Goldfield, E.C.; Richardson, M.J.; Lee, K.G.; Margetts, S., Coordination of sucking, swallowing, and breathing and oxygen saturation during early infant breast-feeding and bottle-feeding, Pediatric Research , 2006, 60, 450-455

Gomaa, A.;Hu, H.;Bellinger, D.;Schwartz, J.;Tsaih, S. W.;Gonzalez-Cossio, T.;Schnaas, L.;Peterson, K.;Aro, A.;Hernandez-Avila, M., Maternal bone lead as an independent risk factor for fetal neurotoxicity: a prospective study, Pediatrics , 2002, 110, 110-118 pubmed

Gomez-Isla, T.;Growdon, W. B.;McNamara, M. J.;Nochlin, D.;Bird, T. D.;Arango, J. C.;Lopera, F.;Kosik, K. S.;Lantos, P. L.;Cairns, N. J.;Hyman, B. T., The impact of different presenilin 1 andpresenilin 2 mutations on amyloid deposition, neurofibrillary changes and neuronal loss in the familial Alzheimer's disease brain: evidence for other phenotype-modifying factors, Brain , 1999, 122, 1709-19

Gonzalez, J. L.;Russo, C. J.;Goldowitz, D.;Sweet, H. O.;Davisson, M. T.;Walsh, C. A., Birthdate and cell marker analysis of scrambler: a novel mutation affecting cortical development with a reeler-like phenotype, J. Neurosci , 1997, 17(23), 9204-11

Gonzalez-Heydrich, J., Alice, D.A., Jame, W., MacMillan, C., Deborah, W., Stephen, V.F., Boyer, K., Christine, M., David, D., Psychiatric disorders and behavioral characterisitics of pediatric patients with both epilepsy and attention-deficit hyperactivity disorder, Epilepsy & Behavior , 2007, 10, 384-388

Gonzalez-Heydrich, J., Alice, D.A., Jame, W., MacMillan, C., Deborah, W., Stephen, V.F., Boyer, K., Christine, M., David, D., Psychiatric disorders and behavioral characterisitics of pediatric patients with both epilepsy and attention-deficit hyperactivity disorder, Epilepsy & Behavior , 2007, 10, 384-388

Gonzalez-Heydrich, J.;DeMaso, D. R.;Irwin, C.;Steingard, R. J.;Kohane, I. S.;Beardslee, W. R., Implementation of an electronic medical record system in a pediatric psychopharmacology program, Int J Med Inf , 2000, 57, 109-16 pubmed

Gonzalez-Heydrich, J.;Steingard, R. J.;Kohane, I., A computer simulation of the hypothalamic-pituitary-adrenal axis, Proc Annu Symp Comput Appl Med Care , 1994, , 1010 pubmed

Gonzalez-Heydrich, J.;Steingard, R. J.;Putnam, F. W.;De Bellis, M. D.;Beardslee, W.;Kohane, I. S., Corticotropin releasing hormone increases apparent potency of adrenocorticotropic hormone stimulation of cortisol secretion, Med Hypotheses , 2001, 57, 544-8 pubmed

Gonzalez-Heydrich, J.;Steingard, R. J.;Putnam, F.;Beardslee, W.;Kohane, I. S., Using \"off the shelf\", computer programs to mine additional insights from published data: diurnal variation in potency of ACTH stimulation of cortisol secretion revealed, Compt Meth Programs Biomed , 1999, 58, 227-238 pubmed

Gonzalez-Navarro H, Vila-Caballer M, Pastor MF, Vinue A, White MF, Burks D, Andres V, Plasma insulin levels predict the development of atherosclerosis when IRS2 deficiency is combined with severe hypercholesterolemia in apolipoprotein E-null mice, Front Biosci , 2007, 12, 2291-8 pubmed

Goodearl, A.;Viehover, A.;Vartanian, T., Neuregulin-induced association of Sos Ras exchange protein with HER2(erbB2)/HER3(erbB3) receptor complexes in Schwann cells through a specific Grb2-HER2(erbB2) interaction, Dev Neurosci , 2001, 23, 25-30 pubmed

Goodman, L. J.;Valverde, J.;Lim, F.;Geswind, M. D.;Federoff, H. J.;Geller, A. I.;Hefti, F., Regulated release and polarized localization of brain-derived neurotrophic factor (BDNF) in hippocampal neurons, Molec. Cell Neurosci. , 1996, 7, 222-238

Goodrich L, Hear, hear for the zebrafish, Neuron , 2005, 45, 3-5 pubmed

Gordon CM, Emans SJ, DuRant RH, Mantzoros C, Grace E, Harper GP, Majzoub JA., Endocrinologic and psychological effects of short-term dexamethasone in anorexia nervosa., Eat Weight Disord. , 2000 , 5(3), 175-82 pubmed

Gordon, C. M.;Dougherty, D. D.;Fischman, A. J.;Emans, S. J.;Grace, E.;Lamm, R.;Alpert, N. M.;Majzoub, J. A.;Rauch, S. L., Neural substrates of anorexia nervosa: a behavioral challenge study with positron emission tomography, J Pediatr , 2001, 139, 51-7 pubmed

Gordon, C. M.;Rowitch, D. H.;Mitchell, M. L.;Kohane, I. S., Topical iodine and neonatal hypothyroidism, Arch Pediatr Adolesc Med , 1995, 149, 1336-9 pubmed

Gordon, Cm;Majzoub, J. A.;Marsh, D. J.;Mulliken, J. B.;Ponder, B. A.;Robinson, B. G.;Eng, C., Four cases of mucosal neuroma syndrome: multiple endocrine neoplasm 2B or not 2B?, J Clin Endocrinol Metabol , 1998, 83, 17-20

Gordon, M. S.;Majzoub, J. A.;Williams, G. H.;Gordon, M. B., Sodium balance modulates thirst in normal man, Endocrine Res , 1997, 23, 377-92

Gorska-Andrzejak, J.;Stowers, R. S.;Borycz, J.;Kostyleva, R.;Schwarz, T. L.;Meinertzhagen, I. A., Mitochondria are redistributed in Drosophila photoreceptors lacking Milton, a kinesin-associated protein, J Comp Neurol , 2003, 463(4), 372-388 pubmed

Gorson K, Adelman L, Pierson C, Beggs AH, Sporadic, adult-onset nemaline myopathy presenting as camptocormia (bent spine syndrome), J Clin Neuromus Dis , 2006, 8, 7-11

Gottlob, I.;Jain, S.;Engle, E. C., Elevation of one eye during tooth brushing, Am J Ophthalmol , 2002, 134, 459-60 pubmed

Goulder, P. J. R.;Brander, C.;Tang, Y.;Tremblay, C.;Colbert, R. A.;Addo, M. M.;Rosenberg, E. S.;Nguyen, T.;Allen, R.;Trocha, A.;Altfeld, M.;He, S.;Bunce, M.;Funkhauser, R.;Pelton, S. I.;Burchett, S. K.;McIntosh, K.;Korber, B. T. M.;Walker, B. D., Evolution and transmission of stable CTL escape mutations in HIV infection, Nature , 2001, 412, 334-348

Goyer, R.; Aposhian, V.; Arab, L.; Bellinger, D.; Burbacher, T.; Burke, T; Jacobson, J.; Knobeloch, L.; Stern, A. and Ryan, L., Toxicological Effects of Methylmercury, , 2000, ,

Grafe, M.;Kinney, H. C., Neuropathology associated with stillbirth, Semin Perinatol , 2002, 26, 83-88

GrandPre, T.;Nakamura, F.;Vartanian, T.;Strittmatter, S. M., Identification of the Nogo inhibitor of axon regeneration as a Reticulon protein, Nature , 2000, 403(6768), 439-444

Grant FD, Gudmundsson K, Hosley CM, Trask LE, Kimberly WT, Luedke CE, Majzoub JA, Vasopressin both inhibits and activates the hypothalamic-pituitary-adrenal axis, submitted , , ,

Grant, F. D.;Ahmadi, A.;Hosley, C. M.;Majzoub, J. A., Two novel mutations of the vasopressin gene associated with familial diabetes insipidus and identification of an asymptomatic carrier infant, J Clin Endocrinol Metabol , 1998, 83(11), 3958-64

Gray PA, Fu H, Luo P, Zhao Q, Yu J, Ferrari A, Tenzen T, Yuk DI, Tsung EF, Cai Z, Alberta JA, Cheng LP, Liu Y, Stenman JM, Valerius MT, Billings N, Kim HA, Greenberg ME, McMahon AP, Rowitch DH, Stiles CD, Ma Q., Mouse brain organization revealed through direct genome-scale TF expression analysis., Science , 2004 , 306(5705), 2255-7 pubmed

Greenberg, M. E.;Bronson, S.;Lock, M.;Neumann, M.;Pavlakis, G. N.;Skowronski, J., Co-localization of HIV-1 Nef with the AP-2 adaptor protein complex correlates with Nef-induced CD4 down-regulation, EMBO J , 1997, 16, 6964-76

Greenberg, M. E.;Iafrate, A. J.;Skowronski, J., The SH3 domain-binding surface and an acidic motif in HIV-1 Nef regulate trafficking of class I MHC complexes, EMBO J , 1998, 17, 2777-89

Greenberg, M. E.;Mathews, M. B., Effects of heterologous downstream sequences on the activity of the HIV-1 promoter and its response to Tat, Nucleic Acids Res , 1997, 25, 5017-24

Greenberg, M. E.;Ostapenko, D. A.;Mathews, M. B., Potentiation of human immunodeficiency virus type 1 Tat by human cellular proteins, J Virol , 1997, 71, 7140-4

Greenberg, S. A.;Sanoudou, D.;Haslett, J. N.;Kohane, I. S.;Kunkel, L. M.;Beggs, A. H.;Amato, A. A., Molecular profiles of inflammatory myopathies, Neurology , 2002, 59, 1170-82 pubmed

Greene, S.;Pomeroy, S. L., Predicting medulloblastoma outcome, Cancer of the Nervous System , 2003, , in press

Greenes, D. S.;Fleisher, G. R.;Kohane, I., Potential impact of a computerized system to report late-arriving laboratory results in the emergency department, Pediatr Emerg Care , 2000, 16, 313-5 pubmed

Greger, V.;Knoll, J. H.;Wagstaff, J.;Woolf, E.;Lieske, P.;Glatt, H.;Benn, P. A.;Rosengren, S. S.;Lalande, M., Angelman syndrome associated with an inversion of chromosome 15q11.2q24.3, Am. J. Hum. Genet. , 1997, 60, 574-80

Greil, G. F.;Stuber, M.;Botnar, R. M.;Kissinger, K. V.;Geva, T.;Newburger, J. W.;Manning, W. J.;Powell, A. J., Coronary magnetic resonance angiography in adolescents and young adults with Kawasaki disease, Circulation , 2002, 105, 908-11 pubmed

Greka A, Navarro B, Oancea E, Duggan A, Clapham DE., TRPC5 is a regulator of hippocampal neurite length and growth cone morphology., Nature Neuroscience , 2003, 6, 837-845 pubmed

Grimson, W. E.;Kikinis, R.;Jolesz, F. A.;Black, P. M., Image-guided surgery, Sci Am , 1999, 280, 62-9

Gronemeyer, D. H.;Jolesz, F. A.;Lufkin, R.;Seibel, R., Image-guided access enhances microtherapy, Diagn Imaging (San Franc) , 1996, Suppl, IR2-5

Gross, F. E.;Koch, R.;Azen, C.;Levy, H.;Hanley, W.;Matalon, R.;Rouse, B.;Trefz, F.;de la Cruz, F., The international collaborative study on maternal phenylketonuria: organization, study design and description of the sample, Eur. J. Pediatr. , 1996, 155, 5158-5161

Growney, J. D.;Scharf, J. M.;Kunkel, L. M.;Dietrich, W. E., Evolutionary divergence of the mouse and human Lgn1/SMA repeat structures, Genomics , 2000, 64, 62-81 pubmed

Gruber, E. M.;Jonas, R. A.;Newburger, J. W.;Zurakowski, D.;Hansen, D. D.;Laussen, P. C., Effect of hematocrit on cerebral blood flow velocity in neonates and infants undergoing deep hypothermic cardiopulmonary bypass, Anesthesia & Analgesia , 1999, 89, 322-327

Gu, Y.;Sekiguchi, J.;Gao, Y.;Dikkes, P.;Frank, K.;Ferguson, D.;Hasty, P.;Chun, J.;Alt, F. W., Defective embryonic neurogenesis in Ku-deficient but not DNA-dependent protein kinase catalytic subunit-deficient mice., Proc Natl Acad Sci U S A , 2000, 97(6), 2668-73 pubmed

Gudbjartsson, H.;Maier, S. E.;Jolesz, F. A., Double line scan diffusion imaging, Magn Reson Med , 1997, 38, 101-9

Gudbjartsson, H.;Maier, S. E.;Mulkern, R. V.;Morocz, I. A.;Patz, S.;Jolesz, F. A., Line scan diffusion imaging, Magn Reson Med , 1996, 36, 509-19

Guldberg, P.;Henriksen, K. F.;Mammen, K. C.;Levy, H. L.;Guttler, F., Large deletions in the phenylalanine hydroxylase gene as a cause of phenylketonuria in India, J Inher Metab Dis , 1997, 20, 845-846

Guldberg, P.;Levy, H. L.;Hanley, W. B.;Koch, R.;Matalon, R.;Rouse, B. M.;Trefz, F.;de la Cruz, F.;Henriksen, F. R.;Guttler, F., Phenylalanine hydroxylase gene mutations in the United States. Report from the Maternal PKU Collaborative Study, Am. J. Hum. Genet. , 1996, 59, 84-94

Guo S, Dunn S, White M, The reciprocal stability of FOXO1 and IRS2 creates a regulatory circuit that controls insulin signaling, Mol Endocrinol , 2006, 20(12), 3389-99 pubmed

Guo W, Jung WE, Marionneau X, Aimond F, XU H, Yamada KA, Schwarz TL, Demolombe S, Nerbonne JM, Targeted deletion of Kv4.2 eliminates I (TO,F) and results in electrical and molecular remodeling, with no evidence of ventricular hypertrophy or myocardial dysfunction, Circ Res , 2005, 12, 1342-50

Gurgel-Giannetti, J.;Reed, U. C.;Zanoteli, E.;Fireman, M. a T.;Oliveira, A. S. B.;Beggs, A. H.;Werneck, L. C.;Marie, S. K.;Zatz, M.;Vainzof, M., Rod distribution and muscle fibers type modification in the progression of nemaline myopathy, J Child Neurol , 2003, , in press

Gurvits, T. V.;Shenton, M. E.;Hokama, H.;Ohta, H.;Lasko, N. B.;Gilbertson, M. W.;Orr, S. P.;Kikinis, R.;Jolesz, F. A.;McCarley, R. W.;Pitman, R. K., Magnetic resonance imaging study of hippocampal volume in chronic, combat-related posttraumatic stress disorder, Biol Psychiatry , 1996, 40, 1091-9

Gussoni, E.;Bennett, R. R.;Muskiewicz, K. R.;Meyerrose, T.;Nolta, J. A.;Gilgoff, I.;Stein, J.;Chan, Y. M.;Lidov, H. G.;Bonnemann, C. G.;Von Moers, A.;Morris, G. E.;Den Dunnen, J. T.;Chamberlain, J. S.;Kunkel, L. M.;Weinberg, K., Long-term persistence of donor nuclei in a Duchenne muscular dystrophy patient receiving bone marrow transplantation, J Clin Invest , 2002, 110, 807-814 pubmed

Gussoni, E.;Blau, H. M.;Kunkel, L. M., The fate of individual myoblasts after transplantation into muscles of DMD patients, Nature Medicine , 1997, 3, 970-7

Gussoni, E.;Soneoka, Y.;Strickland, C. D.;Buzney, E. A.;Khan, M. K.;Flint, A. F.;Kunkel, L. M.;Mulligan, R. C., Dystrophin expression in the mdx mouse restored by stem cell transplantation, Nature , 1999, 401, 390-4

Gussoni, E.;Wang, Y.;Fraefel, C.;Miller, R. G.;Blau, H. M.;Geller, A. I.;Kunkel, L. M., A method to codetect introduced genes and their products in gene therapy protocols, Nature Biotechnol , 1996, 14, 1012-6

Gutman GA, Chandy KG, Adelman JP, Aiyar J, Bayliss DA, Clapham DE, Covarriubias M, Desir GV, Furuichi K, Ganetzky B, Garcia ML, Grissmer S, Jan LY, Karschin A, Kim D, Kuperschmidt S, Kurachi Y, Lazdunski M, Lesage F, Lester HA, McKinnon D, Nichols CG, O\'Kelly I, Robbins J, Robertson GA, Rudy B, Sanguinetti M, Seino S, Stuehmer W, Tamkun MM, Vandenberg CA, Wei A, Wulff H, Wymore RS; International Union of Pharmacology., International Union of Pharmacology. XLI. Compendium of voltage-gated ion channels: potassium channels., Pharmacol Rev. , 2003 , 55(4), 583-6 pubmed

Gutowski NJ, Bosley TM, Engle EC., 110th ENMC International Workshop: the congenital cranial dysinnervation disorders (CCDDs). Naarden, The Netherlands, 25-27 October, 2002., Neuromuscul Disord. , 2003 , 13(7-8), 573-8 pubmed

Guttler, F.;Azen, C.;Guldberg, P.;Romstad, A.;Hanley, W. B.;Levy, H. L.;Matalon, R.;Rouse, B. M.;Trefz, F.;de la Cruz, F.;Koch, R., Relationship among genotype, biochemical phenotype, and cognitive performance in females with phenylalanine hydroxylase deficiency: report from the Maternal Phenylketonuria Collaborative Study, Pediatrics , 1999, 104, 258-62

Guttler, F.;Henriksen, K. F.;Guldberg, P.;Levy, H. L., Confirmatory diagnosis of neonatal phenylalanine hydroxylase deficiency by mutation analysis of Guthrie card DNA, Proceeding Third International Meeting ISNS , 1996, , 15-Dec

Guttmann, C. R.;Jolesz, F. A.;Kikinis, R.;Killiany, R. J.;Moss, M. B.;Sandor, T.;Albert, M. S., White matter changes with normal aging, Neurology , 1998, 50, 972-8

Guttmann, C. R.;Kikinis, R.;Anderson, M. C.;Jakab, M.;Warfield, S. K.;Killiany, R. J.;Weiner, H. L.;Jolesz, F. A., Quantitative follow-up of patients with multiple sclerosis using MRI: reproducibility, J Magn Reson Imaging , 1999, 9, 509-18

Guyon JR, Steffen LS, Howell MH, Pusack TJ, Lawrence C, Kunkel LM, Modeling human muscle disease in zebrafish, Biochim Biophys Acta , 2007, 1772(2), 205-15 pubmed