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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. |
| Waber D, Chiverton A, Pomeroy SL, Kieran M, Rivkin M, Deficits of everyday cogitive function in adolescents and adults treated for craniopharyngioma in children , Manuscript , 2006, submitted, pubmed |
Waber DP, De Moor C, Forbes PW, Almli CR, Botteron KN, Leonard G, Milovan D, Paus T, Rumsey J, The NIH MRI study of normal brain development: performance of a population based sample of healthy children aged 6 to 18 years on a neuropsychological battery, J Int Neuropsychol Soc , 2007, 13(5), 729-46 pubmed |
Waber DP, Turek J, Catania L, Stevenson K, Robaey P, Romero I, Adams H, Alyman C, Jandet-Brunet C, Neuberg DS, Sallan SE, Silverman LB, Neuropsychological outcomes from a randomized trial of triple intrathecal chemotherapy compared with 18 Gy cranial radiation as CNS treatment in acute lymphoblastic leukemia: findings from Dana-Farber Cancer Institute ALL Consortium Protocol 95-01, J Clin Oncol , 2007, 25(31), 4914-21 pubmed |
Waber, D. P.;Strand, K. E., Otitis media: Consistency is the hobgoblin, J. Pediatr. Psych. , 2000, 25, 19-21 pubmed |
Waber, D. P.;Tarbell, N. J., Toxicity of CNS prophylaxis for childhood leukemia, Oncology , 1997, 11, 259-64 |
Waber, D. P.;Wolff, P. H.;Forbes, P. W.;Weiler, M. D., Rapid automatized naming in children referred for evaluation of heterogeneous learning problems: how specific are naming speed deficits to reading disability?, Neuropsychol Dev Cogn Sect C Child Neuropsychol , 2000, 6, 251-261 pubmed |
Waber, D.; Wolff, P.; Weiler, M.; Bellinger, D.; Marcus, D.; Forbes, P., and Wypij, D., Processing of rapid auditory stimuli in school-age children referred for evaluation of learning disorders, Child Development , 2001, 72, 37-49 pubmed |
Waber, D.P., Aberrations in timing in children with impaired reading: Cause, effect or correlate?, Dyslexia, Fluency and the Brain , 2001, , |
Waber, D.P., More good news about neuropsychological late effects in long-term survivors of acute lymphoblastic leukemia, J Pediatr Hem Oncol , 2002, , pubmed |
Waber, D.P.; Carpentieri, S.C.; Klar, N.; Silverman, L.B.; Schwenn, M.; Hurwitz, C.A.; Mullenix, P.J.; Tarbell, N.J.; Sallan, S.E., Cognitive sequelae in children treated for acute lymphoblastic leukemia with dexamethasone or prednisone, J. Pediatr. Hematol. Oncol. , 2000, 22, 206-213 pubmed |
Waber, D.P.; Mullenix, P.J., Neuropsychological sequelae in childhood acute lymphoblastic leukemia (ALL), Pediatric Neuropsychology: Research, Theory and Practice , 1999, , |
Waber, D.P.; Shapiro, B.L.; Carpentieri, S.C.; Gelber, R.D.; Zou, G.; Dufresne, A.; Romero, I.; Tarbell, N.J.; Silverman, L.B.; Sallan, S.E., Excellent therapeutic efficacy and minimal late neurotoxicity in children treated with 18 grays of cranial radiation therapy for high-risk acute lymphoblastic leukemia: a 7-year follow-up study of the Dana-Farber Cancer Institute Consortium Protocol 87-01, Cancer , 2001, 92, 15-22 pubmed |
Waber, D.P.; Weiler, M.D.; Bellinger, D.C.; Marcus, D.J.; Forbes, P.W.; Wypij, D.; Wolff, P.H., Diminished motor timing control in children referred for diagnosis of learning problems, Dev. Neuropscyhol. , 2000, 17, 181-197 pubmed |
Wagner, J.;Akerud, P.;Castro, D.;Holm, P. C.;Snyder, E. Y.;Arenas, E., Type 1 astrocytes induce a midbrain dopaminergic phenotype in Nurr1-overexpressing neural stem cells, Nature Biotech. , 1999, 17, 653-659 |
Waisbren, S. E., Developmental and neuropsychological outcome in children born to mothers with phenylketonuria, MRDD Res. Rev , 1999, 5, 125-131 |
Waisbren, S. E., Phenylketonuria, Handbook of Neurodevelopmental and Genetic Disorders in Children , 1999, , 433-458 |
Waisbren, S. E.;Chang, P.;Levy, H. L.;Shifrin, H.;Allred, E.;Azen, C.;de la Cruz, F.;Hanley, W.;Koch, R.;Matalon, R.;Rouse, B., Neonatal neurological assessment of offspring in maternal phenylketonuria, J Inher Metabol Dis , 1998, 21, 39-48 |
Waisbren, S. E.;Hanley, W.;Levy, H. L.;Shifrin, H.;Allred, E.;Azen, C.;Chang, P. N.;Schmidt, S. C.;de la Cruz, F.;Hall, R.;Matalon, R.;Nanson, J.;Rouse, B.;Trefz, F.;Koch, R., Outcome at age 4 years in offspring of women with maternal phenylketonuria. The maternal PKU collaborative study, JAMA , 2000, 283, 756-762 pubmed |
Waisbren, S. E.;Read, C. Y.;Ampola, M. G.;Brewster, T. G.;Demmer, L. A.;Greenstein, R. M. G.;Ingham, C. L.;Korson, M. S.;Msall, M.;Pueschel, S. M.;Seashore, M. R.;Shih, V. E.;Levy, H. L., Newborn screening compared to clinical identification of biochemical genetic disorders, J Inherit Metab Dis , 2002, 25, 599-600 pubmed |
Waisbren, S. E.;Rokni, H.;Bailey, I.;Rohr, F.;Brown, T.;Warner-Rogers, J., Social factors and the meaning of food in adherence to medical diets: results of a maternal PKU summer camp, J. Inher Metab Dis , 1997, 20, 21-27 |
Waisbren, S.E., Noel, K., Fahbrach, K., Cella, C., Frame, D., Dorenbaum, A., Levy, H., Phenylalanine blood levels and clinical outcomes in phenylketonuria: A systematic literature review and meta-analysis, Molecular Genetics & Metabolism , 2007, , PrePub |
Waisel, D. B.;Fackler, J. C.;Brunner, J. X.;Kohane, I., PEFIOS: an expert closed-loop oxygenation algorithm, Medinfo , 1995, 8 Pt 2, 1132-6 pubmed |
Wallgren-Pettersson, C.;Pelin, K.;Hilpela, P.;Donner, K.;Porfirio, B.;Grazinao, C.;Swoboda, K. J.;Fardeau, M.;Urtizberea, J. a;Muntoni, F.;Sewry, C.;Dubowitz, V.;Iannaccone, S.;Minetti, C.;Pedemonte, M.;Seri, M.;Cusano, R.;Lammens, M.;Castagno-Sloane, A.;Beggs, A. H.;Laing, N. G.;de la Chapelle, A., Clinical and genetic heterogeneity in autosomal recessive nemaline myopathy, Neuromusc. Dis. , 1999, 9, 564-572 |
Walsh, C., Early events in the development of the cerebral cortex, Epilepsy: A Comprehensive Textbook , 1998, , |
Walsh, C. A., Neural development: identical twins separated at birth?, Curr Biol , 1996, 6, 26-8 |
Walsh, C. A., LISsen Up!, Nature Genetics , 1998, 19, 307-308 |
Walsh, C. A., Lineage analysis in the central nervous system, Encyclopedia of Neuroscience , 1998, , |
Walsh, C. A., Genetic malformations of the human cerebral cortex, Neuron , 1999, 23(1), 19-29 |
Walsh, C. A., Genetic Disorders of Human Cerebral Cortical Development, Adv Clin Neurosci , 2002, 12, 515-527 |
Walsh, C. A., Reelin mutations and Lissencephaly with cerebellar hypoplasia, The Metabolic Basis of Developmental Disorders , 2003, , in press |
Walsh, C. A.;Bowler, W. B.;Bilbe, G.;Fraser, W. D.;Gallagher, J. A., Effects of PTH on PTHrP gene expression in human osteoblasts: up-regulation with the kinetics of an immediate early gene, Biochem Biophys Res Commun , 1997, 239, 155-9 |
Walsh, C. A.;Goffinet, A. M., Potential mechanisms of mutations that affect neuronal migration in man and mouse, Curr Opin Genet Dev , 2000, 10, 270-4 pubmed |
Wang G, J.R. Brown, Kanner C, Jackson-Grusby L, Fetal overgrowth caused by global loss of imprinting is rescued by Igf2R reactivation, , , Submitted, |
Wang H, Li J, Follett PL, Zhang Y, Cotanche DA, Jensen FE, Volpe JJ, Rosenberg PA., 12-Lipoxygenase plays a key role in cell death caused by glutathione depletion and arachidonic acid in rat oligodendrocytes., Eur J Neurosci. , 2004 , 20(8), 2049-58 pubmed |
Wang J, Zhai Q, Chen Y, Lin E, Gu W, McBurney MW, He Z, A local mechanism mediates NAD-dependent protection of axon degeneration, Journal of Cell Biology , 2005, , pubmed |
Wang L, Pearlman E, Vujanic G, Zuppan C, Brundler M-A, Cheung J, Clicchio M, Dubois S, Cendron M, Wenger G, Barr F, Collins T, Perez-Atayde A, Kozakewich H, Desmoplastic small round cell tumor of the kidney in childhood, Am J Surg Path , in press, , |
Wang Q, Chen S, Chen Q, Wan X, Shen J, Hoeltge GA, Timur AA, Keating MT, Kirsch GE., The common SCN5A mutation R1193Q causes LQTS-type electrophysiological alterations of the cardiac sodium channel., J Med Genet , 2004 , 41(5), e66 pubmed |
Wang, C.;Jensen, F. E., Age dependence of NMDA receptor involvement in epileptiform activity in rat hippocampal slices, Epilepsy Research , 1996, 23(2), 105-13 |
Wang, C.;Sholas, M. G.;Berde, C. B.;DiCanzio, J.;Zurakowski, D.;Wilder, R. T., Evidence that spinal segmental nitric oxide mediates tachyphylaxis to peripheral local anesthetic nerve block, Acta Anaesthesiol Scand , 2001, 45, 945-53 pubmed |
Wang, G. J.;Chung, H. J.;Schneur, J.;Pratt, K.;Zable, A. C.;Kavanaugh, M. P.;Rosenberg, P. A., High affinity glutamate transport in rat cortical neurons in culture, Molec. Pharmacol. , 1998, 53, 88-96 |
Wang, G. J.;Chung, H. J.;Schnuer, J.;Lea, E.;Robinson, M. B.;Potthoff, W. K.;Aizenman, E.;Rosenberg, P. A., Dihydrokainate-sensitive neuronal glutamate transport is required for protection of rat cortical neurons in culture against synaptically released glutamate, Eur J Neurosci , 1998, 10(8), 2523-31 |
Wang, H.;Clapham, D. E., Conformational changes of the in situ nuclear pore complex, Biophys. J. , 1999, 77, 241-247 |
Wang, H.;Toida, T.;Kim, Y. S.;Capila, I.;Hileman, R. E.;Bernfield, M.;Linhardt, R. J., Glycosaminoglycans can influence fibroblast growth factor-2 mitogenicity without significant growth factor binding, Biochem Biophys Res Commun , 1997, 235, 369-73 |
Wang, K. C.;Kim, J. A.;Sivasankaran, R.;Segal, R. A.;He, Z., p75 interacts with the Nogo receptor as a co-receptor for Nogo, MAG and 0Mgp, Nature , 2002, 420, 74-78 pubmed |
Wang, K. C.;Koprivica, V.;Kim, J. A.;Sivasankaran, R.;Guo, Y.;Neve, R. L.;He, Z., Oligodendrocyte-myelin glycoprotein is a Nogo receptor ligand that inhibits neurite outgrowth, Nature , 2002, 417, 941-944 pubmed |
Wang, K.;Kohane, I.;Bradshaw, K. L.;Fackler, J., A real time patient monitoring system on the World Wide Web, Proc AMIA Annu Fall Symp , 1996, , 729-32 pubmed |
Wang, K.;van Wingerde, F. J.;Bradshaw, K.;Szolovits, P.;Kohane, I., A Java-based multi-institutional medical information retrieval system, Proc AMIA Annu Fall Symp , 1997, , 538-42 pubmed |
Wang, S. M.;Zwaan, J.;Mullaney, P. B.;Jabak, M. H.;Al-Awad, A.;Beggs, A. H.;Engle, E. C., Congenital fibrosis of the extraocular muscles type 2 (CFEOM2), an inherited exotropic strabismum fixus, maps to distal 11q13, Am. J. Hum. Genet , 1998, 63, 517-525 |
Wang, T. F.;Rosenberg, P. A.;Guidotti, G., Characterization of brain ecto-apyrase: evidence for only one ecto-apyrase (CD39) gene, Brain Research , 1997, 47(1-2), 295-302 |
Wang, W. L.;Healy, M. E.;Sattler, M.;Verma, S.;Lin, J.;Maulik, G.;Stiles, C. D.;Griffin, J. D.;Johnson, B. E.;Salgia, R., Growth inhibition and modulation of kinase pathways of small cell lung cancer cell lines by the novel tyrosine kinase inhibitor STI 571, Oncogene , 2000, 19, 352-358 pubmed |
Wang, X.;Chun, S. J.;Treloar, H.;Vartanian, T.;Greer, C. A.;Strittmatter, S. M., Localization of Nogo-A and Nogo-66 receptor proteins at sites of axon-myelin and synaptic contact, J Neurosci , 2002, 22, 550-5-5515 pubmed |
Wang, X.;Zhang, G.;Yang, T.;Zhang, W.;Geller, A. I., A 51 kb HSV-1 plasmid vector can be packaged using a helper virus-free system and supports expression in the rat brain, Biotechniques , 2000, 27, 102-106 pubmed |
Wang, Y.;Sheen, V. L.;Macklis, J. D., Cortical interneurons upregulate neurotrophins in vivo in response to targeted apoptotic degeneration of neighboring pyramidal neurons, Exp Neurol , 1998, 154, 389-402 |
Wang, Y.;Yu, L.;Geller, A. I., Diverse stabilities of expression in the rat brain from different cellular promoters in a helper virus-free HSV-1 vector system, Hum. Gene Ther. , 1999, 10, 1763-1771 |
Wang, Z.;Symons, J. M.;Goldstein, S. L.;McDonald, A.;Miner, J. H.;Kreidberg, J. A., (Alpha)3(beta)1 integrin regulates epithelial cytoskeletal organization, J Cell Sci , 1999, 112 (Pt 17), 2925-35 pubmed |
Warburton, D.;Zhao, J.;Berberich, M. A.;Bernfield, M., Molecular embryology of the lung: then, now, and in the future, Am. J. Physiol. , 1999, 276, L697-704 |
Ware, M. L.;Fox, J. W.;Gonzalez, J. L.;Davis, N. M.;Lambert de Rouvroit, C.;Russo, C. J.;Chua, S. C., Jr.;Goffinet, A. M.;Walsh, C. A., Aberrant splicing of a mouse disabled homolog, mdab1, in the scrambler mouse, Neuron , 1997, 19, 239-49 |
Ware, M. L.;Travasoie, S.;Reid, C. B.;Walsh, C. A., Coexistence of widespread clones and large radial clonal patterns in early ferret cortex, Cerebral Cortex , 1999, 9, 636-645 |
Ware, M. L.;Walsh, C. A., Cell lineage and cell migration in the developing cerebral cortex, Cell Fate and Cell Fate Determination , 1999, , 529-547 |
Warfield SK, Zou KH, Wells WM, Validation of image segmentation by estimating rater bias and variance, Philos Transact A Math Phys Eng Sci , 2008, , pubmed |
Warfield, S. K.;Guimond, A.;Roche, A.;Bharatha, A.;Tei, A.;Talos, F.;Rexilius, J.;Ruiz-Alzola, J.;Westin, C. F.;Haker, S.;Angenent, S.;Tannenbaum, A.;Jolesz, F. A.;Kikinis, R., Advanced nonrigid registration algorithms for image fusion, Brain Mapping: The Methods , 2002, , 661-690 |
Warfield, S. K.;Talos, F.;Tei, A.;Bharatha, A.;Nabavi, A.;Ferrant, M.;Black, P. M.;Jolesz, F. A.;Kikinis, R., Real-time registration of volumetric brain MRI by biomechanical simulation of deformation during image guided neurosurgery, Comput Visual Sc. , 2002, 5, 11-Mar |
Waters, N. S.;Sherman, G. F.;Galaburda, A. M.;Denenberg, V. H., Effects of cortical ectopias on spatial delayed-matching-to-sample performance in BXSB mice, Behav Brain Res , 1997, 84, 23-29 |
Watson F, Puttmann-Holgado R, Thomas F, Lamar D, Hughes M, Kondo M, Rebel V, Schmucker D, Extensive diversity of Ig-superfamily proteins in the immune system of insects, Science , 2005, 309, 1874-8 pubmed |
Watson, F. L.;Heerssen, H. M.;Moheban, D. B.;Lin, M. Z.;Sauvageot, C. M.;Bhattacharyya, A.;Pomeroy, S. L.;Segal, R. A., Rapid nuclear responses to target-derived neurotrophins require retrograde transport of ligand-receptor complex, J Neurosci , 1999, 19, 7889-900 |
Watson, F. L.;Porcionatto, M. A.;Bhattacharyya, A.;Stiles, C. D.;Segal, R. A., TrkA glycosylation regulates receptor localization and activity, J Neurobiol , 1999, 39, 323-36 |
Wattanasirichaigoon, D.;Beggs, A. H., Molecular genetics of long-QT syndrome, Curr. Opin. Pediatr. , 1998, 10, 628-634 |
Wattanasirichaigoon, D.;Swoboda, K. J.;Takada, F.;Tong, H. Q.;Lip, V.;Iannaccone, S. T.;Wallgren-Pettersson, C.;Laing, N. G.;Beggs, A. H., Mutations of the slow muscle alpha-tropomyosin gene, TPM3, are a rare cause of nemaline myopathy, Neurology , 2002, 59, 613-7 pubmed |
Wattanasirichaigoon, D.;Vesely, M. R.;Duggal, P.;Levine, J. C.;Blume, E. D.;Wolff, G. S.;Edwards, S. B.;Beggs, A. H., Sodium channel abnormalities are infrequent in patients with long QT syndrome: Identification of two novel SCN5A mutations, Am. J. Med. Genet. , 1999, 86, 470-476 |
Webb S, Long J, Nelson C, A longitudinal investigation of visual event-related potentials in the first year of life, Developmental Science , 2005, 8, 605-16 pubmed |
Wei Q, Yokota C, Semenov M, Doble B, Woodgett J, He X, R-spondin1 is a high affinity ligand for LRP6 and activates LRP6 phopshorylation and Wnt/beta-catenin signaling, J Biol Chem , 2007, In press, pubmed |
Wei, X.;Henke, V.;Strubing, C.;Clapham, D. E., Real time imaging of nuclear permeation by EGFP in single intact cells, Biophys J , 2003, 84, 1317-1327 pubmed |
Wei, Y.;Eble, J. A.;Wang, Z.;Kreidberg, J. A.;Chapman, H. A., Urokinase receptors promote b1 integrin function through interaction with integrin a3b1, Molec Biol Cell , 2001, 12, 2957-2986 pubmed |
Weiler, M. D.;Bellinger, D. K.;Simmons, E. K.;Rappaport, L. K.;Urion, D. K.;Mitchell, W. J.;Bassett, N. J.;Burke, P. J.;Marmor, J.;Waber, D., Reliability and validity of a DSM-IV based ADHD screener, Child Neuropsychol. , 2000, 6, 3-23 pubmed |
Weiler, M. D.;Bellinger, D.;Marmor, J.;Rancier, S.;Waber, D., Parent and teacher reports of ADHD symptoms: DSM-IV Questionnaire data, J Am Acad Child Adolesc Psychiatr , 1999, 38, 1139-47 |
Weiler, M. D.;Bernstein, J. H.;Bellinger, D. C.;Waber, D. P., Processing speed in children with attention deficit/hyperactivity disorder, inattentive type, Child Neuropsychol. , 2000, 6, 218-34 pubmed |
Weiler, M.D.; Bernstein, J.H.; Bellinger, D.; Kosslyn, S. and Waber, D., Speed of information processing in children referred for learning problems as measured by a visual filtering test, Journal of Learning Dis. , 2000, 33, 538-550 |
Weiler, M.D.; Bernstein, J.H.; Bellinger, D.C.; Waber, D.P., Information processing deficits in children with Attention Deficit/Hyperactivity Disorder, Inattentive Subtype and reading disability, Journal of Learning Dis. , 2002, 35, 448-461 |
Weinberg, M. K.;Tronick, E. Z., Infant affective reactions to the resumption of maternal interaction after the still-face, Child Dev. , 1996, 67, 905-914 |
Weinberg, M. K.;Tronick, E. Z., Maternal depression and infant maladjustment: A failure of mutual regulation, The Handbook of Child and Adolescent Psychiatry , 1997, , |
Weinberg, M. K.;Tronick, E. Z., The impact of maternal psychiatric illness on infant development, J. Clin Psychiatr , 1998, , 53-61 |
Weinberg, M. K.;Tronick, E. Z., Emotional characteristics of infants associated with maternal depression and anxiety, Pediatrics , 1998, 102, 1298-304 pubmed |
Weinberg, M. K.;Tronick, E. Z.;Beeghly, M.;Olson, K. L.;Kernan, H.;Riley, J. M., Subsyndromal depressive symptoms and major depression in postpartum women, Am J Orthopsychiatry , 2001, 71, 87-97 pubmed |
Weinberg, M. K.;Tronick, E. Z.;Cohn, J. F.;Olson, K. L., Gender differences in emotional expressivity and self-regulation during early infancy, Dev Psychol , 1999, 35, 175-88 pubmed |
Weinberg, M. K.;Tronick, E. Z.;Olson, K.;Beeghly, M., Mother-infant self and mutual regulation during face-to-face play at 3 months. The effects of interactive context, infant gender, and maternal depressive symptom statues, Developmental Psychology , 2003, , in press |
Weiner, H. L.;Guttmann, C. R.;Khoury, S. J.;Orav, E. J.;Hohol, M. J.;Kikinis, R.;Jolesz, F. A., Serial magnetic resonance imaging in multiple sclerosis: correlation with attacks, disability, and disease stage [In Process Citation], J Neuroimmunol , 2000, 104, 164-73 pubmed |
Weisberg, E.;Winnier, G. E.;Chen, X.;Farnsworth, C. L.;Hogan, B. L. H.;Whitman, M., A mouse homologue of FAST-1 transduces TGF beta superfamily signals and is expressed during early embryogenesis, Mech. Dev. , 1998, 79, 17-27 |
Weiss B, Bellinger DC, Social ecology of children's vulnerability to environmental pollutants, Environmental Health Perspectives , 2006, 114, 1479-85 pubmed |
Weith, A.;Brodeur, G. M.;Bruns, G. A.;Matise, T. C.;Nischke, D.;Nizetic, D.;Seldin, M. P.;van Roy, M.;Vance, J., Report of the second international workshop on human chromosome 1 mapping 1995, Cytogen Cell Gen. , 1996, 72, 113-154 |
Wen P, Yung W, Lamborn K, Dahia P, Wang Y, Peng B, Abrey L, Raizer J, Cloughesy T, Fink K, Gilbert M, Chang S, Junck L, Schiff D, Lieberman F, Fine H, Mehta M, Robins H, DeAngelis L, Groves M, Puduvalli V, Levin V, Conrad C, Maher E, Aldape K, Hayes M, Letvak L, Egorin M, Capdeville R, Kaplan R, Murgo A, Stiles C, Prados M, Phase I/II study of imatinib mesylate for recurrent malignant gliomas: North American Brain Tumor Consortium Study, Clin Cancer , 2006, 12, 4899-907 pubmed |
Weninger, S. C.;Dunn, A. J.;Muglia, L. J.;Dikkes, P.;Miczek, K. A.;Swiergiel, A. H.;Berridge, C. W.;Majzoub, J. A., Stress-induced behaviors require the corticotropin-releasing hormone (CRH) receptor, but not CRH, Proc. Natl. Acad. Sci. USA , 1999, 96, 8283-8 |
Weninger, S. C.;Muglia, L. J.;Jacobson, L.;Majzoub, J. A., CRH-deficient mice have a normal anoretic response to chronic stress, Regulatory Peptides , 1999, 84, 69-74 |
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Weninger, S. C.;Yankner, B. A., Inflammation and Alkzheimer\'s disease: The good, the bad, and the ugly, Nature Med , 2001, 7, 527-528 pubmed |
Wernovsky, G.; Stiles, K. M.; Gauvreau, K.; Gentles, T. L.; duPlessis, A. J.; Bellinger, D. C.; Walsh, A. Z.; Burnett, J.; Jonas, R. A.; Mayer, J. E., Jr.; Newburger, J. W., Cognitive development after the Fontan operation, Circulation , 2000, 102, 883-9 pubmed |
Wernovsky, G.;Newburger, J. W., Neurologic sequelae of cardiac surgery, Pediatric and Adult Congenital Cardiac Self-Assessment Program , 1997, 6, 203-209 |
Wernovsky, G.;Newburger, J. W., Neurologic and developmental morbidity in children with complex congenital heart disease, J Pediatr , 2003, 142, 8-Jun pubmed |
Westenskow P, Splawski I, Timothy KW, Keating MT, Sanguinetti MC., Compound mutations: a common cause of severe long-QT syndrome, Circulation , 2004 , 109(15), 1834-41 pubmed |
Westin, C. F.;Maier, S. E.;Mamata, H.;Nabavi, A.;Jolesz, F. A.;Kikinis, R., Processing and visualization for diffusion tensor MRI, Med Image Anal , 2002, 6, 93-108 |
Westin, C. F.;Wigstrom, L.;Loock, t;Sjoqvist, L.;Kikinis, R;Knutsson, H., Three-dimensional adaptive filtering in magnetic resonance angiography, J Magn Reson Imaging , 2001, 14, 63-71 pubmed |
Weuve, J.; Kelsey, K.T.; Schwartz, J.; Bellinger, D.; Wright, R.O.; Rajan, P.; Spiro, A.; Sparrow, D.; Aro, A., Delta-aminolevulinic acid dehydratase polymorphism and the relation between low level lead exposure and the Mini-Mental Status Examination in older men: The normative aging study, Occupational and Enviromental Medicine , 2006, 63, 746-753 |
Wey J, Gray M, Belcheva A, NcCarty M, Stoeltzing O, Somico R, Liu W, Evans D, Klagsbrun M, Gallick G, Ellis L, Overexpression of neuropilin-1 promotes constitutive MAPK signaling and chemoresistence in pancreatic cancer cells, British Journal Cancer , 2005, 93, 233-41 pubmed |
White, R. A.;Hughes, R. T.;Adkison, L. R.;Bruns, G.;Zon, L. I., The gene encoding protein kinase SEK1 maps to mouse chromosome 11 and human chromosome 17, Genomics , 1996, 34, 430-2 |
White, T. W.;Sellitto, C.;Paul, D. L.;Goodenough, D. A., Connexin43 and connexin50 are not required for prenatal lens development, Invest Ophthalmol Vis Sci , 2001, 42, 2916-2923 |
White, T.W.; Sellitto, C.; Paul, D.L.; Goodenough, D.A., Connexin diversity in the lens is required for postnatal growth and homeostatis but is not necessary for prenatal development, Invest Ophthalmol Vis Sci , 2001, 42, 2916-2923 |
Whittemore, S. R.;Snyder, E. Y., Physiological relevance and functional potential of central nervous system-derived cell lines, Molec Neurobiol , 1996, 12, 13-38 |
Wible, C. G.;Anderson, J.;Shenton, M. E.;Kricun, A.;Hirayasu, Y.;Tanaka, S.;Levitt, J. J.;O\'Donnell, B. F.;Kikinis, R.;Jolesz, F. A.;McCarley, R. W., Prefrontal cortex, negative symptoms, and schizophrenia: an MRI study, Psychiatry Res , 2001, 108, 65-78 |
Wible, C. G.;Kubicki, M.;Yoo, S. S.;Kacher, D. F.;Salisbury, D. F.;Anderson, M. C.;Shenton, M. E.;Hirayasu, Y.;Kikinis, R.;Jolesz, F. A.;McCarley, R. W., A functional magnetic resonance imaging study of auditory mismatch in schizophrenia, Am J Psychiatry , 2001, 158, 938-943 pubmed |
Wible, C. G.;Shenton, M. E.;Fischer, I. A.;Allard, J. E.;Kikinis, R.;Jolesz, F. A.;Iosifescu, D. V.;McCarley, R. W., Parcellation of the human prefrontal cortex using MRI, Psychiatry Res , 1997, 76, 29-40 |
Wickman K, Karschin C, Karschin A, Picciotto MR, Clapham DE., Brain localization and behavioral impact of the G-protein-gated K+ channel subunit GIRK4., Journal of Neuroscience , 2000, 20, 5608-5615 pubmed |
Wickman, K.;Nemec, J.;Gendler, S.;Clapham, D. E., Abnormal heart rate regulation in GIRK4 knockout mice, Neuron , 1998, 20, 103-114 |
Wickman, K.;Pu, W. T.;Clapham, D. E., Structural characterization of the mouse Girk genes, Gene , 2002, 284(1-2), 241-250 pubmed |
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