Recurrent de novo point mutations in lamin A cause Hutchinson-Gilford progeria syndrome von Collins, Francis S, Eriksson, Maria, Brown, W. Ted, Gordon, Leslie B, Glynn, Michael W, Singer, Joel, Scott, Laura, Erdos, Michael R, Robbins, Christiane M, Moses, Tracy Y, Berglund, Peter, Dutra, Amalia, Pak, Evgenia, Durkin, Sandra, Csoka, Antonei B, Boehnke, Michael, Glover, Thomas W

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Impact of Farnesylation Inhibitors on Survival in Hutchinson-Gilford Progeria Syndrome von GORDON, Leslie B, MASSARO, Joe, D'AGOSTINO, Ralph B, CAMPBELL, Susan E, BRAZIER, Joan, BROWN, W. Ted, KLEINMAN, Monica E, KIERAN, Mark W

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Oxidative stress in autism: Increased lipid peroxidation and reduced serum levels of ceruloplasmin and transferrin - the antioxidant proteins von Chauhan, Abha, Chauhan, Ved, Brown, W. Ted, Cohen, Ira

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Fragile X Premutation Tremor/Ataxia Syndrome: Molecular, Clinical, and Neuroimaging Correlates von Jacquemont, Sébastien, Hagerman, Randi J., Leehey, Maureen, Grigsby, Jim, Zhang, Lin, Brunberg, James A., Greco, Claudia, Des Portes, Vincent, Jardini, Tristan, Levine, Richard, Berry-Kravis, Elizabeth, Brown, W. Ted, Schaeffer, Stephane, Kissel, John, Tassone, Flora, Hagerman, Paul J.

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Decreased GABA A receptor expression in the seizure-prone fragile X mouse von El Idrissi, Abdeslem, Ding, Xiao-Hua, Scalia, Jason, Trenkner, Ekkhart, Brown, W. Ted, Dobkin, Carl

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Fragile X Premutation Carriers: Characteristic MR Imaging Findings of Adult Male Patients with Progressive Cerebellar and Cognitive Dysfunction von Brunberg, James A, Jacquemont, Sebastien, Hagerman, Randi J, Berry-Kravis, Elizabeth M, Grigsby, Jim, Leehey, Maureen A, Tassone, Flora, Brown, W. Ted, Greco, Claudia M, Hagerman, Paul J

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Expansion of the Fragile X CGG Repeat in Females with Premutation or Intermediate Alleles von Nolin, Sarah L., Brown, W. Ted, Glicksman, Anne, Houck, Jr, George E., Gargano, Alice D., Sullivan, Amy, Biancalana, Valérie, Bröndum-Nielsen, Karen, Hjalgrim, Helle, Holinski-Feder, Elke, Kooy, Frank, Longshore, John, Macpherson, James, Mandel, Jean-Louis, Matthijs, Gert, Rousseau, Francois, Steinbach, Peter, Väisänen, Marja-Leena, von Koskull, Harriet, Sherman, Stephanie L.

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Autism severity is associated with child and maternal MAOA genotypes von Cohen, IL, Liu, X, Lewis, MES, Chudley, A, Forster-Gibson, C, Gonzalez, M, Jenkins, EC, Brown, WT, Holden, JJA

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Neuropsychiatric symptoms of fragile X syndrome: Pathophysiology and pharmacotherapy von TSIOURIS, John A, BROWN, W. Ted

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Genetic analysis of first-trimester miscarriages with a combination of cytogenetic karyotyping, microsatellite genotyping and arrayCGH von Zhang, Y-X, Zhang, Y-P, Gu, Y, Guan, F-J, Li, S-L, Xie, J-S, Shen, Y, Wu, B-L, Ju, W, Jenkins, EC, Brown, WT, Zhong, N

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Novel progerin-interactive partner proteins hnRNP E1, EGF, Mel 18, and UBC9 interact with lamin A/C von Zhong, Nanbert, Radu, Gabriel, Ju, Weina, Brown, W. Ted

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Fmr1 knockout mouse has a distinctive strain-specific learning impairment von Dobkin, Carl, Rabe, Ausma, Dumas, Ruth, El Idrissi, Abdeslem, Haubenstock, Harriet, Ted Brown, W

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Association of autism severity with a monoamine oxidase A functional polymorphism von Cohen, IL, Liu, X, Schutz, C, White, BN, Jenkins, EC, Brown, WT, Holden, JJA

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Psychological Theory and Educational Reform: How School Remakes Mind and Society von Brown, William T.

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Apolipoprotein E epsilon 4 allele distributions in late-onset Alzheimer's disease and in other amyloid-forming diseases von Saunders, A M, Schmader, K, Breitner, J C, Benson, M D, Brown, W T, Goldfarb, L, Goldgaber, D, Manwaring, M G, Szymanski, M H, McCown, N

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RNAs That Interact with the Fragile X Syndrome RNA Binding Protein FMRP von Sung, Ying Ju, Conti, James, Currie, Julia R., Brown, W.Ted, Denman, Robert B.

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Metabolism of the 2-oxoaldehyde methylglyoxal by aldose reductase and by glyoxalase-I: roles for glutathione in both enzymes and implications for diabetic complications von Vander Jagt, David L., Hassebrook, Robyn K., Hunsaker, Lucy A., Brown, William M., Royer, Robert E.

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Increased oxidative stress and decreased activities of Ca2+/Mg2+-ATPase and Na+/K+-ATPase in the red blood cells of the hibernating black bear von Chauhan, Ved P.S., Tsiouris, John A., Chauhan, Abha, Sheikh, Ashfaq M., Brown, W.Ted, Vaughan, Michael

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Fragile X gene instability: anchoring AGGs and linked microsatellites von Zhong, N, Yang, W, Dobkin, C, Brown, W T

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Alteration in amino-glycerophospholipids levels in the plasma of children with autism: A potential biochemical diagnostic marker von Chauhan, Ved, Chauhan, Abha, Cohen, Ira L, Brown, W.Ted, Sheikh, Ashfaq

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