Bibliotecas PUC-SP - Busca Integrada

SUT-2 potentiates tau-induced neurotoxicity in Caenorhabditis elegans

Por Guthrie, Chris R., Schellenberg, Gerard D., Kraemer, Brian C.
Publicado em 2009

Genome-wide association reveals genetic effects on human Aβ₄₂and τ protein levels in cerebrospinal fluids: a case control study

Por Schellenberg Gerard D, Han Mi-Ryung, Wang Li-San
Publicado no BMC Neurology (2010-10-01)

Autism risk assessment in siblings of affected children using sex-specific genetic scores

Por Carayol Jerome, Schellenberg Gerard D, Dombroski Beth, Genin Emmanuelle, Rousseau Francis, Dawson Geraldine
Publicado no Molecular Autism (2011-10-01)

Assessing the impact of a combined analysis of four common low-risk genetic variants on autism risk

Por Carayol Jerome, Schellenberg Gerard D, Tores Frederic, Hager Jörg, Ziegler Andreas, Dawson Geraldine
Publicado no Molecular Autism (2010-02-01)

parkin mutation dosage and the phenomenon of anticipation: a molecular genetic study of familial parkinsonism

Por Poorkaj, Parvoneh, Moses, Lina, Montimurro, Jennifer S, Nutt, John G, Schellenberg, Gerard D, Payami, Haydeh
Publicado em 2005

Genetic Investigation of Quantitative Traits Related to Autism: Use of Multivariate Polygenic Models with Ascertainment Adjustment

Por Sung, Yun Ju, Dawson, Geraldine, Munson, Jeffrey, Estes, Annette, Schellenberg, Gerard D., Wijsman, Ellen M.
Publicado em 2005

<it>parkin </it>mutation dosage and the phenomenon of anticipation: a molecular genetic study of familial parkinsonism

Por Schellenberg Gerard D, Nutt John G, Montimurro Jennifer S, Moses Lina, Poorkaj Parvoneh, Payami Haydeh
Publicado no BMC Neurology (2005-02-01)

Neurodegeneration and defective neurotransmission in a Caenorhabditis elegans model of tauopathy

Por Kraemer, Brian C., Zhang, Bin, Leverenz, James B., Thomas, James H., Trojanowski, John Q., Schellenberg, Gerard D.
Publicado em 2003

The Number of Trait Loci in Late-Onset Alzheimer Disease

Por Daw, E. Warwick, Payami, Haydeh, Nemens, Ellen J., Nochlin, David, Bird, Thomas D., Schellenberg, Gerard D., Wijsman, Ellen M.
Publicado em 2000

Missense and silent tau gene mutations cause frontotemporal dementia with parkinsonism-chromosome 17 type, by affecting multiple alternative RNA splicing regulatory elements

Por D’Souza, Ian, Poorkaj, Parvoneh, Hong, Ming, Nochlin, David, Lee, Virginia M.-Y., Bird, Thomas D., Schellenberg, Gerard D.
Publicado em 1999

Preclinical Evidence of Alzheimer Changes: Convergent Cerebrospinal Fluid Biomarker and Fluorodeoxyglucose Positron Emission Tomography Findings

Por Petrie, Eric C., Cross, Donna J., Galasko, Douglas, Schellenberg, Gerard D., Raskind, Murray A., Peskind, Elaine R., Minoshima, Satoshi
Publicado em 2009

p53-Mediated apoptosis is attenuated in Werner syndrome cells

Por Spillare, Elisa A., Robles, Ana I., Wang, Xin Wei, Shen, Jiang-Cheng, Yu, Chang-Eu, Schellenberg, Gerard D., Harris, Curtis C.
Publicado em 1999

Evidence for a Novel Late-Onset Alzheimer Disease Locus on Chromosome 19p13.2

Por Wijsman, Ellen M., Daw, E. Warwick, Yu, Change-En, Payami, Haydeh, Steinbart, Ellen J., Nochlin, David, Conlon, Erin M., Bird, Thomas D., Schellenberg, Gerard D.
Publicado em 2004

Clinical and neuropathological features of the Arctic APP mutation causing early onset Alzheimer's disease

Por Basun, Hans, Bogdanovic, Nenad, Ingelsson, Martin, Almkvist, Ove, Näslund, Jan, Axelman, Karin, Bird, Thomas D., Nochlin, David, Schellenberg, Gerard D., Wahlund, Lars-Olof, Lannfelt, Lars
Publicado em 2008

Comprehensive Analysis of APOE and Selected Proximate Markers for Late-onset Alzheimer Disease: Pattern of Linkage Disequilibrium and Disease/Marker Association

Por Yu, Chang-En, Seltman, Howard, Peskind, Elaine R., Galloway, Nichole, Zhou, Peter X., Rosenthal, Elisabeth, Wijsman, Ellen M., Tsuang, Debby W., Devlin, Bernie, Schellenberg, Gerard D.
Publicado em 2007

Lewy Body Pathology in Familial Alzheimer Disease: Evidence for Disease- and Mutation-Specific Pathologic Phenotype

Por Leverenz, James B., Fishel, Mark A., Peskind, Elaine R., Montine, Thomas J., Nochlin, David, Steinbart, Ellen, Raskind, Murray A., Schellenberg, Gerard D., Bird, Thomas D., Tsuang, Debby
Publicado em 2006

Reduced Hippocampal Insulin-Degrading Enzyme in Late-Onset Alzheimer’s Disease Is Associated with the Apolipoprotein E-ε4 Allele

Por Cook, David G., Leverenz, James B., McMillan, Pamela J., Kulstad, J. Jacob, Ericksen, Sasha, Roth, Richard A., Schellenberg, Gerard D., Jin, Lee-Way, Kovacina, Kristina S., Craft, Suzanne
Publicado em 2003

Clinicopathological concordance and discordance in three monozygotic twin pairs with familial Alzheimer's disease

Por Brickell, Kiri L, Leverenz, James B, Steinbart, Ellen J, Rumbaugh, Malia, Schellenberg, Gerard D, Nochlin, David, Lampe, Thomas H, Holm, Ida E, Van Deerlin, Vivianna, Yuan, Wuxing, Bird, Thomas D
Publicado em 2007

Apolipoprotein E Highly Correlates with AβPP- and Tau-Related Markers in Human Cerebrospinal Fluid

Por Vuletic, Simona, Li, Ge, Peskind, Elaine R., Kennedy, Hal, Marcovina, Santica M., Leverenz, James B., Petrie, Eric C., Lee, Virginia M-Y., Galasko, Douglas, Schellenberg, Gerard D., Albers, John J.
Publicado em 2008

APP717, APP693, and PRIP gene mutations are rare in Alzheimer disease

Por Schellenberg, Gerard D., Anderson, Leojean, O'dahl, Sheldon, Wisjman, Ellen M., Sadovnick, Adele D., Ball, Melvyn J., Larson, Eric B., Kukull, Walter A., Martin, George M., Roses, Allen D., Bird, Thomas D.
Publicado em 1991