An analysis of the role of calcium in facilitation at the frog neuromuscular junction

Por Younkin, S. G.
Publicado em 1974

Neural control of skeletal muscle cholinesterase: a study using organ-cultured rat muscle.

Por Davey, B, Younkin, L H, Younkin, S G
Publicado em 1979

Rheumatoid arthritis-associated polymorphisms are not protective against Alzheimer's disease

Por Simmons, Christopher R, Zou, Fanggeng, Younkin, Steven G, Estus, Steven
Publicado em 2011

Evaluation of the global association between cholesterol-associated polymorphisms and Alzheimer's disease suggests a role for rs3846662 and HMGCR splicing in disease risk

Por Simmons, Christopher R, Zou, Fanggeng, Younkin, Steven G, Estus, Steven
Publicado em 2011

Turnover of acetylcholinesterase in innervated and denervated rat diaphragm.

Por Newman, J R, Virgin, J B, Younkin, L H, Younkin, S G
Publicado em 1984

In situ hybridization of nucleus basalis neurons shows increased beta-amyloid mRNA in Alzheimer disease.

Por Cohen, M L, Golde, T E, Usiak, M F, Younkin, L H, Younkin, S G
Publicado em 1988

Lack of association of hepatic lipase polymorphisms with late onset Alzheimer’s disease

Por Zhu, Haiyan, Taylor, Jennie W., Bennett, David A., Younkin, Steven G., Estus, Steven
Publicado em 2006

Astrocytes in Alzheimer's disease gray matter express alpha 1-antichymotrypsin mRNA.

Por Pasternack, J. M., Abraham, C. R., Van Dyke, B. J., Potter, H., Younkin, S. G.
Publicado em 1989

On multi-marker tests for association in case-control studies

Por Taub, Margaret A., Schwender, Holger R., Younkin, Samuel G., Louis, Thomas A., Ruczinski, Ingo
Publicado em 2013

Multiple Insulin Degrading Enzyme Variants Alter In Vitro Reporter Gene Expression

Por Belbin, Olivia, Crump, Michael, Bisceglio, Gina D., Carrasquillo, Minerva M., Morgan, Kevin, Younkin, Steven G.
Publicado em 2011

Analytic power and sample size calculation for the genotypic transmission/disequilibrium test in case-parent trio studies

Por Neumann, Christoph, Taub, Margaret A., Younkin, Samuel G., Beaty, Terri H., Ruczinski, Ingo, Schwender, Holger
Publicado em 2014

Fast detection of de novo copy number variants from SNP arrays for case-parent trios

Por Scharpf, Robert B, Beaty, Terri H, Schwender, Holger, Younkin, Samuel G, Scott, Alan F, Ruczinski, Ingo
Publicado em 2012

Human neurons derived from a teratocarcinoma cell line express solely the 695-amino acid amyloid precursor protein and produce intracellular beta-amyloid or A4 peptides.

Por Wertkin, A M, Turner, R S, Pleasure, S J, Golde, T E, Younkin, S G, Trojanowski, J Q, Lee, V M
Publicado em 1993

The beta-amyloid protein precursor of Alzheimer disease has soluble derivatives found in human brain and cerebrospinal fluid.

Por Palmert, M R, Podlisny, M B, Witker, D S, Oltersdorf, T, Younkin, L H, Selkoe, D J, Younkin, S G
Publicado em 1989

Activation of PPARδ prevents endothelial dysfunction induced by overexpression of amyloid-β precursor protein

Por d'Uscio, Livius V., Das, Pritam, Santhanam, Anantha V.R., He, Tongrong, Younkin, Steven G., Katusic, Zvonimir S.
Publicado em 2012

Uncoupling of endothelial nitric oxide synthase in cerebral vasculature of Tg2576 mice

Por Santhanam, Anantha Vijay R., d’Uscio, Livius V., He, Tongrong, Das, Pritam, Younkin, Steven G., Katusic, Zvonimir S.
Publicado no J Neurochem (2015)

Expression and processing analyses of wild type and p.R47H TREM2 variant in Alzheimer’s disease brains

Por Ma, Li, Allen, Mariet, Sakae, Nobutaka, Ertekin-Taner, Nilufer, Graff-Radford, Neill R., Dickson, Dennis W., Younkin, Steven G., Sevlever, Daniel
Publicado no Mol Neurodegener (2016)

Genetic variation in PCDH11X is associated with susceptibility to late onset Alzheimer's disease

Por Carrasquillo, Minerva M., Zou, Fanggeng, Pankratz, V. Shane, Wilcox, Samantha L., Ma, Li., Walker, Louise P., Younkin, Samuel G., Younkin, Curtis S., Younkin, Linda H., Bisceglio, Gina D., Ertekin-Taner, Nilufer, Crook, Julia E., Dickson, Dennis W., Petersen, Ronald C., Graff-Radford, Neill R., Younkin, Steven G.
Publicado em 2009

A genome-wide study of de novo deletions identifies a candidate locus for non-syndromic isolated cleft lip/palate risk

Por Younkin, Samuel G, Scharpf, Robert B, Schwender, Holger, Parker, Margaret M, Scott, Alan F, Marazita, Mary L, Beaty, Terri H, Ruczinski, Ingo
Publicado em 2014

Dectecting disease variants in case-parent trio studies using the Bioconductor software package trio

Por Schwender, Holger, Li, Qing, Neumann, Christoph, Taub, Margaret A., Younkin, Samuel G., Berger, Philipp, Scharpf, Robert B., Beaty, Terri H., Ruczinski, Ingo
Publicado em 2014