The Role of Cellular Aging in the Regulation of Free Fatty Acid Induced Cellular Inflammation by Liver X Receptor Alpha

by Schwartz, Charles S
Published 2019

Social credit theory and legislation in Alberta

by Schwartz, Charles.
Published 2012

Social credit theory and legislation in Alberta

by Schwartz, Charles.
Published 2012

A study of heart sound, galvanic skin response, and blood pressure in the measurement of human energy expenditure

by Schwartz, Charles Jay
Published 2008

PCR and serology find no association between xenotropic murine leukemia virus-related virus (XMRV) and autism

by Satterfield Brent C, Garcia Rebecca A, Gurrieri Fiorella, Schwartz Charles E
Published 2010-10-01

Absence of mutations in <it>NR2E1 </it>and <it>SNX3 </it>in five patients with MMEP (microcephaly, microphthalmia, ectrodactyly, and prognathism) and related phenotypes

by Simpson Elizabeth M, Schwartz Charles E, Slavotinek Anne, Morgan Chad T, Everman David B, Kumar Ravinesh A
Published 2007-07-01

TM4SF10 gene sequencing in XLMR patients identifies common polymorphisms but no disease-associated mutation

by Holinski-Feder Elke, Abramowicz Marc J, Gecz Jozef, Kooy Frank, Christophe-Hobertus Christiane, Schwartz Charles, Christophe Daniel
Published 2004-09-01

The <it>FU </it>gene and its possible protein isoforms

by Nöthen Markus M, Mosca Monica, Betz Regina C, Everman David B, Østerlund Torben, Schwartz Charles E, Zaphiropoulos Peter G, Toftgård Rune
Published 2004-07-01

<it>DRD2</it> and <it>PPP1R1B</it> (<it>DARPP-32</it>) polymorphisms independently confer increased risk for autism spectrum disorders and additively predict affected status in mal...

by Hettinger Joe A, Liu Xudong, Hudson Melissa L, Lee Alana, Cohen Ira L, Michaelis Ron C, Schwartz Charles E, Lewis Suzanne ME, Holden Jeanette JA
Published 2012-05-01

XLMR in MRX families 29, 32, 33 and 38 results from the dup24 mutation in the ARX (Aristaless related homeobox) gene

by MacMillan Andrée, Macgregor David, Holinski-Feder Elke, Mangelsdorf Marie, Finnis Merran, Cason A Lauren, Stepp Monica L, Holden Jeanette JA, Gecz Jozef, Stevenson Roger E, Schwartz Charles E
Published 2005-04-01

Multilocus loss of DNA methylation in individuals with mutations in the histone H3 Lysine 4 Demethylase KDM5C

by Grafodatskaya Daria, Chung Barian HY, Butcher Darci T, Turinsky Andrei L, Goodman Sarah J, Choufani Sana, Chen Yi-An, Lou Youliang, Zhao Chunhua, Rajendram Rageen, Abidi Fatima E, Skinner Cindy, Stavropoulos James, Bondy Carolyn A, Hamilton Jill, Wodak Shoshana, Scherer Stephen W, Schwartz Charles E, Weksberg Rosanna
Published 2013-01-01