Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Heather Doelle"'
Autor:
Ruth McPherson, Jonathan Cohen, Heather Doelle, Sybil Hébert, Li Weng, Wendy Schackwitz, Anna Ustaszewska, Len A. Pennacchio, Nihan Kavaslar
Publikováno v:
Journal of Clinical Investigation. 115:1016-1020
Mutations in MEF2A have been implicated in an autosomal dominant form of coronary artery disease (adCAD1). In this study we sought to determine whether severe mutations in MEF2A might also explain sporadic cases of coronary artery disease (CAD). To d
Publikováno v:
Receptors & Clinical Investigation.
The concentration of adenosine nucleotides (ATP&ADP) in the circulation may impact health and disease by controlling cellular metabolic pathways in tissues throughout the body. Fasting plasma nucleotide levels are normally relatively low in healthy s
Autor:
Sherry L. Perkins, Janice Forsythe, Heather Doelle, Eduardo Escares, Claire Pronovost, Susan Taylor-Clapp
Publikováno v:
Clinical Biochemistry. 31:67-71
To evaluate the analytical and clinical performance of the One Touch II and Advantage glucose meters for use in neonatal specimens.For the laboratory evaluation, a total of 96 umbilical cord whole blood specimens were analyzed on the One Touch II and
Autor:
Heather Doelle, Fabienne Benoist, Michael McDonnell, Ruth McPherson, Paulina Lau, Ross W. Milne
Publikováno v:
Journal of Biological Chemistry. 272:23572-23577
We have determined the role of cholesteryl ester transfer protein (CETP) in selective uptake of high density lipoprotein (HDL)-derived cholesteryl esters (CE) by human adipose tissue, using organ culture or collagenase-digested adipocytes. Incubation
A 680 kb duplication at the FTO locus in a kindred with obesity and a distinct body fat distribution
Autor:
Thet Naing, Ruth McPherson, Paulina Lau, Majid Nikpay, Robert Dent, Robert W. Davies, Heather Doelle, Mary-Ellen Harper
Common intronic SNPs in the human fat mass and obesity associated (FTO) gene are strongly associated with body mass index (BMI). In mouse models, inactivation of the Fto gene results in a lean phenotype, whereas overexpression of Fto leads to increas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d8a3f9059aae76e93f14d1603dc0ff6d
https://europepmc.org/articles/PMC3831078/
https://europepmc.org/articles/PMC3831078/
Autor:
Alexandre F Stewart, Ruth McPherson, Li Chen, Kathryn Williams, Heather Doelle, Robbie Davies, Sonny Dandona, Nihan Kavaslar, Julie Ruthberg, Gwen Ewart, Rosemary LaRose, Lan Vo, Yanquing Wang, Paulina Lau, Marino Labinaz, Benjamin Chow, George A Wells, Robert Roberts
Publikováno v:
Circulation. 118
Background : Coronary artery disease (CAD) is the leading cause of death in the western world. The only common genetic risk locus identified to date by us and others in genome wide association studies (GWAS) resides at 9p21.3. Methods: The Ottawa Hea
Autor:
Alexandre F Stewart, Ruth McPherson, Kathryn Williams, Nihan Kavaslar, Julie Rutberg, Heather Doelle, Gwen Ewart, George Wells, Robert Roberts
Publikováno v:
Circulation. 116
Purpose: To identify genes predisposing to Coronary Artery Disease (CAD). Methods: We selected the unbiased approach of using the genome wide scan association case control method. Using the Affymetrix 500K SNP array that that average a marker every 6
Autor:
Len A. Pennacchio, Nadav Ahituv, Robert Dent, Wendy Schackwitz, Heather Doelle, Ruth McPherson, John Michael Collier, Anna Ustaszewska, Sybil Hébert, Nihan Kavaslar
Publikováno v:
Ahituv, Nadav; Kavaslar, Nihan; Schackwitz, Wendy; Ustaszewska, Anna; Collier, John Michael; Hebert, Sybil; et al.(2005). A PYY Q62P variant linked to human obesity. Lawrence Berkeley National Laboratory. Lawrence Berkeley National Laboratory: Lawrence Berkeley National Laboratory. Retrieved from: http://www.escholarship.org/uc/item/2060q8g7
Members of the pancreatic polypeptide family and their receptors have been implicated in the control of food intake in rodents and humans. To investigate whether nucleotide changes in these candidate genes result in abnormal weight in humans, we sequ
Autor:
George A. Wells, Ruth McPherson, Heather Doelle, Li Chen, Robert Roberts, Rosemary LaRose, Kathryn J.H. Williams, Melanie Belanger, Sonny Dandona, Alexandre F.R. Stewart, Olivia Assogba, Gwen Ewart
Publikováno v:
Journal of the American College of Cardiology. 53:1471-1472
To the Editor: To date, the only common genetic variant to consistently associate with risk of coronary artery disease (CAD) or myocardial infarction (MI) is the 9p21.3 variant ([1,2][1]). Several recent reports identified a SNP (rs20455) that alters