Zobrazeno 1 - 8
of 8
pro vyhledávání: '"John Brunzell"'
Autor:
Gail P. Jarvik, Ramakrishnan Rajagopalan, Elisabeth A. Rosenthal, Gertrud Wolfbauer, Laura McKinstry, Aditya Vaze, John Brunzell, Arno G. Motulsky, Deborah A. Nickerson, Patrick J. Heagerty, Ellen M. Wijsman, John J. Albers
Publikováno v:
Journal of Lipid Research, Vol 51, Iss 5, Pp 983-990 (2010)
Phospholipid transfer protein (PLTP) belongs to the lipid transfer/lipopolysaccharide-binding protein gene family. Expression of PLTP has been implicated in the development of atherosclerosis. We evaluated the effects of PLTP region tagging single nu
Externí odkaz:
https://doaj.org/article/237dc7938d4c45df9993e61c372ebe18
Autor:
Baohai Shao, Leila Zelnick, Jake Wimberger, John Brunzell, Jonathan Himmelfarb, Karin E Bornfeldt, Ian H de Boer, Jay W Heinecke
Publikováno v:
Arteriosclerosis, Thrombosis, and Vascular Biology. 37
Patients with type 1 diabetes (T1D) are at high risk of atherosclerotic cardiovascular disease (CVD). Albuminuria is strongly associated with CVD risk and fully accounts for the excess overall mortality risk in some T1D cohorts. One important contrib
Publikováno v:
The Journal of clinical endocrinology and metabolism. 97(9)
Autor:
John Brunzell, Bela F. Asztalos
Publikováno v:
High Density Lipoproteins, Dyslipidemia, and Coronary Heart Disease ISBN: 9781441910585
Low levels of high density lipoprotein (HDL) cholesterol have been associated with an increased risk of coronary heart disease. In the previous chapter, we have described the presence of distinct apolipoprotein A-I containing HDL particles beginning
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::65fc38054d8d6ff103898d879b3fc04f
https://doi.org/10.1007/978-1-4419-1059-2_4
https://doi.org/10.1007/978-1-4419-1059-2_4
Autor:
John Brunzell
Publikováno v:
Polycystic Ovary Syndrome ISBN: 9780824707460
Polycystic Ovary Syndrome
Polycystic Ovary Syndrome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::616a2f5746c813c14552460da23b2f04
https://doi.org/10.1201/9780203910948.ch14
https://doi.org/10.1201/9780203910948.ch14
Autor:
France Mailly, Jutta Palmen, David P.R. Muller, Tracy Gibbs, June Lloyd, John Brunzell, Paul Durrington, Kostas Mitropoulos, John Betteridge, Gerald Watts, Hans Lithell, Franco Angelico, Steve E. Humphries, Philippa J. Talmud
Publikováno v:
Human mutation. 10(6)
The aim of this study was to identify mutations in the lipoprotein lipase (LPL) gene in 20 unrelated patients with familial lipoprotein deficiency (FLLD) and to investigate the genotype/phenotype relationship. The previously reported G188E mutation (
Autor:
Andrew J. Drexler, Richard W. Nesto, Martin J. Abrahamson, George Bakris, David Bell, John Brunzell, Paresh Dandona, Jaime Davidson, Vivian Fonseca, Michael Fowler, Robert Frye, Thomas Giles, Steven Haffner, Norman Hollenberg, Willa Hsueh, Ronald Law, Jorge Plutzky, Robert Ratner, Jane Reusch, Andrew Selwyn
Publikováno v:
Metabolic Syndrome & Related Disorders; Summer2005, Vol. 3 Issue 2, p147-173, 27p
Publikováno v:
Progress in Pediatric Cardiology. 1:76