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Scholar Results 1 - 10 of about 101 related to Weissglas-Volkov: Common Hepatic Nuclear Factor-4α Variants Are Associated With High Serum.... (0.11 sec) 

Common Hepatic Nuclear Factor-4α Variants Are Associated With High Serum …

- diabetesjournals.org
D Weissglas-Volkov, A Huertas-Vazquez, E Suviolahti, … - Diabetes, 2006 - Am Diabetes Assoc
Hepatic nuclear factor-4α (HNF-4α), a transcription factor involved in the regulation of serum
lipid and glucose levels, has recently been associated with type 2 diabetes. The HNF-4α gene
(HNF4A) resides on chromosome 20q12-q13.1, which, in addition to type 2 diabetes, has ...
Cited by 18 - Related articles - BL Direct - All 7 versions

The ABCA1 R230C variant affects hdl-cholesterol levels and body mass index in …


MT Villarreal-Molina, CA Aguilar-Salinas, M Rodriguez- … - Diabetes, 2007 - Am Diabetes Assoc
Short running title: ABCA1 gene variant is associated with obesity ... 1. Unit of Molecular Biology
and Genomic Medicine, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán
(INCMNSZ), Instituto de Investigaciones Biomédicas de la Universidad Nacional ...
Cited by 9 - Related articles

Familial combined hyperlipidemia in Mexicans: association with upstream …

- ahajournals.org
A Huertas-Vazquez, C Aguilar-Salinas, AJ … - … , and vascular biology, 2005 - Am Heart Assoc
From the Unidad de Biología (AH-V., SC-Q., LR-R., TT-L.), Molecular y Medicina Genómica del
Instituto de Investigaciones Biomédicas de la UNAM y del Instituto Nacional de Ciencias Médicas
y Nutrición, Salvador Zubirán, Mexico City, Mexico; the Department of Human Genetics ...
Cited by 42 - Related articles - All 5 versions

Locus for quantitative HDL-cholesterol on chromosome 10q in Finnish families with …

- jlr.org
HE Lilja, E Suviolahti, A Soro-Paavonen, T … - The Journal of Lipid …, 2004 - ASBMB
Decreased HDL-cholesterol (HDL-C) and familial combined hyperlipidemia (FCHL) are the two
most common familial dyslipidemias predisposing to premature coronary heart disease
(CHD). These dyslipidemias share many phenotypic features, suggesting a partially ...
Cited by 20 - Related articles - BL Direct - All 8 versions

A Novel− 192c/g Mutation in the Proximal P2 Promoter of the Hepatocyte Nuclear …

- diabetesjournals.org
J Ek, SP Hansen, M Lajer, C Nicot, TW Boesgaard, S … - Diabetes, 2006 - Am Diabetes Assoc
Recently, it has been shown that mutations in the P2 promoter of the hepatocyte nuclear factor
(HNF)-4α gene (HNF4A) cause maturity-onset diabetes of the young (MODY), while single nucleotide
polymorphisms in this locus are associated with type 2 diabetes. In this study, we ...
Cited by 12 - Related articles - BL Direct - All 6 versions

[CITATION] Programa de Trabajo para dirigir el Instituto Nacional de Medicina Genómica 2004 …


G Jimenez-Sanchez - Fundación Mexicana para la Salud., Mexico DF, 2004
Cited by 2 - Related articles

[CITATION] El Instituto Nacional de Medicina Genómica [The National Institute of Genomic …


G Jimenez-Sanchez, J Valdes Olmedo, G Soberon - Este país, 2002
Cited by 3 - Related articles

Human genomic variation studies and pharmacogenomics are critical for global …


B Seguim, S Essajee, G Jimenez-Sanchez … - Pharmacogenomics …, 2007 - landesbioscience.com
Many people in the world still lack access to essential medicines. The World Health Organization
(WHO) has attempted to address this inequity by creating the essential medicines list (See
http://www.who.int/medicines/publications/essentialmedicines/en/). This list is intended to ...
Cited by 3 - Related articles - Cached - All 4 versions

Two novel apolipoprotein A-IV variants in individuals with familial combined …


SS Deeb, DN Nevin, L Iwasaki, JD Brunzell - Human mutation, 1996 - interscience.wiley.com
It has been suggested that apo A-IV may play a role in modulating the activation of lipoprotein
lipase (LPL) by apo C-II (Goldberg et al., 1990). Therefore, the role of genetic variation at the
apolipoprotein A-IV locus in familial combined hyperlipidemia (FCHL) was investigated. A ...
Cited by 15 - Related articles - BL Direct - All 3 versions

[CITATION] The development of human genetics in Mexico.


F Salamanca, S Armendares - Archives of medical research, 1995 - ncbi.nlm.nih.gov
1: Arch Med Res. 1995;26 Spec No:S55-62. The development of human genetics in Mexico.
Salamanca F, Armendares S. Unidad de Investigación en Genética Humana, Centro Médico
Nacional Siglo XXI, Instituto Mexicano de Seguro Social, México, DF. ...
Cited by 4 - Related articles - BL Direct


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