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Scholar Results 1 - 10 of about 19 citing Kim: Identification of a locus for maturity-onset diabetes of the young on chromosome 8p23. (0.10 sec) 

Tissue-specific transcriptional regulation has diverged significantly between …


DT Odom, RD Dowell, ES Jacobsen, W Gordon, TW … - Nature genetics, 2007 - nature.com
We demonstrate that the binding sites for highly conserved transcription factors vary extensively
between human and mouse. We mapped the binding of four tissue-specific transcription factors
(FOXA2, HNF1A, HNF4A and HNF6) to 4,000 orthologous gene pairs in hepatocytes ...
Cited by 109 - Related articles - BL Direct - All 6 versions

Genetic basis of maturity-onset diabetes of the young


M Vaxillaire, P Froguel - Endocrinology and metabolism clinics of North America, 2006 - Elsevier
Type 2 diabetes mellitus (T2D) is a heterogeneous metabolic disease occurring with concomitant
or interdependent defects of insulin secretion and action [1] and [2]. It generally is accepted that
T2D results from a complex interplay of genetic and environmental factors influencing ...
Cited by 30 - Related articles - All 4 versions

Multiple QTLs influencing triglyceride and HDL and total cholesterol levels …

- gemstudy.ca [PDF] 
Y Yu, DF Wyszynski, DM Waterworth, SD Wilton, … - Science's …, 2005 - stke.sciencemag.org
Abstract: We conducted a genome-wide scan using variance components linkage analysis to
localize quantitative-trait loci (QTLs) influencing triglyceride (TG), high density lipoprotein-cholesterol
(HDL-C), low density lipoprotein-cholesterol, and total cholesterol (TC) levels in 3,071 ...
Cited by 23 - Related articles - BL Direct - All 7 versions

Genes and type 2 diabetes mellitus


MT Tusié Luna - Archives of Medical Research, 2005 - Elsevier
Type 2 diabetes (T2DM) comprises a group of entities with different genetic causes. In most
patients, T2DM results from alterations of various genes, each having a partial and additive
effect. The inheritance pattern is thus complex, and environmental factors play an ...
Cited by 18 - Related articles - All 2 versions

Mutations in the SLC30A8 gene are not a major cause of MODY or other forms of …

- nih.gov
M Borowiec, R Thompson, C Powers, R Xu, T Dickey, A … - Diabetologia, 2007 - Springer
Page 1. RESEARCH LETTER Mutations in the SLC30A8 gene are not a major cause
of MODYor other forms of early-onset, autosomal dominant type 2 diabetes M. Borowiec
& R. Thompson & C. Powers & R. Xu & T. Dickey & A. Doria ...
Cited by 6 - Related articles - BL Direct - All 4 versions

Mutations in MODY genes are not common cause of early-onset type 2 diabetes in …


A Domínguez-López, Á Miliar-García, YX Segura- … - JOP. J Pancreas (Online …, 2005 - joplink.net
Context Maturity-onset diabetes of the young (MODY) is a monogenic form of diabetes mellitus
characterized by autosomal dominant inheritance, early age of onset and a primary insulin secretion
defect. Certain MODY gene sequence variants may be involved in polygenic forms of type ...
Cited by 5 - Related articles - Cached - All 3 versions

Monogenic diabetes in the young, pharmacogenetics and relevance to …

- endojournals.org
M Vaxillaire, P Froguel - Endocrine Reviews, 2008 - Endocrine Soc
Most valuable breakthroughs in the genetics of type 2 diabetes for the past two decades have
arisen from candidate gene studies and familial linkage analysis of maturity-onset diabetes of
the young (MODY), an autosomal dominant form of diabetes typically occurring before 25 ...
Cited by 6 - Related articles - BL Direct - All 6 versions

Genome-wide Linkage Screen for Stature and Body-mass Index in 3.032 Families- …


… , T Hiekkalinna, K Schwander, S Kardia, … - European journal of …, 2009 - pubmedcentral.nih.gov
Stature (adult body height), and body mass index (BMI) have a strong genetic component explaining
observed variation in human populations, however, identifying those genetic components has
been extremely challenging. It seems obvious that sample size is a critical determinant for ...
Cited by 6 - Related articles - All 5 versions

Isolation and functional analysis of human HMBOX1, a homeobox containing …


S Chen, H Saiyin, X Zeng, J Xi, X Liu, X Li, L … - Cytogenet Genome …, 2006 - content.karger.com
We have identified and isolated a novel human gene, HMBOX1 (homeobox containing 1) from
a pancreatic cDNA library. Human HMBOX1 is widely expressed in 18 tissues, and it is highly
expressed in pancreas. According to the genome database, HMBOX1 is located at the ...
Cited by 4 - Related articles - BL Direct - All 5 versions

Examination of PPP1R3B as a candidate gene for the type 2 diabetes and MODY …


JS Dunn, WM Mlynarski, MG Pezzolesi, M … - Annals of Human …, 2006 - interscience.wiley.com
The product of the PPP1R3B gene (G L ) is the regulatory subunit of PP1 - a serine/threonine
phosphatase involved in the modulation of glycogen synthesis in the liver and skeletal
muscle. The PPP1R3B gene is located on chromosome 8p23 in a region that has been ...
Cited by 2 - Related articles - BL Direct - All 3 versions


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