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Scholar Results 1 - 10 of about 101 related to Rogus: High-Density Single Nucleotide Polymorphism Genome-Wide Linkage Scan for Susceptibility.... (0.09 sec) 

High-Density Single Nucleotide Polymorphism Genome-Wide Linkage Scan for Susceptibility …

- nih.gov
JJ Rogus, GD Poznik, MG Pezzolesi, AM … - Diabetes, 2008 - Am Diabetes Assoc
RESEARCH DESIGN AND METHODS— To efficiently search for genomic regions
harboring diabetic nephropathy genes, we conducted a scan using 5,382
informative single nucleotide polymorphisms on 100 sibpairs concordant for ...
Cited by 3 - Related articles - All 4 versions

High-density SNP genome wide linkage scan for susceptibility genes for diabetic nephropathy …

- diabetesjournals.org [PDF] 
JJ Rogus, GD Poznik, MG Pezzolesi, AM … - Diabetes, 2008 - Am Diabetes Assoc
John J. Rogus1, 2, G. David Poznik1, Marcus G. Pezzolesi1,2, Adam M. Smiles1,
Jonathon Dunn1, William Walker1, Krzysztof Wanic1,2, Dariusz Moczulski1,2,3 Luis
Canani1,2,4, Shinichi Araki1,2,5, Yuichiro Makita1,2,6, James H. Warram1, ...
Cited by 1 - Related articles - All 2 versions

Allele A in intron 4 of ecNOS gene will not increase the risk of diabetic nephropathy in type …


S Lin, H Qu, M Qiu - Nephron, 2002 - content.karger.com
Page 1. Letter to the Editor Nephron 2002;91:768 Allele A in Intron 4 of ecNOS
Gene Will Not Increase the Risk of Diabetic Nephropathy in ...
Cited by 4 - Related articles - BL Direct - All 5 versions

Endothelial nitric oxide synthase gene haplotypes and diabetic nephropathy among Asian …


TS Ahluwalia, M Ahuja, TS Rai, HS Kohli, K … - Molecular and Cellular Biochemistry, 2008 - Springer
Abstract Endothelial dysfunction plays a key role in the pathogenesis of
diabetic vascular disease, including dia- betic nephropathy. Endothelial-derived
nitric oxide synthase (eNOS) gene polymorphisms affect eNOS activity and ...
Cited by 3 - Related articles - All 2 versions

Identifying modifier loci in existing genome scan data


EW Daw, Y Lu, AJ Marian, S Shete - Annals of Human Genetics, 2008 - interscience.wiley.com
In many genetic disorders in which a primary disease-causing locus has been
identified, evidence exists for additional trait variation due to genetic
factors. These findings have led to studies seeking secondary 'modifier' ...
Cited by 4 - Related articles - All 3 versions

A novel framework for sib pair linkage analysis

- nih.gov
GD Poznik, K Adamska, X Xu, AS Krolewski, … - The American Journal of Human Genetics, 2006 - Elsevier
Sib pair linkage analysis of a dichotomous trait is a popular method for
narrowing the search for genes that influence complex diseases. Although the
pedigree structures are uncomplicated and the underlying genetic principles ...
Cited by 3 - Related articles - BL Direct - All 8 versions

[PDF] Association of endothelial nitric oxide synthase gene intron 4 polymorphism with end-stage …


M Bellini, MAR Figueira, M Piccoli, JUL … - Nephrology, 2007 - ipen.br
1Division of Nephrology and Geriatrics, Department of Medicine, Universidade
Federal de São Paulo, and 2Instituto de Pesquisas Energéticas e Nucleares,
Cidade Universitária IPEN-CNEN/SP, São Paulo, SP, Brazil
Cited by 4 - Related articles - View as HTML - BL Direct - All 4 versions

Potential genetic modifiers of the cystic fibrosis intestinal inflammatory phenotype on …


O Norkina, RC De Lisle - BMC genetics, 2005 - biomedcentral.com
Although cystic fibrosis is caused by mutations in the cystic fibrosis
transmembrane conductance regulator (CFTR) gene, the severity of disease is
highly variable indicating the influence of modifier genes. The intestines ...
Cited by 5 - Related articles - Cached - All 10 versions

Vitamin D binding protein, a new nutritional marker in cystic fibrosis patients


MM Speeckaert, C Wehlou, S Vandewalle, YE … - Clinical Chemical Laboratory Medicine, 2008 - reference-global.com
Background: Vitamin D binding protein (DBP) is a multifunctional transport
protein with a decreased serum concentration in cystic fibrosis (CF). The pres-
ent study investigates the importance of DBP and its role as an alternative ...
Cited by 6 - Related articles - BL Direct - All 3 versions

A test for genetic association that incorporates information about deviation from Hardy- …

- nih.gov
J Wang, S Shete - The American Journal of Human Genetics, 2008 - Elsevier
For assessment of genetic association between single-nucleotide polymorphisms
(SNPs) and disease status, the logistic-regression model or generalized linear
model is typically employed. However, testing for deviation from ...
Cited by 6 - Related articles - All 6 versions


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