Genome-wide association study of kidney function decline in individuals of European descent - Wikidata - awgldk - TriplyDB

Genome-wide association study of kidney function decline in individuals of European descent

Genome-wide association study of kidney function decline in individuals of European descent

http://www.wikidata.org/entity/Q34453062

about

Genomic and Proteomic Characterization of Acute Kidney Injury Insights into kidney diseases from genome-wide association studies.Genome-wide association studies in pediatric chronic kidney disease.Trans-ethnic Fine Mapping Highlights Kidney-Function Genes Linked to Salt Sensitivity.Development of next generation sequencing panel for UMOD and association with kidney disease.Prediction of the damage-associated non-synonymous single nucleotide polymorphisms in the human MC1R gene A roadmap for the genetic analysis of renal aging Unmet medical needs in lupus nephritis: solutions through evidence-based, personalized medicine Genomics in CKD: Is This the Path Forward?N-acetylgalactosaminyltransferases in cancer.Evidence for extensive pleiotropy among pharmacogenes.Hypertension-attributed nephropathy: what's in a name?Uromodulin: from physiology to rare and complex kidney disorders.Genetic epidemiology in kidney disease.Renal Aging: Causes and Consequences.Uromodulin gene variants and their association with renal function and blood pressure in cats: a pilot study.Genome-Wide Association of CKD Progression: The Chronic Renal Insufficiency Cohort Study.Association between kidney function and genetic polymorphisms in atherosclerotic and chronic kidney diseases: A cross-sectional study in Japanese male workers.Effect of UMOD genotype on long-term graft survival after kidney transplantation in patients treated with cyclosporine-based therapy.The UMOD Locus: Insights into the Pathogenesis and Prognosis of Kidney Disease.Haploinsufficiency of the Transcription Factor Ets-1 Is Renoprotective in Dahl Salt-Sensitive Rats.Genome-wide association studies of albuminuria: towards genetic stratification in diabetes?Lessons from CKD-Related Genetic Association Studies-Moving Forward.PheWAS and Beyond: The Landscape of Associations with Medical Diagnoses and Clinical Measures across 38,662 Individuals from Geisinger.Site-specific O-glycosylation of members of the low-density lipoprotein receptor superfamily enhances ligand interactions.Assessing known chronic kidney disease associated genetic variants in Saudi Arabian populations.

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P2860

Genome-wide association study of kidney function decline in individuals of European descent

http://www.wikidata.org/entity/Q34453062

description

2014 nî lūn-bûn

@nan

2014 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

2014年の論文

@ja

2014年論文

@yue

2014年論文

@zh-hant

2014年論文

@zh-hk

2014年論文

@zh-mo

2014年論文

@zh-tw

2014年论文

@wuu

name

Genome-wide association study ...... ndividuals of European descent

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Genome-wide association study ...... ndividuals of European descent

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Genome-wide association study ...... ndividuals of European descent

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type

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Genome-wide association study ...... ndividuals of European descent

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Genome-wide association study ...... ndividuals of European descent

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Genome-wide association study ...... ndividuals of European descent

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prefLabel

Genome-wide association study ...... ndividuals of European descent

@ast

Genome-wide association study ...... ndividuals of European descent

@en

Genome-wide association study ...... ndividuals of European descent

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Kidney International

P1476

Genome-wide association study ...... ndividuals of European descent

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P2093

Adrienne Tin

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Afshin Parsa

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Andre Franke

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Andrew Johnson

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Audrey Y Chu

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Bamidele O Tayo

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Barbara Kollerits

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Bernhard K Krämer

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Bernhard Paulweber

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Caroline S Fox

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P2860

Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D

The heterotaxy gene GALNT11 glycosylates Notch to orchestrate cilia type and laterality.

Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23

The Usher syndrome proteins cadherin 23 and harmonin form a complex by means of PDZ-domain interactions.

New loci associated with kidney function and chronic kidney disease

Genome-wide association studies of chronic kidney disease: what have we learned?

Mutations in Cdh23, encoding a new type of cadherin, cause stereocilia disorganization in waltzer, the mouse model for Usher syndrome type 1D

Multiple loci associated with indices of renal function and chronic kidney disease

New susceptibility loci associated with kidney disease in type 1 diabetes.

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

P2888

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1017-1029

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scholarly article

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10.1038/KI.2014.361

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5

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87

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Murielle Bochud

Peter Vollenweider

Alexander Teumer

Fernando Rivadeneira

Vilmundur Gudnason

Martina Müller-Nurasyid

André Uitterlinden

Terho Lehtimäki

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2014-12-10T00:00:00Z

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269416816

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1035525597

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25493955

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genome-wide association study

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4425568

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