(Q46865476)

25 December 2017

title

A genome-wide linkage scan for genes controlling variation in urinary albumin excretion in type II diabetes (English)

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25 December 2017

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10

Moczulski D

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25 December 2017

Andrzej S. Krolewski

1

object named as

Krolewski AS

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25 December 2017

author name string

Poznik GD

2

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Placha G

3

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25 December 2017

Canani L

4

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Dunn J

5

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Walker W

6

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Smiles A

7

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25 December 2017

Krolewski B

8

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25 December 2017

Fogarty DG

9

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25 December 2017

Araki S

11

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25 December 2017

Makita Y

12

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25 December 2017

Ng DP

13

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Rogus J

14

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Duggirala R

15

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Rich SS

16

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Warram JH

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language of work or name

English

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publication date

1 January 2006

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25 December 2017

published in

Kidney International

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25 December 2017

volume

69

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25 December 2017

issue

1

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25 December 2017

page(s)

129-136

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25 December 2017

https://scigraph.springernature.com/pub.10.1038/sj.ki.5000023

exact match

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cites work

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Urinary albumin excretion in families with type 2 diabetes is heritable and genetically correlated to blood pressure

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A genome-wide scan for urinary albumin excretion in hypertensive families

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Genome-wide linkage analysis to urinary microalbuminuria in a community-based sample: the Framingham Heart Study

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Segregation analysis of urinary albumin excretion in families with type 2 diabetes

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Nephropathy of type II diabetes: evidence for hereditary factors?

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Familial clustering of diabetic kidney disease. Evidence for genetic susceptibility to diabetic nephropathy

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Population-based assessment of familial clustering of diabetic nephropathy in type 1 diabetes

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Clustering of albumin excretion rate abnormalities in Caucasian patients with NIDDM. The Italian NIDDM Nephropathy Study Group

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7 January 2021

Familial clustering of diabetic nephropathy in Brazilian type 2 diabetic patients.

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A nonlinear effect of hyperglycemia and current cigarette smoking are major determinants of the onset of microalbuminuria in type 1 diabetes

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Determinants of the development of diabetes (maturity-onset diabetes of the young-3) in carriers of HNF-1alpha mutations: evidence for parent-of-origin effect

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Major susceptibility locus for nephropathy in type 1 diabetes on chromosome 3q: results of novel discordant sib-pair analysis

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Risk of advanced diabetic nephropathy in type 1 diabetes is associated with endothelial nitric oxide synthase gene polymorphism

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Endothelial nitric oxide synthase gene polymorphism in intron 4 affects the progression of renal failure in non-diabetic renal diseases

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7 January 2021

Association of the nitric oxide synthase gene polymorphism with an increased risk for progression to diabetic nephropathy in type 2 diabetes

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T-786C polymorphism of the endothelial nitric oxide synthase gene is associated with albuminuria in the diabetes heart study

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7 January 2021

T(-786)-->C polymorphism of the endothelial nitric oxide synthase gene influences the progression of renal disease

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Endothelial nitric oxide synthase gene intron 4 polymorphism in patients with end-stage renal disease

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Nitric oxide synthase gene polymorphisms and diabetic nephropathy

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Sib-pair linkage analysis for susceptibility genes for microvascular complications among Pima Indians with type 2 diabetes. Pima Diabetes Genes Group.

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Gene for susceptibility to diabetic nephropathy in type 2 diabetes maps to 18q22.3-23

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7 January 2021

Exact multipoint quantitative-trait linkage analysis in pedigrees by variance components

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7 January 2021

Variance component methods for detecting complex trait loci

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7 January 2021

Markov chain Monte Carlo segregation and linkage analysis for oligogenic models

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7 January 2021

Extensions to multivariate normal models for pedigree analysis

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Identifiers

DOI

10.1038/SJ.KI.5000023

1 reference

25 December 2017

1 reference

25 December 2017