(Q37778202)

English

The apolipoprotein L1 (APOL1) gene and nondiabetic nephropathy in African Americans

scientific article published on 05 August 2010

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

23 August 2017

1 reference

Europe PubMed Central

The apolipoprotein L1 (APOL1) gene and nondiabetic nephropathy in African Americans (English)

1 reference

Europe PubMed Central

PubMed publication ID

23 August 2017

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Jeffrey B. Kopp

object named as

Jeffrey B Kopp

2

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Cheryl A Winkler

7

object named as

Cheryl A Winkler

1 reference

Europe PubMed Central

PubMed publication ID

23 August 2017

Carl D. Langefeld

3

object named as

Carl D Langefeld

1 reference

Europe PubMed Central

PubMed publication ID

23 August 2017

1

object named as

Barry I Freedman

1 reference

Europe PubMed Central

PubMed publication ID

23 August 2017

Donald W Bowden

8

object named as

Donald W Bowden

1 reference

Europe PubMed Central

PubMed publication ID

23 August 2017

Giulio Genovese

4

object named as

Giulio Genovese

1 reference

Europe PubMed Central

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23 August 2017

author name string

David J Friedman

5

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Europe PubMed Central

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23 August 2017

George W Nelson

6

1 reference

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23 August 2017

Martin R Pollak

9

1 reference

Europe PubMed Central

PubMed publication ID

23 August 2017

publication date

5 August 2010

1 reference

Europe PubMed Central

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23 August 2017

Journal of the American Society of Nephrology

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Europe PubMed Central

PubMed publication ID

23 August 2017

21

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Europe PubMed Central

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23 August 2017

9

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Europe PubMed Central

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23 August 2017

1422-1426

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Europe PubMed Central

PubMed publication ID

23 August 2017

Association of trypanolytic ApoL1 variants with kidney disease in African Americans

1 reference

https://pubmed.ncbi.nlm.nih.gov/20688934

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium

1 reference

https://pubmed.ncbi.nlm.nih.gov/20688934

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Dense mapping of MYH9 localizes the strongest kidney disease associations to the region of introns 13 to 15.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20688934

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The apolipoprotein L gene cluster has emerged recently in evolution and is expressed in human vascular tissue

1 reference

https://pubmed.ncbi.nlm.nih.gov/20688934

12 December 2020

based on heuristic

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High prevalence of sickle cell trait in African Americans with ESRD.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20688934

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A High-Density Admixture Map for Disease Gene Discovery in African Americans

1 reference

https://pubmed.ncbi.nlm.nih.gov/20688934

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphisms in the non-muscle myosin heavy chain 9 gene (MYH9) are strongly associated with end-stage renal disease historically attributed to hypertension in African Americans

1 reference

https://pubmed.ncbi.nlm.nih.gov/20688934

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene

1 reference

https://pubmed.ncbi.nlm.nih.gov/20688934

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The function of apolipoproteins L.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20688934

12 December 2020

based on heuristic

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Human red blood cell polymorphisms and malaria

1 reference

https://pubmed.ncbi.nlm.nih.gov/20688934

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MYH9 is a major-effect risk gene for focal segmental glomerulosclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/20688934

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

MYH9 is associated with nondiabetic end-stage renal disease in African Americans

1 reference

https://pubmed.ncbi.nlm.nih.gov/20688934

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Apolipoprotein L1, a novel Bcl-2 homology domain 3-only lipid-binding protein, induces autophagic cell death

1 reference

https://pubmed.ncbi.nlm.nih.gov/20688934

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Worldwide distribution of the MYH9 kidney disease susceptibility alleles and haplotypes: evidence of historical selection in Africa

1 reference

https://pubmed.ncbi.nlm.nih.gov/20688934

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypertension-associated kidney disease: perhaps no more

1 reference

https://pubmed.ncbi.nlm.nih.gov/20688934

12 December 2020

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inferred from PubMed ID database lookup

Autophagy influences glomerular disease susceptibility and maintains podocyte homeostasis in aging mice

1 reference

https://pubmed.ncbi.nlm.nih.gov/20688934

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The spectrum of MYH9-associated nephropathy

1 reference

https://pubmed.ncbi.nlm.nih.gov/20688934

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1681/ASN.2010070730

1 reference

Europe PubMed Central

PubMed publication ID

23 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

23 August 2017

ResearchGate publication ID

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