A locus for an autosomal dominant form of progressive renal failure and hypertension at chromosome 1q21. (Q34142642)

31 July 2017

A locus for an autosomal dominant form of progressive renal failure and hypertension at chromosome 1q21. (English)

1 reference

31 July 2017

5

Rechavi G

1 reference

31 July 2017

Cohn DH

1

1 reference

31 July 2017

Shohat T

2

1 reference

31 July 2017

Yahav M

3

1 reference

31 July 2017

Ilan T

4

1 reference

31 July 2017

King L

6

1 reference

31 July 2017

Shohat M

7

1 reference

31 July 2017

language of work or name

English

0 references

publication date

4 August 2000

1 reference

American Journal of Human Genetics

31 July 2017

1 reference

31 July 2017

67

1 reference

31 July 2017

3

1 reference

31 July 2017

647-651

1 reference

Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis

31 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287524

Identification of a new locus for medullary cystic disease, on chromosome 16p12.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287524

Hypertension, cardiac hypertrophy, and sudden death in mice lacking natriuretic peptide receptor A

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287524

Familial focal segmental glomerulosclerosis: nine cases in four families and review of the literature

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287524

PKD2, a gene for polycystic kidney disease that encodes an integral membrane protein

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287524

Liddle's syndrome: heritable human hypertension caused by mutations in the beta subunit of the epithelial sodium channel

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287524

Chromosomal distribution of three members of the human natriuretic peptide receptor/guanylyl cyclase gene family

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287524

Glucocorticoid-suppressible hyperaldosteronism results from hybrid genes created by unequal crossovers between CYP11B1 and CYP11B2

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287524

The polycystic kidney disease 1 gene encodes a 14 kb transcript and lies within a duplicated region on chromosome 16. The European Polycystic Kidney Disease Consortium

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1287524

Hereditary nephropathy without deafness

28 October 2018

1 reference

12 December 2020

Autosomal dominant Alport syndrome linked to the type IV collage alpha 3 and alpha 4 genes (COL4A3 and COL4A4)

1 reference

12 December 2020

Chromosome 1 localization of a gene for autosomal dominant medullary cystic kidney disease

1 reference

12 December 2020

Linkage of a Gene Causing Familial Focal Segmental Glomerulosclerosis to Chromosome 11 and Further Evidence of Genetic Heterogeneity

1 reference

12 December 2020

Functional deletion mutation of the 5'-flanking region of type A human natriuretic peptide receptor gene and its association with essential hypertension and left ventricular hypertrophy in the Japanese

1 reference

12 December 2020

Hereditary Occurrence of Cystic Disease of the Renal Medulla

1 reference

12 December 2020

1 reference

12 December 2020

Familial nephritis associated with the nephrotic syndrome. In a family with severe involvement in females

1 reference

12 December 2020

Familial interstitial nephritis

1 reference

12 December 2020

Familial thin basement membrane nephropathy in children with asymptomatic microhematuria

1 reference

12 December 2020

Identifiers

DOI

10.1086/303051

1 reference

release_tut2elnmwrf5djrtfqu4za6xpa

31 July 2017

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/tut2elnmwrf5djrtfqu4za6xpa

24 November 2022

mapped directly with Wikidata item

PMCID

1287524

1 reference

31 July 2017

1 reference