(Q38482164)

English

Variable renal phenotype in a family with an INF2 mutation

scientific article published on 28 August 2010

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Variable renal phenotype in a family with an INF2 mutation (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

1 reference

based on heuristic

inferred from title

author name string

Hyun Kyung Lee

1

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Kyoung Hee Han

2

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Europe PubMed Central

PubMed publication ID

3 September 2017

Yun Hye Jung

3

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Hee Gyung Kang

4

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Kyung Chul Moon

5

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Il Soo Ha

6

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Yong Choi

7

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Hae Il Cheong

8

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

publication date

28 August 2010

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Pediatric Nephrology

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Europe PubMed Central

PubMed publication ID

3 September 2017

26

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PubMed publication ID

3 September 2017

1

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3 September 2017

73-76

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Europe PubMed Central

PubMed publication ID

3 September 2017

https://scigraph.springernature.com/pub.10.1007/s00467-010-1644-5

0 references

Genetics of nephrotic syndrome: connecting molecular genetics to podocyte physiology

1 reference

https://pubmed.ncbi.nlm.nih.gov/20803156

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/20803156

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

INF2 Is a WASP homology 2 motif-containing formin that severs actin filaments and accelerates both polymerization and depolymerization.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20803156

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic kidney diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/20803156

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/20803156

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

TRPC6 is a glomerular slit diaphragm-associated channel required for normal renal function

1 reference

https://pubmed.ncbi.nlm.nih.gov/20803156

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular genetic analysis of podocyte genes in focal segmental glomerulosclerosis--a review

1 reference

https://pubmed.ncbi.nlm.nih.gov/20803156

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

INF2 is an endoplasmic reticulum-associated formin protein.

1 reference

https://pubmed.ncbi.nlm.nih.gov/20803156

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Staying in shape with formins

1 reference

https://pubmed.ncbi.nlm.nih.gov/20803156

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/20803156

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary proteinuria syndromes and mechanisms of proteinuria

1 reference

https://pubmed.ncbi.nlm.nih.gov/20803156

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

WT1 and glomerular diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/20803156

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Nephrotic syndrome in the first year of life: two thirds of cases are caused by mutations in 4 genes (NPHS1, NPHS2, WT1, and LAMB2).

1 reference

https://pubmed.ncbi.nlm.nih.gov/20803156

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/S00467-010-1644-5

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

Dimensions Publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 September 2017

ResearchGate publication ID

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