Diagnosing FSGS without kidney biopsy - a novel INF2-mutation in a family with ESRD of unknown origin (Q36161793)

12 August 2017

0 references

Diagnosing FSGS without kidney biopsy - a novel INF2-mutation in a family with ESRD of unknown origin (English)

1 reference

12 August 2017

Johannes Münch

1

1 reference

12 August 2017

Maik Grohmann

2

1 reference

12 August 2017

Tom H Lindner

3

1 reference

12 August 2017

Carsten Bergmann

4

1 reference

12 August 2017

Jan Halbritter

5

1 reference

12 August 2017

12 October 2016

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12 August 2017

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12 August 2017

17

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12 August 2017

1

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12 August 2017

73

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A single-gene cause in 29.5% of cases of steroid-resistant nephrotic syndrome

12 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5062827

Inverted formin 2 regulates actin dynamics by antagonizing Rho/diaphanous-related formin signaling.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5062827

INF2 mutations in Charcot-Marie-Tooth disease with glomerulopathy

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5062827

Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5062827

Genetics of nephrotic syndrome: connecting molecular genetics to podocyte physiology

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5062827

Modification of mineralocorticoid receptor function by Rac1 GTPase: implication in proteinuric kidney disease

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5062827

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5062827

Staying in shape with formins

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5062827

Mutations in INF2 are a major cause of autosomal dominant focal segmental glomerulosclerosis

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5062827

Aldosterone modulates endothelial permeability and endothelial nitric oxide synthase activity by rearrangement of the actin cytoskeleton

2 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5062827

Novel INF2 mutations in an Italian cohort of patients with focal segmental glomerulosclerosis, renal failure and Charcot-Marie-Tooth neuropathy

23 September 2018

2 references

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=5062827

21 October 2018

https://api.crossref.org/works/10.1186%2FS12881-016-0336-9

Focal segmental glomerular sclerosis in adults: presentation, course, and response to treatment

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/27733133

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/S12881-016-0336-9

1 reference

12 August 2017

1 reference

12 August 2017

PubMed publication ID

27733133

1 reference