Podocyte-specific knockout of myosin 1e disrupts glomerular filtration (Q36312646)

13 August 2017

Podocyte-specific knockout of myosin 1e disrupts glomerular filtration (English)

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13 August 2017

Mira Krendel

6

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author name string

Sharon E Chase

1

1 reference

13 August 2017

Christina V Encina

2

1 reference

13 August 2017

Lindsay R Stolzenburg

3

1 reference

13 August 2017

Arthur H Tatum

4

1 reference

13 August 2017

Lawrence B Holzman

5

1 reference

13 August 2017

18 July 2012

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American Journal of Physiology - Renal Physiology

13 August 2017

1 reference

13 August 2017

303

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13 August 2017

7

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13 August 2017

F1099-106

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describes a project that uses

13 August 2017

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC3469681/fullTextXML

based on heuristic

inferred from PubMed Central ID database lookup

cites work

The podocyte cytoskeleton--key to a functioning glomerulus in health and disease

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469681

CD2AP in mouse and human podocytes controls a proteolytic program that regulates cytoskeletal structure and cellular survival

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469681

Glomerular proteinuria: a complex interplay between unique players

30 September 2017

1 reference

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MYO1E mutations and childhood familial focal segmental glomerulosclerosis

30 September 2017

1 reference

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Podocyte-specific deletion of Myh9 encoding nonmuscle myosin heavy chain 2A predisposes mice to glomerulopathy.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469681

Motor protein Myo1c is a podocyte protein that facilitates the transport of slit diaphragm protein Neph1 to the podocyte membrane

30 September 2017

1 reference

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Cofilin-1 inactivation leads to proteinuria--studies in zebrafish, mice and humans

30 September 2017

1 reference

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Actin-depolymerizing factor cofilin-1 is necessary in maintaining mature podocyte architecture

30 September 2017

1 reference

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Patients with Epstein-Fechtner syndromes owing to MYH9 R702 mutations develop progressive proteinuric renal disease

30 September 2017

1 reference

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The mesangial cell revisited: no cell is an island

30 September 2017

1 reference

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Disruption of Myosin 1e promotes podocyte injury

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469681

Deletion of CD151 results in a strain-dependent glomerular disease due to severe alterations of the glomerular basement membrane

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469681

The actin cytoskeleton of kidney podocytes is a direct target of the antiproteinuric effect of cyclosporine A.

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469681

Actin up: regulation of podocyte structure and function by components of the actin cytoskeleton

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469681

Hereditary proteinuria syndromes and mechanisms of proteinuria

30 September 2017

1 reference

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Nephrin ectodomain engagement results in Src kinase activation, nephrin phosphorylation, Nck recruitment, and actin polymerization

30 September 2017

1 reference

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Nck adaptor proteins link nephrin to the actin cytoskeleton of kidney podocytes

30 September 2017

1 reference

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CD2AP localizes to the slit diaphragm and binds to nephrin via a novel C-terminal domain

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469681

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469681

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

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469681

Human brush border myosin-I and myosin-Ic expression in human intestine and Caco-2BBe cells

30 September 2017

1 reference

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Quantitative trait loci influence renal disease progression in a mouse model of Alport syndrome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3469681

Podocyte-specific expression of cre recombinase in transgenic mice

29 June 2018

1 reference

Crossref

https://api.crossref.org/works/10.1152%2FAJPRENAL.00251.2012

Exome sequencing identified MYO1E and NEIL1 as candidate genes for human autosomal recessive steroid-resistant nephrotic syndrome

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.1152%2FAJPRENAL.00251.2012

10.1152/AJPRENAL.00251.2012

21 January 2018

Identifiers

DOI

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13 August 2017

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13 August 2017

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