Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis (Q24292947)

focal segmental glomerulosclerosis

GOA release 2020-03-11

1 reference

based on heuristic

inferred from title

corrigendum / erratum

Erratum: Corrigendum: Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis

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Joel M Henderson

8

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Henry N. Higgs

object named as

Henry N Higgs

7

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Johannes Schlöndorff

1 reference

ORCID Public Data File 2021

author name string

Elizabeth J Brown

1

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Johannes S Schlöndorff

2

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Daniel J Becker

3

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Hiroyasu Tsukaguchi

4

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Stephen J Tonna

5

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Andrea L Uscinski

6

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Martin R Pollak

Autoinhibition regulates cellular localization and actin assembly activity of the diaphanous-related formins FRLalpha and mDia1.

9

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language of work or name

English

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publication date

January 2010

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published in

Nature Genetics

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volume

42

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page(s)

72-6

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issue

1

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cites work

1 reference

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19 March 2017

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19 March 2017

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Staying in shape with formins

19 March 2017

1 reference

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

19 March 2017

1 reference

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

19 March 2017

1 reference

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The slit diaphragm: a signaling platform to regulate podocyte function

19 March 2017

1 reference

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The mouse Formin mDia1 is a potent actin nucleation factor regulated by autoinhibition

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2980844

INF2 is an endoplasmic reticulum-associated formin protein.

19 March 2017

1 reference

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

27 September 2017

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

27 September 2017

1 reference

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Structure of the autoinhibitory switch in formin mDia1.

27 September 2017

1 reference

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Formin proteins: a domain-based approach.

27 September 2017

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

27 September 2017

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27 September 2017

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The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance

27 September 2017

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Differential distribution of the glutamate transporters GLT-1 and GLAST in tanycytes of the third ventricle

27 September 2017

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The regulation of mDia1 by autoinhibition and its release by Rho*GTP.

30 May 2018

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Structural and mechanistic insights into the interaction between Rho and mammalian Dia.

29 November 2018

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Structural basis of actin filament nucleation and processive capping by a formin homology 2 domain

29 November 2018

1 reference

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Pathologic classification of focal segmental glomerulosclerosis: a working proposal

29 November 2018

1 reference

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Faster linkage analysis computations for pedigrees with loops or unused alleles.

29 November 2018

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29 November 2018

Identifiers

DOI

10.1038/NG.505

1 reference

Dimensions Publication ID

3022766

1044676559

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3022766

1 reference

1 reference

1 reference