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Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis
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scholarly article
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title
Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis
(English)
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main subject
Inverted formin 2
1 reference
stated in
GOA release 2020-03-11
focal segmental glomerulosclerosis
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based on heuristic
inferred from title
corrigendum / erratum
Erratum: Corrigendum: Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis
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author
Joel M Henderson
object named as
Joel M Henderson
series ordinal
8
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Henry N. Higgs
object named as
Henry N Higgs
series ordinal
7
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Johannes Schlöndorff
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stated in
ORCID Public Data File 2021
author name string
Elizabeth J Brown
series ordinal
1
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Johannes S Schlöndorff
series ordinal
2
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Daniel J Becker
series ordinal
3
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Hiroyasu Tsukaguchi
series ordinal
4
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Stephen J Tonna
series ordinal
5
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Andrea L Uscinski
series ordinal
6
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Martin R Pollak
series ordinal
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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issue
1
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page(s)
72-6
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cites work
Autoinhibition regulates cellular localization and actin assembly activity of the diaphanous-related formins FRLalpha and mDia1.
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PubMed Central
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PubMed Central
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PubMed Central
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19 March 2017
Staying in shape with formins
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stated in
PubMed Central
reference URL
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19 March 2017
Mutations in ACTN4, encoding alpha-actinin-4, cause familial focal segmental glomerulosclerosis
1 reference
stated in
PubMed Central
reference URL
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19 March 2017
TRPC6 is a glomerular slit diaphragm-associated channel required for normal renal function
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PubMed Central
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The slit diaphragm: a signaling platform to regulate podocyte function
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19 March 2017
The mouse Formin mDia1 is a potent actin nucleation factor regulated by autoinhibition
1 reference
stated in
PubMed Central
reference URL
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19 March 2017
INF2 is an endoplasmic reticulum-associated formin protein.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2980844
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Actin up: regulation of podocyte structure and function by components of the actin cytoskeleton
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27 September 2017
INF2 Is a WASP homology 2 motif-containing formin that severs actin filaments and accelerates both polymerization and depolymerization.
1 reference
stated in
PubMed Central
reference URL
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27 September 2017
Structure of the autoinhibitory switch in formin mDia1.
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27 September 2017
Formin proteins: a domain-based approach.
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PubMed Central
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27 September 2017
A mutation in the TRPC6 cation channel causes familial focal segmental glomerulosclerosis
1 reference
stated in
PubMed Central
reference URL
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27 September 2017
Efficient multipoint linkage analysis through reduction of inheritance space
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27 September 2017
The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance
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27 September 2017
Differential distribution of the glutamate transporters GLT-1 and GLAST in tanycytes of the third ventricle
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30 May 2018
The regulation of mDia1 by autoinhibition and its release by Rho*GTP.
1 reference
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29 November 2018
Structural and mechanistic insights into the interaction between Rho and mammalian Dia.
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29 November 2018
Structural basis of actin filament nucleation and processive capping by a formin homology 2 domain
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2980844
retrieved
29 November 2018
Pathologic classification of focal segmental glomerulosclerosis: a working proposal
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2980844
retrieved
29 November 2018
Faster linkage analysis computations for pedigrees with loops or unused alleles.
1 reference
stated in
PubMed Central
reference URL
https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2980844
retrieved
29 November 2018
Identifiers
DOI
10.1038/NG.505
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3022766
Dimensions Publication ID
1044676559
0 references
OpenCitations bibliographic resource ID
3022766
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3022766
PMC publication ID
2980844
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3022766
PubMed publication ID
20023659
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
3022766
ResearchGate publication ID
40731149
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