A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2 (Q24291755)

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11 November 2019

title

A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2 (English)

1 reference

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amyotrophic lateral sclerosis

11 November 2019

main subject

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corrigendum / erratum

Erratum: A gene encoding a putative GTPase regulator is mutated in familial amyotrophic lateral sclerosis 2

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author

Collette Hand

2

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11 November 2019

Asako Otomo

5

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11 November 2019

Roshni Singaraja

10

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11 November 2019

Stephen W. Scherer

18

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11 November 2019

Michael R. Hayden

20

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11 November 2019

19

Rouleau GA

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11 November 2019

author name string

Hadano S

1

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11 November 2019

Osuga H

3

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11 November 2019

Yanagisawa Y

4

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11 November 2019

Devon RS

6

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11 November 2019

Miyamoto N

7

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11 November 2019

Showguchi-Miyata J

8

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11 November 2019

Okada Y

9

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11 November 2019

Figlewicz DA

11

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11 November 2019

Kwiatkowski T

12

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11 November 2019

Hosler BA

13

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11 November 2019

Sagie T

14

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11 November 2019

Skaug J

15

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11 November 2019

Nasir J

16

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11 November 2019

Brown RH Jr

17

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11 November 2019

Ikeda JE

21

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11 November 2019

language of work or name

English

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publication date

1 October 2001

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11 November 2019

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11 November 2019

volume

29

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11 November 2019

page(s)

166-173

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11 November 2019

issue

2

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https://scigraph.springernature.com/pub.10.1038/ng1001-166

11 November 2019

exact match

0 references

cites work

Molecular genetic basis of familial ALS.

1 reference

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7 January 2021

Linkage of a gene causing familial amyotrophic lateral sclerosis to chromosome 21 and evidence of genetic-locus heterogeneity

1 reference

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7 January 2021

Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis

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7 January 2021

Linkage of the gene for an autosomal dominant form of juvenile amyotrophic lateral sclerosis to chromosome 9q34.

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7 January 2021

Linkage of recessive familial amyotrophic lateral sclerosis to chromosome 2q33-q35.

1 reference

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7 January 2021

Refined mapping and characterization of the recessive familial amyotrophic lateral sclerosis locus (ALS2) on chromosome 2q33

1 reference

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7 January 2021

Linkage of a commoner form of recessive amyotrophic lateral sclerosis to chromosome 15q15-q22 markers

1 reference

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7 January 2021

Linkage of familial amyotrophic lateral sclerosis with frontotemporal dementia to chromosome 9q21-q22

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7 January 2021

Hereditary motor system diseases (chronic juvenile amyotrophic lateral sclerosis). Conditions combining a bilateral pyramidal syndrome with limb and bulbar amyotrophy

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7 January 2021

A yeast artificial chromosome-based physical map of the juvenile amyotrophic lateral sclerosis (ALS2) critical region on human chromosome 2q33-q34

1 reference

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7 January 2021

Cloning and characterization of three novel genes, ALS2CR1, ALS2CR2, and ALS2CR3, in the juvenile amyotrophic lateral sclerosis (ALS2) critical region at chromosome 2q33-q34: candidate genes for ALS2.

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7 January 2021

Isolation and characterization of the active cDNA of the human cell cycle gene (RCC1) involved in the regulation of onset of chromosome condensation

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7 January 2021

Rho GTPases in neuronal morphogenesis

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7 January 2021

Infantile onset of hereditary ascending spastic paralysis with bulbar involvement

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7 January 2021

A gene (RPGR) with homology to the RCC1 guanine nucleotide exchange factor is mutated in X-linked retinitis pigmentosa (RP3)

1 reference

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7 January 2021

The 1.7 A crystal structure of the regulator of chromosome condensation (RCC1) reveals a seven-bladed propeller

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7 January 2021

Crystal structure of the Dbl and pleckstrin homology domains from the human Son of sevenless protein

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7 January 2021

Vps9p is a guanine nucleotide exchange factor involved in vesicle-mediated vacuolar protein transport

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7 January 2021

A novel Rab5 GDP/GTP exchange factor complexed to Rabaptin-5 links nucleotide exchange to effector recruitment and function

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7 January 2021

Ras-activated endocytosis is mediated by the Rab5 guanine nucleotide exchange activity of RIN1.

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7 January 2021

Generation of GTP-bound Ran by RCC1 is required for chromatin-induced mitotic spindle formation

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7 January 2021

The Rho GTPase and a putative RhoGEF mediate a signaling pathway for the cell shape changes in Drosophila gastrulation

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7 January 2021

Identification of a novel, putative Rho-specific GDP/GTP exchange factor and a RhoA-binding protein: control of neuronal morphology

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7 January 2021

The retinitis pigmentosa GTPase regulator (RPGR) interacts with novel transport-like proteins in the outer segments of rod photoreceptors

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7 January 2021

Kalirin, a cytosolic protein with spectrin-like and GDP/GTP exchange factor-like domains that interacts with peptidylglycine alpha-amidating monooxygenase, an integral membrane peptide-processing enzyme.

1 reference

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7 January 2021

Rho GTPases and the actin cytoskeleton

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7 January 2021

RNA surveillance. Unforeseen consequences for gene expression, inherited genetic disorders and cancer

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https://api.crossref.org/works/10.1038%2FNG1001-166

7 January 2021

Defective axonal transport in a transgenic mouse model of amyotrophic lateral sclerosis

1 reference

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7 January 2021

Slowing of axonal transport is a very early event in the toxicity of ALS-linked SOD1 mutants to motor neurons

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7 January 2021

Gapped BLAST and PSI-BLAST: a new generation of protein database search programs

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7 January 2021

Identifiers

DOI

10.1038/NG1001-166

2 references

Consolidated OpenCitations Corpus – April 2017

3544493

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11586298%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

11 November 2019

1007295188

0 references

3544493

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

2 references

3544493