Reduced expression of the Kinesin-Associated Protein 3 (KIFAP3) gene increases survival in sporadic amyotrophic lateral sclerosis (Q28943310)

43

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Pilar Galan

40

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Shaun Purcell

Ildefonso Rodriguez-Leyva

44

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19

Ildefonso Rodriguez-Leyva

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Claire L Simpson

Claire L. Simpson

34

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Nicola Ticozzi

Nicola Ticozzi

16

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Vincenzo Silani

Vincenzo Silani

17

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Ammar Al-Chalabi

Ammar Al-Chalabi

45

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Orla Hardiman

Orla Hardiman

30

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Vincent Meininger

3

Vincent Meininger

1 reference

14 March 2017

Leonard H van den Berg

5

Leonard H. van den Berg

1 reference

14 March 2017

20

Jan H. Veldink

1 reference

14 March 2017

46

Robert H. Brown

1 reference

14 March 2017

37

Philippe Corcia

1 reference

14 March 2017

32

P. Nigel Leigh

1 reference

14 March 2017

42

H. Robert Horvitz

1 reference

14 March 2017

26

John H. J. Wokke

1 reference

14 March 2017

1

John E. Landers

1 reference

14 March 2017

2

Judith Melki

1 reference

14 March 2017

Jonathan D. Glass

4

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14 March 2017

Michael A. van Es

6

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14 March 2017

Peter C. Sapp

7

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14 March 2017

Paul W. J. van Vught

8

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14 March 2017

Diane M. McKenna-Yasek

9

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Hylke M. Blauw

10

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14 March 2017

Ting-Jan Cho

11

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14 March 2017

Meraida Polak

12

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Lijia Shi

13

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Anne-Marie Wills

14

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14 March 2017

Wendy J. Broom

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Aslihan Ozoguz

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Adrian J. Ivinson

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Betsy A. Hosler

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Alayna Barnes-Nessa

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Nicole Couture

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Thomas J. Kwiatkowski

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Roel A. Ophoff

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Simon Cronin

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Frank P. Diekstra

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Christopher E. Shaw

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Valerie K. Hansen

35

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John F. Powell

36

1 reference

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François Salachas

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Simon Heath

39

1 reference

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Franck Georges

Proceedings of the National Academy of Sciences of the United States of America

41

1 reference

14 March 2017

language of work or name

English

0 references

publication date

2 June 2009

1 reference

14 March 2017

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14 March 2017

106

1 reference

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9004–9009

1 reference

14 March 2017

22

1 reference

14 March 2017

Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683883

Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683883

TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683883

ITPR2 as a susceptibility gene in sporadic amyotrophic lateral sclerosis: a genome-wide association study

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683883

Whole-genome analysis of sporadic amyotrophic lateral sclerosis

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683883

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683883

Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683883

Differential expression of molecular motors in the motor cortex of sporadic ALS

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683883

Genome-wide genotyping in amyotrophic lateral sclerosis and neurologically normal controls: first stage analysis and public release of data

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683883

A genome-wide association study identifies novel risk loci for type 2 diabetes

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683883

A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683883

DNA/RNA helicase gene mutations in a form of juvenile amyotrophic lateral sclerosis (ALS4)

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683883

Sp1- and Krüppel-like transcription factors

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683883

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

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683883

The gene encoding alsin, a protein with three guanine-nucleotide exchange factor domains, is mutated in a form of recessive amyotrophic lateral sclerosis

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683883

Charcot-Marie-Tooth disease type 2A caused by mutation in a microtubule motor KIF1Bbeta

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683883

Epidemiology of mutations in superoxide dismutase in amyotrophic lateral sclerosis

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683883

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

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683883

A genome-wide association study of type 2 diabetes in Finns detects multiple susceptibility variants

16 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683883

Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683883

TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683883

Risk alleles for multiple sclerosis identified by a genomewide study

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683883

A variant in CDKAL1 influences insulin response and risk of type 2 diabetes

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683883

Joint analysis is more efficient than replication-based analysis for two-stage genome-wide association studies

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683883

Mutant SOD1 impairs axonal transport of choline acetyltransferase and acetylcholine release by sequestering KAP3

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683883

Variants of the elongator protein 3 (ELP3) gene are associated with motor neuron degeneration

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683883

Genetic variation in DPP6 is associated with susceptibility to amyotrophic lateral sclerosis

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683883

Genome-wide association studies provide new insights into type 2 diabetes aetiology

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683883

Interleukin 7 receptor alpha chain (IL7R) shows allelic and functional association with multiple sclerosis

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683883

Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individuals

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683883

Increased incidence of the Hfe mutation in amyotrophic lateral sclerosis and related cellular consequences

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683883

Stirring up development with the heterotrimeric kinesin KIF3.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683883

Amyotrophic lateral sclerosis: Part 1. Clinical features, pathology, and ethical issues in management.

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683883

Amyotrophic lateral sclerosis: Part 2. Etiopathogenesis

3 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2683883

Mutant dynactin in motor neuron disease.

3 June 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0812937106

ANG mutations segregate with familial and 'sporadic' amyotrophic lateral sclerosis.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0812937106

VEGF is a modifier of amyotrophic lateral sclerosis in mice and humans and protects motoneurons against ischemic death

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0812937106

A genome-wide association study of sporadic ALS in a homogenous Irish population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0812937106

Variation in interleukin 7 receptor α chain (IL7R) influences risk of multiple sclerosis

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0812937106

When domestiques rebel: kinesins, cadherins and neuronal proliferation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0812937106

Mutations in dynein link motor neuron degeneration to defects in retrograde transport

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.0812937106

Paraoxonase cluster polymorphisms are associated with sporadic ALS

21 January 2018

1 reference

12 December 2020

Paraoxonase gene polymorphisms and sporadic ALS

1 reference

12 December 2020

Differential screening of mutated SOD1 transgenic mice reveals early up-regulation of a fast axonal transport component in spinal cord motor neurons

1 reference

12 December 2020

Homozygous deletion of the survival motor neuron 2 gene is a prognostic factor in sporadic ALS

1 reference

12 December 2020

Familial adult motor neuron disease: amyotrophic lateral sclerosis

1 reference

12 December 2020

Association between centromeric deletions of the SMN gene and sporadic adult-onset lower motor neuron disease

1 reference

12 December 2020

Identifiers

DOI

10.1073/PNAS.0812937106

1 reference

1706279

ADS bibcode

2009PNAS..106.9004L

0 references

1706279

1 reference

1 reference

1 reference