(Q33905231)

29 July 2017

0 references

Identification of two novel loci for dominantly inherited familial amyotrophic lateral sclerosis (English)

1 reference

amyotrophic lateral sclerosis

29 July 2017

main subject

0 references

3

Diane McKenna-Yasek

0 references

Margaret A. Pericak-Vance

13

object named as

Margaret Pericak-Vance

1 reference

29 July 2017

12

Jonathan L Haines

1 reference

29 July 2017

15

H Robert Horvitz

1 reference

29 July 2017

16

Robert H Brown

1 reference

29 July 2017

Peter C Sapp

1

1 reference

29 July 2017

Betsy A Hosler

2

1 reference

29 July 2017

Wendy Chin

4

1 reference

29 July 2017

Amity Gann

5

1 reference

29 July 2017

Hilary Genise

6

1 reference

29 July 2017

Julie Gorenstein

7

1 reference

29 July 2017

Michael Huang

8

1 reference

29 July 2017

Wen Sailer

9

1 reference

29 July 2017

Meg Scheffler

10

1 reference

29 July 2017

Marianne Valesky

11

1 reference

29 July 2017

Teepu Siddique

14

1 reference

29 July 2017

language of work or name

English

0 references

publication date

9 July 2003

1 reference

American Journal of Human Genetics

29 July 2017

published in

1 reference

29 July 2017

volume

73

1 reference

29 July 2017

issue

2

1 reference

29 July 2017

page(s)

397-403

1 reference

Focal loss of the glutamate transporter EAAT2 in a transgenic rat model of SOD1 mutant-mediated amyotrophic lateral sclerosis (ALS).

29 July 2017

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180377

A novel locus for familial amyotrophic lateral sclerosis, on chromosome 18q

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180377

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180377

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180377

Descent graphs in pedigree analysis: applications to haplotyping, location scores, and marker-sharing statistics

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180377

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

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180377

Motor neuron degeneration in mice that express a human Cu,Zn superoxide dismutase mutation

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180377

Transgenic mice expressing an altered murine superoxide dismutase gene provide an animal model of amyotrophic lateral sclerosis

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180377

Strategies for multilocus linkage analysis in humans

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180377

Construction of human linkage maps: likelihood calculations for multilocus linkage analysis.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180377

Estimating the power of a proposed linkage study for a complex genetic trait.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180377

Mutant dynactin in motor neuron disease.

5 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180377

El Escorial World Federation of Neurology criteria for the diagnosis of amyotrophic lateral sclerosis. Subcommittee on Motor Neuron Diseases/Amyotrophic Lateral Sclerosis of the World Federation of Neurology Research Group on Neuromuscular Diseases a

29 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1180377

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

29 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12858291

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Rats expressing human cytosolic copper-zinc superoxide dismutase transgenes with amyotrophic lateral sclerosis: associated mutations develop motor neuron disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12858291

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

An adverse property of a familial ALS-linked SOD1 mutation causes motor neuron disease characterized by vacuolar degeneration of mitochondria

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/12858291

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1086/377158

1 reference

29 July 2017

1 reference

29 July 2017

1 reference