(Q33405616)

English

An extension to a statistical approach for family based association studies provides insights into genetic risk factors for multiple sclerosis in the HLA-DRB1 gene

scientific article published on 4 February 2009

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

1 July 2019

http://europepmc.org/abstract/PMC/2669470

An extension to a statistical approach for family based association studies provides insights into genetic risk factors for multiple sclerosis in the HLA-DRB1 gene (English)

1 reference

Europe PubMed Central

PMC publication ID

1 July 2019

http://europepmc.org/abstract/PMC/2669470

single-nucleotide polymorphism

1 reference

based on heuristic

inferred from title

3

1 reference

Europe PubMed Central

PMC publication ID

12 April 2018

http://europepmc.org/abstract/PMC/2656522

author name string

Sreeram V Ramagopalan

1

1 reference

Europe PubMed Central

PMC publication ID

1 July 2019

http://europepmc.org/abstract/PMC/2669470

Roisin McMahon

2

1 reference

Europe PubMed Central

PMC publication ID

1 July 2019

http://europepmc.org/abstract/PMC/2669470

A Dessa Sadovnick

4

1 reference

Europe PubMed Central

PMC publication ID

1 July 2019

http://europepmc.org/abstract/PMC/2669470

George C Ebers

5

1 reference

Europe PubMed Central

PMC publication ID

1 July 2019

http://europepmc.org/abstract/PMC/2669470

Knut M Wittkowski

6

1 reference

Europe PubMed Central

PMC publication ID

1 July 2019

http://europepmc.org/abstract/PMC/2669470

publication date

4 February 2009

1 reference

Europe PubMed Central

PMC publication ID

1 July 2019

http://europepmc.org/abstract/PMC/2669470

BMC Medical Genetics

1 reference

Europe PubMed Central

PMC publication ID

1 July 2019

http://europepmc.org/abstract/PMC/2669470

10

1 reference

Europe PubMed Central

PMC publication ID

1 July 2019

http://europepmc.org/abstract/PMC/2669470

10

1 reference

Europe PubMed Central

PMC publication ID

1 July 2019

http://europepmc.org/abstract/PMC/2669470

ChickVD: a sequence variation database for the chicken genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2656522

4 July 2018

Calpain 3 is activated through autolysis within the active site and lyses sarcomeric and sarcolemmal components

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2656522

4 July 2018

The calpain system

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2656522

4 July 2018

A New Statistical Method for Haplotype Reconstruction from Population Data

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2656522

4 July 2018

Expression and functional characteristics of calpain 3 isoforms generated through tissue-specific transcriptional and posttranscriptional events

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2656522

4 July 2018

Evidence for implication of muscle-specific calpain (p94) in myofibrillar integrity.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2656522

4 July 2018

Mutations in the proteolytic enzyme calpain 3 cause limb-girdle muscular dystrophy type 2A

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2656522

4 July 2018

Is Z-disk degradation responsible for postmortem tenderization?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2656522

4 July 2018

Molecular cloning of a novel mammalian calcium-dependent protease distinct from both m- and mu-types. Specific expression of the mRNA in skeletal muscle

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2656522

4 July 2018

Multiple sclerosis

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-10

21 January 2018

Environmental factors and multiple sclerosis.

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-10

21 January 2018

Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-10

21 January 2018

Risk alleles for multiple sclerosis identified by a genomewide study

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-10

21 January 2018

The multiple sclerosis- and narcolepsy-associated HLA class II haplotype includes the DRB5*0101 allele

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-10

21 January 2018

The inheritance of resistance alleles in multiple sclerosis

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-10

21 January 2018

The exogenous pathway for antigen presentation on major histocompatibility complex class II and CD1 molecules

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-10

21 January 2018

MHC class II proteins and disease: a structural perspective

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-10

21 January 2018

HLA-DR and -DQ allelic sequences in multiple sclerosis patients are identical to those found in the general population

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-10

21 January 2018

Heterogeneity at the HLA-DRB1 locus and risk for multiple sclerosis

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-10

21 January 2018

IMGT/HLA and IMGT/MHC: sequence databases for the study of the major histocompatibility complex

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-10

21 January 2018

A statistically valid alternative to the TDT

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-10

21 January 2018

The TDT is a statistically valid test: comments on Wittkowski and Liu

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-10

21 January 2018

From genotypes to genes: doubling the sample size

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-10

21 January 2018

HLA class I alleles tag HLA-DRB1*1501 haplotypes for differential risk in multiple sclerosis susceptibility

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-10

21 January 2018

EVI5 is a risk gene for multiple sclerosis

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-10

21 January 2018

A predominant role for the HLA class II region in the association of the MHC region with multiple sclerosis

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-10

21 January 2018

Complex interactions among MHC haplotypes in multiple sclerosis: susceptibility and resistance

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-10

21 January 2018

Friedman-Type Statistics and Consistent Multiple Comparisons for Unbalanced Designs with Missing Data

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-10

21 January 2018

Study on association of single nucleotide polymorphism of CAPN1 gene with muscle fibre and carcass traits in quality chicken populations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2656522

31 October 2018

Possible regulation of the conventional calpain system by skeletal muscle-specific calpain, p94/calpain 3.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2656522

31 October 2018

High-resolution haplotype structure in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2656522

31 October 2018

Calpain 3 mRNA expression in mice after denervation and during muscle regeneration

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2656522

31 October 2018

Calpainopathy-a survey of mutations and polymorphisms

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2656522

31 October 2018

Multiple sclerosis associated amino acids of polymorphic regions relevant for the HLA antigen binding are confined to HLA-DR2

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-10

21 January 2018

Genes for multiple sclerosis

1 reference

https://api.crossref.org/works/10.1186%2F1471-2350-10-10

21 January 2018

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/19193207

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transmission of class I/II multi-locus MHC haplotypes and multiple sclerosis susceptibility: accounting for linkage disequilibrium

1 reference

https://pubmed.ncbi.nlm.nih.gov/19193207

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The genetics of multiple sclerosis: SNPs to pathways to pathogenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19193207

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HLA-DR typing by PCR amplification with sequence-specific primers (PCR-SSP) in 2 hours: an alternative to serological DR typing in clinical practice including donor-recipient matching in cadaveric transplantation

1 reference

https://pubmed.ncbi.nlm.nih.gov/19193207

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM)

1 reference

https://pubmed.ncbi.nlm.nih.gov/19193207

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Association of susceptibility to multiple sclerosis in Sweden with HLA class II DRB1 and DQB1 alleles

1 reference

https://pubmed.ncbi.nlm.nih.gov/19193207

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Importance of HLA-DRB1 and DQA1 genes and of the amino acid polymorphisms in the functional domain of DR beta 1 chain in multiple sclerosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/19193207

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Canadian collaborative project on genetic susceptibility to MS, phase 2: rationale and method. Canadian Collaborative Study Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/19193207

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The DRB1 Val86/Val86 genotype associates with multiple sclerosis in Australian patients

1 reference

https://pubmed.ncbi.nlm.nih.gov/19193207

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1471-2350-10-10

1 reference

https://api.fatcat.wiki/v0/release/myhkd2v27jcnzhbqdewankdd5y

30 July 2022

based on heuristic

mapped directly with Wikidata item

Dimensions Publication ID

1 reference

https://scigraph.springernature.com/pub.10.1186/1471-2350-10-10

9 September 2019

release_myhkd2v27jcnzhbqdewankdd5y

1 reference

https://api.fatcat.wiki/v0/release/myhkd2v27jcnzhbqdewankdd5y

30 July 2022

based on heuristic

mapped directly with Wikidata item

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

1 July 2019

http://europepmc.org/abstract/PMC/2669470

1 reference

https://api.fatcat.wiki/v0/release/myhkd2v27jcnzhbqdewankdd5y

30 July 2022

based on heuristic

mapped directly with Wikidata item

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

1 July 2019

http://europepmc.org/abstract/PMC/2669470

1 reference

https://api.fatcat.wiki/v0/release/myhkd2v27jcnzhbqdewankdd5y

30 July 2022

based on heuristic

mapped directly with Wikidata item

ResearchGate publication ID

0 references

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