An approach to the localization of the susceptibility genes for generalized myasthenia gravis by mapping recombinant ancestral haplotypes (Q43491662)

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scientific article published on January 1, 1992

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English	An approach to the localization of the susceptibility genes for generalized myasthenia gravis by mapping recombinant ancestral haplotypes	scientific article published on January 1, 1992

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scholarly article

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Europe PubMed Central

PubMed publication ID

1349584

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24 November 2017

title

An approach to the localization of the susceptibility genes for generalized myasthenia gravis by mapping recombinant ancestral haplotypes (English)

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stated in

Europe PubMed Central

PubMed publication ID

1349584

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1349584

retrieved

17 September 2022

main subject

myasthenia gravis

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author

Mariapia A Degli-Esposti

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1

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M. A. Degli-Esposti

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Europe PubMed Central

PubMed publication ID

1349584

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1349584

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17 September 2022

author name string

A. Andreas

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2

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Europe PubMed Central

PubMed publication ID

1349584

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1349584

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17 September 2022

F. T. Christiansen

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3

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Europe PubMed Central

PubMed publication ID

1349584

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1349584

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17 September 2022

B. Schalke

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4

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Europe PubMed Central

PubMed publication ID

1349584

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1349584

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17 September 2022

E. Albert

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5

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Europe PubMed Central

PubMed publication ID

1349584

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1349584

retrieved

17 September 2022

R. L. Dawkins

series ordinal

6

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stated in

Europe PubMed Central

PubMed publication ID

1349584

reference URL

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1349584

retrieved

17 September 2022

language of work or name

English

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publication date

1 January 1992

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Europe PubMed Central

PubMed publication ID

1349584

retrieved

24 November 2017

published in

Immunogenetics

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Europe PubMed Central

PubMed publication ID

1349584

retrieved

24 November 2017

volume

35

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stated in

Europe PubMed Central

PubMed publication ID

1349584

retrieved

24 November 2017

issue

6

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stated in

Europe PubMed Central

PubMed publication ID

1349584

retrieved

24 November 2017

page(s)

355-364

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stated in

Europe PubMed Central

PubMed publication ID

1349584

retrieved

24 November 2017

cites work

HLA-A, -B, -C and -D antigens in male patients with myasthenia gravis

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1349584

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Susceptibility to IDDM is marked by MHC supratypes rather than individual alleles

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1349584

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12 December 2020

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inferred from PubMed ID database lookup

Extensive deletions and insertions in different MHC supratypes detected by pusled field gel electrophoresis

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/1349584

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prevalence of ankylosing spondylitis and radiological abnormalities of the sacroiliac joints in HLA-B27 positive individuals

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/1349584

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human major histocompatibility complex contains a minimum of 19 genes between the complement cluster and HLA-B

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/1349584

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Usefulness of densitometry in typing of human complement component C4

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1349584

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Haplotypic polymorphisms of the TNFB gene

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1349584

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HLA-DQ beta-chain polymorphism linked to myasthenia gravis

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1349584

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

High Association of an HL-A Antigen, W27, with Ankylosing Spondylitis

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1349584

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Enhancement of in vivo immune response by tumor necrosis factor

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/1349584

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12 December 2020

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inferred from PubMed ID database lookup

Brief summary of Ninth International Histocompatibility Workshop.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/1349584

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of DR blank alleles by restriction fragment length polymorphism (RFLP)

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1349584

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The diagnostic significance of autoantibodies to the acetylcholine receptor

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1349584

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Different HLA DR-DQ associations in subgroups of idiopathic myasthenia gravis

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1349584

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Polymorphism of the human complement C4 and steroid 21-hydroxylase genes. Restriction fragment length polymorphisms revealing structural deletions, homoduplications, and size variants

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1349584

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A technique for radiolabeling DNA restriction endonuclease fragments to high specific activity

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1349584

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Disease associations with complotypes, supratypes and haplotypes

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/1349584

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12 December 2020

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inferred from PubMed ID database lookup

Rapid transfer of DNA from agarose gels to nylon membranes

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/1349584

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human tumour necrosis factor: precursor structure, expression and homology to lymphotoxin

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/1349584

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HLA and Disease 1982 - A Survey

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1349584

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Autoimmune Response to Acetylcholine Receptor

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1349584

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rearrangement of 21-hydroxylase genes in disease-associated MHC supratypes

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1349584

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Myasthenia gravis and HLA antigens in American blacks and other races

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/1349584

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The structural basis of the multiple forms of human complement component C4.

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/1349584

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

C4 allotyping on plasma or serum: application to routine laboratories

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/1349584

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HLA antigens in Japanese patients with narcolepsy. All the patients were DR2 positive

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/1349584

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Possible evidence for a variant of myasthenia gravis based on HLA and acetylcholine receptor antibody in Chinese patients

1 reference

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/1349584

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HLA and disease--the perils of simplification

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1349584

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structure of human steroid 21-hydroxylase genes

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1349584

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular analysis distinguishes two HLA-DR3-bearing major histocompatibility complex extended haplotypes

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1349584

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Deletion of complement C4 and steroid 21-hydroxylase genes in the HLA class III region

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1349584

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HLA antigens and acetylcholine receptor antibody in the subclassification of myasthenia gravis in Hong Kong Chinese

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1349584

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Characterization of frequent deletions causing steroid 21-hydroxylase deficiency

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1349584

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Some disease-associated ancestral haplotypes carry a polymorphism of TNF.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1349584

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic polymorphism in human glycine-rich beta-glycoprotein

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PubMed

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https://pubmed.ncbi.nlm.nih.gov/1349584

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Complement allotyping in SLE: association with C4A null

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1349584

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Extended HLA/complement allele haplotypes: evidence for T/t-like complex in man.

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1349584

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Pulsed field gel electrophoresis identifies a high degree of variability in the number of tandem 21-hydroxylase and complement C4 gene repeats in 21-hydroxylase deficiency haplotypes

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1349584

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Penicillamine-induced myasthenia in rheumatoid arthritis: its clinical and genetic features

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1349584

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12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Antibody to acetylcholine receptor in myasthenia gravis. Prevalence, clinical correlates, and diagnostic value

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1349584

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Differences in gene copy number carried by different MHC ancestral haplotypes. Quantitation after physical separation of haplotypes by pulsed field gel electrophoresis.

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1349584

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Central MHC genes, IgA deficiency and autoimmune disease

1 reference

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1349584

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HL-A8 and LD-8a in Patients with Myasthenia Gravis

1 reference

stated in

PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1349584

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Molecular genetic analysis of nonclassic steroid 21-hydroxylase deficiency associated with HLA-B14,DR1

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PubMed

reference URL

https://pubmed.ncbi.nlm.nih.gov/1349584

retrieved

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

DOI

10.1007/BF00179791

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1349584

retrieved

24 November 2017

PubMed publication ID

1349584

1 reference

stated in

Europe PubMed Central

PubMed publication ID

1349584

retrieved

24 November 2017

 

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