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

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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17 September 2022

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Mariapia A Degli-Esposti

1

object named as

M. A. Degli-Esposti

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17 September 2022

author name string

A. Andreas

2

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17 September 2022

F. T. Christiansen

3

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17 September 2022

B. Schalke

4

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17 September 2022

E. Albert

5

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17 September 2022

R. L. Dawkins

6

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17 September 2022

language of work or name

English

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publication date

1 January 1992

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24 November 2017

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24 November 2017

volume

35

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24 November 2017

issue

6

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24 November 2017

page(s)

355-364

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

24 November 2017

cites work

1 reference

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

12 December 2020

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

1 reference

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

12 December 2020

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

1 reference

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

12 December 2020

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

1 reference

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

12 December 2020

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

1 reference

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

12 December 2020

Usefulness of densitometry in typing of human complement component C4

1 reference

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

12 December 2020

Haplotypic polymorphisms of the TNFB gene

1 reference

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

12 December 2020

HLA-DQ beta-chain polymorphism linked to myasthenia gravis

1 reference

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

12 December 2020

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

1 reference

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

12 December 2020

Enhancement of in vivo immune response by tumor necrosis factor

1 reference

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

12 December 2020

Brief summary of Ninth International Histocompatibility Workshop.

1 reference

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

12 December 2020

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

1 reference

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

12 December 2020

The diagnostic significance of autoantibodies to the acetylcholine receptor

1 reference

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

12 December 2020

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

1 reference

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

12 December 2020

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

1 reference

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

12 December 2020

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

1 reference

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

12 December 2020

Disease associations with complotypes, supratypes and haplotypes

1 reference

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

12 December 2020

Rapid transfer of DNA from agarose gels to nylon membranes

1 reference

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

12 December 2020

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

1 reference

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

12 December 2020

HLA and Disease 1982 - A Survey

1 reference

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

12 December 2020

Autoimmune Response to Acetylcholine Receptor

1 reference

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

12 December 2020

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

1 reference

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

12 December 2020

Myasthenia gravis and HLA antigens in American blacks and other races

1 reference

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

12 December 2020

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

1 reference

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

12 December 2020

C4 allotyping on plasma or serum: application to routine laboratories

1 reference

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

12 December 2020

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

1 reference

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

12 December 2020

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

1 reference

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

12 December 2020

HLA and disease--the perils of simplification

1 reference

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

12 December 2020

Structure of human steroid 21-hydroxylase genes

1 reference

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

12 December 2020

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

1 reference

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

12 December 2020

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

1 reference

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

12 December 2020

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

1 reference

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

12 December 2020

Characterization of frequent deletions causing steroid 21-hydroxylase deficiency

1 reference

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

12 December 2020

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

1 reference

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

12 December 2020

Genetic polymorphism in human glycine-rich beta-glycoprotein

1 reference

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

12 December 2020

Complement allotyping in SLE: association with C4A null

1 reference

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

12 December 2020

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

1 reference

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

12 December 2020

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

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

12 December 2020

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

1 reference

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

12 December 2020

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

1 reference

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

12 December 2020

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

1 reference

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

12 December 2020

Central MHC genes, IgA deficiency and autoimmune disease

1 reference

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

12 December 2020

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

1 reference

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

12 December 2020

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

1 reference

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

12 December 2020

Identifiers

DOI

10.1007/BF00179791

1 reference

24 November 2017

1 reference