HLA phenotypes and gene polymorphisms in juvenile liver disease associated with α1-antitrypsin deficiency (Q58143773)

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21 September 2019

title

HLA phenotypes and gene polymorphisms in juvenile liver disease associated with alpha 1-antitrypsin deficiency (English)

1 reference

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21 September 2019

1 reference

1

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21 September 2019

author name string

P T Donaldson

2

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21 September 2019

D B Whitehouse

3

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21 September 2019

G Mieli-Vergani

4

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21 September 2019

A Duthie

5

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21 September 2019

D A Hopkinson

6

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A P Mowat

7

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21 September 2019

language of work or name

English

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publication date

1 August 1990

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21 September 2019

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volume

12

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issue

2

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page(s)

218-223

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Molecular basis of alpha-1-antitrypsin deficiency

21 September 2019

cites work

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Outcome of liver disease associated with alpha 1 antitrypsin deficiency (PiZ). Implications for genetic counselling and antenatal diagnosis

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Variation in alpha-1-antitrypsin phenotypes associated with penicillamine therapy

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The genetics of alpha1-antitrypsin: a family study in England and Scotland.

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The natural history of liver disease in alpha 1-antitrypsin deficient children

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Lymphocyte cytotoxicity to autologous hepatocytes in alpha 1-antitrypsin deficiency

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Association of primary sclerosing cholangitis with HLA-B8.

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HLA-DR antigens in HBsAg-positive chronic active liver disease with and without associated delta infection

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HLA A1-B8-DR3 and suppressor cell function in first-degree relatives of patients with autoimmune chronic active hepatitis

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HLA Determinants in Chronic Active Liver Disease: Possible Relation of HLA-Dw3 to Prognosis

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HLA A1, B8, DR3 extended haplotypes in autoimmune chronic hepatitis

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A highly polymorphic locus in human DNA

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Detection of specific sequences among DNA fragments separated by gel electrophoresis

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A DNA-RFLP typing system that positively identifies serologically well-defined and ill-defined HLA-DR and DQ alleles, including DRw10

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HLA-DR allogenotyping using exon-specific cDNA probes and application of rapid minigel methods

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Isolation and identification of a cDNA clone corresponding to an HLA-DR antigen beta chain

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7 January 2021

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

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7 January 2021

DNA-RFLP analysis and genotyping of HLA-DR and DQ antigens

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7 January 2021

HLA in juvenile liver disease with alpha-one-antitrypsin deficiency

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7 January 2021

Adult celiac disease associated with HLA-DRw3 and -DRw7

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7 January 2021

Clinical, pathological, HLA antigen and immunological evidence for disease heterogeneity in myasthenia gravis

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7 January 2021

HLA antigens and Bf allotypes in SLE: evidence for the association being with specific haplotypes

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7 January 2021

HLA-DQ beta gene contributes to susceptibility and resistance to insulin-dependent diabetes mellitus

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7 January 2021

HLA-DQ beta-chain polymorphism linked to myasthenia gravis

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7 January 2021

Family study of the major histocompatibility complex in patients with systemic lupus erythematosus: importance of null alleles of C4A and C4B in determining disease susceptibility

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7 January 2021

An extended HLA-D region haplotype associated with celiac disease.

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7 January 2021

Identifiers

DOI

10.1002/HEP.1840120207

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1975247%20AND%20SRC:MED&resulttype=core&format=json

21 September 2019

1 reference