(Q39059950)

8 September 2017

title

Genetic diversity of the alpha-1-antitrypsin gene in Africans identified using a novel genotyping assay (English)

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8 September 2017

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Vanessa M Hayes

1

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8 September 2017

language of work or name

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1 July 2003

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8 September 2017

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8 September 2017

volume

22

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8 September 2017

issue

1

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8 September 2017

page(s)

59-66

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Alpha-1-antitrypsin PI phenotypes S and Z in Europe: an analysis of the published surveys

8 September 2017

cites work

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https://api.crossref.org/works/10.1002%2FHUMU.10231

7 January 2021

Distribution of alpha1-antitrypsin PI S and PI Z frequencies in countries outside Europe: a meta-analysis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10231

7 January 2021

alpha 1-Antitrypsin Christchurch, 363 Glu----Lys: mutation at the P'5 position does not affect inhibitory activity

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https://api.crossref.org/works/10.1002%2FHUMU.10231

7 January 2021

Human alpha 1-antitrypsin: carbohydrate attachment and sequence homology

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https://api.crossref.org/works/10.1002%2FHUMU.10231

7 January 2021

Alpha 1-antitrypsin deficiency, emphysema, and liver disease. Genetic basis and strategies for therapy

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https://api.crossref.org/works/10.1002%2FHUMU.10231

7 January 2021

Population Genetics of Alpha-1-Antitrypsin Polymorphism in US Whites, US Blacks and African Blacks

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https://api.crossref.org/works/10.1002%2FHUMU.10231

7 January 2021

Alpha-1-antitrypsin variation in Southern Africa.

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https://api.crossref.org/works/10.1002%2FHUMU.10231

7 January 2021

A 30-year perspective on alpha 1-antitrypsin deficiency

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https://api.crossref.org/works/10.1002%2FHUMU.10231

7 January 2021

Identification of DNA polymorphisms associated with the V type alpha1-antitrypsin gene

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10231

7 January 2021

A simple method for identification of point mutations using denaturing gradient gel electrophoresis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10231

7 January 2021

Variants of alpha 1-proteinase inhibitor in black and white South African patients with focal glomerulosclerosis and minimal change nephrotic syndrome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10231

7 January 2021

Improvements in gel composition and electrophoretic conditions for broad-range mutation analysis by denaturing gradient gel electrophoresis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10231

7 January 2021

Molecular analysis of the heterogeneity among the P-family of alpha-1-antitrypsin alleles

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10231

7 January 2021

The amino acid substitutions of human alpha 1-antitrypsin M3, X and Z

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https://api.crossref.org/works/10.1002%2FHUMU.10231

7 January 2021

Computational simulation of DNA melting and its application to denaturing gradient gel electrophoresis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10231

7 January 2021

Mutation detection in the alpha-1 antitrypsin gene (PI) using denaturing gradient gel electrophoresis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10231

7 January 2021

The mechanism of Z alpha 1-antitrypsin accumulation in the liver

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10231

7 January 2021

Complete sequence of the cDNA for human .alpha.1-antitrypsin and the gene for the S variant

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10231

7 January 2021

Characterization of the M1(Ala213) type of alpha 1-antitrypsin, a newly recognized, common "normal" alpha 1-antitrypsin haplotype

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10231

7 January 2021

Rapid analysis of alpha1-antitrypsin PiZ genotype by a real-time PCR approach

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10231

7 January 2021

Mutation of antitrypsin to antithrombin. alpha 1-antitrypsin Pittsburgh (358 Met leads to Arg), a fatal bleeding disorder

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10231

7 January 2021

Antitrypsin and Gc polymorphisms in some populations of Congo: an unusual, highly frequent mutant, PIS, in Bateke and Babenga.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10231

7 January 2021

Clinical features and natural history of severe alpha 1-antitrypsin deficiency. Roger S. Mitchell Lecture

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10231

7 January 2021

Improvement of fragment and primer selection for mutation detection by denaturing gradient gel electrophoresis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10231

7 January 2021

Deletion 14q(q24.3 to q32.1) syndrome: significance of peculiar facial appearance in its diagnosis, and deletion mapping of Pi(alpha 1-antitrypsin)

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.10231

7 January 2021

Identifiers

DOI

10.1002/HUMU.10231

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8 September 2017

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