α1-Antitrypsin TAQ I polymorphism and α1-antichymotrypsin mutations in patients with obstructive pulmonary disease (Q58885905)

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1 November 2019

title

alpha 1-antitrypsin TAQ I polymorphism and alpha 1-antichymotrypsin mutations in patients with obstructive pulmonary disease (English)

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1 November 2019

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1 November 2019

M G Benetazzo

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1 November 2019

L S Gilè

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1 November 2019

C Bombieri

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1 November 2019

M Massobrio

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1 November 2019

P F Pignatti

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1 November 2019

M Luisetti

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1 November 2019

publication date

1 September 1999

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1 November 2019

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1 November 2019

volume

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issue

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1 November 2019

page(s)

648-654

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Genetic risk factors for chronic obstructive pulmonary disease

1 November 2019

cites work

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Animal models of emphysema

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Clinical features of individuals with PI*SZ phenotype of alpha 1-antitrypsin deficiency. alpha 1-Antitrypsin Deficiency Registry Study Group

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7 January 2021

Mutation in the 3' region of the alpha-1-antitrypsin gene and chronic obstructive pulmonary disease

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7 January 2021

Pulmonary function in middle-aged women with heterozygous deficiency of the serine protease inhibitor alpha 1-antichymotrypsin

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7 January 2021

A leucine-to-proline substitution causes a defective alpha 1-antichymotrypsin allele associated with familial obstructive lung disease

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7 January 2021

The defective secretion of a naturally occurring alpha-1-antichymotrypsin variant with a frameshift mutation

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7 January 2021

Point mutation in a 3' flanking sequence of the alpha-1-antitrypsin gene associated with chronic respiratory disease occurs in a regulatory sequence

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7 January 2021

Mis-sense mutation of alpha 1-antichymotrypsin gene associated with chronic lung disease

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The molecular basis of alpha 1-antichymotrypsin deficiency in a heterozygote with liver and lung disease

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7 January 2021

Detection of a new mutant alpha-1-antichymotrypsin in patients with occlusive-cerebrovascular disease

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7 January 2021

Alpha-1-antichymotrypsin variant detected by PCR-single strand conformation polymorphism (PCR-SSCP) and direct sequencing

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7 January 2021

Molecular Approaches for Screening of Genetic Diseases

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The cystic fibrosis gene is not likely to be involved in chronic obstructive pulmonary disease

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Increased incidence of cystic fibrosis gene mutations in adults with disseminated bronchiectasis

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7 January 2021

Mutation in an alpha1-antitrypsin enhancer results in an interleukin-6 deficient acute-phase response due to loss of cooperativity between transcription factors

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7 January 2021

Alpha1-antitrypsin deficiency alleles and the Taq-I G-->A allele in cystic fibrosis lung disease

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7 January 2021

Differences in the prevalence of a TaqI RFLP in the 3‘ flanking region of the α1‐proteinase inhibitor gene between asthmatic and non‐asthmatic black and white South Africans

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7 January 2021

Mis-sense mutation of alpha 1-antichymotrypsin gene and chronic lung disease

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7 January 2021

Alpha 1-antichymotrypsin mutations in patients with chronic obstructive pulmonary disease

1 reference

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7 January 2021

10.1016/S0954-6111(99)90105-1

Identifiers

DOI

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1 November 2019

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