Alpha-1-antitrypsin deficiency: Genetic variations, clinical manifestations and therapeutic interventions-Reference-Cited by-同舟云学术

Alpha-1-antitrypsin deficiency: Genetic variations, clinical manifestations and therapeutic interventions

Published:2017-07 Issue: Volume:773 Page:14-25
ISSN:1383-5742
Container-title:Mutation Research/Reviews in Mutation Research
language:en
Short-container-title:Mutation Research/Reviews in Mutation Research

Author:

Hazari Younis Mohammad,Bashir Arif,Habib Mudasir,Bashir Samirul,Habib Huma,Qasim M. Abul,Shah Naveed Nazir,Haq Ehtishamul,Teckman Jeffrey,Fazili Khalid Majid

Funder

DBT

DST

FIST

UGC-SAP

Publisher

Elsevier BV

Subject

Health, Toxicology and Mutagenesis,Genetics

Reference174 articles.

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2. Accumulation of PiZ alpha 1-antitrypsin causes liver damage in transgenic mice;Carlson;J. Clin. Invest.,1989

3. Cell-specific expression of alpha 1-antitrypsin in human intestinal epithelium;Molmenti;J. Clin. Invest.,1993

4. Biosynthesis of alpha1-proteinase inhibitor by human lung-derived epithelial cells;Cichy;J. Biol. Chem.,1997

5. Z alpha1-antitrypsin polymerizes in the lung and acts as a neutrophil chemoattractant;Mulgrew;Chest,2004

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