The Molecular Defect in a COOH-terminal-modified and shOrtened Mutant of Human Serum Albumin-Reference-Cited by-同舟云学术

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The Molecular Defect in a COOH-terminal-modified and shOrtened Mutant of Human Serum Albumin

Published:1989-02 Issue:6 Volume:264 Page:3385-3389
ISSN:0021-9258
Container-title:Journal of Biological Chemistry
language:en
Short-container-title:Journal of Biological Chemistry

Author:

Minchiotti L,Galliano M,Iadarola P,Meloni M L,Ferri G,Porta F,Castellani A A

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry

Reference36 articles.

1. Complete amino acid sequence of human serum albumin

2. Lipid-Protein Interactions;Brown,1982

3. The human serum albumin gene: structure of a unique locus

4. Molecular structure of the human albumin gene is revealed by nucleotide sequence within q11-22 of chromosome 4.

Cited by 20 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Variations in the Human Serum Albumin Gene: Molecular and Functional Aspects;International Journal of Molecular Sciences;2022-01-21

2. A novel nonsense variation in the albumin gene (c.1309 A>T) causing analbuminaemia;British Journal of Biomedical Science;2020-10-30

3. An intact C-terminal end of albumin is required for its long half-life in humans;Communications Biology;2020-04-20

4. Human serum albumin: From bench to bedside;Molecular Aspects of Medicine;2012-06

5. Mutations and polymorphisms of the gene of the major human blood protein, serum albumin;Human Mutation;2008-08

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