The Region Coding for the Helix Termination Motif and the Adjacent Intron 6 of the Human Type I Hair Keratin Gene hHa2 Contains Three Natural, Closely Spaced Polymorphic Sites-Reference-Cited by-同舟云学术

The Region Coding for the Helix Termination Motif and the Adjacent Intron 6 of the Human Type I Hair Keratin Gene hHa2 Contains Three Natural, Closely Spaced Polymorphic Sites

Published:1996-03 Issue:3 Volume:106 Page:544-548
ISSN:0022-202X
Container-title:Journal of Investigative Dermatology
language:en
Short-container-title:Journal of Investigative Dermatology

Author:

Winter Hermelita,Rogers Michael A.,Mahr Brigitte,Cremer Marion,Krieg Thomas,Navsaria Harshad A.,Leigh Irene M.,Schweizer Jürgen

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

Reference44 articles.

1. Intermediate filaments formed de nova from tail-less cytokeratins in the cytoplasm and in the nucleus;Bader;J Cell Biol,1991

2. Epidermolysis Bullosa Simplex: evidence in two families for keratin abnormalities;Bonifas;Science,1991

3. Mutations of keratin 9 in two families with pantoplantar epidermolytic hyperkeratosis;Bonifas;J Invest Dermatol,1994

4. Mutaion of a type II keratin gene (K6a) in pachyonychia congnita;Bowden;Nat Genet,1995

5. A leucine→proline mutaiton in the H1 subdomain of keratin 1 causes epidermolytic hperkeratosis;Chipev;Cell,1992

Cited by 6 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. Human type I hair keratin pseudogene ? hHaA has functional orthologs in the chimpanzee and gorilla: evidence for recent inactivation of the human gene after the Pan-Homo divergence;Human Genetics;2001-01-22

2. Expression of human hair keratin basic 1 in pilomatrixoma. A study of 128 cases;British Journal of Dermatology;1999-04

3. Characterization of a 190-Kilobase Pair Domain of Human Type I Hair Keratin Genes;Journal of Biological Chemistry;1998-10

4. Cuticle cell defects in lamellar ichthyosis hair and anomalous hair shaft syndromes visualized after detergent extraction;The Anatomical Record;1996-12

5. Human keratin diseases:. Hereditary fragility of specific epithelial tissues;Experimental Dermatology;1996-12