Epidermolysis Bullosa Simplex: Evidence in Two Families for Keratin Gene Abnormalities-Reference-Cited by-同舟云学术

Epidermolysis Bullosa Simplex: Evidence in Two Families for Keratin Gene Abnormalities

Published:1991-11-22 Issue:5035 Volume:254 Page:1202-1205
ISSN:0036-8075
Container-title:Science
language:en
Short-container-title:Science

Author:

Bonifas J. M.¹,Rothman A. L.¹,Epstein E. H.¹

Affiliation:

1. Department of Dermatology, San Francisco General Hospital, University of California, San Francisco, CA 94110.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

Reference35 articles.

1. ALBERS, K, EXPRESSION OF MUTANT KERATIN CDNAS IN EPITHELIAL-CELLS REVEALS POSSIBLE MECHANISMS FOR INITIATION AND ASSEMBLY OF INTERMEDIATE FILAMENTS, JOURNAL OF CELL BIOLOGY 108: 1477 (1989).

2. BADER, B.L., LOW-LEVEL EXPRESSION OF CYTOKERATIN-8, CYTOKERATIN-18 AND CYTOKERATIN-19 IN VASCULAR SMOOTH-MUSCLE CELLS OF HUMAN UMBILICAL-CORD AND IN CULTURED-CELLS DERIVED THEREFROM, WITH AN ANALYSIS OF THE CHROMOSOMAL LOCUS CONTAINING THE CYTOKERATIN-19 GENE, EUROPEAN JOURNAL OF CELL BIOLOGY 47: 300 (1988).

3. BASAZS, I, HUM GENET 68: 57 (1984).

4. BONIFAS, J.M., LINKAGE OF EPIDERMOLYSIS-BULLOSA SIMPLEX TO PROBES IN THE REGION OF KERATIN GENE CLUSTERS ON CHROMOSOME-12Q AND CHROMOSOME-17Q, JOURNAL OF INVESTIGATIVE DERMATOLOGY 96: 550 (1991).

5. BONIFAS J.M. unpublished data.

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