Expression of exon-8-skipped kindlin-1 does not compensate for defects of Kindler syndrome

Journal of Dermatological Science

Volumn 61, Issue 1, 2011, Pages 38-44

  Natsuga, Ken ^a   Nishie, Wataru ^a   Shinkuma, Satoru ^a   Nakamura, Hideki ^a   Matsushima, Yoichiro ^b   Tatsuta, Aya ^c   Komine, Mayumi ^c   Shimizu, Hiroshi ^a  

^a HOKKAIDO UNIVERSITY GRADUATE SCHOOL OF MEDICINE   (Japan)

^b Sano Kosei General Hospital   (Japan)

^c JICHI MEDICAL UNIVERSITY   (Japan)

Author keywords

Basement membrane zone; Epidermolysis bullosa; Exon trapping system; Pseudo ainhum; Skin atrophy

Indexed keywords

BETA1 INTEGRIN; COMPLEMENTARY DNA; GENE PRODUCT; GENOMIC DNA; KINDLIN 1; MESSENGER RNA; UNCLASSIFIED DRUG;

ADULT; ARTICLE; CASE REPORT; EPIDERMOLYSIS BULLOSA; EXON SKIPPING; GENE; GENE DELETION; GENE MUTATION; GENETIC TRANSFECTION; HELA CELL; HUMAN; HUMAN TISSUE; KIND1 GENE; KINDLER SYNDROME; MALE; PATHOGENESIS; POIKILODERMA; PRIORITY JOURNAL; PROTEIN EXPRESSION; RNA SEQUENCE;

ADULT; ANTIGENS, CD29; BLISTER; EPIDERMOLYSIS BULLOSA; EXONS; FEMALE; GENE EXPRESSION; HUMANS; MALE; MEMBRANE PROTEINS; MUTATION; NEOPLASM PROTEINS; PERIODONTAL DISEASES; PHOTOSENSITIVITY DISORDERS; RNA SPLICE SITES; RNA SPLICING; RNA, MESSENGER; SKIN;

EID: 78650679134     PISSN: 09231811     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jdermsci.2010.11.008     Document Type: Article

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