A human keratin 10 knockout causes recessive epidermolytic hyperkeratosis

Human Molecular Genetics

Volumn 15, Issue 7, 2006, Pages 1133-1141

  Müller, Felix B ^a   Huber, Marcel ^b   Kinaciyan, Tamad ^c   Hausser, Ingrid ^d   Schaffrath, Christina ^a   Krieg, Thomas ^a   Hohl, Daniel ^b   Korge, Bernhard P ^a   Arin, Meral J ^a  

^a UNIVERSITY OF COLOGNE   (Germany)

^b LAUSANNE UNIVERSITY HOSPITAL   (Switzerland)

^c Universitatsklinik fur Dermatologie   (Austria)

^d UNIVERSITY OF HEIDELBERG   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

KERATIN; KERATIN 10; KERATIN 16; KERATIN 17; KERATIN 6; SCLEROPROTEIN; UNCLASSIFIED DRUG;

ARTICLE; AUTOSOMAL DOMINANT DISORDER; CASE REPORT; CHILD; CONSANGUINITY; DISEASE SEVERITY; EPIDERMIS; FEMALE; HETEROZYGOSITY; HETEROZYGOTE; HOMOZYGOSITY; HUMAN; HUMAN CELL; HUMAN CELL CULTURE; HUMAN TISSUE; HYPERKERATOSIS; KERATINOCYTE; KNOCKOUT GENE; MALE; NONSENSE MUTATION; PARENT; PHENOTYPE; PRIORITY JOURNAL; PROTEIN AGGREGATION; PROTEIN DEGRADATION; PROTEIN INDUCTION; RECESSIVE INHERITANCE; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SEQUENCE ANALYSIS; STOP CODON; ULTRASTRUCTURE; WESTERN BLOTTING;

3T3 CELLS; CELLS, CULTURED; CHILD; CODON, NONSENSE; EPIDERMIS; EXONS; FEMALE; FIBROBLASTS; FLUORESCENT ANTIBODY TECHNIQUE; GENES, RECESSIVE; GENOTYPE; HOMOZYGOTE; HUMANS; HYPERKERATOSIS, EPIDERMOLYTIC; KERATIN-10; KERATINS; MALE; MICE; MICROSCOPY, ELECTRON; MODELS, BIOLOGICAL; PEDIGREE; PHENOTYPE; RNA, MESSENGER; SKIN;

EID: 33645115691     PISSN: 09646906     EISSN: 14602083     Source Type: Journal    
DOI: 10.1093/hmg/ddl028     Document Type: Article

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