Induction of phenotype modifying cytokines by FERMT1 mutations

Human Mutation

Volumn 32, Issue 4, 2011, Pages 397-406

  Heinemann, Anja ^a   He, Yinghong ^a   Zimina, Elena ^a   Boerries, Melanie ^a   Busch, Hauke ^a   Chmel, Nadja ^a   Kurz, Thorsten ^a   Bruckner Tuderman, Leena ^a   Has, Cristina ^a  

^a UNIVERSITY OF FREIBURG   (Germany)

Author keywords

Cytokine; Epidermolysis bullosa; Fermitin; Fibrosis; Kindler syndrome; Kindlin; TGF

Indexed keywords

ALPHA SMOOTH MUSCLE ACTIN; CONNECTIVE TISSUE GROWTH FACTOR; INTERLEUKIN 1; INTERLEUKIN 20; INTERLEUKIN 24; INTERLEUKIN 6; KINDLIN 1; PLATELET DERIVED GROWTH FACTOR B; REGULATOR PROTEIN; TRANSFORMING GROWTH FACTOR BETA2; UNCLASSIFIED DRUG;

ADULT; ARTICLE; CELL DIFFERENTIATION; CELLULAR STRESS RESPONSE; CHILD; CYTOKINE RELEASE; DERMIS; EPIDERMIS CELL; EPITHELIUM CELL; ERYTHEMA; EXTRACELLULAR MATRIX; FEMALE; FIBROBLAST; GENE MUTATION; HUMAN; HUMAN CELL; HUMAN TISSUE; KERATINOCYTE; MACROPHAGE; MALE; MYOFIBROBLAST; NAIL DYSTROPHY; NOSE MALFORMATION; NUCLEOTIDE SEQUENCE; PARACRINE SIGNALING; PHENOTYPE; POIKILODERMA; PRIORITY JOURNAL; PROTEIN EXPRESSION; PROTEIN SECRETION; SCHOOL CHILD; SKIN ATROPHY; SKIN FIBROSIS; TELANGIECTASIA; UPREGULATION;

ADULT; BLISTER; CHILD; CYTOKINES; EPIDERMOLYSIS BULLOSA; FEMALE; FIBROSIS; HUMANS; KERATINOCYTES; MALE; MEMBRANE PROTEINS; MUTATION; NEOPLASM PROTEINS; PERIODONTAL DISEASES; PHENOTYPE; PHOTOSENSITIVITY DISORDERS; SKIN;

EID: 79952758027     PISSN: 10597794     EISSN: 10981004     Source Type: Journal    
DOI: 10.1002/humu.21449     Document Type: Article

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