Analysis of KIT, SCF, and Initial Screening of SLUG in Patients with Piebaldism

Author:

Murakami Tomoko,Hosomi Naoko,Oiso Naoki,Giovannucci-Uzielli Maria Luisa,Aquaron Robert,Mizoguchi Masako,Kato Atsushi,Ishii Masamitsu,Bitner-Glindzicz Maria,Barnicoat Angela,Wilson Louise,Tsukamoto Katsuhiko,Ueda Hiroshi,Mancini Anthony J.,Suzuki Tamio,Riley Jacquely,Miertus Jan,Camargo Mauricio,Santoro-Zea Alexandra,Atkin Joan,Fukai Kazuyoshi

Publisher

Elsevier BV

Subject

Cell Biology,Dermatology,Molecular Biology,Biochemistry

Reference14 articles.

1. The proto-oncogene c-kit encoding a transmembrane tyrosine kinase receptor maps to the mouse W locus;Chabot;Nature,1988

2. Novel mutations and deletions of the KIT (steel factor receptor) gene in human piebaldism;Ezoe;Am J Hum Genet,1995

3. Mutations in the ligand-binding domain of the kit receptor: An uncommon site in human piebaldism;Fleischman;J Invest Dermatol,1996

4. Deletion of the c-kit protooncogene in the human developmental defect piebald trait;Fleischman;Proc Natl Acad Sci USA,1991

5. Acquired pigmented macules in human piebald lesions. Ultrastructure of melanocytes in hypomelanotic skin;Fukai;Acta Derm-Venereol,1989

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