Analysis of the p16 gene status of non-familial dysplastic nevus syndrome patients

Archives of Dermatological Research

Volumn 293, Issue 10, 2001, Pages

  Matsumura, Yasuhiro ^a   Nishigori, Chikako ^a   Miyachi, Yoshiki ^a  

^a KYOTO UNIVERSITY   (Japan)

Author keywords

Allelic loss; Non familial dysplastic nevus syndrome; p16 gene

Indexed keywords

DNA POLYMERASE; EOSIN; GENOMIC DNA; HEMATOXYLIN; PARAFFIN; POLYACRYLAMIDE; PROTEIN P16; UREA;

ADULT; ALLELE; ANAMNESIS; ARTICLE; AUTORADIOGRAPHY; BODY REGIONS; CANCER SURGERY; CASE REPORT; CAUCASIAN; CELL PROLIFERATION; CELL STRUCTURE; CLINICAL TRIAL; CONTROLLED CLINICAL TRIAL; CONTROLLED STUDY; CORRELATION ANALYSIS; DISEASE CLASSIFICATION; DISEASE COURSE; DISEASE PREDISPOSITION; DNA EXTRACTION; DNA POLYMORPHISM; DYSPLASTIC NEVUS; EXON; FAMILIAL DISEASE; FAMILY HISTORY; FEMALE; FIBROBLAST; GENE MUTATION; GENETIC ANALYSIS; HUMAN; HUMAN TISSUE; JAPAN; MELANOMA; NEVUS CELL; PHENOTYPE; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; SKIN BIOPSY; SKIN CELL; TUMOR SUPPRESSOR GENE; GENETICS; PATHOLOGY; PHYSIOLOGY;

ADULT; ALLELES; DYSPLASTIC NEVUS SYNDROME; FEMALE; FIBROBLASTS; GENES, P16; HUMANS;

EID: 0035544727     PISSN: 03403696     EISSN: None     Source Type: Journal    
DOI: 10.1007/PL00007470     Document Type: Article

References (12)

1. Germline p16 mutations in familial melanoma
2. Homozygotes for CDKN2 (p16) germline mutation in Dutch familial melanoma kindreds
3. Prevalence of p16 and CDK4 germline mutations in 48 melanoma-prone families in France
4. Dysplastic naevi and cutaneous melanoma risk
5. A case of dysplastic nevus
6. High prevalence of mutations in the p53 gene in poorly differentiated squamous cell carcinomas in xeroderma pigmentosum patients
7. Melanoma development in relation to non-functional p16/INK4A protein and dysplastic naevus syndrome in Swedish melanoma kindreds
8. CDKN2A mutations in multiple primary melanomas
9. The genetics of hereditary melanoma and nevi
10. Genetics of familial and sporadic melanoma
11. Deletion mapping of chromosome region 9p21-p22 surrounding the CDKN2 locus in melanoma
12. Definition of the role of chromosome 9p21 in sporadic melanoma through genetic analysis of primary tumours and their metastases