The rise of developing pancreatic cancer in families with familial atypical multiple mole melanoma (FAMMM) associated with a specific 19 bp deletion of P16 (P16 Leiden).

被引:0
|
作者
Vasen, HF
Gruis, NA
Frants, RR
Velden, PA
Hille, E
Bergman, W
机构
[1] LUMC, Dept Gastroenterol, Leiden, Netherlands
[2] Lab Anthropogenet, Leiden, Netherlands
[3] TNO Prevent & Hlth, Leiden, Netherlands
[4] Dept Dermatol, Leiden, Netherlands
关键词
D O I
10.1016/S0016-5085(00)84701-0
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
3263
引用
收藏
页码:A641 / A641
页数:1
相关论文
共 26 条
  • [1] Risk of developing pancreatic cancer in families with familial atypical multiple mole melanoma associated with a specific 19 deletion of p16 (p16-Leiden)
    Vasen, HFA
    Gruis, NA
    Frants, RR
    van der Velden, PA
    Hille, ETM
    Bergman, W
    INTERNATIONAL JOURNAL OF CANCER, 2000, 87 (06) : 809 - 811
  • [2] A locus linked to p16 modifies melanoma risk in Dutch familial atypical multiple mole melanoma (FAMMM) syndrome families
    van der Velden, PA
    Sandkuijl, LA
    Bergman, W
    Hille, ETM
    Frants, RR
    Gruis, NA
    GENOME RESEARCH, 1999, 9 (06) : 575 - 580
  • [3] Clinical and pathological features of pancreatic carcinomas in carriers of a specific 19 deletion of p16 (p16 Leiden)
    De Vos, W
    Offerhaus, J
    Van Puijenbroek, M
    Caspers, E
    Gruis, N
    De Snoo, F
    Griffioen, G
    Bergman, W
    Vasen, H
    Morreau, H
    GASTROENTEROLOGY, 2002, 122 (04) : A488 - A488
  • [4] HOMOZYGOTES FOR CDKN2/P16 GERMLINE MUTATION IN DUTCH FAMILIAL ATYPICAL MULTIPLE MOLE MELANOMA (FAMMM) SYNDROME FAMILIES ARE VIABLE
    GRUIS, NA
    VANDERVELDEN, PA
    SANDKUIJL, LA
    PRINS, DE
    BERGMAN, W
    FRANTS, RR
    VERMEER, BJ
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1995, 104 (04) : 584 - 584
  • [5] Pancreatic carcinoma in carriers of a specific 19 base pair deletion of CDKN2A/p16 (p16-Leiden)
    Cappel, WHDTN
    Offerhaus, GJA
    van Puijenbroek, M
    Caspers, E
    Gruis, NA
    de Snoo, FA
    Lamers, CBHW
    Griffioen, G
    Bergman, W
    Vasen, HFA
    Morreau, H
    CLINICAL CANCER RESEARCH, 2003, 9 (10) : 3598 - 3605
  • [6] VIABILITY OF HOMOZYGOTES FOR A GERMLINE DELETION OF 19 BP IN THE CODING REGION OF THE CDKN2/P16 GENE IN DUTCH MELANOMA FAMILIES
    FRANTS, RR
    VANDERVELDEN, PA
    SANDKUIJL, LA
    PRINS, DE
    BERGMAN, W
    GRUIS, NA
    AMERICAN JOURNAL OF HUMAN GENETICS, 1995, 57 (04) : 338 - 338
  • [7] p16 immunohistochemistry of multiple primary melanomas as screening to identify Familial Melanoma Syndrome
    Ponti, Giovanni
    Luppi, Gabriele
    Losi, Lorena
    Cesinaro, Anna Maria
    Sartori, Giuliana
    Maiorana, Antonio
    Pellacani, Giovanni
    Longo, Caterina
    Boni, Elisa
    Pepe, Patrizia
    Giannetti, Alberto
    Seidenari, Stefania
    Landi, Maria Teresa
    INTERNATIONAL JOURNAL OF DERMATOLOGY, 2012, 51 (04) : 488 - 492
  • [8] MUTATIONS ASSOCIATED WITH FAMILIAL MELANOMA IMPAIR P16(INK4) FUNCTION
    RANADE, K
    HUSSUSSIAN, CJ
    SIKORSKI, RS
    VARMUS, HE
    GOLDSTEIN, AM
    TUCKER, MA
    SERRANO, M
    HANNON, GJ
    BEACH, D
    DRACOPOLI, NC
    NATURE GENETICS, 1995, 10 (01) : 114 - 116
  • [9] Familial melanoma-associated mutations in p16 uncouple its tumor suppressor functions
    Jenkins, N.
    Jung, J.
    Grossman, D.
    JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2012, 132 : S123 - S123
  • [10] Deletion of p16 and p15 genes In schistosomiasis-associated bladder cancer (SABC)
    Eissa, S
    Ali-Labib, R
    Khalifa, A
    CLINICA CHIMICA ACTA, 2000, 300 (1-2) : 159 - 169