메뉴 건너뛰기




Volumn 26, Issue 6 C, 2006, Pages 4885-4888

The CHEK2 1100delC variant in Swedish colorectal cancer

(18)  Djureinovic, Tatjana a   Lindblom, Annika a,d   Dalén, Johan b   Dedorson, Stefan c   Edler, David d   Hjern, Fredrik a   Holm, Jörn e   Lenander, Claes f   Lindforss, Ulrik d   Lundqvist, Nils g   Olivecrona, Hans h   Olsson, Louise a   Påhlman, Lars i   Rutegård, Jörgen j   Smedh, Kennet k   Törnqvist, Anders l   Eiberg, Hans m   Bisgaard, Marie Luise m  


Author keywords

CHEK2; Colorectal cancer

Indexed keywords

CHECKPOINT KINASE 2;

EID: 33845938336     PISSN: 02507005     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (9)

References (14)
  • 2
    • 4944240144 scopus 로고    scopus 로고
    • Genetic predisposition to colorectal cancer
    • de la Chapelle A: Genetic predisposition to colorectal cancer. Nat Rev Cancer 4: 769-780, 2004.
    • (2004) Nat Rev Cancer , vol.4 , pp. 769-780
    • de la Chapelle, A.1
  • 4
    • 18544389716 scopus 로고    scopus 로고
    • Meijers-Heijboer H, van den Ouweland A, Klijn J, Wasielewski M, de Snoo A, Oldenburg R, Hollestelle A, Houben M, Crepin E, van Veghel-Plandsoen M, Elstrodt F, van Duijn C, Bartels C, Meijers C, Schutte M, McGuffog L, Thompson D, Easton D, Sodha N, Seal S, Barfoot R, Mangion J, Chang-Claude J, Eccles D, Eeles R, Evans DG, Houlston R, Murday V, Narod S, Peretz T, Peto J, Phelan C, Zhang HX, Szabo C, Devilee P, Goldgar D, Futreal PA, Nathanson KL, Weber B, Rahman N and Stratton MR: Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations. Nat Genet 31: 55-59, 2002.
    • Meijers-Heijboer H, van den Ouweland A, Klijn J, Wasielewski M, de Snoo A, Oldenburg R, Hollestelle A, Houben M, Crepin E, van Veghel-Plandsoen M, Elstrodt F, van Duijn C, Bartels C, Meijers C, Schutte M, McGuffog L, Thompson D, Easton D, Sodha N, Seal S, Barfoot R, Mangion J, Chang-Claude J, Eccles D, Eeles R, Evans DG, Houlston R, Murday V, Narod S, Peretz T, Peto J, Phelan C, Zhang HX, Szabo C, Devilee P, Goldgar D, Futreal PA, Nathanson KL, Weber B, Rahman N and Stratton MR: Low-penetrance susceptibility to breast cancer due to CHEK2(*)1100delC in noncarriers of BRCA1 or BRCA2 mutations. Nat Genet 31: 55-59, 2002.
  • 7
    • 33144458558 scopus 로고    scopus 로고
    • A genome wide linkage analysis in Swedish families with hereditary non-familial adenomatous polyposis/non-hereditary non-polyposis colorectal cancer
    • Djureinovic T, Skoglund J, Vandrovcova J, Zhou XL, Kalushkova A, Iselius L and Lindblom A: A genome wide linkage analysis in Swedish families with hereditary non-familial adenomatous polyposis/non-hereditary non-polyposis colorectal cancer. Gut 55: 362-366, 2006.
    • (2006) Gut , vol.55 , pp. 362-366
    • Djureinovic, T.1    Skoglund, J.2    Vandrovcova, J.3    Zhou, X.L.4    Kalushkova, A.5    Iselius, L.6    Lindblom, A.7
  • 8
    • 0033991467 scopus 로고    scopus 로고
    • Microsatellite instability as a predictor of a mutation in a DNA mismatch repair gene in familial colorectal cancer
    • Liu T, Wahlberg S, Burek E, Lindblom P, Rubio C and Lindblom A: Microsatellite instability as a predictor of a mutation in a DNA mismatch repair gene in familial colorectal cancer. Genes Chromosomes Cancer 27: 17-25, 2000.
    • (2000) Genes Chromosomes Cancer , vol.27 , pp. 17-25
    • Liu, T.1    Wahlberg, S.2    Burek, E.3    Lindblom, P.4    Rubio, C.5    Lindblom, A.6
  • 9
    • 0032820317 scopus 로고    scopus 로고
    • Various mutation screening techniques in the DNA mismatch repair genes hMSH2 and hMLH1
    • Wahlberg S, Liu T, Lindblom P and Lindblom A: Various mutation screening techniques in the DNA mismatch repair genes hMSH2 and hMLH1. Genet Test 3: 259-264, 1999.
    • (1999) Genet Test , vol.3 , pp. 259-264
    • Wahlberg, S.1    Liu, T.2    Lindblom, P.3    Lindblom, A.4
  • 10
    • 3042582651 scopus 로고    scopus 로고
    • CHEK2*1100delC and susceptibility to breast cancer: A collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10 studies
    • CHEK2 Breast Cancer Case-Control Consortium
    • CHEK2 Breast Cancer Case-Control Consortium: CHEK2*1100delC and susceptibility to breast cancer: a collaborative analysis involving 10,860 breast cancer cases and 9,065 controls from 10 studies. Am J Hum Genet 74: 1175-1182, 2004.
    • (2004) Am J Hum Genet , vol.74 , pp. 1175-1182
  • 11
    • 33645471674 scopus 로고    scopus 로고
    • CHEK2 1100delC in patients with metachronous cancers of the breast and the colorectum
    • Isinger A, Bhat M, Borg A and Nilbert M: CHEK2 1100delC in patients with metachronous cancers of the breast and the colorectum. BMC Cancer 6: 64, 2006.
    • (2006) BMC Cancer , vol.6 , pp. 64
    • Isinger, A.1    Bhat, M.2    Borg, A.3    Nilbert, M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.