메뉴 건너뛰기




Volumn 134, Issue 3, 2012, Pages 1337-1343

Mutational analysis of telomere genes in BRCA1/2-negative breast cancer families with very short telomeres

Author keywords

Familial breast cancer; Genetic variants; Telomere genes; Telomere length

Indexed keywords

TELOMERASE;

EID: 84868214964     PISSN: 01676806     EISSN: 15737217     Source Type: Journal    
DOI: 10.1007/s10549-012-2141-2     Document Type: Article
Times cited : (6)

References (31)
  • 1
    • 0032441791 scopus 로고    scopus 로고
    • The genetics of breast cancer susceptibility
    • Rahman N, Stratton MR (1998) The genetics of breast cancer susceptibility. Annu Rev Genet 32:95-121
    • (1998) Annu Rev Genet , vol.32 , pp. 95-121
    • Rahman, N.1    Stratton, M.R.2
  • 4
    • 37549056200 scopus 로고    scopus 로고
    • The emerging landscape of breast cancer susceptibility
    • Stratton MR, Rahman N (2008) The emerging landscape of breast cancer susceptibility. Nat Genet 40(1):17-22
    • (2008) Nat Genet , vol.40 , Issue.1 , pp. 17-22
    • Stratton, M.R.1    Rahman, N.2
  • 5
    • 52949098309 scopus 로고    scopus 로고
    • Human telomere structure and biology
    • Riethman H (2008) Human telomere structure and biology. Annu Rev Genomics Hum Genet 9:1-19
    • (2008) Annu Rev Genomics Hum Genet , vol.9 , pp. 1-19
    • Riethman, H.1
  • 7
    • 79955039251 scopus 로고    scopus 로고
    • Telomere protein complexes and interactions with telomerase in telomere maintenance
    • Pinto AR, Li H, Nicholls C, Liu JP (2011) Telomere protein complexes and interactions with telomerase in telomere maintenance. Front Biosci 16:187-207
    • (2011) Front Biosci , vol.16 , pp. 187-207
    • Pinto, A.R.1    Li, H.2    Nicholls, C.3    Liu, J.P.4
  • 8
    • 33846850422 scopus 로고    scopus 로고
    • Ten genes for inherited breast cancer
    • Walsh T, King MC (2007) Ten genes for inherited breast cancer. Cancer Cell 11(2):103-105
    • (2007) Cancer Cell , vol.11 , Issue.2 , pp. 103-105
    • Walsh, T.1    King, M.C.2
  • 10
    • 73649113140 scopus 로고    scopus 로고
    • BRCA1 localization to the telomere and its loss from the telomere in response to DNA damage
    • Ballal RD, Saha T, Fan S, Haddad BR, Rosen EM (2009) BRCA1 localization to the telomere and its loss from the telomere in response to DNA damage. J Biol Chem 284(52):36083-36098
    • (2009) J Biol Chem , vol.284 , Issue.52 , pp. 36083-36098
    • Ballal, R.D.1    Saha, T.2    Fan, S.3    Haddad, B.R.4    Rosen, E.M.5
  • 13
    • 70849132066 scopus 로고    scopus 로고
    • Mutational analysis of FANCL, FANCM and the recently identified FANCI suggests that among the 13 known Fanconi anemia genes, only FANCD1/BRCA2 plays a major role in high-risk breast cancer predisposition
    • Garcia MJ, Fernandez V, Osorio A, Barroso A, Fernandez F, Urioste M, Benitez J (2009) Mutational analysis of FANCL, FANCM and the recently identified FANCI suggests that among the 13 known Fanconi anemia genes, only FANCD1/BRCA2 plays a major role in high-risk breast cancer predisposition. Carcinogenesis 30(11):1898-1902
    • (2009) Carcinogenesis , vol.30 , Issue.11 , pp. 1898-1902
    • Garcia, M.J.1    Fernandez, V.2    Osorio, A.3    Barroso, A.4    Fernandez, F.5    Urioste, M.6    Benitez, J.7
  • 16
    • 3543056880 scopus 로고    scopus 로고
    • Functional links between telomeres and proteins of the DNA-damage response
    • D'Adda Di Fagagna F, Teo SH, Jackson SP (2004) Functional links between telomeres and proteins of the DNA-damage response. Genes Dev 18(15):1781-1799
    • (2004) Genes Dev , vol.18 , Issue.15 , pp. 1781-1799
    • D'Adda Di Fagagna, F.1    Teo, S.H.2    Jackson, S.P.3
  • 18
    • 25444519739 scopus 로고    scopus 로고
    • Genetic variation, nucleotide diversity, and linkage disequilibrium in seven telomere stability genes suggest that these genes may be under constraint
    • Savage SA, Stewart BJ, Eckert A, Kiley M, Liao JS, Chanock SJ (2005) Genetic variation, nucleotide diversity, and linkage disequilibrium in seven telomere stability genes suggest that these genes may be under constraint. Hum Mutat 26(4):343-350
    • (2005) Hum Mutat , vol.26 , Issue.4 , pp. 343-350
    • Savage, S.A.1    Stewart, B.J.2    Eckert, A.3    Kiley, M.4    Liao, J.S.5    Chanock, S.J.6
  • 19
    • 0345687981 scopus 로고    scopus 로고
    • Composition and conservation of the telomeric complex
    • Kanoh J, Ishikawa F (2003) Composition and conservation of the telomeric complex. Cell Mol Life Sci 60(11):2295-2302
    • (2003) Cell Mol Life Sci , vol.60 , Issue.11 , pp. 2295-2302
    • Kanoh, J.1    Ishikawa, F.2
  • 20
    • 0034459569 scopus 로고    scopus 로고
    • Human H/ACA small nucleolar RNPs and telomerase share evolutionarily conserved proteins NHP2 and NOP10
    • Pogacic V, Dragon F, Filipowicz W (2000) Human H/ACA small nucleolar RNPs and telomerase share evolutionarily conserved proteins NHP2 and NOP10. Mol Cell Biol 20(23):9028-9040
    • (2000) Mol Cell Biol , vol.20 , Issue.23 , pp. 9028-9040
    • Pogacic, V.1    Dragon, F.2    Filipowicz, W.3
  • 21
    • 2442542173 scopus 로고    scopus 로고
    • Architecture and assembly of mammalian H/ACA small nucleolar and telomerase ribonucleoproteins
    • Wang C, Meier UT (2004) Architecture and assembly of mammalian H/ACA small nucleolar and telomerase ribonucleoproteins. EMBO J 23(8):1857-1867
    • (2004) EMBO J , vol.23 , Issue.8 , pp. 1857-1867
    • Wang, C.1    Meier, U.T.2
  • 22
    • 45849131292 scopus 로고    scopus 로고
    • Mutations in the telomerase component NHP2 cause the premature ageing syndrome dyskeratosis congenita
    • Vulliamy T, Beswick R, Kirwan M, Marrone A, Digweed M, Walne A, Dokal I (2008) Mutations in the telomerase component NHP2 cause the premature ageing syndrome dyskeratosis congenita. Proc Natl Acad Sci USA 105(23):8073-8078
    • (2008) Proc Natl Acad Sci USA , vol.105 , Issue.23 , pp. 8073-8078
    • Vulliamy, T.1    Beswick, R.2    Kirwan, M.3    Marrone, A.4    Digweed, M.5    Walne, A.6    Dokal, I.7
  • 23
    • 0031799895 scopus 로고    scopus 로고
    • X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions
    • Heiss NS, Knight SW, Vulliamy TJ, Klauck SM, Wiemann S, Mason PJ, Poustka A, Dokal I (1998) X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions. Nat Genet 19(1):32-38
    • (1998) Nat Genet , vol.19 , Issue.1 , pp. 32-38
    • Heiss, N.S.1    Knight, S.W.2    Vulliamy, T.J.3    Klauck, S.M.4    Wiemann, S.5    Mason, P.J.6    Poustka, A.7    Dokal, I.8
  • 24
    • 34447307404 scopus 로고    scopus 로고
    • Genetic heterogeneity in autosomal recessive dyskeratosis congenita with one subtype due to mutations in the telomerase-associated protein NOP10
    • Walne AJ, Vulliamy T, Marrone A, Beswick R, Kirwan M, Masunari Y, Al-Qurashi FH, Aljurf M, Dokal I (2007) Genetic heterogeneity in autosomal recessive dyskeratosis congenita with one subtype due to mutations in the telomerase-associated protein NOP10. Hum Mol Genet 16(13):1619-1629
    • (2007) Hum Mol Genet , vol.16 , Issue.13 , pp. 1619-1629
    • Walne, A.J.1    Vulliamy, T.2    Marrone, A.3    Beswick, R.4    Kirwan, M.5    Masunari, Y.6    Al-Qurashi, F.H.7    Aljurf, M.8    Dokal, I.9
  • 28
    • 79953733129 scopus 로고    scopus 로고
    • Genetic variants in telomere-maintaining genes and skin cancer risk
    • Nan H, Qureshi AA, Prescott J, De Vivo I, Han J (2011) Genetic variants in telomere-maintaining genes and skin cancer risk. Hum Genet 129(3):247-253
    • (2011) Hum Genet , vol.129 , Issue.3 , pp. 247-253
    • Nan, H.1    Qureshi, A.A.2    Prescott, J.3    De Vivo, I.4    Han, J.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.