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    Results: 1 to 20 of 129

    1.

    Contribution of BRCA1 germline mutation in patients with sporadic breast cancer.

    Malik FA, Ashraf S, Kayani MA, Jiang WG, Mir A, Ansar M, Baloch IA, Sadiq R.

    Int Semin Surg Oncol. 2008 Aug 29;5:21.PMID: 18759965 [PubMed - in process]Related articlesFree article

    2.

    BRCA1 and BRCA2 germline mutations in Korean patients with sporadic breast cancer.

    Seo JH, Cho DY, Ahn SH, Yoon KS, Kang CS, Cho HM, Lee HS, Choe JJ, Choi CW, Kim BS, Shin SW, Kim YH, Kim JS, Son GS, Lee JB, Koo BH.

    Hum Mutat. 2004 Oct;24(4):350.PMID: 15365993 [PubMed - indexed for MEDLINE]Related articles

    3.

    Mutation screening of the BRCA1 gene in sporadic breast cancer in southern Chinese populations.

    Haitian Z, Yunfei L, Jian Z, Jian L, Qinghua L, Fuqiang W.

    Breast. 2008 Dec;17(6):563-7. Epub 2008 Oct 5.PMID: 18835712 [PubMed - indexed for MEDLINE]Related articles

    4.

    Ovarian cancer BRCA1 mutation detection: Protein truncation test (PTT) outperforms single strand conformation polymorphism analysis (SSCP).

    Geisler JP, Hatterman-Zogg MA, Rathe JA, Lallas TA, Kirby P, Buller RE.

    Hum Mutat. 2001 Oct;18(4):337-44.PMID: 11668617 [PubMed - indexed for MEDLINE]Related articles

    5.

    Novel sequence variants and a high frequency of recurrent polymorphisms in BRCA1 gene in Sri Lankan breast cancer patients and at risk individuals.

    De Silva W, Karunanayake EH, Tennekoon KH, Allen M, Amarasinghe I, Angunawala P, Ziard MH.

    BMC Cancer. 2008 Jul 29;8:214.PMID: 18662409 [PubMed - indexed for MEDLINE]Related articlesFree article

    6.

    BRCA1 mutations in Algerian breast cancer patients: high frequency in young, sporadic cases.

    Uhrhammer N, Abdelouahab A, Lafarge L, Feillel V, Ben Dib A, Bignon YJ.

    Int J Med Sci. 2008 Jul 8;5(4):197-202.PMID: 18645608 [PubMed - indexed for MEDLINE]Related articlesFree article

    7.

    Age-dependent penetrance of different germline mutations in the BRCA1 gene.

    Al-Mulla F, Bland JM, Serratt D, Miller J, Chu C, Taylor GT.

    J Clin Pathol. 2009 Apr;62(4):350-6.PMID: 19329713 [PubMed - indexed for MEDLINE]Related articlesFree article

    8.

    Clustering of variations and haplotype analysis in the highly variable region of exon 11 of BRCA1 in Chinese women with sporadic breast cancer.

    Li Y, Zhang S, Xiao C, Su Z, Zhao Y, Chen W, Zhang G.

    Hum Mutat. 2002 Nov;20(5):404-5.PMID: 12402341 [PubMed - indexed for MEDLINE]Related articles

    9.

    BRCA1 and BRCA2 germline mutation analysis among Indian women from south India: identification of four novel mutations and high-frequency occurrence of 185delAG mutation.

    Vaidyanathan K, Lakhotia S, Ravishankar HM, Tabassum U, Mukherjee G, Somasundaram K.

    J Biosci. 2009 Sep;34(3):415-22.PMID: 19805903 [PubMed - indexed for MEDLINE]Related articlesFree article

    10.

    Five recurrent BRCA1/2 mutations are responsible for cancer predisposition in the majority of Slovenian breast cancer families.

    Krajc M, Teugels E, Zgajnar J, Goelen G, Besic N, Novakovic S, Hocevar M, De Grève J.

    BMC Med Genet. 2008 Sep 10;9:83.PMID: 18783588 [PubMed - indexed for MEDLINE]Related articlesFree article

    11.

    Mutational analysis of BRCA1 and BRCA2 genes in Mexican breast cancer patients.

    Vidal-Millán S, Taja-Chayeb L, Gutiérrez-Hernández O, Ramírez Ugalde MT, Robles-Vidal C, Bargallo-Rocha E, Mohar-Betancourt A, Dueñas-González A.

    Eur J Gynaecol Oncol. 2009;30(5):527-30.PMID: 19899408 [PubMed - indexed for MEDLINE]Related articles

    12.

    Role of BRCA2 mutation status on overall survival among breast cancer patients from Sardinia.

    Budroni M, Cesaraccio R, Coviello V, Sechi O, Pirino D, Cossu A, Tanda F, Pisano M, Palomba G, Palmieri G.

    BMC Cancer. 2009 Feb 20;9:62.PMID: 19232099 [PubMed - indexed for MEDLINE]Related articlesFree article

    13.

    Complete mutation screening and haplotype characterization of BRCA1 gene in Tunisian patients with familial breast cancer.

    Troudi W, Uhrhammer N, Romdhane KB, Sibille C, Amor MB, Khodjet El Khil H, Jalabert T, Mahfoudh W, Chouchane L, Ayed FB, Bignon YJ, Elgaaied AB.

    Cancer Biomark. 2008;4(1):11-8.PMID: 18334730 [PubMed - indexed for MEDLINE]Related articles

    14.

    Low prevalence of BRCA1 exon rearrangements in familial and young sporadic breast cancer patients.

    Ellis D, Patel Y, Yau SC, Hodgson SV, Abbs SJ.

    Fam Cancer. 2006;5(4):323-6. Epub 2006 May 25.PMID: 16724249 [PubMed - indexed for MEDLINE]Related articles

    15.

    Oncogenic pathways in hereditary and sporadic breast cancer.

    Kenemans P, Verstraeten RA, Verheijen RH.

    Maturitas. 2008 Sep-Oct;61(1-2):141-50.PMID: 19434886 [PubMed]Related articles

    16.

    Mutation analysis of the DBC2 gene in sporadic and familial breast cancer.

    Ohadi M, Totonchi M, Maguire P, Lindblom A, Habibi R, Alavi BA, Keyhani E, Najmabadi H.

    Acta Oncol. 2007;46(6):770-2.PMID: 17653899 [PubMed - indexed for MEDLINE]Related articles

    17.

    The prevalence of BRCA1 mutations among young women with triple-negative breast cancer.

    Young SR, Pilarski RT, Donenberg T, Shapiro C, Hammond LS, Miller J, Brooks KA, Cohen S, Tenenholz B, Desai D, Zandvakili I, Royer R, Li S, Narod SA.

    BMC Cancer. 2009 Mar 19;9:86.PMID: 19298662 [PubMed - indexed for MEDLINE]Related articlesFree article

    18.

    [Mutations in the BRCA1 gene (185delAG and 5382insC) are not present in any of the 30 breast cancer patients analyzed from eastern Colombia]

    Sanabria MC, Muñioz G, Vargas CI.

    Biomedica. 2009 Mar;29(1):61-72. Spanish. PMID: 19753840 [PubMed - indexed for MEDLINE]Related articles

    19.

    Contribution of BRCA1 germ-line mutations to breast cancer in Greece: a hospital-based study of 987 unselected breast cancer cases.

    Armaou S, Pertesi M, Fostira F, Thodi G, Athanasopoulos PS, Kamakari S, Athanasiou A, Gogas H, Yannoukakos D, Fountzilas G, Konstantopoulou I.

    Br J Cancer. 2009 Jul 7;101(1):32-7. Epub 2009 Jun 2.PMID: 19491894 [PubMed - indexed for MEDLINE]Related articles

    20.

    Comprehensive mutational analysis of BRCA1/BRCA2 for Korean breast cancer patients: evidence of a founder mutation.

    Seong MW, Cho S, Noh DY, Han W, Kim SW, Park CM, Park HW, Kim SY, Kim JY, Park SS.

    Clin Genet. 2009 Aug;76(2):152-60. Epub 2009 Jul 28.PMID: 19656164 [PubMed - indexed for MEDLINE]Related articles

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