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BRCA2 gene mutations in Greek patients with familial breast cancer.

Armakolas(Athanasios),Ladopoulou(Angela),K... Hum Mutat 2002-02-12

Family history is a well-recognized risk factor for the development of breast cancer. The isolation of BRCA1 and BRCA2 g...

Brca2 (XRCC11) deficiency results in radioresistant DNA synthesis and a highe...

Kraakman-van der Zwet(Maria),Overkamp(Wilh... Mol Cell Biol 2002-01-29

...BRCA2 gene, as well as by the murine Brca2 gene. The Brca2 deficiency in V-C8 cells causes hypersensitivity to various D...

Gene-expression profiles in hereditary breast cancer.

Chinnaiyan(Arul M),Rubin(Mark A) Adv Anat Pathol 2002-02-21

...BRCA2, both of which increase the lifetime risk of developing breast cancer. The genome-wide perspective identified disc...

Clinical management of women with genomic BRCA1 and BRCA2 mutations.

Chang(J),Elledge(R M) Breast Cancer Res Treat 2002-04-02

There is increasing evidence that BRCA1 and BRCA2 associated tumors may differ from sporadic cancers. The purpose of thi...

Novel germline BRCA1 and BRCA2 mutations in breast and breast/ovarian cancer ...

Machackova(E),Damborsky(J),Valik(D),Foreto... Hum Mutat 2002-03-07

...BRCA2 genes. In BRCA1, two novel frame shift mutations were identified as 3761-3762delGA and 2616-2617ins10; in BRCA2, t...

Haplotype analysis in Icelandic and Finnish BRCA2 999del5 breast cancer famil...

Barkardottir(R B),Sarantaus(L),Arason(A),V... Eur J Hum Genet 2002-02-08

The 999del5 mutation is the single, strong BRCA2 founder mutation in Iceland and the most common BRCA1/2 founder mutatio...

The western Swedish BRCA1 founder mutation 3171ins5; a 3.7 cM conserved haplo...

Bergman(A),Einbeigi(Z),Olofsson(U),Taib(Z)... Eur J Hum Genet 2002-02-08

...BRCA2 mutation in Sweden is the BRCA1 mutation 3171ins5. In the western part of Sweden this mutation accounts for as muc...

Psychological impact of genetic counselling and testing in women previously d...

Randall(J),Butow(P),Kirk(J),Tucker(K) Intern Med J 2002-01-10

...BRCA2, now allows women with breast cancer and a family history of breast/ovarian cancer to undergo genetic testing to i...

[Clinical and pathological characteristics and clinical course of patients wi...

Pericay(C),Díez(O),Campos(B),Balmaña(J),Do... Med Clin (Barc) 2002-02-25

...BRCA2 cases. The median follow-up in BRCA1 and BRCA2 BC was 131 and 54 months, respectively.,There were no differences i...

Prevalence of breast cancer predisposition gene mutations in Chinese women an...

Tang(N L),Choy(K W),Pang(C P),Yeo(W),Johns... Clin Chim Acta 2002-01-02

...BRCA2 are high-penetrant cancer predisposition genes, but the prevalence and nature of mutations in these genes appear t...

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