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Breast cancer: genetics, risks, and strategies.

Nogueira(S M),Appling(S E) Nurs Clin North Am 2000-10-12

...BRCA2 genes and related research has increased our understanding of key risk factors. After identifying those who are at...

Comparative genomic hybridization in inherited and sporadic ovarian tumors in...

Patael-Karasik(Y),Daniely(M),Gotlieb(W H),... Cancer Genet Cytogenet 2000-09-08

...BRCA2 mutation carriers), 2 primary peritoneal carcinomatosis, 1 pseudomyxoma peritoneii tumor, and 1 sertoli cell tumor...

Occult ovarian tumors in women with BRCA1 or BRCA2 mutations undergoing proph...

Lu(K H),Garber(J E),Cramer(D W),Welch(W R)... J Clin Oncol 2000-08-01

...BRCA2 testing, each patient's risk of hereditary predisposition was calculated using the Berry-Parmigiani model and fami...

Simultaneous interdisciplinary counseling in German breast/ovarian cancer fam...

Hofferbert(S),Worringen(U),Backe(J),Rücker... Genet Couns 2000-11-21

...BRCA2 mutation analyses render testing in medium to low risk individuals questionable, our findings emphasize the import...

Sequence alterations can mask each other's presence during screening with SSC...

Orban(T I),Csokay(B),Olah(E) Biotechniques 2000-11-09

...BRCA2 genes where the SSCP/HA techniques can produce ambiguous predictions if used to detect known genetic variants comp...

BRCA1 and BRCA2 mutations in Turkish breast/ovarian families and young breast...

Yazici(H),Bitisik(O),Akisik(E),Cabioglu(N)... Br J Cancer 2000-09-28

To date, BRCA1 and BRCA2 mutations in breast and/or ovarian patients have not been characterized in the Turkish populati...

A genome-wide map showing common regions of loss of heterozygosity/allelic im...

Osborne(R J),Hamshere(M G) Cancer Res 2000-08-24

...BRCA2 loci, which confirmed the power of the technique, 24 other regions were identified on 16 different chromosomes.

Genome-wide search for loss of heterozygosity using laser capture microdissec...

Shen(C Y),Yu(J C),Lo(Y L),Kuo(C H),Yue(C T... Cancer Res 2000-08-24

...BRCA2, are involved within the common functional pathway of DSB-related checkpoint/ repair. Because genomic deletion cau...

[Familial ovarian cancer].

Sekine(M),Tanaka(K) Nihon Rinsho 2000-10-19

...BRCA2 are reported to account for around 50% of familial ovarian cancer families. In this paper, we describe the contrib...

Rapid detection of deletion, insertion, and substitution mutations via hetero...

Tian(H),Brody(L C),Landers(J P) Genome Res 2000-10-17

...BRCA2. For this system, the effective fragment size for CE-based HDA was found in the range of 200-300 bp, however, the ...

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