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Overexpression of a set of genes in mesothelioma versus parietal pleura may e...

Roe(O D),Anderssen(E),Helge(E),Hild Hakvaa... J Clin Oncol 0000-00-00

...BRCA2, FANCA, FANCD2, RAD51) were overexpressed in tumour.,Mesothelioma resistance to therapy is reflected in the gene p...

Higher occurrence of childhood cancer in families with germline mutations in ...

Olsson(H),Magnusson(S),Borg(Å),Nilberth(M)... J Clin Oncol 0000-00-00

...BRCA2 (n=43) MMR (MLH1, MSH2 MSH6) (n=31) and CDKN2A (n=15) genes in comparison with population based control families (...

Two common genetic variants increase susceptibility to breast cancer in the S...

Millastre(E),Andres(R),Lambea(J),Serrano(S... J Clin Oncol 0000-00-00

...BRCA2 germline mutations. We aim to detect genetic variants associated with breast cancer susceptibility in Spain.,Withi...

The "BRCAness" syndrome in ovarian cancer: A case-control study describing th...

Tan(D S),Rothermundt Dr(C),Thomas(K),Bancr... J Clin Oncol 0000-00-00

...BRCA2 mutations (BRCA+) were selected from the Royal Marsden Hospital clinical genetics database and matched (1:2) with ...

Impact of BRCA mutation status on the clinical phenotype and survival of here...

Kiechle(M),Engel(C),Schmutzler(R), J Clin Oncol 0000-00-00

...BRCA2 mutation carriers (45 yrs) and women tested negative for BRCA1 and BRCA2 mutations (46 yrs) as well as sporadic br...

A comparison of internet-based models assessing the likelihood of a BRCA muta...

Bordeleau(L J),Ennis(M),Canon(S),Panchal(S... J Clin Oncol 0000-00-00

...BRCA2 genes account for the majority of hereditary breast and ovarian cancer. Various risk assessment models are availab...

BRCA mutation in Chinese population: Preliminary results from the The Hong Ko...

Kwong(A),Wong PhD(C),Ma(E),Ford(J M) J Clin Oncol 0000-00-00

...BRCA2 mutations were found in our population. Further research on the spectrum of the mutations in Chinese will allow th...

The impact of breast cancer morphology on the prediction of a BRCA1 mutation.

Gadzicki(D),Schubert(A),Milde(S),Lehmann(U... J Clin Oncol 0000-00-00

...BRCA2 mutation is causatively related to an individual breast cancer. The aim of this study was to determine in an unsel...

Screening for germline mutations in families at-risk for hereditary breast ca...

Palmero(E I),Hainaut(P),Camey(S A),Filho(C... J Clin Oncol 0000-00-00

...BRCA2, TP53, and CHEK2 mutation analysis.,Of 902 women submitted to GCRA, 214 (23.7%) women from 183 families had pedigr...

Homologous recombination defects in sporadic breast cancers.

Hannemann(J),Mulder(L),Linn(S C),Sonke(G),... J Clin Oncol 0000-00-00

...BRCA2 or by abnormalities in the Fanconi Anemia pathway. In addition, the recently discovered oncogene EMSY is amplified...

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