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Over-representation of two specific haplotypes among chromosomes harbouring B...

Osorio(Ana),de la Hoya(Miguel),Rodríguez-L... Eur J Hum Genet 2004-01-08

The BRCA1 gene is included in a 200-400 kb region that is subjected to a recombination suppression mechanism; this regio...

Identification of differentially expressed genes associated with colorectal c...

Li(S-R),Dorudi(Sina),Bustin(S A) Eur Surg Res 2004-01-28

...BRCA1 tumour suppressor gene. Since promoter methylation is a direct cause of transcription silencing of the BRCA1 gene ...

Mutational analysis of the BRCA1-interacting genes ZNF350/ZBRK1 and BRIP1/BAC...

Rutter(Joni L),Smith(Amelia M),Dávila(Mich... Hum Mutat 2004-02-20

Two potential breast cancer susceptibility genes, encoding the BRCA1-interacting proteins ZNF350 (or ZBRK1) and BRIP1 (o...

Founder mutation in the BRCA1 gene in Malay breast cancer patients from Singa...

Lee(Ann S G),Ho(G H),Oh(P C),Balram(C),Ooi... Hum Mutat 2004-02-20

...BRCA1 gene among ethnic groups from Asia has not been well studied. We investigated the frequency of mutations in the BR...

BRCA1 and BRCA2 mutations in breast/ovarian cancer patients from central Ital...

Stuppia(L),Di Fulvio(P),Aceto(G),Pintor(S)... Hum Mutat 2004-02-20

...BRCA1/BRCA2 mutation was evaluated using the BRCAPRO software. We detected BRCA1/BRCA2 mutations in 8 patients (11.7%). ...

From genotype to phenotype: correlating XRCC1 polymorphisms with mutagen sens...

Wang(Yunfei),Spitz(Margaret R),Zhu(Yong),D... DNA Repair (Amst) 2004-03-30

...BRCA1 C-terminus functional domain and codon 194 is in the linker region of the XRCC1 N-terminal functional domain. To o...

E2F6 negatively regulates BRCA1 in human cancer cells without methylation of ...

Oberley(Matthew J),Inman(David R),Farnham(... J Biol Chem 2004-01-05

...brca1, ctip, art27, hp1alpha, and the rbap48 genes. E2F6 has been postulated to mediate transcriptional repression by re...

Targeted disruption of exons 1 to 6 of the Fanconi Anemia group A gene leads ...

Wong(Jasmine C Y),Alon(Noa),Mckerlie(Colin... Hum Mol Genet 2004-05-20

...Brca1, Fancd2 and Mlh1 appeared normal on Fanca(tm1Hsc) homozygous meiotic chromosomes. Taken together, our results sugg...

Founder mutations in BRCA1/2 are not frequent in Canadian Ashkenazi Jewish me...

Hamel(Nancy),Kotar(Kimberley),Foulkes(Will... BMC Med Genet 2004-05-11

...BRCA1:185delAG, BRCA1:5382insC and BRCA2:6174delT mutations simultaneously using a multiplex sizing assay detecting band...

Clinical, pathological and genetic features of women at high familial risk of...

Scott(C I),Iorgulescu(D G),Thorne(H J),Hen... Clin Genet 2004-03-16

...BRCA1 or BRCA2 mutation positive], identified via family cancer clinics, 49 cases of PM [21 (43%) BRCA1 or BRCA2 mutatio...

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