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1 ere has been very little characterization of BRCA2 protein.
2 2% similarity), respectively, with the human BRCA2 protein.
3 tations predicted to cause truncation of the BRCA2 protein.
4 lic mutations in BRCA2 and express truncated BRCA2 proteins.
5 use cDNA sequence predicts a 3328-amino-acid Brca2 protein, 90 amino acids shorter than the human pro
6        Proximate to the COOH terminus of the BRCA2 protein, a conserved and DNA binding domain (BRCA2
7                                              BRCA2 protein, a product of the breast cancer susceptibi
8                 Our results demonstrate that BRCA2 proteins acetylate primarily H3 and H4 of free his
9                                          The Brca2 proteins also share a potential nuclear localizati
10        Because of the presence of C-terminal BRCA2 protein and atypical clinical features of the misc
11                  Skp2 overexpression reduced BRCA2 protein and promoted cell growth and migration.
12 equenced cDNA for the entire 3329 amino acid Brca2 protein and this has revealed that, like Brca1, Br
13                                The BRCA1 and BRCA2 proteins are important in maintaining genomic stab
14                                The BRCA1 and BRCA2 proteins are involved in the maintenance of genome
15 ow functional significance of restoration of BRCA2 protein by secondary BRCA2 mutations in acquired d
16         This study suggests a requirement of BRCA2 protein for the IR-induced assembly of Rad51 compl
17 ells expressing a carboxy-terminal truncated BRCA2 protein form IR-inducible BRCA2 and FANCD2 foci, b
18           This region is highly conserved in BRCA2 proteins from a variety of mammalian species, but
19                                          The BRCA2 protein has been proposed to function in the repai
20                               Both BRCA1 and BRCA2 proteins have been implicated in the repair of dou
21 ds, which is poorly conserved with mammalian BRCA2 proteins, having only 37% amino acid identity over
22             The mechanistic link between the BRCA2 protein, homologous recombination, and genomic ins
23  appears to diagnose the biochemical loss of BRCA2 protein in cancers (ie, BRCA2-mutant genotype), wh
24 e results demonstrated that the stability of BRCA2 protein in mammalian cells depends on the presence
25 tudies provide evidence for key roles of the BRCA2 protein in mammalian gametogenesis and meiotic suc
26 tissue truncation test to identify truncated BRCA2 proteins in breast cancer tissue biopsies in vivo
27                                              BRCA2 protein interacts directly with the RAD51 recombin
28  eight BRC repeats would affect the way that BRCA2 protein interacts with the RAD51 filament.
29 er development, at least in part because the BRCA2 protein is required for the maintenance of genomic
30 ss either phospho-Ser7-FANCG, or full length BRCA2 protein, lack the interactions amongst the four co
31 ssibility, we examined the alteration of the BRCA2 protein level in human cell lines after UV irradia
32           Mitomycin C (MMC) led to decreased BRCA2 protein levels associated with increased ubiquitin
33 ar phenotype was observed after reduction of BRCA2 protein levels using specific BRCA2 small-interfer
34 able of binding to two separate sites in the BRCA2 protein, located either side of the BRC repeats.
35  in human cell lines led to dramatic loss of BRCA2 protein, mainly due to its increased degradation.
36                         We demonstrated that Brca2 protein prevents single-stranded DNA gap accumulat
37                                              BRCA2 protein regulates recombinational repair by intera
38                 Although the function of the BRCA2 protein remains to be determined, murine cells hom
39 n-truncating mutations, a test for truncated BRCA2 proteins should identify most BRCA2 hereditary can
40      Lastly, we demonstrate that full-length BRCA2 protein stimulates DMC1-mediated DNA strand exchan
41 f human Rad51 to the conserved BRC repeat of BRCA2 protein, the RecB-domain may be one of several str
42 iduals by promoting degradation of wild-type BRCA2 protein, thereby predisposing them to genomic inst
43 e in the cancer, which indicated that intact BRCA2 protein was present in this cancer.
44 s this question, the expression of wild-type BRCA2 protein was reconstituted, in an either constituti
45             Residues 3196-3232 of the murine BRCA2 protein were shown to be involved in this interact
46 ript lacking exons 4-7, encoding an in-frame BRCA2 protein with an internal deletion of 105 amino aci
47 defined and an interaction identified of the Brca2 protein with the DNA-repair protein Rad51.

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