Found: 8
Select item for more details and to access through your institution.
Preinvasive colorectal lesion transcriptomes correlate with endoscopic morphology (polypoid vs. nonpolypoid).
- Published in:
- EMBO Molecular Medicine, 2011, v. 3, n. 6, p. 334, doi. 10.1002/emmm.201100141
- By:
- Publication type:
- Article
Apoptotic effect of ethyl-4-isothiocyanatobutanoate is associated with DNA damage, proteasomal activity and induction of p53 and p21<sup>cip1/waf1</sup>.
- Published in:
- Apoptosis, 2006, v. 11, n. 8, p. 1299, doi. 10.1007/s10495-006-8760-5
- By:
- Publication type:
- Article
The Escherichia coli RecA protein complements recombination defective phenotype of the Saccharomyces cerevisiae rad52 mutant cells.
- Published in:
- Yeast, 2003, v. 20, n. 5, p. 389, doi. 10.1002/yea.971
- By:
- Publication type:
- Article
Novel MLH1 and MSH2 germline mutations in the first HNPCC families identified in Slovakia (Communicated by Mark H. Paalman) Online Citation: Human Mutation, Mutation in Brief #598 (2002) Online http://www.interscience.wiley.com/humanmutation/pdf/mutation/598.pdf)
- Published in:
- Human Mutation, 2003, v. 21, n. 4, p. 449, doi. 10.1002/humu.9127
- By:
- Publication type:
- Article
Novel MLH1 and MSH2 germline mutations in the first HNPCC families identified in SlovakiaCommunicated by Mark H. PaalmanOnline Citation: Human Mutation, Mutation in Brief #598 (2002) Onlinehttp://www.interscience.wiley.com/humanmutation/pdf/mutation/598.pdf
- Published in:
- Human Mutation, 2003, v. 21, n. 4, p. 449, doi. 10.1002/humu.9127
- By:
- Publication type:
- Article
Comprehensive genetic characterization of hereditary breast/ovarian cancer families from Slovakia.
- Published in:
- Breast Cancer Research & Treatment, 2011, v. 126, n. 1, p. 119, doi. 10.1007/s10549-010-1325-x
- By:
- Publication type:
- Article
Identification of rare complete BRCA1 gene deletion using a combination of SNP haplotype analysis, MLPA and array-CGH techniques.
- Published in:
- Breast Cancer Research & Treatment, 2008, v. 109, n. 3, p. 581, doi. 10.1007/s10549-007-9670-0
- By:
- Publication type:
- Article
High-Resolution Breakpoint Analysis Provides Evidence for the Sequence-Directed Nature of Genome Rearrangements in Hereditary Disorders.
- Published in:
- Human Mutation, 2015, v. 36, n. 2, p. 250, doi. 10.1002/humu.22734
- By:
- Publication type:
- Article