Found: 12
Select item for more details and to access through your institution.
Efficiency of the revised Bethesda guidelines (2003) for the detection of mutations in mismatch repair genes in Austrian HNPCC patients.
- Published in:
- International Journal of Cancer, 2006, v. 118, n. 6, p. 1465, doi. 10.1002/ijc.21524
- By:
- Publication type:
- Article
[Cp<sub>2</sub>Ti(PMe<sub>3</sub>)<sub>2</sub>]-A Versatile Source of Titanocene Derivatives.
- Published in:
- Angewandte Chemie International Edition, 1985, v. 24, n. 5, p. 394, doi. 10.1002/anie.198503941
- By:
- Publication type:
- Article
Impacts of Telomeric Length, Chronic Hypoxia, Senescence, and Senescence-Associated Secretory Phenotype on the Development of Thoracic Aortic Aneurysm.
- Published in:
- International Journal of Molecular Sciences, 2022, v. 23, n. 24, p. 15498, doi. 10.3390/ijms232415498
- By:
- Publication type:
- Article
Spectrum of germ-line MLH1 and MSH2 mutations in Austrian patients with hereditary nonpolyposis colorectal cancer.
- Published in:
- Wiener Klinische Wochenschrift, 2005, v. 117, n. 7/8, p. 269, doi. 10.1007/s00508-005-0337-8
- By:
- Publication type:
- Article
TP53 germline mutation may affect response to anticancer treatments: analysis of an intensively treated Li-Fraumeni family.
- Published in:
- Breast Cancer Research & Treatment, 2015, v. 151, n. 3, p. 671, doi. 10.1007/s10549-015-3424-1
- By:
- Publication type:
- Article
Strategy for prevention of cancers of the esophagus.
- Published in:
- Annals of the New York Academy of Sciences, 2014, v. 1325, n. 1, p. 108, doi. 10.1111/nyas.12529
- 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
• Pancho trial (p53-adapted neoadjuvant chemotherapy for resectable esophageal cancer) completed—mutation rate of the marker higher than expected.
- Published in:
- European Surgery: ACA Acta Chirurgica Austriaca, 2018, v. 50, n. 4, p. 160, doi. 10.1007/s10353-018-0527-z
- By:
- Publication type:
- Article
Validity of assessing level walking with the 2D motion analysis software TEMPLO and reliability of 3D marker application.
- Published in:
- Scientific Reports, 2024, v. 14, n. 1, p. 1, doi. 10.1038/s41598-024-52053-z
- By:
- Publication type:
- Article
Conducting Design Research Internationally: A Dutch-German Approach.
- Published in:
- Design Management Review, 2012, v. 23, n. 1, p. 64, doi. 10.1111/j.1948-7169.2012.00172.x
- By:
- Publication type:
- Article
Potential of DNA methylation in rectal cancer as diagnostic and prognostic biomarkers.
- Published in:
- 2015
- By:
- Publication type:
- journal article