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Familial Cancer|October 10, 2024
MSH6-proficient crypt foci in MSH6 constitutional mismatch repair deficiency: reversion of a frameshifted coding microsatellite to its wild-type sequenceJinru Shia, Francisco Sanchez-Vega, Stanley Cho, et al.Hereditary Cancer in Clinical Practice|June 14, 2024
Modifiable risk factors for cancer among people with lynch syndrome: an international, cross-sectional surveyRobert F Power, Damien E Doherty, Roberta Horgan, et al.Cancer Research|May 19, 2006
MDM2 SNP309 accelerates tumor formation in a gender-specific and hormone-dependent mannerGareth L Bond, Kim M Hirshfield, Tomas Kirchhoff, et al.Sports Medicine - Open|June 23, 2026
Injury Patterns in Soccer-Induced Maxillofacial Fractures and Ocular Trauma: A Narrative ReviewAnaas M Mergoum, Jacob Lentner, Brooke Echter, et al.International Journal of Cancer|October 2, 2003
MSH6 germline mutations are rare in colorectal cancer familiesPaolo Peterlongo, Khedoudja Nafa, Gabriel S Lerman, et al.Cancer Research|August 4, 2004
Increased progesterone receptor expression in benign epithelium of BRCA1-related breast cancersTari A King, Mary L Gemignani, Weiwei Li, et al.Human Molecular Genetics|January 15, 2005
Functional and genomic approaches reveal an ancient CHEK2 allele associated with breast cancer in the Ashkenazi Jewish populationAvraham Shaag, Tom Walsh, Paul Renbaum, et al.Annals of Surgical Oncology|June 29, 2007
Heterogenic loss of the wild-type BRCA allele in human breast tumorigenesisTari A King, Weiwei Li, Edi Brogi, et al.Breast Cancer Research and Treatment|January 23, 2022
Perceptions of patients and medical oncologists toward biospecimen donation in the setting of abnormal breast imaging findingsDavinia S Seah, Nabihah Tayob, Jose Pablo Leone, et al.Cancer|January 9, 2019
Ampullary cancer: Evaluation of somatic and germline genetic alterations and association with clinical outcomesWinston Wong, Maeve A Lowery, Michael F Berger, et al.Pageof 61