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Gastroenterology|November 16, 2005
MLH1 germline epimutations as a factor in hereditary nonpolyposis colorectal cancerMegan Hitchins, Rachel Williams, Kayfong Cheong, et al.
BMC Health Services Research|March 11, 2024
The impact of a regionally based translational cancer research collaborative in Australia using the FAIT methodologyChristine L Paul, Nicole M Verrills, Stephen Ackland, et al.
Eclinicalmedicine|December 16, 2025
Sertraline to reduce recidivism in impulsive violent offenders (ReINVEST): a randomised double blind clinical trialTony Butler, Emaediong I Akpanekpo, Lee Knight, et al.
Journal of B.U.ON. : Official Journal of the Balkan Union of Oncology|November 6, 2007
Breast cancer susceptibility genesJan Lubinski, Marcin Korzen, Bohdan Gorski, et al.
Nature Communications|November 27, 2019
LncRNA REG1CP promotes tumorigenesis through an enhancer complex to recruit FANCJ helicase for REG3A transcriptionHamed Yari, Lei Jin, Liu Teng, et al.
Antioxidants (Basel, Switzerland)|July 27, 2024
Antioxidant Properties of Zinc and Copper-Blood Zinc-to Copper-Ratio as a Marker of Cancer Risk BRCA1 Mutation CarriersMilena Matuszczak, Adam Kiljańczyk, Wojciech Marciniak, et al.
Human Molecular Genetics|July 19, 2015
A rare P2X7 variant Arg307Gln with absent pore formation function protects against neuroinflammation in multiple sclerosisBen J Gu, Judith Field, Sébastien Dutertre, et al.
Hereditary Cancer in Clinical Practice|September 19, 2024
Blood molybdenum level as a marker of cancer risk on BRCA1 carriersMilena Matuszczak, Adam Kiljańczyk, Wojciech Marciniak, et al.
International Journal of Cancer|July 20, 2020
The "unnatural" history of colorectal cancer in Lynch syndrome: Lessons from colonoscopy surveillanceAysel Ahadova, Toni T Seppälä, Christoph Engel, et al.
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