Showing results (1-10 of 24) with videos related to

Sort By:
Pageof 3
Oncotarget|September 14, 2020
Paradox breaker BRAF inhibitors have comparable potency and MAPK pathway reactivation to encorafenib in BRAF mutant colorectal cancerOliver J Pickles, Aneta Drozd, Louise Tee, et al.
Journal of Medical Genetics|July 2, 2013
Comparison of the clinical scoring systems in Silver-Russell syndrome and development of modified diagnostic criteria to guide molecular genetic testingRenuka P Dias, Peter Nightingale, Carol Hardy, et al.
Clinical Epigenetics|July 2, 2014
Methylation analysis and diagnostics of Beckwith-Wiedemann syndrome in 1,000 subjectsAbdulla Ibrahim, Gail Kirby, Carol Hardy, et al.
Nature Structural & Molecular Biology|November 23, 2023
Intra-promoter switch of transcription initiation sites in proliferation signaling-dependent RNA metabolismJoseph W Wragg, Paige-Louise White, Yavor Hadzhiev, et al.
Brain Communications|February 26, 2021
Evidence that autosomal recessive spastic cerebral palsy-1 (CPSQ1) is caused by a missense variant in HPDLNeil V Morgan, Bryndis Yngvadottir, Mary O'Driscoll, et al.
Radiation Oncology (London, England)|July 14, 2021
Complete response to neoadjuvant chemoradiotherapy in rectal cancer is associated with RAS/AKT mutations and high tumour mutational burdenJoanne D Stockton, Louise Tee, Celina Whalley, et al.
International Journal of Cancer|January 8, 2003
The patched polymorphism Pro1315Leu (C3944T) may modulate the association between use of oral contraceptives and breast cancer riskJenny Chang-Claude, Alison Dunning, Udo Schnitzbauer, et al.
Clinical Epigenetics|December 12, 2013
Epimutation profiling in Beckwith-Wiedemann syndrome: relationship with assisted reproductive technologyLouise Tee, Derek Hk Lim, Renuka P Dias, et al.
Human Genetics|June 17, 2005
Locus heterogeneity in autosomal recessive congenital cataracts: linkage to 9q and germline HSF4 mutationsTim Forshew, Colin A Johnson, Shagufta Khaliq, et al.
Human Reproduction (Oxford, England)|December 17, 2008
Clinical and molecular genetic features of Beckwith-Wiedemann syndrome associated with assisted reproductive technologiesDerek Lim, Sarah C Bowdin, Louise Tee, et al.
Pageof 3