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Structure (London, England : 1993)|February 27, 2018
Disease Variants of FGFR3 Reveal Molecular Basis for the Recognition and Additional Roles for Cdc37 in Hsp90 Chaperone SystemTom D Bunney, Alison J Inglis, Domenico Sanfelice, et al.
The Journal of Investigative Dermatology|August 4, 2019
Frequent and Persistent PLCG1 Mutations in Sézary Cells Directly Enhance PLCγ1 Activity and Stimulate NFκB, AP-1, and NFAT SignalingVarsha M Patel, Charlotte E Flanagan, Marta Martins, et al.
Frontiers in Immunology|January 9, 2019
Novel PLCG2 Mutation in a Patient With APLAID and Cutis LaxaJoão Farela Neves, Rainer Doffinger, Gabriela Barcena-Morales, et al.
Molecular Cell|April 28, 2009
Structural insights into formation of an active signaling complex between Rac and phospholipase C gamma 2Tom D Bunney, Olaniyi Opaleye, S Mark Roe, et al.
Oncotarget|June 4, 2016
Quantitative in vivo optical tomography of cancer progression & vasculature development in adult zebrafishSunil Kumar, Nicola Lockwood, Marie-Christine Ramel, et al.
Molecular and Cellular Biology|January 20, 2011
Membrane environment exerts an important influence on rac-mediated activation of phospholipase Cγ2Katy L Everett, Anja Buehler, Tom D Bunney, et al.
Molecular Cell|February 18, 2006
Structural and mechanistic insights into ras association domains of phospholipase C epsilonTom D Bunney, Richard Harris, Natalia Lamuño Gandarillas, et al.
Oncotarget|March 19, 2016
Landscape of activating cancer mutations in FGFR kinases and their differential responses to inhibitors in clinical useHarshnira Patani, Tom D Bunney, Nethaji Thiyagarajan, et al.
American Journal of Human Genetics|September 25, 2012
A hypermorphic missense mutation in PLCG2, encoding phospholipase Cγ2, causes a dominantly inherited autoinflammatory disease with immunodeficiencyQing Zhou, Geun-Shik Lee, Jillian Brady, et al.
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