Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Lindsey Millard"'
Autor:
Kevin Hudson, Richard Mott, Richard A. Ward, Jonathan D. Wrigley, Stephen W. Peters, Ian M. Hardern, Lindsey Millard, Thorsten Nowak, Peter B. Simpson, Kay Eckersley, Michael Walters
Publikováno v:
Cell Biochemistry and Biophysics. 60:99-111
USP7 (HAUSP) is a deubiquitinating enzyme, which plays a crucial role in regulating the levels of the p53 tumour suppressor protein, through its ability to prevent the proteasomal degradation of the Ubiquitin ligase for p53, Hdm2. Supporting evidence
Autor:
James P. Dean, Jack W. Singer, Sherri Amberg, Huafeng Zhou, Lindsey Millard, Suliman Al-Fayoumi
Publikováno v:
Cancer Research. 76:CT159-CT159
Introduction: Dysregulation in tyrosine kinase signaling has been implicated in development of hematologic malignancies including myelofibrosis and lymphomas. Pacritinib is an oral kinase inhibitor with specificity for JAK2, FLT3, CSF1R, and IRAK1. I
Autor:
Suliman Al-Fayoumi, Huafeng Zhou, James P. Dean, Mary S. Campbell, Sherri Amberg, Lindsey Millard
Publikováno v:
Blood. 126:5178-5178
Introduction: PAC is a kinase inhibitor with specificity for JAK2, FLT3, IRAK1, and CFS1R that does not inhibit JAK1. PAC has demonstrated activity in phase (Ph) 1-3 clinical studies. Nonclinical and clinical pharmacokinetic (PK) and pharmacodynamic
Autor:
Kay Eckersley, Helen Plant, Peter B. Simpson, David M. Andrews, Kevin Hudson, Lindsey Millard, Marian Preston, Ian M. Hardern, Thorsten Nowak, Jonathan D. Wrigley
Publikováno v:
Cancer Research. 71:4043-4043
Deubiquitinating enzymes (DUBs) represent promising opportunities for therapeutic intervention in oncology, and this study reports key information about the catalytic activity, assaying and inhibition of this novel enzyme class. The DUBs are protease