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British Journal of Cancer
|
July 23, 2022
Genomic architecture of FGFR2 fusions in cholangiocarcinoma and its implication for molecular testing
Olaf Neumann, Timothy C Burn, Michael Allgäuer, et al.
The Journal of Biological Chemistry
|
January 5, 2002
Absence of post-translational aspartyl beta-hydroxylation of epidermal growth factor domains in mice leads to developmental defects and an increased incidence of intestinal neoplasia
Joseph E Dinchuk, Richard J Focht, Jennifer A Kelley, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 10, 1997
Polycystin: in vitro synthesis, in vivo tissue expression, and subcellular localization identifies a large membrane-associated protein
O Ibraghimov-Beskrovnaya, W R Dackowski, L Foggensteiner, et al.
Journal of Medicinal Chemistry
|
July 16, 2021
Discovery of Pemigatinib: A Potent and Selective Fibroblast Growth Factor Receptor (FGFR) Inhibitor
Liangxing Wu, Colin Zhang, Chunhong He, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
April 6, 2010
Selective inhibition of JAK1 and JAK2 is efficacious in rodent models of arthritis: preclinical characterization of INCB028050
Jordan S Fridman, Peggy A Scherle, Robert Collins, et al.
Blood
|
March 4, 2010
Selective inhibition of IDO1 effectively regulates mediators of antitumor immunity
Xiangdong Liu, Niu Shin, Holly K Koblish, et al.
Plos One
|
April 22, 2020
INCB054828 (pemigatinib), a potent and selective inhibitor of fibroblast growth factor receptors 1, 2, and 3, displays activity against genetically defined tumor models
Phillip C C Liu, Holly Koblish, Liangxing Wu, et al.
Journal of Medicinal Chemistry
|
June 23, 2006
Potent benzimidazole sulfonamide protein tyrosine phosphatase 1B inhibitors containing the heterocyclic (S)-isothiazolidinone phosphotyrosine mimetic
Andrew P Combs, Wenyu Zhu, Matthew L Crawley, et al.
ACS Medicinal Chemistry Letters
|
May 20, 2017
INCB24360 (Epacadostat), a Highly Potent and Selective Indoleamine-2,3-dioxygenase 1 (IDO1) Inhibitor for Immuno-oncology
Eddy W Yue, Richard Sparks, Padmaja Polam, et al.
The Journal of Biological Chemistry
|
August 7, 1999
Cloning and characterization of ADAMTS11, an aggrecanase from the ADAMTS family
I Abbaszade, R Q Liu, F Yang, et al.
Page
of 13
Search research articles
Search
Showing results (111-120 of 128) with videos related to
Sort By:
Page
of 13
British Journal of Cancer
|
July 23, 2022
Genomic architecture of FGFR2 fusions in cholangiocarcinoma and its implication for molecular testing
Olaf Neumann, Timothy C Burn, Michael Allgäuer, et al.
The Journal of Biological Chemistry
|
January 5, 2002
Absence of post-translational aspartyl beta-hydroxylation of epidermal growth factor domains in mice leads to developmental defects and an increased incidence of intestinal neoplasia
Joseph E Dinchuk, Richard J Focht, Jennifer A Kelley, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
June 10, 1997
Polycystin: in vitro synthesis, in vivo tissue expression, and subcellular localization identifies a large membrane-associated protein
O Ibraghimov-Beskrovnaya, W R Dackowski, L Foggensteiner, et al.
Journal of Medicinal Chemistry
|
July 16, 2021
Discovery of Pemigatinib: A Potent and Selective Fibroblast Growth Factor Receptor (FGFR) Inhibitor
Liangxing Wu, Colin Zhang, Chunhong He, et al.
Journal of Immunology (Baltimore, Md. : 1950)
|
April 6, 2010
Selective inhibition of JAK1 and JAK2 is efficacious in rodent models of arthritis: preclinical characterization of INCB028050
Jordan S Fridman, Peggy A Scherle, Robert Collins, et al.
Blood
|
March 4, 2010
Selective inhibition of IDO1 effectively regulates mediators of antitumor immunity
Xiangdong Liu, Niu Shin, Holly K Koblish, et al.
Plos One
|
April 22, 2020
INCB054828 (pemigatinib), a potent and selective inhibitor of fibroblast growth factor receptors 1, 2, and 3, displays activity against genetically defined tumor models
Phillip C C Liu, Holly Koblish, Liangxing Wu, et al.
Journal of Medicinal Chemistry
|
June 23, 2006
Potent benzimidazole sulfonamide protein tyrosine phosphatase 1B inhibitors containing the heterocyclic (S)-isothiazolidinone phosphotyrosine mimetic
Andrew P Combs, Wenyu Zhu, Matthew L Crawley, et al.
ACS Medicinal Chemistry Letters
|
May 20, 2017
INCB24360 (Epacadostat), a Highly Potent and Selective Indoleamine-2,3-dioxygenase 1 (IDO1) Inhibitor for Immuno-oncology
Eddy W Yue, Richard Sparks, Padmaja Polam, et al.
The Journal of Biological Chemistry
|
August 7, 1999
Cloning and characterization of ADAMTS11, an aggrecanase from the ADAMTS family
I Abbaszade, R Q Liu, F Yang, et al.
Page
of 13