Results 211 to 220 of about 35,836 (258)
The multi-kinase inhibitor tinengotinib as monotherapy or combined with atezolizumab in advanced solid tumors: a phase Ib/II trial. [PDF]
Zhang P +17 more
europepmc +1 more source
<i>FGFR3</i> Gene Alterations and Protein Expression in Paired TURBT and Radical Cystectomy Archival Specimens of Muscle-Invasive Bladder Cancer. [PDF]
Miyake M +14 more
europepmc +1 more source
Ex Vivo Tumor-Derived Organoid Pharmacotyping Identifies Personalized Therapeutic Options for Patients with Biliary Tract Cancer. [PDF]
Richardson AB +14 more
europepmc +1 more source
FGFR Inhibitors in Oncology: Insight on the Management of Toxicities in Clinical Practice
Fibroblast Growth Factor receptor (FGFR) pathway aberrations have been implicated in approximately 7% of the malignancies. As our knowledge of FGFR aberrations in cancer continues to evolve, FGFR inhibitors emerged as potential targeted therapeutic ...
Sri Harsha Tella +2 more
exaly +2 more sources
FGFR a promising druggable target in cancer: Molecular biology and new drugs
Introduction The Fibroblast Growth Factor Receptor (FGFR) family consists of Tyrosine Kinase Receptors (TKR) involved in several biological functions.
Tindara Franchina +2 more
exaly +2 more sources
Hepatocellular carcinoma (HCC) is the most common type of primary liver cancer, ranking third in cancer deaths worldwide. Over the last decade, several studies have emphasized the development of tyrosine kinase inhibitors (TKIs) to target the aberrant ...
Yijun Wang, Tongyue Zhang, Limin Xia
exaly +2 more sources
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FGFR Mutations and Plagiocephaly
Journal of Craniofacial Surgery, 2008FGFR genes have important effects on bone development, and mutations in 4 "hot spot" exons of FGFR1-3 are found in many patients with craniosynostosis and some with synostotic plagiocephaly. To test the hypothesis that sequence variation in those exons predisposes toward developmental bone deformation, we assayed 160 children with nonsynostotic ...
Valairat, Dhamcharee, Richard G, Boles
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