Results 201 to 210 of about 37,664 (239)
GALNT3 is a novel target driving lymphomagenesis via O-glycosylation of FGFR2. [PDF]
Sun R +7 more
europepmc +1 more source
Prenatal diagnosis of apert syndrome at 23 weeks: a case report with isolated syndactyly and sacrococcygeal appendage preceding cranial malformation. [PDF]
Ge S, Lai Q, Yuan D, McGrath E.
europepmc +1 more source
Role of lipid rafts in the FGFR2c-mediated oncogenic signaling by involvement of TRPA1 channel in pancreatic ductal adenocarcinoma cells. [PDF]
Mancini V +7 more
europepmc +1 more source
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Digestive Diseases and Sciences, 2021
FGFR2 genomic alterations are observed in 10-20% of cholangiocarcinoma (CCA). Although FGFR2 fusions are an important actionable target, FGFR2 protein expression has not been thoroughly characterized.To evaluate FGFR2 protein expression in cholangiocarcinoma harboring FGFR2 genomic alterations.FGFR2 protein expression was evaluated in 99 CCA cases with
Pedro Usón Junior +2 more
exaly +3 more sources
FGFR2 genomic alterations are observed in 10-20% of cholangiocarcinoma (CCA). Although FGFR2 fusions are an important actionable target, FGFR2 protein expression has not been thoroughly characterized.To evaluate FGFR2 protein expression in cholangiocarcinoma harboring FGFR2 genomic alterations.FGFR2 protein expression was evaluated in 99 CCA cases with
Pedro Usón Junior +2 more
exaly +3 more sources
The Lancet Gastroenterology and Hepatology, 2021
BACKGROUND Treatment options are sparse for patients with advanced cholangiocarcinoma after progression on first-line gemcitabine-based therapy.
M. Javle +22 more
semanticscholar +1 more source
BACKGROUND Treatment options are sparse for patients with advanced cholangiocarcinoma after progression on first-line gemcitabine-based therapy.
M. Javle +22 more
semanticscholar +1 more source
Journal of Clinical Oncology, 2023
4009 Background: Oncogenic FGFR2 alterations (fusions/rearrangements (f/r), amplifications, mutations) represent a broad therapeutic opportunity as they drive multiple solid tumors, particularly cholangiocarcinoma (CCA). However, off-isoform toxicity and
M. Borad +19 more
semanticscholar +1 more source
4009 Background: Oncogenic FGFR2 alterations (fusions/rearrangements (f/r), amplifications, mutations) represent a broad therapeutic opportunity as they drive multiple solid tumors, particularly cholangiocarcinoma (CCA). However, off-isoform toxicity and
M. Borad +19 more
semanticscholar +1 more source
Discovery of a Selective and Orally Bioavailable FGFR2 Degrader for Treating Gastric Cancer.
Journal of Medicinal Chemistry, 2023Abnormal activation of fibroblast growth factor receptors (FGFRs) results in the development and progression of human cancers. FGFR2 is frequently amplified or mutated in cancers; therefore, it is an attractive target for tumor therapy.
Lin Ma +12 more
semanticscholar +1 more source
American Journal of Medical Genetics Part A, 2014
Craniosynostosis is a congenital anomaly that can occur as an isolated condition or as part of a syndrome. Although several genes are known to cause syndromic craniosynostosis, only 24% can be attributed to known genes. Therefore, it is likely that more mutations and other genes are involved.
Goos, Jacqueline +7 more
openaire +3 more sources
Craniosynostosis is a congenital anomaly that can occur as an isolated condition or as part of a syndrome. Although several genes are known to cause syndromic craniosynostosis, only 24% can be attributed to known genes. Therefore, it is likely that more mutations and other genes are involved.
Goos, Jacqueline +7 more
openaire +3 more sources
Modulation of the expression of the FGFR2-IIIb and FGFR2-IIIc molecules in dermatofibroma
Journal of Dermatological Science, 2008[No abstract available]
SKROZA, Nevena +7 more
openaire +3 more sources
Journal of Clinical Oncology, 2022
4009 Background: Survival outcomes are historically poor in patients (pts) with advanced/metastatic iCCA, with median overall survival (mOS) times of approximately 1 year with first-line gemcitabine plus cisplatin and approximately 6 months with second ...
L. Goyal +19 more
semanticscholar +1 more source
4009 Background: Survival outcomes are historically poor in patients (pts) with advanced/metastatic iCCA, with median overall survival (mOS) times of approximately 1 year with first-line gemcitabine plus cisplatin and approximately 6 months with second ...
L. Goyal +19 more
semanticscholar +1 more source

