Results 11 to 20 of about 24,353 (179)

K-Ras and β-catenin mutations cooperate with Fgfr3 mutations in mice to promote tumorigenesis in the skin and lung, but not in the bladder [PDF]

open access: yesDisease Models & Mechanisms, 2011
SUMMARY The human fibroblast growth factor receptor 3 (FGFR3) gene is frequently mutated in superficial urothelial cell carcinoma (UCC). To test the functional significance of FGFR3 activating mutations as a ‘driver’ of UCC, we targeted the expression of
Imran Ahmad   +8 more
doaj   +2 more sources

FGFR3 signaling and function in triple negative breast cancer [PDF]

open access: yesCell Communication and Signaling, 2020
Background Triple negative breast cancer (TNBC) accounts for 16% of breast cancers and represents an aggressive subtype that lacks targeted therapeutic options.
Nicole J. Chew   +9 more
doaj   +2 more sources

Generation of Fgfr3 Conditional Knockout Mice

open access: yesInternational Journal of Biological Sciences, 2010
Fibroblast growth factor receptor 3 (FGFR3), highly conserved in both humans and murine, is one of key tyrosine kinase receptors for FGF. FGFR3 is expressed in different tissues, including cartilage, brain, kidney, and intestine at different development ...
Nan Su, Xiaoling Xu, Cuiling Li, Qifen He, Ling Zhao, Can Li, Siyu Chen, Fengtao Luo, Lingxian Yi, Xiaolan Du, Haiyang Huang, Chuxia Deng, Lin Chen
doaj   +1 more source

Роль мутационного статуса гена FGFR3 в предсказании прогрессирования рака мочевого пузыря без мышечной инвазии [PDF]

open access: yes, 2015
A prospective study was conducted to assess the prognostic value of FGFR3 gene mutation status in patients with non-muscle invasive bladder cancer. A total of 265 patients were included in the study. FGFR3 gene mutations were found in 168 (63.4 %) cases.
R. I. Goncharova   +7 more
core   +1 more source

THE MOLECULAR PATHOGENESIS OF BLADDER CANCER

open access: yesAlʹmanah Kliničeskoj Mediciny, 2016
The review describes the current views on urothelial carcinoma carcinogenesis. Based on the up-todate genetic studies, molecular pathways determining the development of superficial and invasive bladder cancers are considered. It was demonstrated that the
M. V. Nemtsova, N. E. Kushlinskii
doaj   +1 more source

Loss of FGFR3 Delays Acute Myeloid Leukemogenesis by Programming Weakly Pathogenic CD117-Positive Leukemia Stem-Like Cells

open access: yesFrontiers in Pharmacology, 2021
Chemotherapeutic patients with leukemia often relapse and produce drug resistance due to the existence of leukemia stem cells (LSCs). Fibroblast growth factor receptor 3 (FGFR3) signaling mediates the drug resistance of LSCs in chronic myeloid leukemia ...
Chen Guo   +9 more
doaj   +1 more source

The Prognostic Value of FGFR3 Expression in Patients with T1 Non-Muscle Invasive Bladder Cancer

open access: yesCancer Management and Research, 2021
Danijel Sikic,1,2 Helge Taubert,1,2 Johannes Breyer,3 Markus Eckstein,2,4 Veronika Weyerer,2,4 Bastian Keck,1,2 Jennifer Kubon,1,2 Wolfgang Otto,3 Thomas S Worst,5 Maximilian C Kriegmair,5 Philipp Erben,5 Arndt Hartmann,2,4 Bernd Wullich,1,2 Ralph M ...
Sikic D   +14 more
doaj  

Activated FGFR3 suppresses bone regeneration and bone mineralization in an ovariectomized mouse model

open access: yesBMC Musculoskeletal Disorders, 2023
Background Postmenopausal osteoporosis is a widespread health concern due to its prevalence among older adults and an associated high risk of fracture. The downregulation of bone regeneration delays fracture healing.
Itaru Kawashima   +8 more
doaj   +1 more source

FGFR3 expression in primary invasive bladder cancers and matched lymph node metastases. [PDF]

open access: yes, 2015
PURPOSE: FGFR3 is considered a good therapeutic target for bladder cancer. However, to our knowledge it is unknown whether the FGFR3 status of primary tumors is a surrogate for related metastases, which must be targeted by FGFR targeted systemic ...
Achim Fleischmann   +23 more
core   +2 more sources

The utility of molecular genetic techniques in craniosynostosis cases associated with intellectual disability

open access: yesRomanian Journal of Laboratory Medicine, 2018
Molecular genetic testing in craniosynostosis leads to the detection of the mutations in the genes encoding fibroblast growth factor receptors (FGFR), providing information about the etiology of the genetic disorder.
Bogliş Alina   +2 more
doaj   +1 more source

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