نتایج جستجو برای: fgfr2 gene

تعداد نتایج: 1142053  

2017
Takashi Okuda Tomohiko Taki Kazuhiro Nishida Yoshiaki Chinen Hisao Nagoshi Chouhei Sakakura Masafumi Taniwaki

Several novel fusion transcripts were identified by next-generation sequencing in gastric cancer; however, the breakpoint junctions have yet to be characterized. The present study characterized a plethora of APIP-FGFR2 genomic breakpoints in the SNU-16 gastric cancer cell line, which harbored homogeneously staining regions (hsrs) and double minute chromosomes. Oligonucleotide microarrays reveal...

Journal: :Journal of medical genetics 1997
D Steinberger H Collmann B Schmalenberger U Müller

We identified a novel mutation in members of a family with signs of Crouzon syndrome and plagiocephaly. In affected members of the family an A-->G transition was found at position 886 in exon 5 of the fibroblast growth factor receptor 2 (FGFR2) gene. The base change results in the replacement of a lysine by glutamic acid in Ig-like loop III of FGFR2. The unusual finding of plagiocephaly in thes...

Journal: :The FASEB Journal 2021

Continuous fossil discoveries and recent analysis of genomic data are revealing that anatomically modern traits evolved following a complex evolutionary path. Our current understanding human evolution considers the skull likely as mosaic correlated whose development is in turn integrated with other organs, such brain. However, we still know little about complexity genetic networks supervising t...

Journal: :Molecular cancer therapeutics 2015
Yeonui Kwak Hanna Cho Wooyoung Hur Taebo Sim

Uncontrolled activation of FGFRs induces the progression of various cancers. It was recently reported that FGFR2-activating mutants are implicated in about 12% of endometrial carcinomas. AZD4547, a potent pan-FGFR inhibitor, is currently being evaluated in clinical trials for several FGFR-driven cancers. However, AZD4547 has not been examined yet against FGFR2 mutant-driven endometrial cancers....

2012
Yoko Matsuda Junji Ueda Toshiyuki Ishiwata

The fibroblast growth factor receptor (FGFR) family consists of four members, named FGFR1, 2, 3, and 4. All 4 FGFRs and their ligands, fibroblast growth factors (FGFs), are expressed in colorectal cancer (CRC). Recent studies have shown that FGFR2 plays important roles in cancer progression; therefore, it is of great interest as a novel target for cancers. Expression of FGFR2 regulates migratio...

2016
Thomas M. Campbell Mauro A.A. Castro Ines de Santiago Michael N.C. Fletcher Silvia Halim Radhika Prathalingam Bruce A.J. Ponder Kerstin B. Meyer

The fibroblast growth factor receptor 2 (FGFR2) locus is consistently the top hit in genome-wide association studies for oestrogen receptor-positive (ER(+)) breast cancer. Yet, its mode of action continues to be controversial. Here, we employ a systems biology approach to demonstrate that signalling via FGFR2 counteracts cell activation by oestrogen. In the presence of oestrogen, the oestrogen ...

Journal: :Molecular cancer therapeutics 2013
Gottfried E Konecny Teodora Kolarova Neil A O'Brien Boris Winterhoff Guorong Yang Jingwei Qi Zhengdong Qi Natarajan Venkatesan Raul Ayala Tong Luo Richard S Finn Jessica Kristof Chad Galderisi Diana Graus Porta Lee Anderson Michael M Shi Alejandro Yovine Dennis J Slamon

The recent identification of activating fibroblast growth factor receptor 2 (FGFR2) mutations in endometrial cancer has generated an opportunity for a novel target-based therapy. Here, we explore the therapeutic potential of 2 FGFR inhibitors, the multikinase inhibitor dovitinib (TKI258) and the more selective FGFR inhibitor NVP-BGJ398 for the treatment of endometrial cancer. We examined the ef...

2013
Kenneth A. Walker Sunder Sims-Lucas Valeria E. Di Giovanni Caitlin Schaefer Whitney M. Sunseri Tatiana Novitskaya Mark P. de Caestecker Feng Chen Carlton M. Bates

PURPOSE Pax3cre-mediated deletion of fibroblast growth factor receptor 2 (Fgfr2) broadly in renal and urinary tract mesenchyme led to ureteric bud (UB) induction defects and vesicoureteral reflux (VUR), although the mechanisms were unclear. Here, we investigated whether Fgfr2 acts specifically in peri-Wolffian duct stroma (ST) to regulate UB induction and development of VUR and the mechanisms o...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 2007
Yuna Kim Nathan Bingham Ryohei Sekido Keith L Parker Robin Lovell-Badge Blanche Capel

Targeted mutagenesis of Fgf9 in mice causes male-to-female sex reversal. Among the four FGF receptors, FGFR2 showed two highly specific patterns based on antibody staining, suggesting that it might be the receptor-mediating FGF9 signaling in the gonad. FGFR2 was detected at the plasma membrane in proliferating coelomic epithelial cells and in the nucleus in Sertoli progenitor cells. This expres...

نمودار تعداد نتایج جستجو در هر سال

با کلیک روی نمودار نتایج را به سال انتشار فیلتر کنید