نتایج جستجو برای: fgfr3

تعداد نتایج: 1106  

2014
Manal Mustafa Nabil Moghrabi Bassam Bin-Abbas

FGFR3 mutations cause wide spectrum of disorders ranging from skeletal dysplasias (hypochondroplasia, achondroplasia, and thanatophoric dysplasia), benign skin tumors (epidermal nevi, seborrhaeic keratosis, and acanthosis nigricans), and epithelial malignancies (multiple myeloma and prostate and bladder carcinoma). Hypochondroplasia is the most common type of short-limb dwarfism in children res...

2001
Haiyan Dai Ruth Holm Gunnar B. Kristensen Vera M. Abeler Anne‐Lise Børresen‐Dale Åslaug Helland

Fibroblast growth factor receptor 3 (FGFR3) seems to play an inhibitory role in bone development, as activating mutations in the gene underlie disorders such as achondroplasia and thanatophoric dysplasia. Findings from multiple myeloma (MM) indicate that FGFR3 also can act as an oncogene, and mutation of codon 249 in the fibroblast growth factor receptor 3 (FGFR3) gene was recently detected in ...

2013
Sarah V. Williams Carolyn D. Hurst Margaret A. Knowles

FGF receptor 3 (FGFR3) is activated by mutation or over-expression in many bladder cancers. Here, we identify an additional mechanism of activation via chromosomal re-arrangement to generate constitutively activated fusion genes. FGFR3-transforming acid coiled coil 3 (TACC3) fusions resulting from 4p16.3 re-arrangements and a t(4;7) that generates a FGFR3-BAI1-associated protein 2-like 1 (BAIAP...

2012
Daniel M Silverberg

BACKGROUND Upper urinary tract cancer is typically diagnosed with urine cytology and imaging techniques. These assays can be limited by sensitivity, specificity, or technical issues making some diagnoses difficult. CASE PRESENTATION A 73-year old man presented to the clinic with a right renal pelvis filling defect that was detected by a CT-scan performed for unrelated reasons. Urine cytology ...

Journal: :Cancer research 2004
Chengliu Jin Fen Wang Xiaochong Wu Chundong Yu Yongde Luo Wallace L McKeehan

Tissue homeostasis in normal prostate and two-compartment nonmalignant prostate tumors depends on harmonious two-way communications between epithelial and stromal compartments. Within the fibroblast growth factor (FGF) family, signaling to an epithelial cell-specific FGF receptor (FGFR) 2IIIb-heparan sulfate complex from stromal-specific FGF7 and FGF10 delivers directionally specific instructio...

Journal: :Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology 2009
Peter J Wild Thomas Fuchs Robert Stoehr Dieter Zimmermann Simona Frigerio Barbara Padberg Inbal Steiner Ellen C Zwarthoff Maximilian Burger Stefan Denzinger Ferdinand Hofstaedter Glen Kristiansen Thomas Hermanns Hans-Helge Seifert Maurizio Provenzano Tullio Sulser Volker Roth Joachim M Buhmann Holger Moch Arndt Hartmann

PURPOSE To evaluate molecular and immunohistochemical markers to develop a molecular grading of urothelial bladder cancer and to test these markers in voided urine samples. EXPERIMENTAL DESIGN 255 consecutive biopsies from primary bladder cancer patients were evaluated on a tissue microarray. The clinical parameters gender, age, adjacent carcinoma in situ, and multifocality were collected. Ur...

2013
Fenghao Chen Sarvenaz Sarabipour Kalina Hristova

The A391E mutation in fibroblast growth factor receptor 3 (FGFR3) is the genetic cause for Crouzon syndrome with Acanthosis Nigricans. Here we investigate the effect of this mutation on FGFR3 activation in HEK 293 T cells over a wide range of fibroblast growth factor 1 concentrations using a physical-chemical approach that deconvolutes the effects of the mutation on dimerization, ligand binding...

2004
Chengliu Jin Fen Wang Xiaochong Wu Chundong Yu Yongde Luo Wallace L. McKeehan

Tissue homeostasis in normal prostate and two-compartment nonmalignant prostate tumors depends on harmonious two-way communications between epithelial and stromal compartments. Within the fibroblast growth factor (FGF) family, signaling to an epithelial cell-specific FGF receptor (FGFR) 2IIIb-heparan sulfate complex from stromal-specific FGF7 and FGF10 delivers directionally specific instructio...

Journal: :The Journal of clinical investigation 2016
Davide Komla-Ebri Emilie Dambroise Ina Kramer Catherine Benoist-Lasselin Nabil Kaci Cindy Le Gall Ludovic Martin Patricia Busca Florent Barbault Diana Graus-Porta Arnold Munnich Michaela Kneissel Federico Di Rocco Martin Biosse-Duplan Laurence Legeai-Mallet

Achondroplasia (ACH) is the most frequent form of dwarfism and is caused by gain-of-function mutations in the fibroblast growth factor receptor 3-encoding (FGFR3-encoding) gene. Although potential therapeutic strategies for ACH, which aim to reduce excessive FGFR3 activation, have emerged over many years, the use of tyrosine kinase inhibitor (TKI) to counteract FGFR3 hyperactivity has yet to be...

2006
Mitsukazu Mamada Tohru Yorifuji Keiji Kurokawa Masahiko Kawai Toru Momoi Tatsutoshi Nakahata

FGFR3 (fibroblast growth factor receptor 3) is a gene responsible for the most common form of osteodysplasia, achondroplasia, which results in extreme short stature. An allelic disorder, hypochondroplasia, however, presents with a much milder phenotype and is sometimes indistinguishable from idiopathic short stature. In this study, in order to test the possibility of the mildest end of hypochon...

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