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FGFR3
| Symbol: | FGFR3 | | Name(s): | fibroblast growth factor receptor 3 (achondroplasia, thanatophoric dwarfism) | | Type: | protein-coding | | Organism: | Homo sapiens | | Synonyms: | ACH, CD333, CEK2, HSFGFR3EX, JTK4 | | Links: |
Pubmed,
Entrez Gene,
GeneCards,
BioGPS,
Map Viewer.
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Gene Information from Publications |
| Publication Link |
Summary of findings |
| 18199430 |
Observational study of genetic testing. (HuGE Navigator) |
| 18072261 |
Strong immunohistochemical expression of FGFR3, a superficial staining pattern of CK20, and a low proliferative activity define those papillary urothelial neoplasms of low malignant potential that do not recur. |
| 15221641 |
Observational study of genetic testing. (HuGE Navigator) |
| 15915095 |
Observational study of gene-disease association. (HuGE Navigator) |
| 16061860 |
Observational study of gene-disease association. (HuGE Navigator) |
| 16434832 |
Observational study of genetic testing. (HuGE Navigator) |
| 16877735 |
Observational study of gene-disease association. (HuGE Navigator) |
| 17343269 |
Observational study of gene-disease association. (HuGE Navigator) |
| 17683901 |
Observational study of genetic testing. (HuGE Navigator) |
| 17867592 |
Observational study of genotype prevalence and gene-disease association. (HuGE Navigator) | →View more information from publications. |
Recent Publications on FGFR3: |  |
Germline mutation screening of the Saethre-Chotzen-associated genes TWIST1 and FGFR3 in families with BRCA1/2-negative breast cancer.
Saethre-Chotzen syndrome is one of the most common craniosynostosis... | 30th October, 2009
| Lundberg Laboratory for Cancer Research, Department of Pathology, The
| Scand J Plast Reconstr Surg Hand Surg. 2009;43(5):251-5.
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Pfeiffer-like syndrome with holoprosencephaly: a newborn with maternal smoking and alcohol exposure.
We report the case of a female infant with Pfeiffer-like syndrome and... | 28th October, 2009
| Division of Genetics, Department of Pediatrics, Chung Shan Medical
| Pediatr Neonatol. 2009 Oct;50(5):234-8.
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Activating mutations in FGFR3 and HRAS reveal a shared genetic origin for congenital disorders and testicular tumors.
Genes mutated in congenital malformation syndromes are frequently... | 27th October, 2009
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| Nat Genet. 2009 Nov;41(11):1247-52. Epub 2009 Oct 25.
DOI Direct Link |
FGFR3 and PIK3CA mutations in stucco keratosis and dermatosis papulosa nigra.
Summary Background Stucco keratosis (STK) and dermatosis papulosa nigra... | 23rd October, 2009
| Department of Dermatology, University of Regensburg,
| Br J Dermatol. 2009 Sep 1.
DOI Direct Link |
Distinct microRNA alterations characterize high- and low-grade bladder cancer.
Urothelial carcinoma of the bladder (UCC) is a common disease that arises... | 22nd October, 2009
| Academic Urology Unit, University of Sheffield, Sheffield, United Kingdom.
| Cancer Res. 2009 Nov 1;69(21):8472-81. Epub 2009 Oct 20.
DOI Direct Link |
→View more research publications. |
Press Releases on FGFR3:
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| Data for EntreMed's ENMD-2076 to Be Presented at the Upcoming AACR-NCI-EORTC Conference |
3rd November, 2009 |
EntreMed |
-- Poster Session: Wednesday, November 18, 2009 - 12:30 p.m. - 2:30 p.m.
Abstract No: C75, "A novel multi-targeted Aurora A and VEGFR2 kinase
inhibitor, ENMD-2076,
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| Entremed Presents Results of ENMD-2076 Phase 1 Study in Advanced Cancer Patients |
1st June, 2009 |
EntreMed, Inc. |
Recently Expanded Clinical Program Now Includes Solid and Hematological Malignancies
ROCKVILLE, Md., June 1 /PRNewswire-FirstCall/ -- EntreMed, Inc. (Nasdaq: ENMD), a
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FGFR3 results (if any) from reagent suppliers | 
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