Skip Nav Destination
Close Modal
Update search
Filter
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
Filter
- Title
- Author
- Author Affiliations
- Full Text
- Abstract
- Keyword
- DOI
- ISBN
- EISBN
- ISSN
- EISSN
- Issue
- Volume
- References
NARROW
Format
Subjects
Journal
Article Type
TOC Section
Date
Availability
1-3 of 3
Keywords: Fgfr3
Close
Follow your search
Access your saved searches in your account
Would you like to receive an alert when new items match your search?
Sort by
Journal Articles
In collection:
Developmental Disorders
Martin Biosse Duplan, Emilie Dambroise, Valentin Estibals, Joelle Veziers, Jérome Guicheux, Laurence Legeai-Mallet
Journal:
Disease Models & Mechanisms
Dis Model Mech (2021) 14 (4): dmm048272.
Published: 23 April 2021
...Martin Biosse Duplan; Emilie Dambroise; Valentin Estibals; Joelle Veziers; Jérome Guicheux; Laurence Legeai-Mallet ABSTRACT Achondroplasia (ACH), the most common form of dwarfism, is caused by a missense mutation in the gene coding for fibroblast growth factor receptor 3 ( FGFR3 ). The resulting...
Includes: Supplementary data
Journal Articles
In collection:
Cancer
Yongjun Yin, Xiaodi Ren, Craig Smith, Qianxu Guo, Maria Malabunga, Ilhem Guernah, Yiwei Zhang, Juqun Shen, Haijun Sun, Nabil Chehab, Nick Loizos, Dale L. Ludwig, David M. Ornitz
Journal:
Disease Models & Mechanisms
Dis Model Mech (2016) 9 (5): 563–571.
Published: 1 May 2016
...Yongjun Yin; Xiaodi Ren; Craig Smith; Qianxu Guo; Maria Malabunga; Ilhem Guernah; Yiwei Zhang; Juqun Shen; Haijun Sun; Nabil Chehab; Nick Loizos; Dale L. Ludwig; David M. Ornitz ABSTRACT Activating mutations in fibroblast growth factor receptor 3 (FGFR3) have been identified in multiple types...
Includes: Supplementary data
Journal Articles
Rizwan Yousaf, Qinghang Meng, Robert B. Hufnagel, Ying Xia, Chandrakala Puligilla, Zubair M. Ahmed, Saima Riazuddin
Journal:
Disease Models & Mechanisms
Dis Model Mech (2015) 8 (12): 1543–1553.
Published: 1 December 2015
..., Map3k1 tm1Yxia mutant mice have supernumerary functional outer hair cells (OHCs) and Deiters' cells. Loss of MAP3K1 function resulted in the downregulation of Fgfr3 , Fgf8 , Fgf10 and Atf3 expression in the inner ear. Fgfr3, Fgf8 and Fgf10 have a role in induction of the otic placode or in otic...
Includes: Supplementary data