These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
261 related articles for article (PubMed ID: 33952673)
1. An RNA aptamer restores defective bone growth in FGFR3-related skeletal dysplasia in mice. Kimura T; Bosakova M; Nonaka Y; Hruba E; Yasuda K; Futakawa S; Kubota T; Fafilek B; Gregor T; Abraham SP; Gomolkova R; Belaskova S; Pesl M; Csukasi F; Duran I; Fujiwara M; Kavkova M; Zikmund T; Kaiser J; Buchtova M; Krakow D; Nakamura Y; Ozono K; Krejci P Sci Transl Med; 2021 May; 13(592):. PubMed ID: 33952673 [TBL] [Abstract][Full Text] [Related]
2. A novel tyrosine kinase inhibitor restores chondrocyte differentiation and promotes bone growth in a gain-of-function Fgfr3 mouse model. Jonquoy A; Mugniery E; Benoist-Lasselin C; Kaci N; Le Corre L; Barbault F; Girard AL; Le Merrer Y; Busca P; Schibler L; Munnich A; Legeai-Mallet L Hum Mol Genet; 2012 Feb; 21(4):841-51. PubMed ID: 22072392 [TBL] [Abstract][Full Text] [Related]
3. FGFR3 induces degradation of BMP type I receptor to regulate skeletal development. Qi H; Jin M; Duan Y; Du X; Zhang Y; Ren F; Wang Y; Tian Q; Wang X; Wang Q; Zhu Y; Xie Y; Liu C; Cao X; Mishina Y; Chen D; Deng CX; Chang Z; Chen L Biochim Biophys Acta; 2014 Jul; 1843(7):1237-47. PubMed ID: 24657641 [TBL] [Abstract][Full Text] [Related]
4. Constitutive activation of MEK1 in chondrocytes causes Stat1-independent achondroplasia-like dwarfism and rescues the Fgfr3-deficient mouse phenotype. Murakami S; Balmes G; McKinney S; Zhang Z; Givol D; de Crombrugghe B Genes Dev; 2004 Feb; 18(3):290-305. PubMed ID: 14871928 [TBL] [Abstract][Full Text] [Related]
5. Meclozine facilitates proliferation and differentiation of chondrocytes by attenuating abnormally activated FGFR3 signaling in achondroplasia. Matsushita M; Kitoh H; Ohkawara B; Mishima K; Kaneko H; Ito M; Masuda A; Ishiguro N; Ohno K PLoS One; 2013; 8(12):e81569. PubMed ID: 24324705 [TBL] [Abstract][Full Text] [Related]
6. HDAC6 deficiency or inhibition blocks FGFR3 accumulation and improves bone growth in a model of achondroplasia. Ota S; Zhou ZQ; Romero MP; Yang G; Hurlin PJ Hum Mol Genet; 2016 Oct; 25(19):4227-4243. PubMed ID: 27506979 [TBL] [Abstract][Full Text] [Related]
10. Meckel's and condylar cartilages anomalies in achondroplasia result in defective development and growth of the mandible. Biosse Duplan M; Komla-Ebri D; Heuzé Y; Estibals V; Gaudas E; Kaci N; Benoist-Lasselin C; Zerah M; Kramer I; Kneissel M; Porta DG; Di Rocco F; Legeai-Mallet L Hum Mol Genet; 2016 Jul; 25(14):2997-3010. PubMed ID: 27260401 [TBL] [Abstract][Full Text] [Related]
11. Repression of hedgehog signaling and BMP4 expression in growth plate cartilage by fibroblast growth factor receptor 3. Naski MC; Colvin JS; Coffin JD; Ornitz DM Development; 1998 Dec; 125(24):4977-88. PubMed ID: 9811582 [TBL] [Abstract][Full Text] [Related]
12. Meclozine promotes longitudinal skeletal growth in transgenic mice with achondroplasia carrying a gain-of-function mutation in the FGFR3 gene. Matsushita M; Hasegawa S; Kitoh H; Mori K; Ohkawara B; Yasoda A; Masuda A; Ishiguro N; Ohno K Endocrinology; 2015 Feb; 156(2):548-54. PubMed ID: 25456072 [TBL] [Abstract][Full Text] [Related]
13. Intermittent PTH (1-34) injection rescues the retarded skeletal development and postnatal lethality of mice mimicking human achondroplasia and thanatophoric dysplasia. Xie Y; Su N; Jin M; Qi H; Yang J; Li C; Du X; Luo F; Chen B; Shen Y; Huang H; Xian CJ; Deng C; Chen L Hum Mol Genet; 2012 Sep; 21(18):3941-55. PubMed ID: 22634226 [TBL] [Abstract][Full Text] [Related]
14. A Ser(365)-->Cys mutation of fibroblast growth factor receptor 3 in mouse downregulates Ihh/PTHrP signals and causes severe achondroplasia. Chen L; Li C; Qiao W; Xu X; Deng C Hum Mol Genet; 2001 Mar; 10(5):457-65. PubMed ID: 11181569 [TBL] [Abstract][Full Text] [Related]
15. PTH has the potential to rescue disturbed bone growth in achondroplasia. Ueda K; Yamanaka Y; Harada D; Yamagami E; Tanaka H; Seino Y Bone; 2007 Jul; 41(1):13-8. PubMed ID: 17466614 [TBL] [Abstract][Full Text] [Related]
16. Statin treatment rescues FGFR3 skeletal dysplasia phenotypes. Yamashita A; Morioka M; Kishi H; Kimura T; Yahara Y; Okada M; Fujita K; Sawai H; Ikegawa S; Tsumaki N Nature; 2014 Sep; 513(7519):507-11. PubMed ID: 25231866 [TBL] [Abstract][Full Text] [Related]
17. ARQ 087 inhibits FGFR signaling and rescues aberrant cell proliferation and differentiation in experimental models of craniosynostoses and chondrodysplasias caused by activating mutations in FGFR1, FGFR2 and FGFR3. Balek L; Gudernova I; Vesela I; Hampl M; Oralova V; Kunova Bosakova M; Varecha M; Nemec P; Hall T; Abbadessa G; Hatch N; Buchtova M; Krejci P Bone; 2017 Dec; 105():57-66. PubMed ID: 28826843 [TBL] [Abstract][Full Text] [Related]
18. C-Type Natriuretic Peptide Analog as Therapy for Achondroplasia. Legeai-Mallet L Endocr Dev; 2016; 30():98-105. PubMed ID: 26684019 [TBL] [Abstract][Full Text] [Related]
19. Tyrosine kinase inhibitor NVP-BGJ398 functionally improves FGFR3-related dwarfism in mouse model. Komla-Ebri D; Dambroise E; Kramer I; Benoist-Lasselin C; Kaci N; Le Gall C; Martin L; Busca P; Barbault F; Graus-Porta D; Munnich A; Kneissel M; Di Rocco F; Biosse-Duplan M; Legeai-Mallet L J Clin Invest; 2016 May; 126(5):1871-84. PubMed ID: 27064282 [TBL] [Abstract][Full Text] [Related]
20. In vitro and in vivo characterization of Recifercept, a soluble fibroblast growth factor receptor 3, as treatment for achondroplasia. Gonçalves D; Rignol G; Dellugat P; Hartmann G; Sarrazy Garcia S; Stavenhagen J; Santarelli L; Gouze E; Czech C PLoS One; 2020; 15(12):e0244368. PubMed ID: 33370388 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]