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Journal Abstract Search

295 related items for PubMed ID: 12929929

  • 1. PTHrP rescues ATDC5 cells from apoptosis induced by FGF receptor 3 mutation.
    Yamanaka Y, Tanaka H, Koike M, Nishimura R, Seino Y.
    J Bone Miner Res; 2003 Aug; 18(8):1395-403. PubMed ID: 12929929
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  • 8. FGFR3 down-regulates PTH/PTHrP receptor gene expression by mediating JAK/STAT signaling in chondrocytic cell line.
    Li M, Seki Y, Freitas PH, Nagata M, Kojima T, Sultana S, Ubaidus S, Maeda T, Shimomura J, Henderson JE, Tamura M, Oda K, Liu Z, Guo Y, Suzuki R, Yamamoto T, Takagi R, Amizuka N.
    J Electron Microsc (Tokyo); 2010 Aug; 59(3):227-36. PubMed ID: 20356821
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  • 10. The biological action of parathyroid hormone-related peptide (PTHrP) and fibroblast growth factor receptor 3 (FGFR3) on bone and cartilage.
    Amizuka N, Ozawa H, Sasaki T.
    Kaibogaku Zasshi; 2000 Oct; 75(5):415-25. PubMed ID: 11155687
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  • 12. Signalling by fibroblast growth factor receptor 3 and parathyroid hormone-related peptide coordinate cartilage and bone development.
    Amizuka N, Davidson D, Liu H, Valverde-Franco G, Chai S, Maeda T, Ozawa H, Hammond V, Ornitz DM, Goltzman D, Henderson JE.
    Bone; 2004 Jan; 34(1):13-25. PubMed ID: 14751559
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  • 13. 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 01; 18(3):290-305. PubMed ID: 14871928
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  • 17. Overexpression of FGFR3, Stat1, Stat5 and p21Cip1 correlates with phenotypic severity and defective chondrocyte differentiation in FGFR3-related chondrodysplasias.
    Legeai-Mallet L, Benoist-Lasselin C, Munnich A, Bonaventure J.
    Bone; 2004 Jan 01; 34(1):26-36. PubMed ID: 14751560
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  • 18. Transformation and Stat activation by derivatives of FGFR1, FGFR3, and FGFR4.
    Hart KC, Robertson SC, Kanemitsu MY, Meyer AN, Tynan JA, Donoghue DJ.
    Oncogene; 2000 Jul 06; 19(29):3309-20. PubMed ID: 10918587
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  • 20. 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 15; 21(18):3941-55. PubMed ID: 22634226
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