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Journal Abstract Search

407 related items for PubMed ID: 24850862

  • 41.
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  • 42. Haploinsufficiency of osterix in chondrocytes impairs skeletal growth in mice.
    Cheng S, Xing W, Zhou X, Mohan S.
    Physiol Genomics; 2013 Oct 01; 45(19):917-23. PubMed ID: 23943855
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  • 44. Sox9 directs hypertrophic maturation and blocks osteoblast differentiation of growth plate chondrocytes.
    Dy P, Wang W, Bhattaram P, Wang Q, Wang L, Ballock RT, Lefebvre V.
    Dev Cell; 2012 Mar 13; 22(3):597-609. PubMed ID: 22421045
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  • 47. Targeting Runx2 expression in hypertrophic chondrocytes impairs endochondral ossification during early skeletal development.
    Ding M, Lu Y, Abbassi S, Li F, Li X, Song Y, Geoffroy V, Im HJ, Zheng Q.
    J Cell Physiol; 2012 Oct 13; 227(10):3446-56. PubMed ID: 22223437
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  • 48. Skeletal Deformities in Osterix-Cre;Tgfbr2f/f Mice May Cause Postnatal Death.
    Corps K, Stanwick M, Rectenwald J, Kruggel A, Peters SB.
    Genes (Basel); 2021 Jun 25; 12(7):. PubMed ID: 34202311
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  • 49. Zfp521 controls bone mass by HDAC3-dependent attenuation of Runx2 activity.
    Hesse E, Saito H, Kiviranta R, Correa D, Yamana K, Neff L, Toben D, Duda G, Atfi A, Geoffroy V, Horne WC, Baron R.
    J Cell Biol; 2010 Dec 27; 191(7):1271-83. PubMed ID: 21173110
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  • 52. Cbfa1: a molecular switch in osteoblast biology.
    Ducy P.
    Dev Dyn; 2000 Dec 27; 219(4):461-71. PubMed ID: 11084646
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  • 53. Abnormal bone remodelling activity of dental follicle cells from a cleidocranial dysplasia patient.
    Liu Y, Zhang X, Sun X, Wang X, Zhang C, Zheng S.
    Oral Dis; 2018 Oct 27; 24(7):1270-1281. PubMed ID: 29787635
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  • 54. Osteogenesis requires FAK-dependent collagen synthesis by fibroblasts and osteoblasts.
    Rajshankar D, Wang Y, McCulloch CA.
    FASEB J; 2017 Mar 27; 31(3):937-953. PubMed ID: 27881487
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  • 55. SATB2 is a multifunctional determinant of craniofacial patterning and osteoblast differentiation.
    Dobreva G, Chahrour M, Dautzenberg M, Chirivella L, Kanzler B, Fariñas I, Karsenty G, Grosschedl R.
    Cell; 2006 Jun 02; 125(5):971-86. PubMed ID: 16751105
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  • 56. Core Binding Factor-β Knockdown Alters Ovarian Gene Expression and Function in the Mouse.
    Wilson K, Park J, Curry TE, Mishra B, Gossen J, Taniuchi I, Jo M.
    Mol Endocrinol; 2016 Jul 02; 30(7):733-47. PubMed ID: 27176614
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  • 57. microRNA-31 inhibition partially ameliorates the deficiency of bone marrow stromal cells from cleidocranial dysplasia.
    Xu L, Fu Y, Zhu W, Xu R, Zhang J, Zhang P, Cheng J, Jiang H.
    J Cell Biochem; 2019 Jun 02; 120(6):9472-9486. PubMed ID: 30506733
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  • 58. Dysregulation of chondrogenesis in human cleidocranial dysplasia.
    Zheng Q, Sebald E, Zhou G, Chen Y, Wilcox W, Lee B, Krakow D.
    Am J Hum Genet; 2005 Aug 02; 77(2):305-12. PubMed ID: 15952089
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  • 59. Epiphyseal chondrocyte secondary ossification centers require thyroid hormone activation of Indian hedgehog and osterix signaling.
    Xing W, Cheng S, Wergedal J, Mohan S.
    J Bone Miner Res; 2014 Oct 02; 29(10):2262-75. PubMed ID: 24753031
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  • 60. The cleidocranial dysplasia-related R131G mutation in the Runt-related transcription factor RUNX2 disrupts binding to DNA but not CBF-beta.
    Han MS, Kim HJ, Wee HJ, Lim KE, Park NR, Bae SC, van Wijnen AJ, Stein JL, Lian JB, Stein GS, Choi JY.
    J Cell Biochem; 2010 May 02; 110(1):97-103. PubMed ID: 20225274
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