386 related articles for article (PubMed ID: 24850862)
1. Cbfβ deletion in mice recapitulates cleidocranial dysplasia and reveals multiple functions of Cbfβ required for skeletal development.
Chen W; Ma J; Zhu G; Jules J; Wu M; McConnell M; Tian F; Paulson C; Zhou X; Wang L; Li YP
Proc Natl Acad Sci U S A; 2014 Jun; 111(23):8482-7. PubMed ID: 24850862
[TBL] [Abstract][Full Text] [Related]
2. Core binding factor beta (Cbfβ) controls the balance of chondrocyte proliferation and differentiation by upregulating Indian hedgehog (Ihh) expression and inhibiting parathyroid hormone-related protein receptor (PPR) expression in postnatal cartilage and bone formation.
Tian F; Wu M; Deng L; Zhu G; Ma J; Gao B; Wang L; Li YP; Chen W
J Bone Miner Res; 2014 Jul; 29(7):1564-1574. PubMed ID: 24821091
[TBL] [Abstract][Full Text] [Related]
3. Chondrocyte-specific knockout of Cbfβ reveals the indispensable function of Cbfβ in chondrocyte maturation, growth plate development and trabecular bone formation in mice.
Wu M; Li YP; Zhu G; Lu Y; Wang Y; Jules J; McConnell M; Serra R; Shao JZ; Chen W
Int J Biol Sci; 2014; 10(8):861-72. PubMed ID: 25170300
[TBL] [Abstract][Full Text] [Related]
4. Deletion of core-binding factor β (Cbfβ) in mesenchymal progenitor cells provides new insights into Cbfβ/Runxs complex function in cartilage and bone development.
Wu M; Li C; Zhu G; Wang Y; Jules J; Lu Y; McConnell M; Wang YJ; Shao JZ; Li YP; Chen W
Bone; 2014 Aug; 65():49-59. PubMed ID: 24798493
[TBL] [Abstract][Full Text] [Related]
5. Core-binding factor beta interacts with Runx2 and is required for skeletal development.
Yoshida CA; Furuichi T; Fujita T; Fukuyama R; Kanatani N; Kobayashi S; Satake M; Takada K; Komori T
Nat Genet; 2002 Dec; 32(4):633-8. PubMed ID: 12434152
[TBL] [Abstract][Full Text] [Related]
6. Nell-1, a key functional mediator of Runx2, partially rescues calvarial defects in Runx2(+/-) mice.
Zhang X; Ting K; Bessette CM; Culiat CT; Sung SJ; Lee H; Chen F; Shen J; Wang JJ; Kuroda S; Soo C
J Bone Miner Res; 2011 Apr; 26(4):777-91. PubMed ID: 20939017
[TBL] [Abstract][Full Text] [Related]
7. Runx1 is a central regulator of osteogenesis for bone homeostasis by orchestrating BMP and WNT signaling pathways.
Tang CY; Wu M; Zhao D; Edwards D; McVicar A; Luo Y; Zhu G; Wang Y; Zhou HD; Chen W; Li YP
PLoS Genet; 2021 Jan; 17(1):e1009233. PubMed ID: 33476325
[TBL] [Abstract][Full Text] [Related]
8. Cbfb regulates bone development by stabilizing Runx family proteins.
Qin X; Jiang Q; Matsuo Y; Kawane T; Komori H; Moriishi T; Taniuchi I; Ito K; Kawai Y; Rokutanda S; Izumi S; Komori T
J Bone Miner Res; 2015 Apr; 30(4):706-14. PubMed ID: 25262822
[TBL] [Abstract][Full Text] [Related]
9. Runt-related transcription factor 1 is required for murine osteoblast differentiation and bone formation.
Tang J; Xie J; Chen W; Tang C; Wu J; Wang Y; Zhou XD; Zhou HD; Li YP
J Biol Chem; 2020 Aug; 295(33):11669-11681. PubMed ID: 32571873
[TBL] [Abstract][Full Text] [Related]
10. Runx1 up-regulates chondrocyte to osteoblast lineage commitment and promotes bone formation by enhancing both chondrogenesis and osteogenesis.
Tang CY; Chen W; Luo Y; Wu J; Zhang Y; McVicar A; McConnell M; Liu Y; Zhou HD; Li YP
Biochem J; 2020 Jul; 477(13):2421-2438. PubMed ID: 32391876
[TBL] [Abstract][Full Text] [Related]
11. Core binding factor β of osteoblasts maintains cortical bone mass via stabilization of Runx2 in mice.
Lim KE; Park NR; Che X; Han MS; Jeong JH; Kim SY; Park CY; Akiyama H; Kim JE; Ryoo HM; Stein JL; Lian JB; Stein GS; Choi JY
J Bone Miner Res; 2015 Apr; 30(4):715-22. PubMed ID: 25358268
[TBL] [Abstract][Full Text] [Related]
12. Core Binding Factor β Plays a Critical Role During Chondrocyte Differentiation.
Park NR; Lim KE; Han MS; Che X; Park CY; Kim JE; Taniuchi I; Bae SC; Choi JY
J Cell Physiol; 2016 Jan; 231(1):162-71. PubMed ID: 26058470
[TBL] [Abstract][Full Text] [Related]
13. Cbfβ governs osteoblast-adipocyte lineage commitment through enhancing β-catenin signaling and suppressing adipogenesis gene expression.
Wu M; Wang Y; Shao JZ; Wang J; Chen W; Li YP
Proc Natl Acad Sci U S A; 2017 Sep; 114(38):10119-10124. PubMed ID: 28864530
[TBL] [Abstract][Full Text] [Related]
14. Inactivation of Ihh in Sp7-Expressing Cells Inhibits Osteoblast Proliferation, Differentiation, and Bone Formation, Resulting in a Dwarfism Phenotype with Severe Skeletal Dysplasia in Mice.
Wang Y; Dong Z; Yang R; Zong S; Wei X; Wang C; Guo L; Sun J; Li H; Li P
Calcif Tissue Int; 2022 Nov; 111(5):519-534. PubMed ID: 35731246
[TBL] [Abstract][Full Text] [Related]
15. An analysis of skeletal development in osteoblast-specific and chondrocyte-specific runt-related transcription factor-2 (Runx2) knockout mice.
Takarada T; Hinoi E; Nakazato R; Ochi H; Xu C; Tsuchikane A; Takeda S; Karsenty G; Abe T; Kiyonari H; Yoneda Y
J Bone Miner Res; 2013 Oct; 28(10):2064-9. PubMed ID: 23553905
[TBL] [Abstract][Full Text] [Related]
16. Targeted reversion of induced pluripotent stem cells from patients with human cleidocranial dysplasia improves bone regeneration in a rat calvarial bone defect model.
Saito A; Ooki A; Nakamura T; Onodera S; Hayashi K; Hasegawa D; Okudaira T; Watanabe K; Kato H; Onda T; Watanabe A; Kosaki K; Nishimura K; Ohtaka M; Nakanishi M; Sakamoto T; Yamaguchi A; Sueishi K; Azuma T
Stem Cell Res Ther; 2018 Jan; 9(1):12. PubMed ID: 29357927
[TBL] [Abstract][Full Text] [Related]
17. A Runx2 threshold for the cleidocranial dysplasia phenotype.
Lou Y; Javed A; Hussain S; Colby J; Frederick D; Pratap J; Xie R; Gaur T; van Wijnen AJ; Jones SN; Stein GS; Lian JB; Stein JL
Hum Mol Genet; 2009 Feb; 18(3):556-68. PubMed ID: 19028669
[TBL] [Abstract][Full Text] [Related]
18. CCAAT/enhancer-binding protein beta promotes osteoblast differentiation by enhancing Runx2 activity with ATF4.
Tominaga H; Maeda S; Hayashi M; Takeda S; Akira S; Komiya S; Nakamura T; Akiyama H; Imamura T
Mol Biol Cell; 2008 Dec; 19(12):5373-86. PubMed ID: 18843047
[TBL] [Abstract][Full Text] [Related]
19. Cbfbeta interacts with Runx2 and has a critical role in bone development.
Kundu M; Javed A; Jeon JP; Horner A; Shum L; Eckhaus M; Muenke M; Lian JB; Yang Y; Nuckolls GH; Stein GS; Liu PP
Nat Genet; 2002 Dec; 32(4):639-44. PubMed ID: 12434156
[TBL] [Abstract][Full Text] [Related]
20. Inhibition of miR338 rescues cleidocranial dysplasia in Runx2 mutant mice partially via the Hif1a-Vegfa axis.
Jin R; Zhang H; Lin C; Guo J; Zou W; Chen Z; Liu H
Exp Mol Med; 2023 Jan; 55(1):69-80. PubMed ID: 36599929
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]