201 related articles for article (PubMed ID: 23925499)
1. Disorders with similar clinical phenotypes reveal underlying genetic interaction: SATB2 acts as an activator of the UPF3B gene.
Leoyklang P; Suphapeetiporn K; Srichomthong C; Tongkobpetch S; Fietze S; Dorward H; Cullinane AR; Gahl WA; Huizing M; Shotelersuk V
Hum Genet; 2013 Dec; 132(12):1383-93. PubMed ID: 23925499
[TBL] [Abstract][Full Text] [Related]
2. Osteoblast-specific transcription factor Osterix (Osx) is an upstream regulator of Satb2 during bone formation.
Tang W; Li Y; Osimiri L; Zhang C
J Biol Chem; 2011 Sep; 286(38):32995-3002. PubMed ID: 21828043
[TBL] [Abstract][Full Text] [Related]
3. [Study progress of special AT-rich sequence binding protein 2].
Qian YY; Wang HJ; Ma D
Yi Chuan; 2011 Sep; 33(9):947-52. PubMed ID: 21951795
[TBL] [Abstract][Full Text] [Related]
4. Heterozygous nonsense mutation SATB2 associated with cleft palate, osteoporosis, and cognitive defects.
Leoyklang P; Suphapeetiporn K; Siriwan P; Desudchit T; Chaowanapanja P; Gahl WA; Shotelersuk V
Hum Mutat; 2007 Jul; 28(7):732-8. PubMed ID: 17377962
[TBL] [Abstract][Full Text] [Related]
5. 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; 125(5):971-86. PubMed ID: 16751105
[TBL] [Abstract][Full Text] [Related]
6. Disruption of SATB2 or its long-range cis-regulation by SOX9 causes a syndromic form of Pierre Robin sequence.
Rainger JK; Bhatia S; Bengani H; Gautier P; Rainger J; Pearson M; Ansari M; Crow J; Mehendale F; Palinkasova B; Dixon MJ; Thompson PJ; Matarin M; Sisodiya SM; Kleinjan DA; Fitzpatrick DR
Hum Mol Genet; 2014 May; 23(10):2569-79. PubMed ID: 24363063
[TBL] [Abstract][Full Text] [Related]
7. Special AT-rich binding protein-2 (SATB2) differentially affects disease-causing p63 mutant proteins.
Chung J; Grant RI; Kaplan DR; Irwin MS
J Biol Chem; 2011 Nov; 286(47):40671-80. PubMed ID: 21965674
[TBL] [Abstract][Full Text] [Related]
8. Antisense suppression of the nonsense mediated decay factor Upf3b as a potential treatment for diseases caused by nonsense mutations.
Huang L; Low A; Damle SS; Keenan MM; Kuntz S; Murray SF; Monia BP; Guo S
Genome Biol; 2018 Jan; 19(1):4. PubMed ID: 29334995
[TBL] [Abstract][Full Text] [Related]
9. SATB2-LEMD2 interaction links nuclear shape plasticity to regulation of cognition-related genes.
Feurle P; Abentung A; Cera I; Wahl N; Ablinger C; Bucher M; Stefan E; Sprenger S; Teis D; Fischer A; Laighneach A; Whitton L; Morris DW; Apostolova G; Dechant G
EMBO J; 2021 Feb; 40(3):e103701. PubMed ID: 33319920
[TBL] [Abstract][Full Text] [Related]
10. Further supporting evidence for the SATB2-associated syndrome found through whole exome sequencing.
Zarate YA; Perry H; Ben-Omran T; Sellars EA; Stein Q; Almureikhi M; Simmons K; Klein O; Fish J; Feingold M; Douglas J; Kruer MC; Si Y; Mao R; McKnight D; Gibellini F; Retterer K; Slavotinek A
Am J Med Genet A; 2015 May; 167A(5):1026-32. PubMed ID: 25885067
[TBL] [Abstract][Full Text] [Related]
11. Roles of SATB2 in osteogenic differentiation and bone regeneration.
Zhang J; Tu Q; Grosschedl R; Kim MS; Griffin T; Drissi H; Yang P; Chen J
Tissue Eng Part A; 2011 Jul; 17(13-14):1767-76. PubMed ID: 21385070
[TBL] [Abstract][Full Text] [Related]
12. In the developing cerebral cortex: axonogenesis, synapse formation, and synaptic plasticity are regulated by SATB2 target genes.
Guo Q; Wang Y; Wang Q; Qian Y; Jiang Y; Dong X; Chen H; Chen X; Liu X; Yu S; Zhu J; Shan S; Wu B; Zhou W; Wang H
Pediatr Res; 2023 May; 93(6):1519-1527. PubMed ID: 36028553
[TBL] [Abstract][Full Text] [Related]
13. The UPF3B gene, implicated in intellectual disability, autism, ADHD and childhood onset schizophrenia regulates neural progenitor cell behaviour and neuronal outgrowth.
Jolly LA; Homan CC; Jacob R; Barry S; Gecz J
Hum Mol Genet; 2013 Dec; 22(23):4673-87. PubMed ID: 23821644
[TBL] [Abstract][Full Text] [Related]
14. Cellular transformation of human mammary epithelial cells by SATB2.
Yu W; Ma Y; Ochoa AC; Shankar S; Srivastava RK
Stem Cell Res; 2017 Mar; 19():139-147. PubMed ID: 28167342
[TBL] [Abstract][Full Text] [Related]
15. Metformin reduces SATB2-mediated osteosarcoma stem cell-like phenotype and tumor growth via inhibition of N-cadherin/NF-kB signaling.
Xu HY; Fang W; Huang ZW; Lu JC; Wang YQ; Tang QL; Song GH; Kang Y; Zhu XJ; Zou CY; Yang HL; Shen JN; Wang J
Eur Rev Med Pharmacol Sci; 2017 Oct; 21(20):4516-4528. PubMed ID: 29131265
[TBL] [Abstract][Full Text] [Related]
16. Satb2 haploinsufficiency phenocopies 2q32-q33 deletions, whereas loss suggests a fundamental role in the coordination of jaw development.
Britanova O; Depew MJ; Schwark M; Thomas BL; Miletich I; Sharpe P; Tarabykin V
Am J Hum Genet; 2006 Oct; 79(4):668-78. PubMed ID: 16960803
[TBL] [Abstract][Full Text] [Related]
17. SATB2 suppresses the progression of colorectal cancer cells via inactivation of MEK5/ERK5 signaling.
Mansour MA; Hyodo T; Ito S; Kurita K; Kokuryo T; Uehara K; Nagino M; Takahashi M; Hamaguchi M; Senga T
FEBS J; 2015 Apr; 282(8):1394-405. PubMed ID: 25662172
[TBL] [Abstract][Full Text] [Related]
18. The AT-rich DNA-binding protein SATB2 promotes expression and physical association of human (G)γ- and (A)γ-globin genes.
Zhou LQ; Wu J; Wang WT; Yu W; Zhao GN; Zhang P; Xiong J; Li M; Xue Z; Wang X; Xie XM; Guo ZC; Lv X; Liu DP
J Biol Chem; 2012 Aug; 287(36):30641-52. PubMed ID: 22825848
[TBL] [Abstract][Full Text] [Related]
19. Satb2 regulates proliferation and nuclear integrity of pre-osteoblasts.
Dowrey T; Schwager EE; Duong J; Merkuri F; Zarate YA; Fish JL
Bone; 2019 Oct; 127():488-498. PubMed ID: 31325654
[TBL] [Abstract][Full Text] [Related]
20. SATB2 targeted by methylated miR-34c-5p suppresses proliferation and metastasis attenuating the epithelial-mesenchymal transition in colorectal cancer.
Gu J; Wang G; Liu H; Xiong C
Cell Prolif; 2018 Aug; 51(4):e12455. PubMed ID: 29701273
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
