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2. Twist1 homodimers enhance FGF responsiveness of the cranial sutures and promote suture closure. Connerney J; Andreeva V; Leshem Y; Mercado MA; Dowell K; Yang X; Lindner V; Friesel RE; Spicer DB Dev Biol; 2008 Jun; 318(2):323-34. PubMed ID: 18471809 [TBL] [Abstract][Full Text] [Related]
3. Mutations in TCF12, encoding a basic helix-loop-helix partner of TWIST1, are a frequent cause of coronal craniosynostosis. Sharma VP; Fenwick AL; Brockop MS; McGowan SJ; Goos JA; Hoogeboom AJ; Brady AF; Jeelani NO; Lynch SA; Mulliken JB; Murray DJ; Phipps JM; Sweeney E; Tomkins SE; Wilson LC; Bennett S; Cornall RJ; Broxholme J; Kanapin A; ; Johnson D; Wall SA; van der Spek PJ; Mathijssen IM; Maxson RE; Twigg SR; Wilkie AO Nat Genet; 2013 Mar; 45(3):304-7. PubMed ID: 23354436 [TBL] [Abstract][Full Text] [Related]
4. Computational modeling of the bHLH domain of the transcription factor TWIST1 and R118C, S144R and K145E mutants. Maia AM; da Silva JH; Mencalha AL; Caffarena ER; Abdelhay E BMC Bioinformatics; 2012 Jul; 13():184. PubMed ID: 22839202 [TBL] [Abstract][Full Text] [Related]
5. Interrelationship of cranial suture fusion, basicranial development, and resynostosis following suturectomy in twist1(+/-) mice, a murine model of Saethre-Chotzen syndrome. Hermann CD; Lee CS; Gadepalli S; Lawrence KA; Richards MA; Olivares-Navarrete R; Williams JK; Schwartz Z; Boyan BD Calcif Tissue Int; 2012 Oct; 91(4):255-66. PubMed ID: 22903506 [TBL] [Abstract][Full Text] [Related]
6. Oxidative stress drives disulfide bond formation between basic helix-loop-helix transcription factors. Danciu TE; Whitman M J Cell Biochem; 2010 Feb; 109(2):417-24. PubMed ID: 19950203 [TBL] [Abstract][Full Text] [Related]
7. Jagged1 functions downstream of Twist1 in the specification of the coronal suture and the formation of a boundary between osteogenic and non-osteogenic cells. Yen HY; Ting MC; Maxson RE Dev Biol; 2010 Nov; 347(2):258-70. PubMed ID: 20727876 [TBL] [Abstract][Full Text] [Related]
8. Recombinant mouse periostin ameliorates coronal sutures fusion in Twist1 Bai S; Li D; Xu L; Duan H; Yuan J; Wei M J Transl Med; 2018 Apr; 16(1):103. PubMed ID: 29665811 [TBL] [Abstract][Full Text] [Related]
10. EphA4 as an effector of Twist1 in the guidance of osteogenic precursor cells during calvarial bone growth and in craniosynostosis. Ting MC; Wu NL; Roybal PG; Sun J; Liu L; Yen Y; Maxson RE Development; 2009 Mar; 136(5):855-64. PubMed ID: 19201948 [TBL] [Abstract][Full Text] [Related]
11. Mutations in snail family genes enhance craniosynostosis of Twist1 haplo-insufficient mice: implications for Saethre-Chotzen Syndrome. Oram KF; Gridley T Genetics; 2005 Jun; 170(2):971-4. PubMed ID: 15802514 [TBL] [Abstract][Full Text] [Related]
12. Quantitative Morphologic Analysis of Cranial Vault in Twist1+/- Mice: Implications in Craniosynostosis. Nuri T; Ota M; Ueda K; Iseki S Plast Reconstr Surg; 2022 Jan; 149(1):28e-37e. PubMed ID: 34936613 [TBL] [Abstract][Full Text] [Related]
13. TWIST1 Homodimers and Heterodimers Orchestrate Lineage-Specific Differentiation. Fan X; Waardenberg AJ; Demuth M; Osteil P; Sun JQJ; Loebel DAF; Graham M; Tam PPL; Fossat N Mol Cell Biol; 2020 May; 40(11):. PubMed ID: 32179550 [TBL] [Abstract][Full Text] [Related]
14. Cell mixing at a neural crest-mesoderm boundary and deficient ephrin-Eph signaling in the pathogenesis of craniosynostosis. Merrill AE; Bochukova EG; Brugger SM; Ishii M; Pilz DT; Wall SA; Lyons KM; Wilkie AO; Maxson RE Hum Mol Genet; 2006 Apr; 15(8):1319-28. PubMed ID: 16540516 [TBL] [Abstract][Full Text] [Related]
15. Ablepharon and craniosynostosis in a patient with a localized TWIST1 basic domain substitution. Takenouchi T; Sakamoto Y; Sato H; Suzuki H; Uehara T; Ohsone Y; Kosaki K Am J Med Genet A; 2018 Dec; 176(12):2777-2780. PubMed ID: 30450715 [TBL] [Abstract][Full Text] [Related]
16. Twist is required for establishment of the mouse coronal suture. Yoshida T; Phylactou LA; Uney JB; Ishikawa I; Eto K; Iseki S J Anat; 2005 May; 206(5):437-44. PubMed ID: 15857364 [TBL] [Abstract][Full Text] [Related]
17. Altered bone growth dynamics prefigure craniosynostosis in a zebrafish model of Saethre-Chotzen syndrome. Teng CS; Ting MC; Farmer DT; Brockop M; Maxson RE; Crump JG Elife; 2018 Oct; 7():. PubMed ID: 30375332 [TBL] [Abstract][Full Text] [Related]
18. A role for fibroblast growth factor receptor-2 in the altered osteoblast phenotype induced by Twist haploinsufficiency in the Saethre-Chotzen syndrome. Guenou H; Kaabeche K; Mée SL; Marie PJ Hum Mol Genet; 2005 Jun; 14(11):1429-39. PubMed ID: 15829502 [TBL] [Abstract][Full Text] [Related]
19. Roles of FGFR2 and twist in human craniosynostosis: insights from genetic mutations in cranial osteoblasts. Marie PJ; Kaabeche K; Guenou H Front Oral Biol; 2008; 12():144-159. PubMed ID: 18391499 [TBL] [Abstract][Full Text] [Related]
20. Integration of FGF and TWIST in calvarial bone and suture development. Rice DP; Aberg T; Chan Y; Tang Z; Kettunen PJ; Pakarinen L; Maxson RE; Thesleff I Development; 2000 May; 127(9):1845-55. PubMed ID: 10751173 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]