322 related articles for article (PubMed ID: 23354436)
1. 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]
2. 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]
3. Clinical spectrum and outcomes in families with coronal synostosis and TCF12 mutations.
di Rocco F; Baujat G; Arnaud E; Rénier D; Laplanche JL; Daire VC; Collet C
Eur J Hum Genet; 2014 Dec; 22(12):1413-6. PubMed ID: 24736737
[TBL] [Abstract][Full Text] [Related]
4. Twist1 dimer selection regulates cranial suture patterning and fusion.
Connerney J; Andreeva V; Leshem Y; Muentener C; Mercado MA; Spicer DB
Dev Dyn; 2006 May; 235(5):1345-57. PubMed ID: 16502419
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Embryonic requirements for Tcf12 in the development of the mouse coronal suture.
Ting MC; Farmer DT; Teng CS; He J; Chai Y; Crump JG; Maxson RE
Development; 2022 Jan; 149(1):. PubMed ID: 34878091
[TBL] [Abstract][Full Text] [Related]
7. A craniosynostosis massively parallel sequencing panel study in 309 Australian and New Zealand patients: findings and recommendations.
Lee E; Le T; Zhu Y; Elakis G; Turner A; Lo W; Venselaar H; Verrenkamp CA; Snow N; Mowat D; Kirk EP; Sachdev R; Smith J; Brown NJ; Wallis M; Barnett C; McKenzie F; Freckmann ML; Collins F; Chopra M; Gregersen N; Hayes I; Rajagopalan S; Tan TY; Stark Z; Savarirayan R; Yeung A; Adès L; Gattas M; Gibson K; Gabbett M; Amor DJ; Lattanzi W; Boyd S; Haan E; Gianoutsos M; Cox TC; Buckley MF; Roscioli T
Genet Med; 2018 Sep; 20(9):1061-1068. PubMed ID: 29215649
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Expanding the mutation spectrum in 182 Spanish probands with craniosynostosis: identification and characterization of novel TCF12 variants.
Paumard-Hernández B; Berges-Soria J; Barroso E; Rivera-Pedroza CI; Pérez-Carrizosa V; Benito-Sanz S; López-Messa E; Santos F; García-Recuero II; Romance A; Ballesta-Martínez JM; López-González V; Campos-Barros Á; Cruz J; Guillén-Navarro E; Sánchez Del Pozo J; Lapunzina P; García-Miñaur S; Heath KE
Eur J Hum Genet; 2015 Jul; 23(7):907-14. PubMed ID: 25271085
[TBL] [Abstract][Full Text] [Related]
10. Phosphoregulation of Twist1 provides a mechanism of cell fate control.
Firulli AB; Conway SJ
Curr Med Chem; 2008; 15(25):2641-7. PubMed ID: 18855684
[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. NGS targeted screening of 100 Scandinavian patients with coronal synostosis.
Topa A; Rohlin A; Andersson MK; Fehr A; Lovmar L; Stenman G; Kölby L
Am J Med Genet A; 2020 Feb; 182(2):348-356. PubMed ID: 31837199
[TBL] [Abstract][Full Text] [Related]
13. Altered Twist1 and Hand2 dimerization is associated with Saethre-Chotzen syndrome and limb abnormalities.
Firulli BA; Krawchuk D; Centonze VE; Vargesson N; Virshup DM; Conway SJ; Cserjesi P; Laufer E; Firulli AB
Nat Genet; 2005 Apr; 37(4):373-81. PubMed ID: 15735646
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. 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]
16. 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]
17. Saethre-Chotzen syndrome: a case report.
Peña WA; Slavotinek A; Oberoi S
Cleft Palate Craniofac J; 2010 May; 47(3):318-21. PubMed ID: 19860490
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Molecular genetic analysis of TWIST1 and FGFR3 genes in Korean patients with coronal synostosis: identification of three novel TWIST1 mutations.
Ko JM; Jeong SY; Yang JA; Park DH; Yoon SH
Plast Reconstr Surg; 2012 May; 129(5):814e-821e. PubMed ID: 22544111
[TBL] [Abstract][Full Text] [Related]
20. The natural history of patients treated for TWIST1-confirmed Saethre-Chotzen syndrome.
Foo R; Guo Y; McDonald-McGinn DM; Zackai EH; Whitaker LA; Bartlett SP
Plast Reconstr Surg; 2009 Dec; 124(6):2085-2095. PubMed ID: 19952666
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
