181 related articles for article (PubMed ID: 17868088)
1. Generation of a Twist1 conditional null allele in the mouse.
Chen YT; Akinwunmi PO; Deng JM; Tam OH; Behringer RR
Genesis; 2007 Sep; 45(9):588-92. PubMed ID: 17868088
[TBL] [Abstract][Full Text] [Related]
2. Craniofacial shape variation in Twist1+/- mutant mice.
Parsons TE; Weinberg SM; Khaksarfard K; Howie RN; Elsalanty M; Yu JC; Cray JJ
Anat Rec (Hoboken); 2014 May; 297(5):826-33. PubMed ID: 24585549
[TBL] [Abstract][Full Text] [Related]
3. The mesenchymal architecture of the cranial mesoderm of mouse embryos is disrupted by the loss of Twist1 function.
Bildsoe H; Loebel DA; Jones VJ; Hor AC; Braithwaite AW; Chen YT; Behringer RR; Tam PP
Dev Biol; 2013 Feb; 374(2):295-307. PubMed ID: 23261931
[TBL] [Abstract][Full Text] [Related]
4. 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]
5. 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]
6. 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]
7. 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]
8. Specific inactivation of Twist1 in the mandibular arch neural crest cells affects the development of the ramus and reveals interactions with hand2.
Zhang Y; Blackwell EL; McKnight MT; Knutsen GR; Vu WT; Ruest LB
Dev Dyn; 2012 May; 241(5):924-40. PubMed ID: 22411303
[TBL] [Abstract][Full Text] [Related]
9. Generation of an Frs2alpha conditional null allele.
Lin Y; Zhang J; Zhang Y; Wang F
Genesis; 2007 Sep; 45(9):554-9. PubMed ID: 17868091
[TBL] [Abstract][Full Text] [Related]
10. Intercellular Genetic Interaction Between Irf6 and Twist1 during Craniofacial Development.
Fakhouri WD; Metwalli K; Naji A; Bakhiet S; Quispe-Salcedo A; Nitschke L; Kousa YA; Schutte BC
Sci Rep; 2017 Aug; 7(1):7129. PubMed ID: 28769044
[TBL] [Abstract][Full Text] [Related]
11. The variable expressivity and incomplete penetrance of the twist-null heterozygous mouse phenotype resemble those of human Saethre-Chotzen syndrome.
Bourgeois P; Bolcato-Bellemin AL; Danse JM; Bloch-Zupan A; Yoshiba K; Stoetzel C; Perrin-Schmitt F
Hum Mol Genet; 1998 Jun; 7(6):945-57. PubMed ID: 9580658
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. Generation of mice with a conditional Lbh null allele.
Lindley LE; Briegel KJ
Genesis; 2013 Jul; 51(7):491-7. PubMed ID: 23495064
[TBL] [Abstract][Full Text] [Related]
14. Prenatal diagnosis of a 7p15-p21 deletion encompassing the TWIST1 gene involved in Saethre-Chotzen syndrome.
Spaggiari E; Aboura A; Sinico M; Mabboux P; Dupont C; Delezoide AL; Guimiot F
Eur J Med Genet; 2012; 55(8-9):498-501. PubMed ID: 22569119
[TBL] [Abstract][Full Text] [Related]
15. An ENU-induced mutation in Twist1 transactivation domain causes hindlimb polydactyly with complete penetrance and dominant-negatively impairs E2A-dependent transcription.
Chen RZ; Cheng X; Tan Y; Chang TC; Lv H; Jia Y
Sci Rep; 2020 Feb; 10(1):2501. PubMed ID: 32051525
[TBL] [Abstract][Full Text] [Related]
16. 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]
17. Unraveling the transcriptional regulation of TWIST1 in limb development.
Hirsch N; Eshel R; Bar Yaacov R; Shahar T; Shmulevich F; Dahan I; Levaot N; Kaplan T; Lupiáñez DG; Birnbaum RY
PLoS Genet; 2018 Oct; 14(10):e1007738. PubMed ID: 30372441
[TBL] [Abstract][Full Text] [Related]
18. Generation of mice with a novel conditional null allele of the Sox9 gene.
Yap SP; Xing X; Kraus P; Sivakamasundari V; Chan HY; Lufkin T
Biotechnol Lett; 2011 Aug; 33(8):1551-8. PubMed ID: 21484342
[TBL] [Abstract][Full Text] [Related]
19. 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]
20. Twist1 Is Essential for Tooth Morphogenesis and Odontoblast Differentiation.
Meng T; Huang Y; Wang S; Zhang H; Dechow PC; Wang X; Qin C; Shi B; D'Souza RN; Lu Y
J Biol Chem; 2015 Dec; 290(49):29593-602. PubMed ID: 26487719
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]