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7. Structure-function studies of the bHLH phosphorylation domain of TWIST1 in prostate cancer cells. Gajula RP; Chettiar ST; Williams RD; Nugent K; Kato Y; Wang H; Malek R; Taparra K; Cades J; Annadanam A; Yoon AR; Fertig E; Firulli BA; Mazzacurati L; Burns TF; Firulli AB; An SS; Tran PT Neoplasia; 2015 Jan; 17(1):16-31. PubMed ID: 25622896 [TBL] [Abstract][Full Text] [Related]
8. A twisted hand: bHLH protein phosphorylation and dimerization regulate limb development. Cai J; Jabs EW Bioessays; 2005 Nov; 27(11):1102-6. PubMed ID: 16237669 [TBL] [Abstract][Full Text] [Related]
9. 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]
10. Mutations within helix I of Twist1 result in distinct limb defects and variation of DNA binding affinities. Firulli BA; Redick BA; Conway SJ; Firulli AB J Biol Chem; 2007 Sep; 282(37):27536-27546. PubMed ID: 17652084 [TBL] [Abstract][Full Text] [Related]
11. 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]
12. Functional analysis of natural mutations in two TWIST protein motifs. Funato N; Twigg SR; Higashihori N; Ohyama K; Wall SA; Wilkie AO; Nakamura M Hum Mutat; 2005 Jun; 25(6):550-6. PubMed ID: 15880747 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. 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]
15. The Heterodimeric TWIST1-E12 Complex Drives the Oncogenic Potential of TWIST1 in Human Mammary Epithelial Cells. Jacqueroud L; Bouard C; Richard G; Payen L; Devouassoux-Shisheboran M; Spicer DB; Caramel J; Collin G; Puisieux A; Tissier A; Ansieau S Neoplasia; 2016 May; 18(5):317-327. PubMed ID: 27237323 [TBL] [Abstract][Full Text] [Related]
16. 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]
17. 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]
18. 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]
20. A Twist-Box domain of the C. elegans Twist homolog, HLH-8, plays a complex role in transcriptional regulation. Gruss MJ; O'Callaghan C; Donnellan M; Corsi AK Genetics; 2023 Aug; 224(4):. PubMed ID: 37067863 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]