These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
6. Setleis syndrome: genetic and clinical findings in a new case with epilepsy. Giordano L; Desnick RJ; Molinaro A; Uliana V; Forzano F; Edelmann L; Nazarenko I; Pinelli L; Accorsi P; Faravelli F Pediatr Neurol; 2014 Apr; 50(4):389-91. PubMed ID: 24486222 [TBL] [Abstract][Full Text] [Related]
7. Mechanisms of Regulation of the Casasnovas-Nieves JJ; Rodríguez Y; Franco HL; Cadilla CL Genes (Basel); 2023 Aug; 14(9):. PubMed ID: 37761873 [TBL] [Abstract][Full Text] [Related]
8. Focal facial dermal dysplasias type III: Two families with Setleis syndrome in China. Cao Q; Zhang S; Wang J; Wang Y; Pan C; Wang X; Zhao A; Chen X; Qin P; Zhang S; Yao Z; Lv D; Yang Y; Li M J Dermatol; 2022 Oct; 49(10):1057-1061. PubMed ID: 35713327 [TBL] [Abstract][Full Text] [Related]
9. Setleis syndrome in Mexican-Nahua sibs due to a homozygous TWIST2 frameshift mutation and partial expression in heterozygotes: review of the focal facial dermal dysplasias and subtype reclassification. Cervantes-Barragán DE; Villarroel CE; Medrano-Hernández A; Durán-McKinster C; Bosch-Canto V; Del-Castillo V; Nazarenko I; Yang A; Desnick RJ J Med Genet; 2011 Oct; 48(10):716-20. PubMed ID: 21931173 [TBL] [Abstract][Full Text] [Related]
10. A novel frameshift mutation in TWIST2 gene causing Setleis syndrome. Girisha KM; Bidchol AM; Sarpangala MK; Satyamoorthy K Indian J Pediatr; 2014 Mar; 81(3):302-4. PubMed ID: 24127007 [TBL] [Abstract][Full Text] [Related]
11. De novo triplication at 1p36.23p36.22 further refines the dosage sensitive region of overlap in Setleis syndrome (focal facial dermal dysplasia type III). Oh RY; Chun K; Kowalski PE; Chitayat D Am J Med Genet A; 2023 Jun; 191(6):1607-1613. PubMed ID: 36942595 [TBL] [Abstract][Full Text] [Related]
12. Twist1- and Twist2-haploinsufficiency results in reduced bone formation. Huang Y; Meng T; Wang S; Zhang H; Mues G; Qin C; Feng JQ; D'Souza RN; Lu Y PLoS One; 2014; 9(6):e99331. PubMed ID: 24971743 [TBL] [Abstract][Full Text] [Related]
13. The TWIST2 mutation causes Setleis syndrome: a rare clinical case report. Ayaz A; Yalcintepe S; Ozalp Yuregir O; Sahin Y; Ozer A; Eser M; Celik U Clin Dysmorphol; 2017 Apr; 26(2):128-131. PubMed ID: 27750268 [No Abstract] [Full Text] [Related]
14. LINC01235-TWIST2 feedback loop facilitates epithelial-mesenchymal transition in gastric cancer by inhibiting THBS2. Tan YE; Xing Y; Ran BL; Zhang C; Pan SW; An W; Chen QC; Xu HM Aging (Albany NY); 2020 Nov; 12(24):25060-25075. PubMed ID: 33206629 [TBL] [Abstract][Full Text] [Related]
15. Recurrent Mutations in the Basic Domain of TWIST2 Cause Ablepharon Macrostomia and Barber-Say Syndromes. Marchegiani S; Davis T; Tessadori F; van Haaften G; Brancati F; Hoischen A; Huang H; Valkanas E; Pusey B; Schanze D; Venselaar H; Vulto-van Silfhout AT; Wolfe LA; Tifft CJ; Zerfas PM; Zambruno G; Kariminejad A; Sabbagh-Kermani F; Lee J; Tsokos MG; Lee CC; Ferraz V; da Silva EM; Stevens CA; Roche N; Bartsch O; Farndon P; Bermejo-Sanchez E; Brooks BP; Maduro V; Dallapiccola B; Ramos FJ; Chung HY; Le Caignec C; Martins F; Jacyk WK; Mazzanti L; Brunner HG; Bakkers J; Lin S; Malicdan MC; Boerkoel CF; Gahl WA; de Vries BB; van Haelst MM; Zenker M; Markello TC Am J Hum Genet; 2015 Jul; 97(1):99-110. PubMed ID: 26119818 [TBL] [Abstract][Full Text] [Related]
16. Biological function and molecular mechanism of Twist2. Zhao CX; Yang Z Yi Chuan; 2015 Jan; 37(1):17-24. PubMed ID: 25608809 [TBL] [Abstract][Full Text] [Related]
17. Regulation of p21 by TWIST2 contributes to its tumor-suppressor function in human acute myeloid leukemia. Zhang X; Ma W; Cui J; Yao H; Zhou H; Ge Y; Xiao L; Hu X; Liu BH; Yang J; Li YY; Chen S; Eaves CJ; Wu D; Zhao Y Oncogene; 2015 Jun; 34(23):3000-10. PubMed ID: 25088197 [TBL] [Abstract][Full Text] [Related]
18. Ocular adnexal phenotype and management of a patient with mosaic expression of a mutation in TWIST2. De Niear MA; Law JJ; Abel TW; Mawn LA Orbit; 2022 Dec; 41(6):779-782. PubMed ID: 34092176 [TBL] [Abstract][Full Text] [Related]
20. TWIST2 and the PPAR signaling pathway are important in the progression of nonalcoholic steatohepatitis. Zhang Y; Ge X; Li Y; Zhang B; Wang P; Hao M; Gao P; Zhao Y; Sun T; Lu S; Ma W Lipids Health Dis; 2021 Apr; 20(1):39. PubMed ID: 33879188 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]