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.
245 related articles for article (PubMed ID: 12668638)
1. Mammary gland, limb and yolk sac defects in mice lacking Tbx3, the gene mutated in human ulnar mammary syndrome. Davenport TG; Jerome-Majewska LA; Papaioannou VE Development; 2003 May; 130(10):2263-73. PubMed ID: 12668638 [TBL] [Abstract][Full Text] [Related]
2. A dominant repression domain in Tbx3 mediates transcriptional repression and cell immortalization: relevance to mutations in Tbx3 that cause ulnar-mammary syndrome. Carlson H; Ota S; Campbell CE; Hurlin PJ Hum Mol Genet; 2001 Oct; 10(21):2403-13. PubMed ID: 11689487 [TBL] [Abstract][Full Text] [Related]
3. A de novo TBX3 mutation presenting as dorsalization of the little fingers: A forme fruste phenotype of ulnar-mammary syndrome. Al-Qattan MM; Maddirevula S; Alkuraya FS Eur J Med Genet; 2020 Jan; 63(1):103615. PubMed ID: 30654152 [TBL] [Abstract][Full Text] [Related]
4. Tbx3, the ulnar-mammary syndrome gene, and Tbx2 interact in mammary gland development through a p19Arf/p53-independent pathway. Jerome-Majewska LA; Jenkins GP; Ernstoff E; Zindy F; Sherr CJ; Papaioannou VE Dev Dyn; 2005 Dec; 234(4):922-33. PubMed ID: 16222716 [TBL] [Abstract][Full Text] [Related]
5. The ulnar-mammary syndrome gene, Tbx3, is a direct target of the retinoic acid signaling pathway, which regulates its expression during mouse limb development. Ballim RD; Mendelsohn C; Papaioannou VE; Prince S Mol Biol Cell; 2012 Jun; 23(12):2362-72. PubMed ID: 22535523 [TBL] [Abstract][Full Text] [Related]
6. Interactions between FGF and Wnt signals and Tbx3 gene expression in mammary gland initiation in mouse embryos. Eblaghie MC; Song SJ; Kim JY; Akita K; Tickle C; Jung HS J Anat; 2004 Jul; 205(1):1-13. PubMed ID: 15255957 [TBL] [Abstract][Full Text] [Related]
7. Mutations in human TBX3 alter limb, apocrine and genital development in ulnar-mammary syndrome. Bamshad M; Lin RC; Law DJ; Watkins WC; Krakowiak PA; Moore ME; Franceschini P; Lala R; Holmes LB; Gebuhr TC; Bruneau BG; Schinzel A; Seidman JG; Seidman CE; Jorde LB Nat Genet; 1997 Jul; 16(3):311-5. PubMed ID: 9207801 [TBL] [Abstract][Full Text] [Related]
8. Development of a subset of forelimb muscles and their attachment sites requires the ulnar-mammary syndrome gene Tbx3. Colasanto MP; Eyal S; Mohassel P; Bamshad M; Bonnemann CG; Zelzer E; Moon AM; Kardon G Dis Model Mech; 2016 Nov; 9(11):1257-1269. PubMed ID: 27491074 [TBL] [Abstract][Full Text] [Related]
9. TBX3, the gene mutated in ulnar-mammary syndrome, promotes growth of mammary epithelial cells via repression of p19ARF, independently of p53. Platonova N; Scotti M; Babich P; Bertoli G; Mento E; Meneghini V; Egeo A; Zucchi I; Merlo GR Cell Tissue Res; 2007 May; 328(2):301-16. PubMed ID: 17265068 [TBL] [Abstract][Full Text] [Related]
10. The T-box transcription factors TBX2 and TBX3 in mammary gland development and breast cancer. Douglas NC; Papaioannou VE J Mammary Gland Biol Neoplasia; 2013 Jun; 18(2):143-7. PubMed ID: 23624936 [TBL] [Abstract][Full Text] [Related]
11. Haploinsufficiency of TBX3 causes ulnar-mammary syndrome in a large Turkish family. Wollnik B; Kayserili H; Uyguner O; Tukel T; Yuksel-Apak M Ann Genet; 2002; 45(4):213-7. PubMed ID: 12668170 [TBL] [Abstract][Full Text] [Related]
12. TBX3 over-expression causes mammary gland hyperplasia and increases mammary stem-like cells in an inducible transgenic mouse model. Liu J; Esmailpour T; Shang X; Gulsen G; Liu A; Huang T BMC Dev Biol; 2011 Oct; 11():65. PubMed ID: 22039763 [TBL] [Abstract][Full Text] [Related]
13. Phenotype of a patient with contiguous deletion of TBX5 and TBX3: expanding the disease spectrum. Bogarapu S; Bleyl SB; Calhoun A; Viskochil D; Saarel EV; Everitt MD; Frank DU Am J Med Genet A; 2014 May; 164A(5):1304-9. PubMed ID: 24664963 [TBL] [Abstract][Full Text] [Related]
14. Novel TBX3 mutation data in families with ulnar-mammary syndrome indicate a genotype-phenotype relationship: mutations that do not disrupt the T-domain are associated with less severe limb defects. Meneghini V; Odent S; Platonova N; Egeo A; Merlo GR Eur J Med Genet; 2006; 49(2):151-8. PubMed ID: 16530712 [TBL] [Abstract][Full Text] [Related]
15. Ulnar-mammary syndrome with dysmorphic facies and mental retardation caused by a novel 1.28 Mb deletion encompassing the TBX3 gene. Klopocki E; Neumann LM; Tönnies H; Ropers HH; Mundlos S; Ullmann R Eur J Hum Genet; 2006 Dec; 14(12):1274-9. PubMed ID: 16896345 [TBL] [Abstract][Full Text] [Related]
16. The spectrum of mutations in TBX3: Genotype/Phenotype relationship in ulnar-mammary syndrome. Bamshad M; Le T; Watkins WS; Dixon ME; Kramer BE; Roeder AD; Carey JC; Root S; Schinzel A; Van Maldergem L; Gardner RJ; Lin RC; Seidman CE; Seidman JG; Wallerstein R; Moran E; Sutphen R; Campbell CE; Jorde LB Am J Hum Genet; 1999 Jun; 64(6):1550-62. PubMed ID: 10330342 [TBL] [Abstract][Full Text] [Related]
17. The role of Tbx2 and Tbx3 in mammary development and tumorigenesis. Rowley M; Grothey E; Couch FJ J Mammary Gland Biol Neoplasia; 2004 Apr; 9(2):109-18. PubMed ID: 15300007 [TBL] [Abstract][Full Text] [Related]
18. Molecular interactions between Tbx3 and Bmp4 and a model for dorsoventral positioning of mammary gland development. Cho KW; Kim JY; Song SJ; Farrell E; Eblaghie MC; Kim HJ; Tickle C; Jung HS Proc Natl Acad Sci U S A; 2006 Nov; 103(45):16788-93. PubMed ID: 17071745 [TBL] [Abstract][Full Text] [Related]
19. Mouse TBX3 mutants suggest novel molecular mechanisms for Ulnar-mammary syndrome. Frank DU; Emechebe U; Thomas KR; Moon AM PLoS One; 2013; 8(7):e67841. PubMed ID: 23844108 [TBL] [Abstract][Full Text] [Related]
20. Regulation of Tbx3 expression by anteroposterior signalling in vertebrate limb development. Tümpel S; Sanz-Ezquerro JJ; Isaac A; Eblaghie MC; Dobson J; Tickle C Dev Biol; 2002 Oct; 250(2):251-62. PubMed ID: 12376101 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]