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348 related items for PubMed ID: 15614781
1. Xenopus aristaless-related homeobox (xARX) gene product functions as both a transcriptional activator and repressor in forebrain development. Seufert DW, Prescott NL, El-Hodiri HM. Dev Dyn; 2005 Feb; 232(2):313-24. PubMed ID: 15614781 [Abstract] [Full Text] [Related]
2. The vertebrate ortholog of Aristaless is regulated by Dlx genes in the developing forebrain. Cobos I, Broccoli V, Rubenstein JL. J Comp Neurol; 2005 Mar 14; 483(3):292-303. PubMed ID: 15682394 [Abstract] [Full Text] [Related]
3. Mouse orthologue of ARX, a gene mutated in several X-linked forms of mental retardation and epilepsy, is a marker of adult neural stem cells and forebrain GABAergic neurons. Colombo E, Galli R, Cossu G, Gécz J, Broccoli V. Dev Dyn; 2004 Nov 14; 231(3):631-9. PubMed ID: 15376319 [Abstract] [Full Text] [Related]
4. The Xenopus arx gene is expressed in the developing rostral forebrain. El-Hodiri HM, Qi XL, Seufert DW. Dev Genes Evol; 2003 Jan 14; 212(12):608-12. PubMed ID: 12536326 [Abstract] [Full Text] [Related]
5. xArx2: an aristaless homolog that regulates brain regionalization during development in Xenopus laevis. Wolanski M, Khosrowshahian F, Kelly LE, El-Hodiri HM, Crawford MJ. Genesis; 2009 Jan 14; 47(1):19-31. PubMed ID: 19006070 [Abstract] [Full Text] [Related]
6. LIM-homeodomain genes as developmental and adult genetic markers of Xenopus forebrain functional subdivisions. Moreno N, Bachy I, Rétaux S, González A. J Comp Neurol; 2004 Apr 19; 472(1):52-72. PubMed ID: 15024752 [Abstract] [Full Text] [Related]
7. Comparative functional analysis provides evidence for a crucial role for the homeobox gene Nkx2.1/Titf-1 in forebrain evolution. van den Akker WM, Brox A, Puelles L, Durston AJ, Medina L. J Comp Neurol; 2008 Jan 10; 506(2):211-23. PubMed ID: 18022953 [Abstract] [Full Text] [Related]
8. Expression of murine Lhx5 suggests a role in specifying the forebrain. Sheng HZ, Bertuzzi S, Chiang C, Shawlot W, Taira M, Dawid I, Westphal H. Dev Dyn; 1997 Feb 10; 208(2):266-77. PubMed ID: 9022063 [Abstract] [Full Text] [Related]
9. Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans. Kitamura K, Yanazawa M, Sugiyama N, Miura H, Iizuka-Kogo A, Kusaka M, Omichi K, Suzuki R, Kato-Fukui Y, Kamiirisa K, Matsuo M, Kamijo S, Kasahara M, Yoshioka H, Ogata T, Fukuda T, Kondo I, Kato M, Dobyns WB, Yokoyama M, Morohashi K. Nat Genet; 2002 Nov 10; 32(3):359-69. PubMed ID: 12379852 [Abstract] [Full Text] [Related]
10. Lhx5 promotes forebrain development and activates transcription of secreted Wnt antagonists. Peng G, Westerfield M. Development; 2006 Aug 10; 133(16):3191-200. PubMed ID: 16854974 [Abstract] [Full Text] [Related]
11. The function of the Aristaless-related homeobox (Arx) gene product as a transcriptional repressor is diminished by mutations associated with X-linked mental retardation (XLMR). Fullenkamp AN, El-Hodiri HM. Biochem Biophys Res Commun; 2008 Dec 05; 377(1):73-8. PubMed ID: 18835247 [Abstract] [Full Text] [Related]
12. Xenopus Zic4: conservation and diversification of expression profiles and protein function among the Xenopus Zic family. Fujimi TJ, Mikoshiba K, Aruga J. Dev Dyn; 2006 Dec 05; 235(12):3379-86. PubMed ID: 16871625 [Abstract] [Full Text] [Related]
13. The role of ARX in cortical development. Friocourt G, Poirier K, Rakić S, Parnavelas JG, Chelly J. Eur J Neurosci; 2006 Feb 05; 23(4):869-76. PubMed ID: 16519652 [Abstract] [Full Text] [Related]
14. Three human ARX mutations cause the lissencephaly-like and mental retardation with epilepsy-like pleiotropic phenotypes in mice. Kitamura K, Itou Y, Yanazawa M, Ohsawa M, Suzuki-Migishima R, Umeki Y, Hohjoh H, Yanagawa Y, Shinba T, Itoh M, Nakamura K, Goto Y. Hum Mol Genet; 2009 Oct 01; 18(19):3708-24. PubMed ID: 19605412 [Abstract] [Full Text] [Related]
15. ARX: a gene for all seasons. Gécz J, Cloosterman D, Partington M. Curr Opin Genet Dev; 2006 Jun 01; 16(3):308-16. PubMed ID: 16650978 [Abstract] [Full Text] [Related]
16. Distinct roles for Distal-less genes Dlx3 and Dlx5 in regulating ectodermal development in Xenopus. Luo T, Matsuo-Takasaki M, Sargent TD. Mol Reprod Dev; 2001 Nov 01; 60(3):331-7. PubMed ID: 11599044 [Abstract] [Full Text] [Related]
17. The proneural determinant MASH1 regulates forebrain Dlx1/2 expression through the I12b intergenic enhancer. Poitras L, Ghanem N, Hatch G, Ekker M. Development; 2007 May 01; 134(9):1755-65. PubMed ID: 17409112 [Abstract] [Full Text] [Related]
18. Xtbx6r, a novel T-box gene expressed in the paraxial mesoderm, has anterior neural-inducing activity. Yabe S, Tazumi S, Yokoyama J, Uchiyama H. Int J Dev Biol; 2006 May 01; 50(8):681-9. PubMed ID: 17051478 [Abstract] [Full Text] [Related]
19. Developmental analysis of activin-like kinase receptor-4 (ALK4) expression in Xenopus laevis. Chen Y, Whitaker LL, Ramsdell AF. Dev Dyn; 2005 Feb 01; 232(2):393-8. PubMed ID: 15614766 [Abstract] [Full Text] [Related]
20. Zebrafish genes rx1 and rx2 help define the region of forebrain that gives rise to retina. Chuang JC, Raymond PA. Dev Biol; 2001 Mar 01; 231(1):13-30. PubMed ID: 11180949 [Abstract] [Full Text] [Related] Page: [Next] [New Search]