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.
230 related articles for article (PubMed ID: 16754645)
1. Ube3a expression is not altered in Mecp2 mutant mice. Jordan C; Francke U Hum Mol Genet; 2006 Jul; 15(14):2210-5. PubMed ID: 16754645 [TBL] [Abstract][Full Text] [Related]
2. Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3. Samaco RC; Hogart A; LaSalle JM Hum Mol Genet; 2005 Feb; 14(4):483-92. PubMed ID: 15615769 [TBL] [Abstract][Full Text] [Related]
3. Cerebellar gene expression profiles of mouse models for Rett syndrome reveal novel MeCP2 targets. Jordan C; Li HH; Kwan HC; Francke U BMC Med Genet; 2007 Jun; 8():36. PubMed ID: 17584923 [TBL] [Abstract][Full Text] [Related]
4. Ube3a mRNA and protein expression are not decreased in Mecp2R168X mutant mice. Lawson-Yuen A; Liu D; Han L; Jiang ZI; Tsai GE; Basu AC; Picker J; Feng J; Coyle JT Brain Res; 2007 Nov; 1180():1-6. PubMed ID: 17936729 [TBL] [Abstract][Full Text] [Related]
5. MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression. Makedonski K; Abuhatzira L; Kaufman Y; Razin A; Shemer R Hum Mol Genet; 2005 Apr; 14(8):1049-58. PubMed ID: 15757975 [TBL] [Abstract][Full Text] [Related]
6. MECP2 mutations in Rett syndrome adversely affect lymphocyte growth, but do not affect imprinted gene expression in blood or brain. Balmer D; Arredondo J; Samaco RC; LaSalle JM Hum Genet; 2002 Jun; 110(6):545-52. PubMed ID: 12107440 [TBL] [Abstract][Full Text] [Related]
7. Exploring the possible link between MeCP2 and oxidative stress in Rett syndrome. Filosa S; Pecorelli A; D'Esposito M; Valacchi G; Hajek J Free Radic Biol Med; 2015 Nov; 88(Pt A):81-90. PubMed ID: 25960047 [TBL] [Abstract][Full Text] [Related]
8. MECP2 mutations and clinical correlations in Greek children with Rett syndrome and associated neurodevelopmental disorders. Psoni S; Sofocleous C; Traeger-Synodinos J; Kitsiou-Tzeli S; Kanavakis E; Fryssira-Kanioura H Brain Dev; 2012 Jun; 34(6):487-95. PubMed ID: 21982064 [TBL] [Abstract][Full Text] [Related]
9. The disease progression of Mecp2 mutant mice is affected by the level of BDNF expression. Chang Q; Khare G; Dani V; Nelson S; Jaenisch R Neuron; 2006 Feb; 49(3):341-8. PubMed ID: 16446138 [TBL] [Abstract][Full Text] [Related]
10. Abnormalities of cell packing density and dendritic complexity in the MeCP2 A140V mouse model of Rett syndrome/X-linked mental retardation. Jentarra GM; Olfers SL; Rice SG; Srivastava N; Homanics GE; Blue M; Naidu S; Narayanan V BMC Neurosci; 2010 Feb; 11():19. PubMed ID: 20163734 [TBL] [Abstract][Full Text] [Related]
11. Investigation of UBE3A and MECP2 in Angelman syndrome (AS) and patients with features of AS. Hitchins MP; Rickard S; Dhalla F; Fairbrother UL; de Vries BB; Winter R; Pembrey ME; Malcolm S Am J Med Genet A; 2004 Mar; 125A(2):167-72. PubMed ID: 14981718 [TBL] [Abstract][Full Text] [Related]
12. Touchscreen learning deficits in Ube3a, Ts65Dn and Mecp2 mouse models of neurodevelopmental disorders with intellectual disabilities. Leach PT; Crawley JN Genes Brain Behav; 2018 Jul; 17(6):e12452. PubMed ID: 29266714 [TBL] [Abstract][Full Text] [Related]
13. Altered somatosensory barrel cortex refinement in the developing brain of Mecp2-null mice. Moroto M; Nishimura A; Morimoto M; Isoda K; Morita T; Yoshida M; Morioka S; Tozawa T; Hasegawa T; Chiyonobu T; Yoshimoto K; Hosoi H Brain Res; 2013 Nov; 1537():319-26. PubMed ID: 24060648 [TBL] [Abstract][Full Text] [Related]
15. Neuroanatomy in mouse models of Rett syndrome is related to the severity of Mecp2 mutation and behavioral phenotypes. Allemang-Grand R; Ellegood J; Spencer Noakes L; Ruston J; Justice M; Nieman BJ; Lerch JP Mol Autism; 2017; 8():32. PubMed ID: 28670438 [TBL] [Abstract][Full Text] [Related]
16. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2. Amir RE; Van den Veyver IB; Wan M; Tran CQ; Francke U; Zoghbi HY Nat Genet; 1999 Oct; 23(2):185-8. PubMed ID: 10508514 [TBL] [Abstract][Full Text] [Related]
17. Downregulation of CNPase in a MeCP2 deficient mouse model of Rett syndrome. Wu W; Gu W; Xu X; Shang S; Zhao Z Neurol Res; 2012 Mar; 34(2):107-13. PubMed ID: 22334035 [TBL] [Abstract][Full Text] [Related]
18. Partial rescue of MeCP2 deficiency by postnatal activation of MeCP2. Giacometti E; Luikenhuis S; Beard C; Jaenisch R Proc Natl Acad Sci U S A; 2007 Feb; 104(6):1931-6. PubMed ID: 17267601 [TBL] [Abstract][Full Text] [Related]
19. Methyl CpG-binding protein 2 (a mutation of which causes Rett syndrome) directly regulates insulin-like growth factor binding protein 3 in mouse and human brains. Itoh M; Ide S; Takashima S; Kudo S; Nomura Y; Segawa M; Kubota T; Mori H; Tanaka S; Horie H; Tanabe Y; Goto Y J Neuropathol Exp Neurol; 2007 Feb; 66(2):117-23. PubMed ID: 17278996 [TBL] [Abstract][Full Text] [Related]
20. A mouse Mecp2-null mutation causes neurological symptoms that mimic Rett syndrome. Guy J; Hendrich B; Holmes M; Martin JE; Bird A Nat Genet; 2001 Mar; 27(3):322-6. PubMed ID: 11242117 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]