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Functions of site-specific histone acetylation and deacetylation.
Shahbazian MD, Grunstein M. Shahbazian MD, et al. Annu Rev Biochem. 2007;76:75-100. doi: 10.1146/annurev.biochem.76.052705.162114. Annu Rev Biochem. 2007. PMID: 17362198 Review.
Histone H2B ubiquitylation controls processive methylation but not monomethylation by Dot1 and Set1.
Shahbazian MD, Zhang K, Grunstein M. Shahbazian MD, et al. Mol Cell. 2005 Jul 22;19(2):271-7. doi: 10.1016/j.molcel.2005.06.010. Mol Cell. 2005. PMID: 16039595 Free article.
Insight into Rett syndrome: MeCP2 levels display tissue- and cell-specific differences and correlate with neuronal maturation.
Shahbazian MD, Antalffy B, Armstrong DL, Zoghbi HY. Shahbazian MD, et al. Hum Mol Genet. 2002 Jan 15;11(2):115-24. doi: 10.1093/hmg/11.2.115. Hum Mol Genet. 2002. PMID: 11809720
Identification of MeCP2 mutations in a series of females with autistic disorder.
Carney RM, Wolpert CM, Ravan SA, Shahbazian M, Ashley-Koch A, Cuccaro ML, Vance JM, Pericak-Vance MA. Carney RM, et al. Among authors: shahbazian m. Pediatr Neurol. 2003 Mar;28(3):205-11. doi: 10.1016/s0887-8994(02)00624-0. Pediatr Neurol. 2003. PMID: 12770674
Molecular genetics of Rett syndrome and clinical spectrum of MECP2 mutations.
Shahbazian MD, Zoghbi HY. Shahbazian MD, et al. Curr Opin Neurol. 2001 Apr;14(2):171-6. doi: 10.1097/00019052-200104000-00006. Curr Opin Neurol. 2001. PMID: 11262731 Review.
Reduction of Purkinje cell pathology in SCA1 transgenic mice by p53 deletion.
Shahbazian MD, Orr HT, Zoghbi HY. Shahbazian MD, et al. Neurobiol Dis. 2001 Dec;8(6):974-81. doi: 10.1006/nbdi.2001.0444. Neurobiol Dis. 2001. PMID: 11741393
Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3.
Shahbazian M, Young J, Yuva-Paylor L, Spencer C, Antalffy B, Noebels J, Armstrong D, Paylor R, Zoghbi H. Shahbazian M, et al. Neuron. 2002 Jul 18;35(2):243-54. doi: 10.1016/s0896-6273(02)00768-7. Neuron. 2002. PMID: 12160743
Rett syndrome and MeCP2: linking epigenetics and neuronal function.
Shahbazian MD, Zoghbi HY. Shahbazian MD, et al. Am J Hum Genet. 2002 Dec;71(6):1259-72. doi: 10.1086/345360. Epub 2002 Nov 19. Am J Hum Genet. 2002. PMID: 12442230 Free PMC article. Review. No abstract available.
Balanced X chromosome inactivation patterns in the Rett syndrome brain.
Shahbazian MD, Sun Y, Zoghbi HY. Shahbazian MD, et al. Am J Med Genet. 2002 Aug 1;111(2):164-8. doi: 10.1002/ajmg.10557. Am J Med Genet. 2002. PMID: 12210344
Infantile hypotonia as a presentation of Rett syndrome.
Heilstedt HA, Shahbazian MD, Lee B. Heilstedt HA, et al. Among authors: shahbazian md. Am J Med Genet. 2002 Aug 15;111(3):238-42. doi: 10.1002/ajmg.10633. Am J Med Genet. 2002. PMID: 12210319
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