Mona D. Shahbazian
Affiliations: | Acrometrix, Benicia, CA, United States |
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"Mona Shahbazian"Mean distance: 16.34 (cluster 11) | S | N | B | C | P |
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| Watson CM, Pelka GJ, Radziewic T, et al. (2005) Reduced proportion of Purkinje cells expressing paternally derived mutant Mecp2308 allele in female mouse cerebellum is not due to a skewed primary pattern of X-chromosome inactivation. Human Molecular Genetics. 14: 1851-61 |
| Carney RM, Wolpert CM, Ravan SA, et al. (2003) Identification of MeCP2 mutations in a series of females with autistic disorder. Pediatric Neurology. 28: 205-11 |
| Shahbazian MD, Zoghbi HY. (2002) Rett syndrome and MeCP2: linking epigenetics and neuronal function. American Journal of Human Genetics. 71: 1259-72 |
| Shahbazian MD, Sun Y, Zoghbi HY. (2002) Balanced X chromosome inactivation patterns in the Rett syndrome brain. American Journal of Medical Genetics. 111: 164-8 |
| Heilstedt HA, Shahbazian MD, Lee B. (2002) Infantile hypotonia as a presentation of Rett syndrome. American Journal of Medical Genetics. 111: 238-42 |
| Shahbazian M, Young J, Yuva-Paylor L, et al. (2002) Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3. Neuron. 35: 243-54 |
| Shahbazian MD, Antalffy B, Armstrong DL, et al. (2002) Insight into Rett syndrome: MeCP2 levels display tissue- and cell-specific differences and correlate with neuronal maturation. Human Molecular Genetics. 11: 115-24 |
| Shahbazian MD, Orr HT, Zoghbi HY. (2001) Reduction of Purkinje cell pathology in SCA1 transgenic mice by p53 deletion. Neurobiology of Disease. 8: 974-81 |
| Shahbazian MD, Zoghbi HY. (2001) Molecular genetics of Rett syndrome and clinical spectrum of MECP2 mutations. Current Opinion in Neurology. 14: 171-6 |