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Keywords: Mecp2
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Journal Articles
Journal Articles
Journal Articles
Journal Articles
Dis Model Mech (2017) 10 (12): 1439–1451.
Published: 1 December 2017
...M. van der Vaart; O. Svoboda; B. G. Weijts; R. Espín-Palazón; V. Sapp; T. Pietri; M. Bagnat; A. R. Muotri; D. Traver ABSTRACT Mutations in MECP2 cause Rett syndrome, a severe neurological disorder with autism-like features. Duplication of MECP2 also causes severe neuropathology. Both diseases...
Includes: Supplementary data
Journal Articles
Dis Model Mech (2017) 10 (7): 837–845.
Published: 1 July 2017
...Wei Li; Alba Bellot-Saez; Mary L. Phillips; Tao Yang; Frank M. Longo; Lucas Pozzo-Miller ABSTRACT Rett syndrome (RTT) is a neurodevelopmental disorder caused by mutations in methyl-CpG-binding protein-2 ( MECP2 ), a transcriptional regulator of many genes, including brain-derived neurotrophic...
Includes: Supplementary data
Journal Articles
Dis Model Mech (2015) 8 (4): 363–371.
Published: 1 April 2015
... into human clinical trials. Notably, in our study Mecp2 Null/Y mice treated with phenytoin showed an increase in activity and hyperventilation, whereas these effects were not observed in the less-severe female Mecp2 Null/+ mice. However, both male Mecp2 Null/Y and female Mecp2 Null/+ mice...
Includes: Supplementary data
Journal Articles