Results 211 to 220 of about 33,901 (278)

Revealing function-altering MECP2 mutations in individuals with autism spectrum disorder using yeast and Drosophila. [PDF]

Genetics
Chen E, Schmitt J, McIntosh G, Young BP, Lian T, Liu J, Chen KK, Liston JB, MacDonald L, Wang B, Medina Giro S, Boehme B, Das M, Indran S, Chao JT, Rogic S, Pavlidis P, Allan DW, Loewen CJR.   +18 more
europepmc   +1 more source

Cell-type- and locus-specific epigenetic editing of memory expression. [PDF]

Nat Genet
Coda DM, Watt L, Glauser L, Batiuk MY, Burns AM, Stahl CL, Wong LY, Gräff J.   +7 more
europepmc   +1 more source

A small-molecule TrkB ligand improves dendritic spine phenotypes and atypical behaviors in female Rett syndrome mice

Disease Models & Mechanisms
Destynie Medeiros, Karen Ayala-Baylon, Hailey Egido-Betancourt, Eric Miller, Christopher Chapleau, Holly Robinson, Mary L. Phillips, Tao Yang, Frank M. Longo, Wei Li, Lucas Pozzo-Miller   +10 more
doaj   +1 more source

Neurodegeneration Within the Spectrum of Pervasive Developmental Disorders. [PDF]

Cureus
Mihalcea D, Iordache MP, Angelescu C.
europepmc   +1 more source

Loss of MeCP2 in aminergic neurons causes cell-autonomous defects in neurotransmitter synthesis and specific behavioral abnormalities

, 2009
Rodney C. Samaco, Caleigh Mandel‐Brehm, Hsiao-Tuan Chao, Christopher Ward, Sharyl L. Fyffe-Maricich, Jun Ren, Keith Hyland, Christina Thaller, Stephen M. Maricich, Peter Humphreys, John J. Greer, Alan K. Percy, Daniel G. Glaze, Huda Y. Zoghbi, Jeffrey L. Neul   +14 more
openalex   +1 more source

Author Correction: Engineering novel CRISPRi repressors for highly efficient mammalian gene regulation. [PDF]

Genome Biol
Kristof A, Karunakaran K, Allen C, Mizote P, Briggs S, Jian Z, Nash P, Blazeck J.   +7 more
europepmc   +1 more source

Acute MeCP2 loss in adult mice reveals transcriptional and chromatin changes that precede neurological dysfunction and inform pathogenesis

Sameer S. Bajikar, Jian Zhou, Ryan O’Hara, Harini P Tirumala, Mark A. Durham, Alexander J. Trostle, Michelle Dias, Yingyao Shao, Hu Chen, Wei Wang, Hari Krishna Yalamanchili, Ying‐Wooi Wan, Laura A. Banaszynski, Zhandong Liu, Huda Y. Zoghbi   +14 more
openalex   +1 more source

Functional skills in MECP2 duplication syndrome: developmental dynamics and regression. [PDF]

Orphanet J Rare Dis
Ta D, Downs J, Baynam G, Richmond P, Wilson A, Leonard H.   +5 more
europepmc   +1 more source

Presence of phosphodiester backbone, but not nucleobases, in the guide's 3' terminal region is necessary for RISC loading and target cleavage in vitro and in vivo. [PDF]

Nucleic Acids Res
O'Reilly D, Furgal RC, Ross VM, Luu E, Gross KY, Hariharan V, Summers A, Cooper D, Allen S, Dahlke C, Rachid MO, Chan IL, Fakih HH, Alterman JF, Echeverria D, Watts JK, Khvorova A.   +16 more
europepmc   +1 more source

Enhancing cognitive-motor recovery in Rett syndrome: effects of integrated intervention on neuropsychological and motor outcome. [PDF]

Front Psychol
Fabio RA, Semino M, Perina M.
europepmc   +1 more source