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Matthew J Lyst

Showing results (1-10 of 11) with videos related to

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Nature Reviews. Genetics|March 4, 2015
Rett syndrome: a complex disorder with simple rootsMatthew J Lyst, Adrian Bird
The EMBO Journal|October 27, 2006
Regulation of MBD1-mediated transcriptional repression by SUMO and PIAS proteinsMatthew J Lyst, Xinsheng Nan, Irina Stancheva
FEBS Letters|July 28, 2016
Sequence-specific DNA binding by AT-hook motifs in MeCP2Matthew J Lyst, John Connelly, Cara Merusi, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 29, 2017
Structure of the MeCP2-TBLR1 complex reveals a molecular basis for Rett syndrome and related disordersValdeko Kruusvee, Matthew J Lyst, Ceitidh Taylor, et al.
Cell Reports|August 30, 2018
Affinity for DNA Contributes to NLS Independent Nuclear Localization of MeCP2Matthew J Lyst, Robert Ekiert, Jacky Guy, et al.
Genes & Development|November 23, 2018
Toxicity of overexpressed MeCP2 is independent of HDAC3 activityMartha V Koerner, Laura FitzPatrick, Jim Selfridge, et al.
Scientific Reports|March 8, 2023
A screen for MeCP2-TBL1 interaction inhibitors using a luminescence-based assayBeatrice Alexander-Howden, Li Zhang, Almer M van der Sloot, et al.
Nature Communications|May 16, 2026
Dysfunction of a SET3-like complex underlies a family of related neurological disordersKatie M Paton, Beatrice Alexander-Howden, Jenna I Hare, et al.
Nature|June 18, 2013
Activity-dependent phosphorylation of MeCP2 threonine 308 regulates interaction with NCoRDaniel H Ebert, Harrison W Gabel, Nathaniel D Robinson, et al.
Nature Neuroscience|June 18, 2013
Rett syndrome mutations abolish the interaction of MeCP2 with the NCoR/SMRT co-repressorMatthew J Lyst, Robert Ekiert, Daniel H Ebert, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Nature Reviews. Genetics|March 4, 2015
Rett syndrome: a complex disorder with simple rootsMatthew J Lyst, Adrian Bird
The EMBO Journal|October 27, 2006
Regulation of MBD1-mediated transcriptional repression by SUMO and PIAS proteinsMatthew J Lyst, Xinsheng Nan, Irina Stancheva
FEBS Letters|July 28, 2016
Sequence-specific DNA binding by AT-hook motifs in MeCP2Matthew J Lyst, John Connelly, Cara Merusi, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 29, 2017
Structure of the MeCP2-TBLR1 complex reveals a molecular basis for Rett syndrome and related disordersValdeko Kruusvee, Matthew J Lyst, Ceitidh Taylor, et al.
Cell Reports|August 30, 2018
Affinity for DNA Contributes to NLS Independent Nuclear Localization of MeCP2Matthew J Lyst, Robert Ekiert, Jacky Guy, et al.
Genes & Development|November 23, 2018
Toxicity of overexpressed MeCP2 is independent of HDAC3 activityMartha V Koerner, Laura FitzPatrick, Jim Selfridge, et al.
Scientific Reports|March 8, 2023
A screen for MeCP2-TBL1 interaction inhibitors using a luminescence-based assayBeatrice Alexander-Howden, Li Zhang, Almer M van der Sloot, et al.
Nature Communications|May 16, 2026
Dysfunction of a SET3-like complex underlies a family of related neurological disordersKatie M Paton, Beatrice Alexander-Howden, Jenna I Hare, et al.
Nature|June 18, 2013
Activity-dependent phosphorylation of MeCP2 threonine 308 regulates interaction with NCoRDaniel H Ebert, Harrison W Gabel, Nathaniel D Robinson, et al.
Nature Neuroscience|June 18, 2013
Rett syndrome mutations abolish the interaction of MeCP2 with the NCoR/SMRT co-repressorMatthew J Lyst, Robert Ekiert, Daniel H Ebert, et al.
Pageof 2