MeCP2_E1 N-terminal modifications affect its degradation rate and are disrupted by the Ala2Val Rett mutation
Abstract Methyl CpG-binding protein 2 (MeCP2), the mutated protein in Rett syndrome
(RTT), is a crucial chromatin-modifying and gene-regulatory protein that has two main …
(RTT), is a crucial chromatin-modifying and gene-regulatory protein that has two main …
MeCP2_E1 N-terminal modifications affect its degradation rate and are disrupted by the Ala2Val Rett mutation
TI Sheikh, AM de Paz, S Akhtar, J Ausió… - Human Molecular …, 2017 - academic.oup.com
Abstract Methyl CpG-binding protein 2 (MeCP2), the mutated protein in Rett syndrome
(RTT), is a crucial chromatin-modifying and gene-regulatory protein that has two main …
(RTT), is a crucial chromatin-modifying and gene-regulatory protein that has two main …
MeCP2_E1 N-terminal modifications affect its degradation rate and are disrupted by the Ala2Val Rett mutation
TI Sheikh, AM de Paz, S Akhtar, J Ausio… - Human Molecular …, 2017 - hero.epa.gov
Abstract Methyl CpG-binding protein 2 (MeCP2), the mutated protein in Rett syndrome
(RTT), is a crucial chromatin-modifying and gene-regulatory protein that has two main …
(RTT), is a crucial chromatin-modifying and gene-regulatory protein that has two main …
[PDF][PDF] MeCP2_E1 N-terminal modifications affect its degradation rate and are disrupted by the Ala2Val Rett mutation
TI Sheikh, AM de Paz, S Akhtar, J Ausio… - Human Molecular …, 2017 - researchgate.net
Abstract Methyl CpG-binding protein 2 (MeCP2), the mutated protein in Rett syndrome
(RTT), is a crucial chromatin-modifying and gene-regulatory protein that has two main …
(RTT), is a crucial chromatin-modifying and gene-regulatory protein that has two main …
[HTML][HTML] MeCP2_E1 N-terminal modifications affect its degradation rate and are disrupted by the Ala2Val Rett mutation
TI Sheikh, AM de Paz, S Akhtar, J Ausió… - Human Molecular …, 2017 - ncbi.nlm.nih.gov
Abstract Methyl CpG-binding protein 2 (MeCP2), the mutated protein in Rett syndrome
(RTT), is a crucial chromatin-modifying and gene-regulatory protein that has two main …
(RTT), is a crucial chromatin-modifying and gene-regulatory protein that has two main …
MeCP2_E1 N-terminal modifications affect its degradation rate and are disrupted by the Ala2Val Rett mutation.
TI Sheikh, A Martínez de Paz, S Akhtar… - Human Molecular …, 2017 - search.ebscohost.com
Abstract Methyl CpG-binding protein 2 (MeCP2), the mutated protein in Rett syndrome
(RTT), is a crucial chromatin-modifying and gene-regulatory protein that has two main …
(RTT), is a crucial chromatin-modifying and gene-regulatory protein that has two main …
MeCP2_E1 N-terminal modifications affect its degradation rate and are disrupted by the Ala2Val Rett mutation.
TI Sheikh, AM de Paz, S Akhtar, J Ausió… - Human Molecular …, 2017 - europepmc.org
Abstract Methyl CpG-binding protein 2 (MeCP2), the mutated protein in Rett syndrome
(RTT), is a crucial chromatin-modifying and gene-regulatory protein that has two main …
(RTT), is a crucial chromatin-modifying and gene-regulatory protein that has two main …
MeCP2_E1 N-terminal modifications affect its degradation rate and are disrupted by the Ala2Val Rett mutation
TI Sheikh, AM de Paz, S Akhtar… - Human molecular …, 2017 - pubmed.ncbi.nlm.nih.gov
Methyl CpG-binding protein 2 (MeCP2), the mutated protein in Rett syndrome (RTT), is a
crucial chromatin-modifying and gene-regulatory protein that has two main isoforms …
crucial chromatin-modifying and gene-regulatory protein that has two main isoforms …