Pages that link to "Q34307505"
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The following pages link to A previously unidentified MECP2 open reading frame defines a new protein isoform relevant to Rett syndrome (Q34307505):
Displaying 50 items.
- Identification of the imprinted KLF14 transcription factor undergoing human-specific accelerated evolution (Q21092496) (← links)
- A mono-allelic bivalent chromatin domain controls tissue-specific imprinting at Grb10 (Q24652620) (← links)
- The odyssey of MeCP2 and parental imprinting (Q24671994) (← links)
- Modifiers and Readers of DNA Modifications and Their Impact on Genome Structure, Expression, and Stability in Disease (Q26742136) (← links)
- MeCP2 and the enigmatic organization of brain chromatin. Implications for depression and cocaine addiction (Q26747013) (← links)
- Developmental Dynamics of Rett Syndrome (Q26768284) (← links)
- The Utility of Next-Generation Sequencing in Gene Discovery for Mutation-Negative Patients with Rett Syndrome (Q26800087) (← links)
- Rett syndrome - biological pathways leading from MECP2 to disorder phenotypes (Q28025533) (← links)
- A review of Rett syndrome (RTT) with induced pluripotent stem cells (Q28072303) (← links)
- Novel mutations in the CDKL5 gene, predicted effects and associated phenotypes (Q28236247) (← links)
- Molecular genetics of Rett syndrome: when DNA methylation goes unrecognized (Q28240924) (← links)
- MeCP2: the chromatin connection and beyond (Q28256925) (← links)
- Mechanisms of disease: neurogenetics of MeCP2 deficiency (Q28260093) (← links)
- MECP2 and CDKL5 gene mutation analysis in Chinese patients with Rett syndrome (Q28272755) (← links)
- Dexamethasone induces a putative repressor complex and chromatin modifications in the CRH promoter (Q28576128) (← links)
- A partial loss of function allele of methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndrome (Q28586765) (← links)
- Enhanced cell death in MeCP2 null cerebellar granule neurons exposed to excitotoxicity and hypoxia (Q28589283) (← links)
- Analysis of protein domains and Rett syndrome mutations indicate that multiple regions influence chromatin-binding dynamics of the chromatin-associated protein MECP2 in vivo (Q28591033) (← links)
- Ex Vivo Treatment with a Novel Synthetic Aminoglycoside NB54 in Primary Fibroblasts from Rett Syndrome Patients Suppresses MECP2 Nonsense Mutations (Q28743688) (← links)
- IUGR differentially alters MeCP2 expression and H3K9Me3 of the PPARγ gene in male and female rat lungs during alveolarization (Q28909812) (← links)
- Bdnf overexpression in hippocampal neurons prevents dendritic atrophy caused by Rett-associated MECP2 mutations (Q28941188) (← links)
- A Model for Neural Development and Treatment of Rett Syndrome Using Human Induced Pluripotent Stem Cells (Q29619964) (← links)
- Beyond Widespread Mecp2 Deletions to Model Rett Syndrome: Conditional Spatio-Temporal Knockout, Single-Point Mutations and Transgenic Rescue Mice (Q30450914) (← links)
- Mice with an isoform-ablating Mecp2 exon 1 mutation recapitulate the neurologic deficits of Rett syndrome (Q30575472) (← links)
- Over-expression of either MECP2_e1 or MECP2_e2 in neuronally differentiated cells results in different patterns of gene expression (Q31155726) (← links)
- Expression profiling of clonal lymphocyte cell cultures from Rett syndrome patients (Q33251357) (← links)
- Reduced MeCP2 expression is frequent in autism frontal cortex and correlates with aberrant MECP2 promoter methylation (Q33283941) (← links)
- High levels of MeCP2 depress MHC class I expression in neuronal cells (Q33312371) (← links)
- Mecp2-null mice provide new neuronal targets for Rett syndrome. (Q33383191) (← links)
- MECP2 isoform-specific vectors with regulated expression for Rett syndrome gene therapy (Q33497321) (← links)
- Preferential transfer of certain plasma membrane proteins onto T and B cells by trogocytosis (Q33525562) (← links)
- Experimental Autoimmune Encephalomyelitis (EAE)-Induced Elevated Expression of the E1 Isoform of Methyl CpG Binding Protein 2 (MeCP2E1): Implications in Multiple Sclerosis (MS)-Induced Neurological Disability and Associated Myelin Damage (Q33838894) (← links)
- Recent advances in MeCP2 structure and function (Q33867993) (← links)
- Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation. (Q33910551) (← links)
- Ocular MECP2 protein expression in patients with and without Rett syndrome. (Q34047370) (← links)
- A partial MECP2 duplication in a mildly affected adult male: a putative role for the 3' untranslated region in the MECP2 duplication phenotype. (Q34375828) (← links)
- Cellular commitment in the developing cerebellum (Q34460069) (← links)
- Novel MeCP2 isoform-specific antibody reveals the endogenous MeCP2E1 expression in murine brain, primary neurons and astrocytes (Q34490485) (← links)
- Rett syndrome diagnostic criteria: lessons from the Natural History Study (Q34496045) (← links)
- Rett syndrome: a Rosetta stone for understanding the molecular pathogenesis of autism (Q34499035) (← links)
- Setdb1-mediated histone H3K9 hypermethylation in neurons worsens the neurological phenotype of Mecp2-deficient mice (Q34511024) (← links)
- Experimental models of Rett syndrome based on Mecp2 dysfunction. (Q34686591) (← links)
- MeCP2 is required for global heterochromatic and nucleolar changes during activity-dependent neuronal maturation. (Q34988096) (← links)
- miRNA-132 orchestrates chromatin remodeling and translational control of the circadian clock (Q35047068) (← links)
- Complexities of Rett Syndrome and MeCP2: Figure 1 (Q35080184) (← links)
- Brain region-specific expression of MeCP2 isoforms correlates with DNA methylation within Mecp2 regulatory elements. (Q35110620) (← links)
- MECP2e1 isoform mutation affects the form and function of neurons derived from Rett syndrome patient iPS cells (Q35235695) (← links)
- CAGE-defined promoter regions of the genes implicated in Rett Syndrome. (Q35533684) (← links)
- Transgenic complementation of MeCP2 deficiency: phenotypic rescue of Mecp2-null mice by isoform-specific transgenes (Q35603659) (← links)
- Partial rescue of MeCP2 deficiency by postnatal activation of MeCP2. (Q35629499) (← links)