Pages that link to "Q28593334"
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The following pages link to MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression (Q28593334):
Displaying 50 items.
- Methyl CpG binding protein 2 (Q21499136) (← links)
- Maternal disruption of Ube3a leads to increased expression of Ube3a-ATS in trans (Q24531844) (← links)
- The comorbidity of autism with the genomic disorders of chromosome 15q11.2-q13 (Q24594577) (← links)
- The ubiquitin proteasome system in neuropathology (Q24644208) (← links)
- The odyssey of MeCP2 and parental imprinting (Q24671994) (← links)
- DLX5 and DLX6 expression is biallelic and not modulated by MeCP2 deficiency (Q24677959) (← links)
- 15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders (Q24683678) (← links)
- DNA modifications: function and applications in normal and disease States (Q26829214) (← links)
- Abnormalities of the DNA methylation mark and its machinery: an emerging cause of neurologic dysfunction (Q27003875) (← links)
- Genetic modifiers of MeCP2 function in Drosophila (Q27313791) (← links)
- Molecular genetics of Rett syndrome: when DNA methylation goes unrecognized (Q28240924) (← links)
- Mechanisms of disease: neurogenetics of MeCP2 deficiency (Q28260093) (← links)
- Mecp2-null mice provide new neuronal targets for Rett syndrome. (Q33383191) (← links)
- CpG and Non-CpG Methylation in Epigenetic Gene Regulation and Brain Function (Q33836737) (← links)
- Pre-administration of G9a/GLP inhibitor during synaptogenesis prevents postnatal ethanol-induced LTP deficits and neurobehavioral abnormalities in adult mice. (Q34325299) (← links)
- Rett syndrome: a Rosetta stone for understanding the molecular pathogenesis of autism (Q34499035) (← links)
- Synaptic determinants of rett syndrome. (Q34689838) (← links)
- Truncation of Ube3a-ATS unsilences paternal Ube3a and ameliorates behavioral defects in the Angelman syndrome mouse model (Q35079892) (← links)
- CB1-receptor knockout neonatal mice are protected against ethanol-induced impairments of DNMT1, DNMT3A, and DNA methylation. (Q35153976) (← links)
- Ethanol exposure induces neonatal neurodegeneration by enhancing CB1R Exon1 histone H4K8 acetylation and up-regulating CB1R function causing neurobehavioral abnormalities in adult mice (Q35224267) (← links)
- Partial rescue of MeCP2 deficiency by postnatal activation of MeCP2. (Q35629499) (← links)
- Dynamic changes in Histone H3 lysine 9 acetylation localization patterns during neuronal maturation require MeCP2. (Q35762162) (← links)
- Increased copy number for methylated maternal 15q duplications leads to changes in gene and protein expression in human cortical samples (Q35779834) (← links)
- Mechanisms of activation of the paternally expressed genes by the Prader-Willi imprinting center in the Prader-Willi/Angelman syndromes domains (Q35983002) (← links)
- Adult Phenotypes in Angelman- and Rett-Like Syndromes (Q36006568) (← links)
- Ube3a-ATS is an atypical RNA polymerase II transcript that represses the paternal expression of Ube3a (Q36301671) (← links)
- Non-Coding RNAs at the Gnas and Snrpn-Ube3a Imprinted Gene Loci and Their Involvement in Hereditary Disorders (Q36433565) (← links)
- How imprinting centres work (Q36436525) (← links)
- Imprinting in neurons (Q36436581) (← links)
- Intracytoplasmic sperm injection--an assisted reproduction technique that should make us cautious about imprinting deregulation (Q36524664) (← links)
- X-linked mental retardation and epigenetics (Q36663018) (← links)
- G9a-mediated histone methylation regulates ethanol-induced neurodegeneration in the neonatal mouse brain. (Q36850801) (← links)
- Advances in behavioral genetics: mouse models of autism (Q36937876) (← links)
- MECP2 genomic structure and function: insights from ENCODE (Q36959606) (← links)
- Smchd1 regulates a subset of autosomal genes subject to monoallelic expression in addition to being critical for X inactivation (Q37000934) (← links)
- Ube3a mRNA and protein expression are not decreased in Mecp2R168X mutant mice (Q37251436) (← links)
- Cell cloning-based transcriptome analysis in Rett patients: relevance to the pathogenesis of Rett syndrome of new human MeCP2 target genes (Q37295711) (← links)
- Genes related to mitochondrial functions, protein degradation, and chromatin folding are differentially expressed in lymphomonocytes of Rett syndrome patients (Q37422466) (← links)
- MicroRNAs and epigenetic regulation in the mammalian inner ear: implications for deafness (Q37624422) (← links)
- Ethanol induced acetylation of histone at G9a exon1 and G9a-mediated histone H3 dimethylation leads to neurodegeneration in neonatal mice. (Q37638056) (← links)
- Evolving role of MeCP2 in Rett syndrome and autism (Q37754018) (← links)
- Genetic and epigenetic dysregulation of imprinted genes in the brain (Q37961799) (← links)
- Autism spectrum disorders: the quest for genetic syndromes (Q38104700) (← links)
- E6AP in the brain: one protein, dual function, multiple diseases (Q38148981) (← links)
- The contribution of epigenetics to understanding genetic factors in autism (Q38152705) (← links)
- MeCP2 Deficiency in Neuroglia: New Progress in the Pathogenesis of Rett Syndrome (Q42372796) (← links)
- Epigenetics and cerebral organoids: promising directions in autism spectrum disorders (Q47562578) (← links)
- Evaluation of autism traits in Angelman syndrome: a resource to unfold autism genes (Q50313899) (← links)
- A survey of seizures and current treatments in 15q duplication syndrome (Q50343349) (← links)
- Germline correction of an epimutation related to Silver-Russell syndrome (Q50597783) (← links)