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SAMACO, RODNEY
One or more keywords matched the following items that are connected to SAMACO, RODNEY
Item TypeName
Academic Article MECP2 mutations in Rett syndrome adversely affect lymphocyte growth, but do not affect imprinted gene expression in blood or brain.
Academic Article X-Chromosome inactivation ratios affect wild-type MeCP2 expression within mosaic Rett syndrome and Mecp2-/+ mouse brain.
Academic Article Multiple pathways regulate MeCP2 expression in normal brain development and exhibit defects in autism-spectrum disorders.
Academic Article Complexities of Rett syndrome and MeCP2.
Academic Article A partial loss of function allele of methyl-CpG-binding protein 2 predicts a human neurodevelopmental syndrome.
Academic Article Dysfunction in GABA signalling mediates autism-like stereotypies and Rett syndrome phenotypes.
Academic Article Epigenetic overlap in autism-spectrum neurodevelopmental disorders: MECP2 deficiency causes reduced expression of UBE3A and GABRB3.
Academic Article Adult neural function requires MeCP2.
Academic Article Preclinical research in Rett syndrome: setting the foundation for translational success.
Concept Rett Syndrome
Academic Article Forniceal deep brain stimulation rescues hippocampal memory in Rett syndrome mice.
Academic Article Loss of MeCP2 in the rat models regression, impaired sociability and transcriptional deficits of Rett syndrome.
Academic Article Loss of MeCP2 Causes Urological Dysfunction and Contributes to Death by Kidney Failure in Mouse Models of Rett Syndrome.
Grant Neurobehavioral and biochemical outcome measures in Rett syndrome rodent models
Academic Article Improving clinical trial readiness to accelerate development of new therapeutics for Rett syndrome.
Search Criteria
  • Rett Syndrome