Pages that link to "Q74009717"
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The following pages link to MeCP2 mutations in children with and without the phenotype of Rett syndrome (Q74009717):
Displayed 50 items.
- Rett syndrome and MeCP2: linking epigenetics and neuronal function (Q24616417) (← links)
- Rett syndrome: clinical review and genetic update (Q24674633) (← links)
- Clinical Genetic Aspects of ASD Spectrum Disorders (Q26769819) (← links)
- Rett Syndrome: Reaching for Clinical Trials (Q27337778) (← links)
- Neurodevelopmental disorders in males related to the gene causing Rett syndrome in females (MECP2) (Q28180155) (← links)
- Review article: breaking new ground with Rett syndrome (Q28187714) (← links)
- Mutations and polymorphisms in the human methyl CpG-binding protein MECP2 (Q28188406) (← links)
- Identification of MeCP2 mutations in a series of females with autistic disorder (Q28207072) (← links)
- Mechanisms of disease: neurogenetics of MeCP2 deficiency (Q28260093) (← links)
- Alternative polyadenylation of MeCP2: Influence of cis-acting elements and trans-acting factors (Q28646094) (← links)
- Postnatal Neurodevelopmental Disorders: Meeting at the Synapse? (Q29616332) (← links)
- Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3 (Q29616516) (← links)
- Annual Research Review: Transgenic mouse models of childhood-onset psychiatric disorders (Q30469044) (← links)
- InterRett, a model for international data collection in a rare genetic disorder (Q30717719) (← links)
- A decade of high-resolution liquid chromatography of nucleic acids on styrene-divinylbenzene copolymers (Q30718645) (← links)
- Functional Profiling of Human MeCP2 by Automated Data Comparison Analysis and Computerized Expression Pathway Modeling (Q31097619) (← links)
- Effects of sedation on auditory brainstem response in Rett syndrome (Q33804114) (← links)
- Mutations of CDKL5 cause a severe neurodevelopmental disorder with infantile spasms and mental retardation. (Q33910551) (← links)
- X-chromosome inactivation patterns are unbalanced and affect the phenotypic outcome in a mouse model of rett syndrome (Q33911020) (← links)
- Epilepsy in autism (Q33966993) (← links)
- Temporal and regional alterations in NMDA receptor expression in Mecp2-null mice (Q34004048) (← links)
- Ocular MECP2 protein expression in patients with and without Rett syndrome. (Q34047370) (← links)
- Rethinking the fate of males with mutations in the gene that causes Rett syndrome (Q34460580) (← links)
- Genetic effects on human cognition: lessons from the study of mental retardation syndromes (Q34542327) (← links)
- MeCP2 and other methyl-CpG binding proteins (Q34733505) (← links)
- Associations between MeCP2 mutations, X-chromosome inactivation, and phenotype (Q34733527) (← links)
- Clinical trials and treatment prospects (Q34733540) (← links)
- Perspectives on analyses of nucleic acid constituents: the basis of genomics (Q34865906) (← links)
- Rett syndrome. Current status and new vistas (Q35077740) (← links)
- The Use of Denaturing High-Performance Liquid Chromatography (DHPLC) for the Analysis of Genetic Variations: Impact for Diagnostics and Pharmacogenetics (Q35127771) (← links)
- Two new Rett syndrome families and review of the literature: expanding the knowledge of MECP2 frameshift mutations. (Q35213632) (← links)
- Describing the phenotype in Rett syndrome using a population database (Q35273721) (← links)
- Heterogeneity in residual function of MeCP2 carrying missense mutations in the methyl CpG binding domain (Q35443072) (← links)
- Selective cerebral volume reduction in Rett syndrome: a multiple-approach MR imaging study (Q35492515) (← links)
- Paradoxical role of methyl-CpG-binding protein 2 in Rett syndrome. (Q35671678) (← links)
- Rapid genotyping of common MeCP2 mutations with an electronic DNA microchip using serial differential hybridization (Q35870262) (← links)
- Correlation of the vesicular acetylcholine transporter densities in the striata to the clinical abilities of women with Rett syndrome (Q36344561) (← links)
- Functional outcomes in Rett syndrome (Q36414822) (← links)
- The relationship of Rett syndrome and MECP2 disorders to autism. (Q36443010) (← links)
- Rett syndrome: new clinical and molecular insights. (Q36545755) (← links)
- The association between behavior and genotype in Rett syndrome using the Australian Rett Syndrome Database. (Q36922496) (← links)
- Very mild cases of Rett syndrome with skewed X inactivation (Q36927070) (← links)
- Brain metabolism in Rett syndrome: age, clinical, and genotype correlations (Q37178721) (← links)
- GlyT2-Dependent Preservation of MECP2-Expression in Inhibitory Neurons Improves Early Respiratory Symptoms but Does Not Rescue Survival in a Mouse Model of Rett Syndrome. (Q37246898) (← links)
- A common MECP2 haplotype associates with reduced cortical surface area in humans in two independent populations (Q37340881) (← links)
- Role of conserved cis-regulatory elements in the post-transcriptional regulation of the human MECP2 gene involved in autism (Q37352229) (← links)
- MicroRNAs and epigenetic regulation in the mammalian inner ear: implications for deafness (Q37624422) (← links)
- Analysis of the Serotonergic System in a Mouse Model of Rett Syndrome Reveals Unusual Upregulation of Serotonin Receptor 5b (Q37685373) (← links)
- Rett syndrome and MeCP2. (Q38194967) (← links)
- A novel hypomorphic MECP2 point mutation is associated with a neuropsychiatric phenotype (Q38359244) (← links)