Pages that link to "Q28302378"

The following pages link to Novel JARID1C/SMCX mutations in patients with X-linked mental retardation (Q28302378):

Displaying 49 items.

• The X-linked mental retardation gene SMCX/JARID1C defines a family of histone H3 lysine 4 demethylases (Q24298299) (← links)
• PHF8, a gene associated with cleft lip/palate and mental retardation, encodes for an Nepsilon-dimethyl lysine demethylase (Q24309265) (← links)
• Structural and Evolutionary Basis for the Dual Substrate Selectivity of Human KDM4 Histone Demethylase Family (Q27673793) (← links)
• Erasing the methyl mark: histone demethylases at the center of cellular differentiation and disease (Q29617086) (← links)
• Sex-specific expression of the X-linked histone demethylase gene Jarid1c in brain (Q33348587) (← links)
• Methamphetamine-associated memory is regulated by a writer and an eraser of permissive histone methylation. (Q33624077) (← links)
• A distinctive gene expression fingerprint in mentally retarded male patients reflects disease-causing defects in the histone demethylase KDM5C. (Q33698314) (← links)
• PHD fingers: epigenetic effectors and potential drug targets (Q33819263) (← links)
• The JmjN domain of Jhd2 is important for its protein stability, and the plant homeodomain (PHD) finger mediates its chromatin association independent of H3K4 methylation (Q34042577) (← links)
• Proliferating cell nuclear antigen is required for loading of the SMCX/KMD5C histone demethylase onto chromatin (Q34047729) (← links)
• Chromatin and oxygen sensing in the context of JmjC histone demethylases (Q34103385) (← links)
• The genetic basis of non-syndromic intellectual disability: a review (Q34283901) (← links)
• Identification and characterization of two novel JARID1C mutations: suggestion of an emerging genotype-phenotype correlation (Q34328652) (← links)
• The hidden genetics of epilepsy-a clinically important new paradigm (Q34415194) (← links)
• Multilocus loss of DNA methylation in individuals with mutations in the histone H3 lysine 4 demethylase KDM5C. (Q34565537) (← links)
• The histone H3K4 demethylase SMCX links REST target genes to X-linked mental retardation. (Q34624060) (← links)
• Reversible histone methylation regulates brain gene expression and behavior (Q34879560) (← links)
• Epigenetic Regulation by Lysine Demethylase 5 (KDM5) Enzymes in Cancer. (Q34897761) (← links)
• Epigenetic gene regulation in the adult mammalian brain: Multiple roles in memory formation (Q35036368) (← links)
• Disrupted intricacy of histone H3K4 methylation in neurodevelopmental disorders (Q35849485) (← links)
• A cell-permeable ester derivative of the JmjC histone demethylase inhibitor IOX1 (Q35854599) (← links)
• Epileptogenesis: can the science of epigenetics give us answers? (Q36008878) (← links)
• Mutations in the KDM5C ARID Domain and Their Plausible Association with Syndromic Claes-Jensen-Type Disease (Q36324695) (← links)
• Histone demethylases and cancer (Q36421138) (← links)
• NRSF and BDNF polymorphisms as biomarkers of cognitive dysfunction in adults with newly diagnosed epilepsy (Q36520757) (← links)
• Xp11.2 microduplications including IQSEC2, TSPYL2 and KDM5C genes in patients with neurodevelopmental disorders (Q36591206) (← links)
• Histone lysine demethylases: emerging roles in development, physiology and disease (Q36957469) (← links)
• Mutations in JARID1C are associated with X-linked mental retardation, short stature and hyperreflexia (Q37013268) (← links)
• Chromatin-bound RNA and the neurobiology of psychiatric disease (Q37351175) (← links)
• The histone demethylase Dmel\Kdm4A controls genes required for life span and male-specific sex determination in Drosophila (Q37480775) (← links)
• Epigenetic mechanisms underlying human epileptic disorders and the process of epileptogenesis (Q37699484) (← links)
• Physiological roles of class I HDAC complex and histone demethylase. (Q37806964) (← links)
• Errors in Erasure: Links Between Histone Lysine Methylation Removal and Disease (Q37818082) (← links)
• Epigenetic Treatments for Cognitive Impairments (Q37877119) (← links)
• Role of H3K4 demethylases in complex neurodevelopmental diseases (Q37961732) (← links)
• Molecular mechanisms and potential functions of histone demethylases (Q37999690) (← links)
• Histone methylation in the nervous system: functions and dysfunctions (Q38060650) (← links)
• Histone lysine demethylases as targets for anticancer therapy (Q38162717) (← links)
• Jumonji family histone demethylases in neural development. (Q38221959) (← links)
• The retinoblastoma binding protein RBP2 is an H3K4 demethylase (Q38304373) (← links)
• Histone H3K4 trimethylation: dynamic interplay with pre-mRNA splicing (Q38583533) (← links)
• Patient Mutations of the Intellectual Disability Gene KDM5C Downregulate Netrin G2 and Suppress Neurite Growth in Neuro2a Cells (Q38757954) (← links)
• Analysis of SCN1A mutation and parental origin in patients with Dravet syndrome. (Q42658858) (← links)
• A Drosophila Model of Intellectual Disability Caused by Mutations in the Histone Demethylase KDM5. (Q50421548) (← links)
• Altered Gene-Regulatory Function of KDM5C by a Novel Mutation Associated With Autism and Intellectual Disability. (Q52579275) (← links)
• High frequency of mosaic pathogenic variants in genes causing epilepsy-related neurodevelopmental disorders. (Q55022100) (← links)
• Epigenetic Mechanisms of Mental Retardation (Q56501909) (← links)
• Molecular mechanisms and potential functions of histone demethylases (Q59540864) (← links)
• Sex Chromosome Effects on Male-Female Differences in Mammals (Q59794873) (← links)