Histone H3 lysine methylation in cognition and intellectual disability disorders

Learning and Memory

Volumn 20, Issue 10, 2013, Pages 570-579

  Parkel, Sven ^a   Lopez Atalaya, Jose P ^a   Barco, Angel ^a  

^a INSTITUTO DE NEUROCIENCIAS   (Spain)

Author keywords

[No Author keywords available]

Indexed keywords

CELL NUCLEUS RECEPTOR; FLAVINE ADENINE NUCLEOTIDE; HISTONE H3; HISTONE METHYLTRANSFERASE; LYSINE; NONHISTONE PROTEIN; TRANSCRIPTION FACTOR EZH2;

ALTERNATIVE RNA SPLICING; AMINO TERMINAL SEQUENCE; AMNESIA; AUTISM; BRAIN CELL; CLAES JENSEN TYPE SYNDROMIC X LINKED INTELLECTUAL DISABILITY; COGNITION; COGNITIVE DEFECT; CONDITIONING; DEMETHYLATION; DNA REPLICATION; ENTORHINAL CORTEX; ENZYME SPECIFICITY; EPIGENETICS; FEAR; GENE EXPRESSION; GENE EXPRESSION REGULATION; GENE INACTIVATION; GENE REPRESSION; GENE SILENCING; GENETIC TRANSCRIPTION; HIPPOCAMPAL CA1 REGION; HIPPOCAMPUS; HISTONE ACETYLATION; HISTONE METHYLATION; HUMAN; INTELLECTUAL IMPAIRMENT; KABUKI MAKEUP SYNDROME; KLEEFSTRA SYNDROME; LEARNING; LONG TERM MEMORY; LONG TERM POTENTIATION; MEMORY; MEMORY CONSOLIDATION; MENTAL DEVELOPMENT; MUTANT DROSOPHILA; NERVE CELL DIFFERENTIATION; NERVE CELL PLASTICITY; NONHUMAN; POINT MUTATION; PREFRONTAL CORTEX; PRIORITY JOURNAL; PROMOTER REGION; PROTEIN DOMAIN; PROTEIN FAMILY; PROTEIN PROCESSING; REVIEW; RNA GENE; SOTOS SYNDROME; STOP CODON; SYDERIUS X LINKED INTELLECTUAL DISABILITY; SYNAPTIC TRANSMISSION; WOLF HIRSCHHORN SYNDROME; X CHROMOSOME LINKED DISORDER;

ANIMALS; COGNITION DISORDERS; EPIGENESIS, GENETIC; HISTONES; HUMANS; INTELLECTUAL DISABILITY; LYSINE; METHYLATION; PROTEIN PROCESSING, POST-TRANSLATIONAL;

EID: 84885122834     PISSN: 10720502     EISSN: 15495485     Source Type: Journal    
DOI: 10.1101/lm.029363.112     Document Type: Review

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