Pages that link to "Q34643439"
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The following pages link to Molecular and comparative genetics of mental retardation (Q34643439):
Displayed 50 items.
- Our Fragile Intellect (Q7110639) (← links)
- A multi-platform draft de novo genome assembly and comparative analysis for the Scarlet Macaw (Ara macao) (Q21090760) (← links)
- A functional link between the histone demethylase PHF8 and the transcription factor ZNF711 in X-linked mental retardation (Q24304870) (← links)
- CNTNAP2 and NRXN1 are mutated in autosomal-recessive Pitt-Hopkins-like mental retardation and determine the level of a common synaptic protein in Drosophila (Q24315560) (← links)
- Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13 (Q24612956) (← links)
- A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation (Q24613870) (← links)
- Population genetic analysis of the N-acylsphingosine amidohydrolase gene associated with mental activity in humans (Q24647682) (← links)
- Genetic enhancement of cognition in a kindred with cone-rod dystrophy due to RIMS1 mutation (Q24657752) (← links)
- Nonvesicular release of glutamate by glial xCT transporters suppresses glutamate receptor clustering in vivo (Q24675057) (← links)
- The role of neuronal complexes in human X-linked brain diseases (Q24680472) (← links)
- Advances in understanding - genetic basis of intellectual disability (Q26748977) (← links)
- Child development and molecular genetics: 14 years later (Q26853446) (← links)
- A targeted glycan-related gene screen reveals heparan sulfate proteoglycan sulfation regulates WNT and BMP trans-synaptic signaling (Q27330302) (← links)
- Evaluating historical candidate genes for schizophrenia (Q28082318) (← links)
- Genetic foundations of human intelligence (Q28238449) (← links)
- The genetic and environmental origins of learning abilities and disabilities in the early school years (Q28256888) (← links)
- Genome-wide association analysis identifies 13 new risk loci for schizophrenia (Q28297287) (← links)
- Animal models of autism spectrum disorders: information for neurotoxicologists (Q28385566) (← links)
- The Rho-linked mental retardation protein oligophrenin-1 controls synapse maturation and plasticity by stabilizing AMPA receptors (Q28574269) (← links)
- X-linked mental retardation gene CUL4B targets ubiquitylation of H3K4 methyltransferase component WDR5 and regulates neuronal gene expression (Q28578733) (← links)
- Evolutionary genomics of human intellectual disability (Q28729961) (← links)
- MEF2C regulates cortical inhibitory and excitatory synapses and behaviors relevant to neurodevelopmental disorders. (Q30370553) (← links)
- Sex differences in protein expression in the mouse brain and their perturbations in a model of Down syndrome (Q30398962) (← links)
- Enhanced tethered-flight duration and locomotor activity by overexpression of the human gene SOD1 in Drosophila motorneurons (Q30411883) (← links)
- Gene expression in cortical interneuron precursors is prescient of their mature function (Q30486244) (← links)
- Control of cognition and adaptive behavior by the GLP/G9a epigenetic suppressor complex (Q30492948) (← links)
- Whole transcriptome analysis of a reversible neurodegenerative process in Drosophila reveals potential neuroprotective genes. (Q30528302) (← links)
- Alteration in basal and depolarization induced transcriptional network in iPSC derived neurons from Timothy syndrome. (Q30596522) (← links)
- Assessing Relevance of External Cognitive Measures (Q31172442) (← links)
- Origin and evolution of candidate mental retardation genes on the human X chromosome (MRX) (Q33318140) (← links)
- Molecular cytogenetics and cytogenomics of brain diseases (Q33464340) (← links)
- Forging links between human mental retardation-associated CNVs and mouse gene knockout models (Q33474855) (← links)
- Heritability and genomics of gene expression in peripheral blood (Q33575322) (← links)
- Aversive phototaxic suppression: evaluation of a short-term memory assay in Drosophila melanogaster. (Q33582826) (← links)
- Conserved family of glycerol kinase loci in Drosophila melanogaster (Q33595210) (← links)
- Single exon-resolution targeted chromosomal microarray analysis of known and candidate intellectual disability genes (Q33620872) (← links)
- The genetics of autism: key issues, recent findings, and clinical implications (Q33739608) (← links)
- A mental retardation gene, motopsin/neurotrypsin/prss12, modulates hippocampal function and social interaction (Q33790196) (← links)
- Memory consolidation and gene expression in Periplaneta americana (Q33835496) (← links)
- Alterations in CDH15 and KIRREL3 in patients with mild to severe intellectual disability (Q33845730) (← links)
- Genetic architectures of psychiatric disorders: the emerging picture and its implications (Q33949729) (← links)
- A genomewide scan for intelligence identifies quantitative trait loci on 2q and 6p. (Q34015456) (← links)
- Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits (Q34024006) (← links)
- Disruption of an EHMT1-associated chromatin-modification module causes intellectual disability (Q34283663) (← links)
- A cell-based fascin bioassay identifies compounds with potential anti-metastasis or cognition-enhancing functions. (Q34392217) (← links)
- Genome-wide DNA methylation and gene expression analyses of monozygotic twins discordant for intelligence levels (Q34451972) (← links)
- Genetics of intelligence (Q34529957) (← links)
- Genetics and pathophysiology of mental retardation (Q34529963) (← links)
- Understanding intellectual disability through RASopathies (Q34558084) (← links)
- Mutations in autism susceptibility candidate 2 (AUTS2) in patients with mental retardation. (Q34599654) (← links)