Found: 22
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CDK19 is disrupted in a female patient with bilateral congenital retinal folds, microcephaly and mild mental retardation.
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- Human Genetics, 2010, v. 128, n. 3, p. 281, doi. 10.1007/s00439-010-0848-x
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- Article
Restoring polyamines protects from age-induced memory impairment in an autophagy-dependent manner.
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- Nature Neuroscience, 2013, v. 16, n. 10, p. 1453, doi. 10.1038/nn.3512
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- Article
The Epigenetic Regulator G9a Mediates Tolerance to RNA Virus Infection in Drosophila.
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- PLoS Pathogens, 2015, v. 11, n. 4, p. 1, doi. 10.1371/journal.ppat.1004692
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- Article
Regulation of cell differentiation and function by the euchromatin histone methyltranserfases G9a and GLP.
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- Biochemistry & Cell Biology, 2016, v. 94, n. 1, p. 26, doi. 10.1139/bcb-2015-0017
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- Article
The histone methyltransferase G9a regulates tolerance to oxidative stress–induced energy consumption.
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- PLoS Biology, 2019, v. 17, n. 3, p. 1, doi. 10.1371/journal.pbio.2006146
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- Article
Conditional depletion of intellectual disability and Parkinsonism candidate gene ATP6AP2 in fly and mouse induces cognitive impairment and neurodegeneration.
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- Human Molecular Genetics, 2015, v. 24, n. 23, p. 6736, doi. 10.1093/hmg/ddv380
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- Article
CEP89 is required for mitochondrial metabolism and neuronal function in man and fly.
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- Human Molecular Genetics, 2013, v. 22, n. 15, p. 3138, doi. 10.1093/hmg/ddt170
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- Article
Homozygous and heterozygous disruptions of ANK3: at the crossroads of neurodevelopmental and psychiatric disorders.
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- Human Molecular Genetics, 2013, v. 22, n. 10, p. 1960, doi. 10.1093/hmg/ddt043
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- Article
SLC29A3 gene is mutated in pigmented hypertrichosis with insulin-dependent diabetes mellitus syndrome and interacts with the insulin signaling pathway.
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- Human Molecular Genetics, 2009, v. 18, n. 12, p. 2257, doi. 10.1093/hmg/ddp161
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- Article
Ubiquitin Ligase HUWE1 Regulates Axon Branching through the Wnt/β-Catenin Pathway in a <i>Drosophila</i> Model for Intellectual Disability.
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- PLoS ONE, 2013, v. 8, n. 11, p. 1, doi. 10.1371/journal.pone.0081791
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- Article
Mitigation of TDP-43 toxic phenotype by an RGNEF fragment in amyotrophic lateral sclerosis models.
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- Brain: A Journal of Neurology, 2024, v. 147, n. 6, p. 2053, doi. 10.1093/brain/awae078
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- Article
Mutations in the chromatin modifier gene KANSL1 cause the 17q21.31 microdeletion syndrome.
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- Nature Genetics, 2012, v. 44, n. 6, p. 639, doi. 10.1038/ng.2262
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- Article
Epigenetic Regulation of Learning and Memory by Drosophila EHMT/G9a.
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- PLoS Biology, 2011, v. 9, n. 1, p. 1, doi. 10.1371/journal.pbio.1000569
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- Article
Altered GPM6A/M6 Dosage Impairs Cognition and Causes Phenotypes Responsive to Cholesterol in Human and Drosophila.
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- Human Mutation, 2014, v. 35, n. 12, p. 1495, doi. 10.1002/humu.22697
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- Article
Optimal RNA isolation method and primer design to detect gene knockdown by qPCR when validating Drosophila transgenic RNAi lines.
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- BMC Research Notes, 2017, v. 10, p. 1, doi. 10.1186/s13104-017-2959-0
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- Article
Epigenetic regulation of memory: implications in human cognitive disorders.
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- Biomolecular Concepts, 2013, v. 4, n. 1, p. 1, doi. 10.1515/bmc-2012-0026
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- Article
Conserved regulation of neurodevelopmental processes and behavior by FoxP in Drosophila.
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- PLoS ONE, 2019, v. 14, n. 2, p. 1, doi. 10.1371/journal.pone.0211652
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- Article
Identification of a novel synaptic protein, TMTC3, involved in periventricular nodular heterotopia with intellectual disability and epilepsy.
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- Human Molecular Genetics, 2017, v. 26, n. 21, p. 4278, doi. 10.1093/hmg/ddx316
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- Article
foxo is required for resistance to amino acid starvation in Drosophila.
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- Genome, 2008, v. 51, n. 8, p. 668, doi. 10.1139/G08-047
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- Article
Expression of Drosophila FOXO regulates growth and can phenocopy starvation.
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- BMC Developmental Biology, 2003, v. 3, p. 5, doi. 10.1186/1471-213X-3-5
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- Article
The epigenetic regulator G9a attenuates stress-induced resistance and metabolic transcriptional programs across different stressors and species.
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- BMC Biology, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s12915-021-01025-0
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- Article
Functional convergence of histone methyltransferases EHMT1 and KMT2C involved in intellectual disability and autism spectrum disorder.
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- PLoS Genetics, 2017, v. 13, n. 10, p. 1, doi. 10.1371/journal.pgen.1006864
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- Article