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Transcriptome Analysis of the Cerebellum of Mice Fed a Manganese-Deficient Diet.
- Published in:
- Frontiers in Genetics, 2020, v. 11, p. N.PAG, doi. 10.3389/fgene.2020.558725
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- Article
Activation of Xist by an evolutionarily conserved function of KDM5C demethylase.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-30352-1
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- Article
Altered Gene-Regulatory Function of KDM5C by a Novel Mutation Associated With Autism and Intellectual Disability.
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- Frontiers in Molecular Neuroscience, 2018, p. 1, doi. 10.3389/fnmol.2018.00104
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- Article
ATRX ADD domain links an atypical histone methylation recognition mechanism to human mental-retardation syndrome.
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- Nature Structural & Molecular Biology, 2011, v. 18, n. 7, p. 769, doi. 10.1038/nsmb.2062
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- Article
Patient Mutations of the Intellectual Disability Gene KDM5C Downregulate Netrin G2 and Suppress Neurite Growth in Neuro2a Cells.
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- Journal of Molecular Neuroscience, 2016, v. 60, n. 1, p. 33, doi. 10.1007/s12031-016-0770-3
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- Article
Alcohol-specific transcriptional dynamics of memory reconsolidation and relapse.
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- Translational Psychiatry, 2023, v. 13, n. 1, p. 1, doi. 10.1038/s41398-023-02352-2
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- Article
The manganese transporter SLC39A8 links alkaline ceramidase 1 to inflammatory bowel disease.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-49049-8
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- Article
Quiescence enables unrestricted cell fate in naive embryonic stem cells.
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- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-46121-1
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- Publication type:
- Article
Quiescence enables unrestricted cell fate in naive embryonic stem cells.
- Published in:
- Nature Communications, 2024, v. 15, n. 1, p. 1, doi. 10.1038/s41467-024-46121-1
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- Publication type:
- Article
A neurodegeneration gene, WDR45, links impaired ferritinophagy to iron accumulation.
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- Journal of Neurochemistry, 2022, v. 160, n. 3, p. 356, doi. 10.1111/jnc.15548
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- Article
An atypical 12q24.31 microdeletion implicates six genes including a histone demethylase KDM2B and a histone methyltransferase SETD1B in syndromic intellectual disability.
- Published in:
- Human Genetics, 2016, v. 135, n. 7, p. 757, doi. 10.1007/s00439-016-1668-4
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- Article
Identification and characterization of two novel JARID1C mutations: suggestion of an emerging genotype-phenotype correlation.
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- European Journal of Human Genetics, 2012, v. 20, n. 9, p. 1010, doi. 10.1038/ejhg.2012.114
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- Publication type:
- Article
Identification and characterization of two novel JARID1C mutations: suggestion of an emerging genotype–phenotype correlation.
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- European Journal of Human Genetics, 2010, v. 18, n. 3, p. 330, doi. 10.1038/ejhg.2009.175
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- Article
Soma‐to‐germline transformation in chromatin‐linked neurodevelopmental disorders?
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- FEBS Journal, 2022, v. 289, n. 8, p. 2301, doi. 10.1111/febs.16196
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- Article
A histone H3 lysine 27 demethylase regulates animal posterior development.
- Published in:
- Nature, 2007, v. 449, n. 7163, p. 689, doi. 10.1038/nature06192
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- Article
Author Correction: Mutually suppressive roles of KMT2A and KDM5C in behaviour, neuronal structure, and histone H3K4 methylation.
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- 2020
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- Correction Notice
Mutually suppressive roles of KMT2A and KDM5C in behaviour, neuronal structure, and histone H3K4 methylation.
- Published in:
- Communications Biology, 2020, v. 3, n. 1, p. 1, doi. 10.1038/s42003-020-1001-6
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- Publication type:
- Article
Correction: Identification of lysine methylation in the core GTPase domain by GoMADScan.
- Published in:
- 2019
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- Publication type:
- Correction Notice
Impact of dietary manganese on experimental colitis in mice.
- Published in:
- FASEB Journal, 2020, v. 34, n. 2, p. 2929, doi. 10.1096/fj.201902396R
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- Publication type:
- Article
Ferroportin disease mutations influence manganese accumulation and cytotoxicity.
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- FASEB Journal, 2019, v. 33, n. 2, p. 2228, doi. 10.1096/fj.201800831R
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- Article
X chromosome dosage of histone demethylase KDM5C determines sex differences in adiposity.
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- 2020
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- Publication type:
- journal article
Sequencing of first-strand cDNA library reveals full-length transcriptomes.
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- Nature Communications, 2015, v. 6, n. 1, p. 6002, doi. 10.1038/ncomms7002
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- Publication type:
- Article
Modulation of chromatin architecture influences the neuronal nucleus through activity-regulated gene expression.
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- Biochemical Society Transactions, 2023, v. 51, n. 2, p. 703, doi. 10.1042/BST20220889
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- Publication type:
- Article
Sexually Dimorphic Alterations in the Transcriptome and Behavior with Loss of Histone Demethylase KDM5C.
- Published in:
- Cells (2073-4409), 2023, v. 12, n. 4, p. 637, doi. 10.3390/cells12040637
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- Publication type:
- Article
Epigenetic Etiology of Intellectual Disability.
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- Journal of Neuroscience, 2017, v. 37, n. 45, p. 10773, doi. 10.1523/JNEUROSCI.1840-17.2017
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- Publication type:
- Article
CRISPR-based genome editing of a diurnal rodent, Nile grass rat (Arvicanthis niloticus).
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- BMC Biology, 2024, v. 22, n. 1, p. 1, doi. 10.1186/s12915-024-01943-9
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- Publication type:
- Article
Identification of lysine methylation in the core GTPase domain by GoMADScan.
- Published in:
- PLoS ONE, 2019, v. 14, n. 8, p. 1, doi. 10.1371/journal.pone.0219436
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- Publication type:
- Article
A component of BRAF-HDAC complex, BHC80, is required for neonatal survival in mice
- Published in:
- FEBS Letters, 2006, v. 580, n. 13, p. 3129, doi. 10.1016/j.febslet.2006.04.065
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- Article