Found: 17
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De Novo Variants Found in Three Distinct Schizophrenia Populations Hit a Common Core Gene Network Related to Microtubule and Actin Cytoskeleton Gene Ontology Classes.
- Published in:
- Life (2075-1729), 2024, v. 14, n. 2, p. 244, doi. 10.3390/life14020244
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- Publication type:
- Article
Looking beyond the usual suspects: sulfide stress in schizophrenia pathophysiology.
- Published in:
- EMBO Molecular Medicine, 2019, v. 11, n. 12, p. N.PAG, doi. 10.15252/emmm.201910983
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- Publication type:
- Article
HENA, heterogeneous network-based data set for Alzheimer's disease.
- Published in:
- Scientific Data, 2019, v. 6, n. 1, p. N.PAG, doi. 10.1038/s41597-019-0152-0
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- Article
Netrin G1: its downregulation in the nucleus accumbens of cocaine-conditioned mice and genetic association in human cocaine dependence.
- Published in:
- 2018
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- Publication type:
- journal article
Somatostatin-IRES-Cre Mice: Between Knockout and Wild-Type?
- Published in:
- Frontiers in Endocrinology, 2017, p. 1, doi. 10.3389/fendo.2017.00131
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- Article
Genetics of dopamine receptors and drug addiction.
- Published in:
- Human Genetics, 2012, v. 131, n. 6, p. 803, doi. 10.1007/s00439-012-1145-7
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- Publication type:
- Article
SMARCA2 and other genome-wide supported schizophrenia-associated genes: regulation by REST/NRSF, network organization and primate-specific evolution.
- Published in:
- Human Molecular Genetics, 2010, v. 19, n. 14, p. 2841, doi. 10.1093/hmg/ddq184
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- Publication type:
- Article
Convergent evidence identifying MAP/microtubule affinity-regulating kinase 1 (MARK1) as a susceptibility gene for autism.
- Published in:
- Human Molecular Genetics, 2008, v. 17, n. 16, p. 2541, doi. 10.1093/hmg/ddn154
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- Publication type:
- Article
The fragile X mental retardation protein is a molecular adaptor between the neurospecific KIF3C kinesin and dendritic RNA granules.
- Published in:
- Human Molecular Genetics, 2007, v. 16, n. 24, p. 3047, doi. 10.1093/hmg/ddm263
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- Publication type:
- Article
Survival motor neuron SMN1 and SMN2 gene promoters: identical sequences and differential expression in neurons and non-neuronal cells.
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- European Journal of Human Genetics, 2004, v. 12, n. 9, p. 729, doi. 10.1038/sj.ejhg.5201217
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- Publication type:
- Article
Identification of a novel brain-specific and reelin-regulated gene that encodes a protein colocalized with synapsin.
- Published in:
- European Journal of Neuroscience, 2004, v. 20, n. 3, p. 603, doi. 10.1111/j.1460-9568.2004.03473.x
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- Publication type:
- Article
Noradrenergic neuronal development is impaired by mutation of the proneural HASH-1 gene in congenital central hypoventilation syndrome (Ondine's curse).
- Published in:
- Human Molecular Genetics, 2003, v. 12, n. 23, p. 3173, doi. 10.1093/hmg/ddg339
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- Publication type:
- Article
Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome.
- Published in:
- Nature Genetics, 2003, v. 33, n. 4, p. 459, doi. 10.1038/ng1130
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- Publication type:
- Article
Murine peripherin gene sequences direct Cre recombinase expression to peripheral neurons in transgenic mice
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- FEBS Letters, 2002, v. 523, n. 1-3, p. 68, doi. 10.1016/S0014-5793(02)02936-8
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- Publication type:
- Article
Caffeine-induced Telencephalic Vesicle Evagination in Early Post-implantation Mouse Embryos Involves cAMP-dependent Protein Kinase (PKA) Inhibition.
- Published in:
- Cerebral Cortex, 2001, v. 11, n. 4, doi. 10.1093/cercor/11.4.343
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- Publication type:
- Article
CRE and TRE sequences of the rat tyrosine hydroxylase promoter are required for TH basal expression in adult mice but not in the embryo.
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- European Journal of Neuroscience, 1998, v. 10, n. 2, p. 508, doi. 10.1046/j.1460-9568.1998.00059.x
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- Publication type:
- Article
Both upstream and intragenic sequences of the human neurofilament light gene direct expression of lacZ in neurons of transgenic mouse embryos.
- Published in:
- Journal of Molecular Neuroscience, 1994, v. 5, n. 4, p. 273, doi. 10.1007/BF02736727
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- Publication type:
- Article