×
Entrez Id:
3458
Gene Symbol:
IFNG
IFNG
0.310
AlteredExpression
group
BEFREE
This mechanism might contribute to cognitive impairment in chronic brain disease featuring elevated IFN-γ levels, blood-brain barrier leakage, and/or T cell infiltration, well before neurodegeneration occurs.
30782788
2019
×
Entrez Id:
7040
Gene Symbol:
TGFB1
TGFB1
0.310
Biomarker
group
CTD_human
Human TGF-β1 deficiency causes severe inflammatory bowel disease and encephalopathy.
29483653
2018
×
Entrez Id:
351
Gene Symbol:
APP
APP
0.310
Biomarker
group
BEFREE
Amyloid-β precursor protein (APP ) correlates with the pathogenesis of certain brain diseases , such as Alzheimer disease (AD).
29777707
2018
×
Entrez Id:
7248
Gene Symbol:
TSC1
TSC1
0.310
Biomarker
group
CTD_human
Tsc2 gene inactivation causes a more severe epilepsy phenotype than Tsc1 inactivation in a mouse model of tuberous sclerosis complex.
21062901
2011
×
Entrez Id:
3458
Gene Symbol:
IFNG
IFNG
0.310
Therapeutic
group
CTD_human
Protective effects of interferon-gamma against methamphetamine-induced neurotoxicity.
18282668
2008
×
Entrez Id:
11277
Gene Symbol:
TREX1
TREX1
0.310
GeneticVariation
group
BEFREE
Mutations in the TREX1 gene are an underlying cause of the neurological brain disease Aicardi-Goutières syndrome implicating TREX1 dysfunction in an aberrant immune response.
17293595
2007
×
Entrez Id:
7248
Gene Symbol:
TSC1
TSC1
0.310
Biomarker
group
LHGDN
These results indicate that hamartin binds to NADE to regulate neuronal cell function and loss of this association is likely to contribute to the brain pathology in TSC.
17355907
2007
×
Entrez Id:
11277
Gene Symbol:
TREX1
TREX1
0.310
Biomarker
group
CTD_human
Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 cause Aicardi-Goutières syndrome at the AGS1 locus.
16845398
2006
×
Entrez Id:
8851
Gene Symbol:
CDK5R1
CDK5R1
0.310
Biomarker
group
BEFREE
Malfunctioning of cyclin-dependent kinase 5 (CDK5) through aberrant proteolytic cleavage of its neuronal activators p35 and p39 is involved in neurodegeneration in Alzheimer's disease (AD) and other neurodegenerative brain diseases .
15917097
2005
×
Entrez Id:
8851
Gene Symbol:
CDK5R1
CDK5R1
0.310
Biomarker
group
CTD_human
Increased activity of cyclin-dependent kinase 5 leads to attenuation of cocaine-mediated dopamine signaling.
15665076
2005
×
Entrez Id:
3456
Gene Symbol:
IFNB1
IFNB1
0.310
Biomarker
group
BEFREE
Interferon beta (IFNbeta ) has been shown to decrease clinical relapses, reduce brain disease activity, and possibly slow progression of disability.
12618863
2003
×
Entrez Id:
351
Gene Symbol:
APP
APP
0.310
Biomarker
group
CTD_human
However, when stained with beta-amyloid precursor protein , multifocal axonal injury was evident in the brain , spinal cord, and nerve roots.
11800653
2002
×
Entrez Id:
3456
Gene Symbol:
IFNB1
IFNB1
0.310
Biomarker
group
CTD_human
In vitro assessment for neurotoxicity of antitumor agents before local administration into central nervous system.
8615598
1996
×
Entrez Id:
7040
Gene Symbol:
TGFB1
TGFB1
0.310
Biomarker
group
BEFREE
Involvement of TGF-beta 1 in these human brain disorders is discussed in relation to the potent effects of TGF-beta 1 on wound healing and inflammatory responses in peripheral tissues.
8300749
1993
×
Entrez Id:
3785
Gene Symbol:
KCNQ2
KCNQ2
0.300
Biomarker
group
CTD_human
KCNQ2 encephalopathy: Features, mutational hot spots, and ezogabine treatment of 11 patients.
27602407
2016
×
Entrez Id:
9152
Gene Symbol:
SLC6A5
SLC6A5
0.300
Biomarker
group
CTD_human
Molecular basis of the dominant negative effect of a glycine transporter 2 mutation associated with hyperekplexia.
25480793
2015
×
Entrez Id:
10617
Gene Symbol:
STAMBP
STAMBP
0.300
Biomarker
group
CTD_human
Mutations in STAMBP, encoding a deubiquitinating enzyme, cause microcephaly-capillary malformation syndrome.
23542699
2013
×
Entrez Id:
4353
Gene Symbol:
MPO
MPO
0.300
Biomarker
group
CTD_human
Resveratrol confers protection against rotenone-induced neurotoxicity by modulating myeloperoxidase levels in glial cells.
23593274
2013
×
Entrez Id:
4968
Gene Symbol:
OGG1
OGG1
0.300
Biomarker
group
CTD_human
Multiple cellular and molecular events were involved in the manifestation of brain defects due primarily to the lack of ogg1 .
24075420
2013
×
Entrez Id:
6341
Gene Symbol:
SCO1
SCO1
0.300
Biomarker
group
CTD_human
COX19 mediates the transduction of a mitochondrial redox signal from SCO1 that regulates ATP7A-mediated cellular copper efflux.
23345593
2013
×
Entrez Id:
1548
Gene Symbol:
CYP2A6
CYP2A6
0.300
Biomarker
group
CTD_human
CYP2A6 plays a key role in nicotine metabolism and oxidative stress in astrocytes, and this has implications in nicotine-associated brain toxicity.
22498344
2012
×
Entrez Id:
6505
Gene Symbol:
SLC1A1
SLC1A1
0.300
Biomarker
group
CTD_human
Taken together, this study implicates EAAC1 -dependent cysteine uptake as an endogenous source of enhancing antioxidant function and zinc homeostasis in neurons in the ischemic brain .
22575539
2012
×
Entrez Id:
80169
Gene Symbol:
CTC1
CTC1
0.300
Biomarker
group
CTD_human
Mutations in CTC1, encoding conserved telomere maintenance component 1, cause Coats plus.
22267198
2012
×
Entrez Id:
7249
Gene Symbol:
TSC2
TSC2
0.300
Biomarker
group
CTD_human
Tsc2 gene inactivation causes a more severe epilepsy phenotype than Tsc1 inactivation in a mouse model of tuberous sclerosis complex.
21062901
2011
×
Entrez Id:
10319
Gene Symbol:
LAMC3
LAMC3
0.300
Biomarker
group
CTD_human
In human but not mouse fetal brain , LAMC3 is enriched in postmitotic cortical plate neurons, localizing primarily to the somatodendritic compartment.
21572413
2011