MIRROR MOVEMENTS 4
|
0.400 |
GeneticVariation
|
disease |
UNIPROT |
Mutations in the netrin-1 gene cause congenital mirror movements.
|
28945198 |
2017 |
MIRROR MOVEMENTS 4
|
0.400 |
CausalMutation
|
disease |
CLINVAR |
|
|
|
Subarachnoid Hemorrhage
|
0.350 |
Biomarker
|
disease |
BEFREE |
The endovascular perforation SAH model was constructed using male C57BL/6J mice, and recombinant NTN-1 was administrated intravenously.
|
30614619 |
2019 |
Subarachnoid Hemorrhage
|
0.350 |
Biomarker
|
disease |
BEFREE |
This study was designed to discern the utility of serum netrin-1 as a biomarker for assessing the severity and prognosis of patients with aneurysmal SAH.
|
31047878 |
2019 |
Subarachnoid Hemorrhage
|
0.350 |
AlteredExpression
|
disease |
BEFREE |
Our results showed that endogenous NTN-1 and its receptor UNC5B level were increased after SAH.
|
29162556 |
2018 |
Subarachnoid Hemorrhage
|
0.350 |
Biomarker
|
disease |
CTD_human |
Recombinant Netrin-1 binding UNC5B receptor attenuates neuroinflammation and brain injury via PPARγ/NFκB signaling pathway after subarachnoid hemorrhage in rats.
|
29162556 |
2018 |
Subarachnoid Hemorrhage
|
0.350 |
AlteredExpression
|
disease |
BEFREE |
The expression of endogenous NTN-1 and its receptor Deleted in Colorectal Cancer were increased after SAH.
|
28526701 |
2017 |
Subarachnoid Hemorrhage
|
0.350 |
AlteredExpression
|
disease |
BEFREE |
Our results revealed that endogenous NTN-1 level was increased after SAH.
|
28347836 |
2017 |
Cerebral Edema
|
0.300 |
Therapeutic
|
phenotype |
CTD_human |
Knockdown of endogenous NTN-1 increased expression of pro-inflammatory mediators and MPO, and aggravated neuroinflammation and brain edema.
|
29162556 |
2018 |
Perinatal Subarachnoid Hemorrhage
|
0.300 |
Biomarker
|
phenotype |
CTD_human |
Recombinant Netrin-1 binding UNC5B receptor attenuates neuroinflammation and brain injury via PPARγ/NFκB signaling pathway after subarachnoid hemorrhage in rats.
|
29162556 |
2018 |
Subarachnoid Hemorrhage, Spontaneous
|
0.300 |
Biomarker
|
phenotype |
CTD_human |
Recombinant Netrin-1 binding UNC5B receptor attenuates neuroinflammation and brain injury via PPARγ/NFκB signaling pathway after subarachnoid hemorrhage in rats.
|
29162556 |
2018 |
Vasogenic Cerebral Edema
|
0.300 |
Therapeutic
|
phenotype |
CTD_human |
Recombinant Netrin-1 binding UNC5B receptor attenuates neuroinflammation and brain injury via PPARγ/NFκB signaling pathway after subarachnoid hemorrhage in rats.
|
29162556 |
2018 |
Cytotoxic Cerebral Edema
|
0.300 |
Therapeutic
|
phenotype |
CTD_human |
Recombinant Netrin-1 binding UNC5B receptor attenuates neuroinflammation and brain injury via PPARγ/NFκB signaling pathway after subarachnoid hemorrhage in rats.
|
29162556 |
2018 |
Neurobehavioral Manifestations
|
0.300 |
Therapeutic
|
phenotype |
CTD_human |
Recombinant Netrin-1 binding UNC5B receptor attenuates neuroinflammation and brain injury via PPARγ/NFκB signaling pathway after subarachnoid hemorrhage in rats.
|
29162556 |
2018 |
Vasogenic Brain Edema
|
0.300 |
Therapeutic
|
phenotype |
CTD_human |
Recombinant Netrin-1 binding UNC5B receptor attenuates neuroinflammation and brain injury via PPARγ/NFκB signaling pathway after subarachnoid hemorrhage in rats.
|
29162556 |
2018 |
Cytotoxic Brain Edema
|
0.300 |
Therapeutic
|
phenotype |
CTD_human |
Recombinant Netrin-1 binding UNC5B receptor attenuates neuroinflammation and brain injury via PPARγ/NFκB signaling pathway after subarachnoid hemorrhage in rats.
|
29162556 |
2018 |
Subarachnoid Hemorrhage, Aneurysmal
|
0.300 |
Biomarker
|
phenotype |
CTD_human |
Recombinant Netrin-1 binding UNC5B receptor attenuates neuroinflammation and brain injury via PPARγ/NFκB signaling pathway after subarachnoid hemorrhage in rats.
|
29162556 |
2018 |
Subarachnoid Hemorrhage, Intracranial
|
0.300 |
Biomarker
|
phenotype |
CTD_human |
Recombinant Netrin-1 binding UNC5B receptor attenuates neuroinflammation and brain injury via PPARγ/NFκB signaling pathway after subarachnoid hemorrhage in rats.
|
29162556 |
2018 |
Brain Edema
|
0.300 |
Therapeutic
|
phenotype |
CTD_human |
Knockdown of endogenous NTN-1 increased expression of pro-inflammatory mediators and MPO, and aggravated neuroinflammation and brain edema.
|
29162556 |
2018 |
Cleft upper lip
|
0.110 |
Biomarker
|
disease |
BEFREE |
NTN1 gene was risk to non-syndromic cleft lip only among Han Chinese population.
|
30506619 |
2019 |
Cleft upper lip
|
0.110 |
GeneticVariation
|
disease |
GWASCAT |
Genome-wide meta-analyses of nonsyndromic orofacial clefts identify novel associations between FOXE1 and all orofacial clefts, and TP63 and cleft lip with or without cleft palate.
|
28054174 |
2017 |
Mirror movements disorder
|
0.110 |
GeneticVariation
|
disease |
BEFREE |
Mutations in the netrin-1 gene cause congenital mirror movements.
|
28945198 |
2017 |
Cleft upper lip
|
0.110 |
GeneticVariation
|
disease |
GWASCAT |
Genome-wide association study identifies a new susceptibility locus for cleft lip with or without a cleft palate.
|
25775280 |
2015 |
Cleft upper lip
|
0.110 |
GeneticVariation
|
disease |
GWASDB |
Genome-wide meta-analyses of nonsyndromic cleft lip with or without cleft palate identify six new risk loci.
|
22863734 |
2012 |
Cleft upper lip
|
0.110 |
GeneticVariation
|
disease |
GWASDB |
A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4.
|
20436469 |
2010 |