Intellectual Disability
|
0.110 |
AlteredExpression
|
group |
BEFREE |
We previously described a patient with intellectual disability (ID) and seizures (Patient 1), carrying a de novo chromosome translocation affecting the CNS-expressed MAPK10/JNK3 gene.
|
23329067 |
2013 |
Intellectual Disability
|
0.110 |
Biomarker
|
group |
HPO |
|
|
|
Personality Disorders
|
0.100 |
Biomarker
|
group |
HPO |
|
|
|
Encephalopathies
|
0.100 |
Biomarker
|
group |
HPO |
|
|
|
Neurodegenerative Disorders
|
0.050 |
Biomarker
|
group |
BEFREE |
All of these indicated <b>J30-8</b> as proved isoform-selective JNK3 inhibitors that might serve as a useful tool for further JNK3 studies with AD as well as for the development of JNK3 inhibitors for the potential treatment of neurodegenerative diseases.
|
31268308 |
2019 |
Neurodegenerative Disorders
|
0.050 |
Biomarker
|
group |
BEFREE |
Therefore, targeting JNK3 is a reasonable strategy for drug discovery in neurodegenerative diseases.
|
28372912 |
2017 |
Neurodegenerative Disorders
|
0.050 |
Biomarker
|
group |
BEFREE |
JNK3 is predominantly found in the CNS neurons, making it an attractive target for neurodegenerative disorders.
|
26505831 |
2015 |
Neurodegenerative Disorders
|
0.050 |
PosttranslationalModification
|
group |
BEFREE |
It has been shown that c-Jun N-terminal kinase-3 (JNK3) becomes activated by phosphorylation in various neurodegenerative diseases and phosphorylates outer mitochondrion associated proteins leading to neuronal apoptosis.
|
28676395 |
2017 |
Neurodegenerative Disorders
|
0.050 |
Biomarker
|
group |
BEFREE |
The kinase c-Jun N-terminal Kinase 3 (JNK3) plays an important role in neurodegenerative diseases.
|
31158642 |
2019 |
Brain Diseases
|
0.010 |
GeneticVariation
|
group |
BEFREE |
These interactions are likely affected by a truncated JNK3 protein, and thereby provide an explanation for the link between alterations in MAP kinase signal transduction and brain disorders.
|
16249883 |
2006 |
Brain Neoplasms
|
0.010 |
Biomarker
|
group |
BEFREE |
Together with prior evidence that, in JNK3-deficient mice, the JNK3 signaling pathway mediates apoptosis in central nervous tissue, our results suggest that loss of expression of the JNK3 gene may play an important role in the development of brain tumors in humans.
|
11322657 |
2001 |
Cardiovascular Diseases
|
0.010 |
GeneticVariation
|
group |
BEFREE |
We used instrumental variable analysis based on two single nucleotide polymorphism (SNPs) HSD17B13/MAPK10 (rs6834314) and PNPLA3/SAMM50 (rs738409) to assess the associations of ALT (U/L) with IHD, diabetes and other CVD risk factors in the Guangzhou Biobank Cohort Study (GBCS).
|
28007909 |
2017 |
Cognition Disorders
|
0.010 |
GeneticVariation
|
group |
BEFREE |
Characterisation of de novo MAPK10/JNK3 truncation mutations associated with cognitive disorders in two unrelated patients.
|
23329067 |
2013 |
Metabolic Diseases
|
0.010 |
Biomarker
|
group |
BEFREE |
This reveals AD as a metabolic disease that is under tight control by JNK3.
|
22958823 |
2012 |
Neoplasms
|
0.010 |
Biomarker
|
group |
BEFREE |
The conclusion that JNK can act as a tumor suppressor is consistent with the presence of loss-of-function mutations in JNK pathway components (Jnk3 and Mkk4) in human tumors.
|
12734425 |
2003 |
nervous system disorder
|
0.010 |
Biomarker
|
group |
BEFREE |
JNK3 is a widely studied target for small-drugs used to treat a variety of neurological disorders.
|
29930333 |
2018 |
Hyperactive behavior
|
0.110 |
Biomarker
|
phenotype |
HPO |
|
|
|
Hyperactive behavior
|
0.110 |
GeneticVariation
|
phenotype |
BEFREE |
Over-expression of this hyperactive mutant in transgenic parasites led to a dominant negative effect causing massive cell death during amastigote differentiation, demonstrating the essential nature of MPK10 auto-inhibition for parasite viability.
|
25232945 |
2014 |
Accidental Falls
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Aggressive behavior
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Myoclonus
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Respiratory Function Tests
|
0.100 |
GeneticVariation
|
phenotype |
GWASDB |
Genome-wide association studies identify CHRNA5/3 and HTR4 in the development of airflow obstruction.
|
22837378 |
2012 |
Mental deterioration
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Seizures, Focal
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|
Generalized tonic seizures
|
0.100 |
Biomarker
|
phenotype |
HPO |
|
|
|