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UnknownFrequent somatic mutations in MAP3K5 and MAP3K9 in metastatic melanoma identified by exome sequencing.
Not available
S-EPMC3267896 | biostudies-literature
UnknownSomatic mutations in MAP3K5 attenuate its proapoptotic function in melanoma through increased binding to thioredoxin.
Not available
S-EPMC3947167 | biostudies-literature
UnknownThe Epstein-Barr Virus-encoded miR-BART22 targets MAP3K5 to promote host cell proliferative and invasive abilities in nasopharyngeal carcinoma.
Not available
S-EPMC5327380 | biostudies-literature
UnknownDifferential expression of apoptotic genes PDIA3 and MAP3K5 distinguishes between low- and high-risk prostate cancer.
Not available
S-EPMC2807430 | biostudies-literature
UnknownCetylpyridinium chloride triggers paraptosis to suppress pancreatic tumor growth via the ERN1-MAP3K5-p38 pathway.
Not available
S-EPMC11357866 | biostudies-literature
UnknownExosome-mediated delivery of gga-miR-20a-5p regulates immune response of chicken macrophages by targeting IFNGR2, MAPK1, MAP3K5, and MAP3K14.
Not available
S-EPMC10164535 | biostudies-literature
UnknownLifespan extension conferred by mitogen-activated protein kinase kinase kinase 5 (MAP3K5) longevity-associated gene variation is confined to at-risk men with a cardiometabolic disease.
Not available
S-EPMC8034933 | biostudies-literature
TranscriptomicsDNA methylome signature in rheumatoid arthritis
Objectives: Epigenetics can influence disease susceptibility and severity. While DNA methylation of individual genes has been explored in autoimmunity, no unbiased systematic analyses have been reported. Therefore, a genome-wide evaluation of DNA methylation loci in fibroblast-like synoviocytes (FLS...
ORGANISM(S): Homo sapiens 
2013-04-25 | E-GEOD-46364 | biostudies-arrayexpress
TranscriptomicsTranscription profiling by array of human clonal primary fibroblasts from patients with CDKL5 mutations
Mutations in the human CDKL5 gene have been shown to cause infantile spasms, as well as Rett syndrome-like phenotype. Because CDKL5 is subjected to X chromosome inactivation (XCI), individual cells from CDKL5 mutation girls either express the wild-type or mutant allele, likely resulting in different...
ORGANISM(S): Homo sapiens 
2011-07-23 | E-MEXP-2833 | biostudies-arrayexpress
UnknownAnalysis of Polymorphisms in 59 Potential Candidate Genes for Association With Human Longevity.
Not available
S-EPMC6175033 | biostudies-literature
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