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38 Possible Causes for Ddx5, human, protein

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  • Mental Retardation

    Therefore, in this study, we identified DDX5, FUS, EWSR1 and LSM14A as TAD-interacting proteins sensitive to F32L and/or Y96L mutation by pull-down assays and mass spectrometry[ncbi.nlm.nih.gov] To examine this hypothesis, we have studied normal human brainstem tissue with immunohistochemical techniques and confocal microscopy.[ncbi.nlm.nih.gov] Altered expression of ADH has also been reported in Drosophila Fragile-X mental retardation protein (DFMRP) mutant flies.[ncbi.nlm.nih.gov]

  • Calcitriol

    […] the induction of DDX5.[ncbi.nlm.nih.gov] Calcitriol activates its receptor and enhances the synthesis of important human antibiotics like cathelicidin and β2-defensin while inhibiting hepcidin.[ncbi.nlm.nih.gov] Being highly lipid soluble, both calcifediol and calcitriol travel in the bloodstream on carriage proteins, principally on vitamin D-binding protein.[ncbi.nlm.nih.gov]

  • Temozolomide

    Further, the most significant module consisted of 28 downregulated proteins that were filtered from the PPI network, and 9 proteins (DHX9, HNRNPR, RPL3, HNRNPA3, SF1, DDX5[ncbi.nlm.nih.gov] We found that FTY720 suppressed the protein and mRNA levels of Nrf2 in human U251MG and U87MG glioblastoma cells lines.[ncbi.nlm.nih.gov] These findings suggest that TMZ may be effective for pediatric refractory anaplastic ependymoma with low MGMT protein expression.[ncbi.nlm.nih.gov]

  • Cockayne Syndrome

    Immunoprecipitation studies confirmed the reciprocal interaction of CAND1, CSTF1, DDX3X, DDX5, DDX17, DDX23, DHX36, HDAC1, HNRNPU, MTA2, PRPF3, PSMD3, RBBP4, SFPQ, SMARCA1[journals.plos.org] Cockayne syndrome (CS) is a rare human disorder characterized by pathologies of premature aging, neurological abnormalities, sensorineural hearing loss and cachectic dwarfism[ncbi.nlm.nih.gov] The Cockayne syndrome complementation group B (CSB) protein is an ATP-dependent chromatin remodeler with an essential function in transcription-coupled DNA repair, and mutations[ncbi.nlm.nih.gov]

  • Entamoeba Histolytica

    […] di-snRNP component CP6; the U4/U6.U5 tri-snRNP components SAD1 and Prp38; and the nineteen complex (NTC) components Prp19, KIAA0560/Aquarius intron-binding spliceosomal factor, DDX5[frontiersin.org] E. histolytica is also a zoonotic protozoan parasite with the potential to infect non-human primates.[ncbi.nlm.nih.gov] EhADH emerged as an extended peripheral membrane protein with high fluctuation in Bro1 and V shape domains. 500 ns-long MDS and protein-protein docking predictions evidenced[ncbi.nlm.nih.gov]

  • Calcium Glucarate

    Resveratrol directly targets DDX5 resulting in suppression of the mTORC1 pathway in prostate cancer Cell Death Dis. 2016 May 5;7:e2211.[produitsnaturelsgammaforce.com] However, humans can only handle so many toxins. The human body is involved fending off xenoestrogens, air pollutants, chronic infections, and mycotoxins.[blog.bulletproof.com] Today, all humans have to deal with toxins from foods, fossil fuels and other pollutants on a regular basis.[blueskyvitamin.com]

  • Atypical HSD10 Disease

    HSD17B2; RDH8; HSD17B12; HSD17B8; HSD17B12B; HSD17B11; HSD17B7; HSD17B14 Function estrogen receptor binding Related Protein FUS; PPID; STRN; CNOT1; DDX54; WIPI1; NSD1; PPARG; DDX5[creativebiomart.net] Datasheet Description Recombinant Human HSD17B10 / CAMR was expressed from HEK293. Its molecular weight is 28KD.[speedbiosystems.com] Synonyms Hydroxyacyl CoA Dehydrogenase type II protein, ER associated amyloid beta-binding protein protein, SCHAD protein, HSD17B10 protein, Type II HADH protein, Type 10[fitzgerald-fii.com]

  • Familial Congenital Mirror Movements 2

    FHIT, ERG, FBXO11, ERC1, FCRL4, FGF6, FEV, ELF4, ECT2L, EPS15, EPHA5, DOT1L, EBF1, EPHA3, EIF4A2, PER1, ELK4, EPHB1, PDCD1LG2, DDX10, PAFAH1B2, DAXX, DDIT3, PBRM1, PDCD1, DDX5[mendelian.co] Human RAD51 shows predominant expression in testis, ovary, and lymphoid tissue.[sigmaaldrich.com] Multiple protein interactions have been demonstrated for the mammalian Rad51 protein.[mskcc.org]

  • Pseudopseudohypoparathyroidism

    FHIT, ERG, FBXO11, ERC1, FCRL4, FGF6, FEV, ELF4, ECT2L, EPS15, EPHA5, DOT1L, EBF1, EPHA3, EIF4A2, PER1, ELK4, EPHB1, PDCD1LG2, DDX10, PAFAH1B2, DAXX, DDIT3, PBRM1, PDCD1, DDX5[mendelian.co] This central region of mouse chromosome 1 shares a region of homology with the long arm of human chromosome 2, suggesting that the human homologue of Stk25 would also map[ncbi.nlm.nih.gov] […] pseudohypoparathyroidism (PHP) type Ia and Albright's hereditary osteodystrophy (AHO) is associated with deficient activity of the stimulatory guanine nucleotide-binding protein[ncbi.nlm.nih.gov]

  • Congenital Cataract - Microcornea - Corneal Opacity

    Inhibitory effects are additive with GADD45 proteins but occurs also in the absence of GADD45 proteins.[string-db.org] Learn more about how to achieve it with Mendelian Learn more Other genes that you may find interesting DENND1A DDX5 MIP[mendelian.co] Recombinant Human PXDN protein, His-tagged Cat.No.: PXDN-1930H Product Overview: Recombinant Human PXDN aa.[creativebiomart.net]