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226 Possible Causes for Rdx, mouse, protein

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  • Formaldehyde

    Both mouse strains were divided into two main groups: the non-sensitized group and the OVA-sensitized group.[ncbi.nlm.nih.gov] Nitration of methenamine gives the explosive cyclonite , or RDX.[britannica.com] “On one hand, damage to proteins in the nucleus could impair the stress responses to and repair of DNA damage, and on the other hand accumulation of damaged proteins could[news.brown.edu]

  • Shock

    […] promoted, the progression of Hsp90 chaperone cycling and client maturation, resulting in an increment of cell apoptosis by the combination of simvastatin and LBH589 in a mouse[ncbi.nlm.nih.gov] […] nitroglycerine) 7,700 m/s — active ingredient in dynamite TATB (triaminotrinitrobenzene) 7,350 m/s — used to trigger nuclear weapons, insensitive to accidental detonation RDX[physics.info] The prepared nanocomposites were also used to screen proteins from a mixture of cellular extracts, and five proteins from HeLa cells were identified as potential client proteins[ncbi.nlm.nih.gov]

  • X-Linked Alport Syndrome

    A mouse model of this disorder was generated by targeting a human nonsense mutation, G5X, to the mouse Col4a5 gene.[ncbi.nlm.nih.gov] MYH14, MYH9, MYO15A, MYO3A, MYO6, MYO7A, NDP, NLRP3, OPA1, OSBPL2, OTOA, OTOF, OTOG, OTOGL, P2RX2, PAX3, PCDH15, PDZD7, PMP22, PNPT1, POLR1D, POU3F4, POU4F3, PRPS1, PTPRQ, RDX[genedx.com] Abstract Although the evidence indicates that mutation of the gene for the alpha 5 chain of type IV collagen, alpha 5-(IV), is the primary defect in X-linked Alport syndrome, protein[ncbi.nlm.nih.gov]

  • Usher Syndrome

    Institute on Deafness and Other Communication Disorders (NIDCD), NIH, Bethesda, MD 20892, USA. 2 Laboratory of Molecular Genetics, NIDCD, NIH, Bethesda, MD 20892, USA. 3 Mouse[ncbi.nlm.nih.gov] MYH14, MYH9, MYO15A, MYO3A, MYO6, MYO7A, NDP, NLRP3, OPA1, OSBPL2, OTOA, OTOF, OTOG, OTOGL, P2RX2, PAX3, PCDH15, PDZD7, PMP22, PNPT1, POLR1D, POU3F4, POU4F3, PRPS1, PTPRQ, RDX[genedx.com] PDZ domain-containing 7 protein (PDZD7) is a paralog of the scaffolding proteins harmonin and whirlin, which are implicated in Usher type 1 and type 2 syndromes.[ncbi.nlm.nih.gov]

  • Bardet-Biedl Syndrome 10

    "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences" . Proc. Natl. Acad. Sci.[en.wikipedia.org] GIPC3, GJB2, GJB3, GJB6, GPSM2, GRXCR1, HGF, ILDR1, KCNJ10, LHFPL5, LOXHD1, LRTOMT, MARVELD2, MSRB3, MYO15A, MYO3A, MYO6, MYO7A, OTOA, OTOF, PCDH15, POU3F4, PRPS1, PTPRQ, RDX[centogene.com] (version 88.38) Entrez gene 79738 UniProt Q8TAM1 (UniProt - Evidence at protein level) neXtProt NX_Q8TAM1 Antibodypedia BBS10 antibodies PROTEIN BROWSER i BBS10-001 PROTEIN[proteinatlas.org]

  • Bardet-Biedl Syndrome 2

    Datasheet References Protocols Product name Description Mouse polyclonal to BBS2 Host species Mouse Tested applications Species reactivity Reacts with: Recombinant fragment[abcam.com] GIPC3, GJB2, GJB3, GJB6, GPSM2, GRXCR1, HGF, ILDR1, KCNJ10, LHFPL5, LOXHD1, LRTOMT, MARVELD2, MSRB3, MYO15A, MYO3A, MYO6, MYO7A, OTOA, OTOF, PCDH15, POU3F4, PRPS1, PTPRQ, RDX[centogene.com] The protein encoded by this gene forms a multiprotein BBSome complex with seven other BBS proteins.[genecards.org]

  • Dynamite Poisoning

    Non-genotoxicity of 2,4,6trinitrotoluene (TNT) to the mouse bone marrow and the rat liver: implications for its carcinogenicity. Arch. Toxicol. ‏ الصفحة 63 - Sorsa, M.[books.google.com] The yield of HMX per mole of hexamine is about 55-60%, as compared to 80-85% in the manufacture of RDX (193-196). ‏[books.google.com] Cassava roots are very rich in starch, and contain significant amounts of protein, minerals, vitamins A, B and C.[pyroenergen.com]

  • Nitroglycerin

    […] metabolism* Nitroglycerin/pharmacokinetics* Nitroglycerin/pharmacology Swine Substances Isoflavones Nitric Oxide Chloral Hydrate daidzin ALDH2 protein, human ALDH2 protein, mouse[ncbi.nlm.nih.gov] The undiluted form it is one of the most powerful high explosives, analogous to military explosives RDX and PETN, along with the plastic explosive C-4.[chm.bris.ac.uk] In its undiluted form, it is one of the world's most powerful explosives, comparable to the more recently developed RDX and PETN .[en.wikipedia.org]

  • Spondyloepiphyseal Dysplasia Congenita

    A missense mutation in the mouse Col2a1 gene has been discovered, resulting in a mouse phenotype with similarities to human spondyloepiphyseal dysplasia (SED) congenita.[ncbi.nlm.nih.gov] ESPN, P2RX2, SIX5, SNAI2, SLC17A8, SERPINB6, SOX10, STRC, SLC19A2, TCOF1, SLC4A11, MT-TS1, MT-TS2, TECTA, TMPRSS3, RIPOR2, CEMIP, LARS2, MCM2, PRPS1, KCNE1, KCNQ1, PTPRQ, RDX[mendelian.co] PSACH results from mutations in the cartilage oligomeric matrix protein (COMP) gene, while SEDC is caused by mutations in the gene for type II procollagen (COL2A1).[ncbi.nlm.nih.gov]

  • Usher Syndrome Type I

    We recently reported tight linkage on mouse chromosome 7 of OMP to the shaker-1 deafness mutant, between the tyrosinase and globin loci.[ncbi.nlm.nih.gov] MYH14, MYH9, MYO15A, MYO3A, MYO6, MYO7A, NDP, NLRP3, OPA1, OSBPL2, OTOA, OTOF, OTOG, OTOGL, P2RX2, PAX3, PCDH15, PDZD7, PMP22, PNPT1, POLR1D, POU3F4, POU4F3, PRPS1, PTPRQ, RDX[genedx.com] […] network formed by the USH1B, C, D and G proteins is responsible for the correct cohesion of the hair bundle.[ncbi.nlm.nih.gov]