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9,056 Possible Causes for mutation

  • Influenza

    […] site/48 h  8,760 h 2.6 10 3 mutations/site/year and 0.4 10 5 mutations/site/71 h 8,760 h 0.5 10 3 mutations/site/year, respectively.[doi.org] A total of 813,663 nucleotides were sequenced, giving rates of 2.0 x 10(-6) and 0.6 x 10(-6) mutations per site per infectious cycle, which, when extended to 1 year, agree[ncbi.nlm.nih.gov] 10 5 mutations/site/7 infectious cycles 0.6 10 6 mutations/site/infectious cycle, respectively.[doi.org]

  • Upper Respiratory Infection

    .: Emergence of macrolide-resistant Mycoplasma pneumoniae with a 23S rRNA gene mutation . Antimicrob Agents Chemother 2005, 49: 2302–2306.[link.springer.com]

  • Acute Gastroenteritis

    A whole genome sequencing revealed that all of the viral genome segments were highly similar to those of the Rotarix virus, with the exception of five amino acid mutations[ncbi.nlm.nih.gov] The clinical characteristics of patients were studied, and the rplD, rplV, and 23S rRNA domain V genes were sequenced to detected resistance-related mutations.[ncbi.nlm.nih.gov] Further identification of unique amino acid mutations in both VP1 and RdRp of NoV strain as shown in this report may provide insight in explaining its structural and antigenic[ncbi.nlm.nih.gov]

  • Viral Lower Respiratory Infection

    To study the effect of IFIH1 on RSV and HRV replication, we used Huh7.5 cells, which lack endogenous expression of IFIH1 and express a mutated, inactive form of RIG-I, and[pnas.org] GPR56 homozygous nonsense mutation p.R271* associated with phenotypic variability in bilateral frontoparietal polymicrogyria.[turkishjournalpediatrics.org] Antibiotic resistance is when bacteria is regularly exposed to the same drug over time and will eventually mutate and develop resistance to this drug.[europeanlung.org]

  • Urinary Tract Infection

    For women with an average risk of ovarian cancer (defined as women who do not have a document germline mutation or who do not have a strong family history suspicious for a[choosingwisely.org] In other words, even if both infections are caused by E. coli , the second is likely a mutation or separate form of E. coli .[plushcare.com] Poltorak A, He X, Smirnova I, Liu MY, Huffel CV, Du X, Birdwell D, Alejos E, Silva M, Galanos C et al (1998) Defective LPS signaling in C3H/HeJ and C57BL/10ScCr mice: mutations[doi.org]

  • Adrenal Insufficiency

    The X-linked form is related to mutations in the DAX1 (NROB1) gene.[ncbi.nlm.nih.gov] All mutations resulted in reduced or absent SGPL1 protein and/or enzyme activity.[ncbi.nlm.nih.gov] The mutation was confirmed in the CYP11A1 gene.[ncbi.nlm.nih.gov]

  • Skin Infection

    In contrast, only 13% of the control group reported FLG mutations (22 heterozygous variants).[ncbi.nlm.nih.gov] RESULTS: Compared with those without the FLG-null mutations, patients with AD who had FLG mutation(s) had approximately a seven times increased risk of more than four episodes[ncbi.nlm.nih.gov] The construction of infectious VZV recombinants that have deletions or targeted mutations of viral genes or their promoters and the evaluation of VZV mutants in T cell and[ncbi.nlm.nih.gov]

  • Sinusitis

    Increased prevalence of chronic rhinosinusitis in carriers of a cystic fibrosis mutation .Arch Otolaryngol Head Neck Surg. 2005 ;131: 237 - 40 Google Scholar Crossref Medline[doi.org] Cystic fibrosis gene mutations F508 and 394delTT in patients with chronic sinusitis in Finland .Acta Otolaryngol. 2001 ;121: 945 - 7 Google Scholar Crossref Medline ISI Armenaka[doi.org]

  • Sunburn

    Sometimes the cells with sun-caused mutated DNA do turn into problem cells, however, that do not call it quits and keep proliferating as cancers.[livescience.com] This mutated DNA may eventually lead to skin cancer. The warmth of a sunburn generally stems from increased blood flow to the exposed site.[scientificamerican.com] A novel XPD mutation in a compound heterozygote; the mutation in the second allele is present in three homozygous patients with mild sun sensitivity.[ncbi.nlm.nih.gov]

  • Osteoporosis

    BACKGROUND AND OBJECTIVES: Plastin 3 (PLS3) mutations are associated with an X-linked osteoporosis.[ncbi.nlm.nih.gov] Patients carrying homozygous WNT1 mutations have more frequent fractures while heterozygous carriers of the mutation in WNT1 gene are also found to have early onset osteoporosis[ncbi.nlm.nih.gov] Mutations in PLS3 have been identified as a cause of bone fragility in children, but the bone phenotype associated with PLS3 mutations has not been reported in detail.[ncbi.nlm.nih.gov]

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