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10,423 Possible Causes for TRNAK1, gene

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  • Influenza

    […] into the human virus gene pool.[pubmedcentral.nih.gov] Figure 2 Phylogenetic tree of the influenza virus HA gene segment, HA1.[dx.doi.org] […] triple-reassortant influenza A virus with a HA that resembles H3 of human seasonal influenza from 2004 to 2005, N2 from influenza A virus already established in swine, and the internal gene[ncbi.nlm.nih.gov]

    Missing: TRNAK1
  • Acute Gastroenteritis

    KEYWORDS: full genome analysis; human rotavirus A; non-structural genes; structural genes[ncbi.nlm.nih.gov] VP4 and VP7 genes from a subset of samples were sequenced for phylogenetic analysis.[ncbi.nlm.nih.gov] The evolutionary rate of VP1 gene of GII.2 was distinctly higher than that of the partial polymerase region of GII.16.[ncbi.nlm.nih.gov]

    Missing: TRNAK1
  • Upper Respiratory Infection

    T2R38 is encoded by the TAS2R38 gene, which has several common genetic polymorphisms that result in altered receptor functionality.[ncbi.nlm.nih.gov] Moreover, common polymorphisms of the TAS2R38 gene were linked to significant differences in the ability of upper respiratory cells to clear and kill bacteria.[ncbi.nlm.nih.gov] — Asthma risk increased 17 times when children who had bronchiolitis in the first two years of life also had a common variation of the Plasminogen activator inhibitor-1 gene[sciencedaily.com]

    Missing: TRNAK1
  • Urinary Tract Infection

    We report here that UPEC upregulates the expression of ethanolamine utilization genes during uncomplicated UTIs in humans.[ncbi.nlm.nih.gov] In present study we investigate genetic variation of these genes in diabetic patients (3 to 4 times higher prevalence of UTI in comparison to general population).[ncbi.nlm.nih.gov] Maybe that yet unknown gene polymorphisms together with geographical and /or socio-economic differences can influence on the development of RS.[ncbi.nlm.nih.gov]

    Missing: TRNAK1
  • Connective Tissue Disease

    Glycine Metabolism Disorders Disease (OMIM Number) Defective Proteins or Enzymes Defective Gene or Genes (Chromosomal Location) Comments Nonketotic hyperglycinemia (605899[merck.com] Other diseases of connective tissue cannot be regularly defined by selected gene abnormalities, such as systemic lupus erythematosus or scleroderma .[medicinenet.com] This is caused by a mutation in the gene TGFBR on either chromosome 3 or 9 depending on the type. These are also referred to as systemic autoimmune diseases.[en.wikipedia.org]

    Missing: TRNAK1
  • Insect Bite

    Immunophenotyping, direct immunofluorescence (DIF) tests, and IgH gene rearrangement studies were performed in the lesions associated with MCL only.[ncbi.nlm.nih.gov] […] insensitive to permethrin is discussed along with the surprising contrary clinical evidence from Europe about efficacy of permethrin in children with head lice carrying kdr-like gene[ncbi.nlm.nih.gov]

    Missing: TRNAK1
  • Viral Lower Respiratory Infection

    The samples were tested using a Rotor-Gene 6000 (Qiagen) and the following conditions: (1) hold at 95 C for 15 min; and (2) 45 cycles of (a) step 1, 95 C hold for 15 s; (b[thorax.bmj.com] This in turn initiates a signaling cascade that results in type 1 IFN production and activation of antiviral genes ( 23 ).[pnas.org] Shift (major antigenic change) Influenza viruses have segmented genomes (each gene is on a separate gene segment).[virology.uct.ac.za]

    Missing: TRNAK1
  • Malignant Neoplasm

    The Ataxia-telangiectasia mutated gene and breast cancer: gene expression profiles and sequence variants. Cancer Lett. 2005 Sep 28;227(2):105-14. Epub 2005 Jan 8.[ghr.nlm.nih.gov] In addition to mutations, which can be either inherited or somatically acquired, epigenetic silencing of DNA repair genes may promote tumorigenesis.[ncbi.nlm.nih.gov] […] of gene function in cancer.[doi.org]

    Missing: TRNAK1
  • Skin Infection

    There was also increased expression of genes encoding virulence factors, namely secreted toxins and fibronectin and/or fibrinogen-binding proteins.[ncbi.nlm.nih.gov] The VZV genome has at least 70 known or predicted open reading frames (ORFs), but understanding how these gene products function in virulence is difficult because VZV is a[ncbi.nlm.nih.gov] Leukocyte adhesion deficiency (LAD) I is a well-described genetic disorder in which leukocytes are unable to migrate to sites of inflammation due to mutations in the ITGB2 gene[ncbi.nlm.nih.gov]

    Missing: TRNAK1
  • Osteoporosis

    Gene ontology enrichment analysis and Kyoto Encyclopedia of Genes and Genomes pathway enrichment analyses were conducted.[ncbi.nlm.nih.gov] […] the TNFα gene are associated with postmenopausal osteoporosis susceptibility in some populations; however, the exact molecular mechanism remains unknown.[ncbi.nlm.nih.gov] CONCLUSION: Each ERα and ERβ gene polymorphism might have different impact on PMOP risk and BMD in various ethnicities.[ncbi.nlm.nih.gov]

    Missing: TRNAK1

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