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7,255 Possible Causes for Allele, RAPGEF1, wt

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  • Viral Lower Respiratory Infection

    Cotransfection of IFIH1-wt with each of the mutant IFIH1 isoforms showed interference with IFIH1-wt-induced IFNβ production ( P 0.05, Fig. 2 A ).[pnas.org] The T allele at rs35732034 leads to skipping of exon 14. The G allele at rs35337543 leads to skipping of exon 8.[pnas.org] IFIH1-wt is more stable than the alternate IFIH1 isoforms, and the stability of IFIH1-wt is reduced upon coexpression with any of the alternate isoforms.[pnas.org]

    Missing: RAPGEF1
  • Influenza

    Each antigenic type is designated as “ ij ” by virtue of containing allele i at one locus and allele j at the other.[pnas.org] The middle panel s hows the wt M2 channel in the open state.[doi.org] Our results indicated increased risk of both severe and mild influenza in subjects carrying the IFITM3 rs12252 polymorphism in the allele contrast C vs.[ncbi.nlm.nih.gov]

    Missing: RAPGEF1
  • Urinary Tract Infection

    Similarly CT genotype and T allele of TLR4 rs4986791 are also significantly associated with UTI in both groups.[ncbi.nlm.nih.gov] Maccioli GA, Dorman T, Brown BR, Mazuski JE, McLean BA, Kuszaj JM, Rosenbaum SH, Frankel LR, Devlin JW, Govert JA, Smith B, Peruzzi WT; American College of Critical Care Medicine[choosingwisely.org] Wang CH, Fang CC, Chen NC, Liu SS, Yu PH, Wu TY, Chen WT, Lee CC, Chen SC (July 9, 2012).[en.wikipedia.org]

    Missing: RAPGEF1
  • Acute Bronchitis

    Barbee RA, Halonen M, Kaltenborn WT, Burrows B. A longitudinal study of respiratory symptoms in a community population sample.[doi.org] Estimated numbers and prevalence of PI*S and PI*Z alleles of alpha1-antitrypsin deficiency in European countries. Eur Respir J 2006 ;27: 77 –84. 30.[ajrccm.atsjournals.org] Eiser N, Denman WT, West C, Luce P. Oral diamorphine: lack of effect on dyspnoea and exercise tolerance in the “pink puffer” syndrome.[ajrccm.atsjournals.org]

    Missing: RAPGEF1
  • Dementia

    The clinical presentation of C9orf72 patients with pathogenic ATXN2 alleles ( 35 CAG-repeats) is unknown.[ncbi.nlm.nih.gov] Cooke WT, Smith WT (1966) Neurological disorders associated with adult coeliac disease. Brain 89(4):683–722 CrossRef PubMed Google Scholar 28.[doi.org] Hu WT, Murray JA, Greenaway MC, et al.: Cognitive impairment and celiac disease . Arch Neurol 2006, 63: 1440–1446. PubMed CrossRef Google Scholar 33.[doi.org]

    Missing: RAPGEF1
  • Osteoporosis

    Clinical Relevance Table for Fracture ‐ Primary Prevention Trials Outcome # Patients # Trials Control Event Rate Wt Absolute RD Wt Rel % Change NNT B Statistical Sig Quality[doi.org] Thus, we provide further evidence of bone phenotypes beyond those typically associated with SATB2-associated syndrome in individuals with potential dominant-negative SATB2 alleles[ncbi.nlm.nih.gov] BACKGROUND: Previous studies have suggested that tumor necrosis factor α (TNF-α), encoded by the TNFα gene, can increase osteoclast formation, and that specific alleles of[ncbi.nlm.nih.gov]

    Missing: RAPGEF1
  • Infectious Mononucleosis

    Aronson MD, Komaroff AL, Pass TM, Ervin CT, Branch WT. Heterophil antibody in adults with sore throat: frequency and clinical presentation.[aafp.org] By logistic regression, HLA-A*01 alleles [odds ratio (OR) per allele, 2.15; 95% CI, 1.60–2.88] were associated with increased and HLA-A*02 alleles (OR per allele, 0.70; 95%[dx.doi.org] The figure includes the cleavage sites for XhoI (X) and the expected fragment sizes after restriction analysis of EBV-wt and ΔBLLF1 genomes.[dx.doi.org]

    Missing: RAPGEF1
  • Otitis Media

    OBJECTIVE VS: T 39C, RR 18, HR 84, BP 116/74, SpO2 99%, Wt 18.2kg, Ht 110cm General: Well nourished, no acute distress HEENT: PERRLA, sclera white, conjunctiva pink.[npstudent.com] We also identified a second hypomorphic allele, V33A, with only modest increases in auditory thresholds and reduced incidence of OM.[ncbi.nlm.nih.gov]

    Missing: RAPGEF1
  • Endocrine Dysfunction

    Neuromuscular fxn Hyperthyroidism & cardiovascular fxn -increased ventilation, HR, blood volume, cardiac output -vasodilation -feel hot all the time -increased appetite -wt[quizlet.com] Co-occurring diagnoses among FMR1 premutation allele carriers. Clin.[mdpi.com] DHEA for women Endocrine disorders and PT implications -refer medical workup if: abnl height sexual maturity hair growth or loss abnl sexual fxn menstruation unexplained wt[quizlet.com]

    Missing: RAPGEF1
  • Mephenytoin

    wt) was greater than that in those heterozygous (wt/m1 and wt/m2) (203.9 /- 42.5% vs 69.6 /- 4.1%). 0-8 h urinary mephenytoin S/R ratio of those PMs with m1 mutation was[ncbi.nlm.nih.gov] […] of Caucasian poor metabolizer alleles.[ncbi.nlm.nih.gov] One PMs was D6-wt/D6-B, another PMs had the genotype D6-wt/ and hence both were misclassified as EMs.[ncbi.nlm.nih.gov]

    Missing: RAPGEF1