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8,284 Possible Causes for phenotype

  • Upper Respiratory Infection

    BACKGROUND: Asthma has several phenotypical features, including recurrent exacerbations and recurrent episodes of upper respiratory infection (URI).[]

  • Influenza

    Phenotypic susceptibility testing by the NA-Star assay indicated a highly reduced inhibition by oseltamivir and normal inhibition by zanamivir.[] We used reverse-genetics to demonstrate that a single egg-adapted HA RBS mutation (Q226R) was responsible for this phenotype. Copyright 2018 Elsevier Ltd.[]

  • Pharyngitis

    ) and its associated M phenotype were recorded in 40.9 % of the cases.[] M phenotype was the most common (71.8%), followed by iMLS (18.4%) and cMLS (9.7%).[] […] present investigation was deliberately aimed at evaluating the biofilm-forming ability of 63 clinical MRSA isolates recovered from pharyngitis patients through different phenotypic[]

  • Urinary Tract Infection

    We geno- and phenotypically characterized three EHEC isolates obtained from the urine of hospitalized patients suffering from UTIs.[] Out of the 198 confirmed isolates of K. pneumonia, 62 cases (31.3%) have the gene phenotype of broad spectrum β-lactamase enzymes and highest frequency of gene phenotype was[] Our data support the translational utility of this murine model to cUTI in humans as humanized exposures produced microbiologic outcomes consistent with the phenotypic profiles[]

  • Sunburn

    OBJECTIVES: To investigate sunscreen use in relation to demographic and phenotypic characteristics among women in Norway, as well as solar UV exposure, sunburn experience[]

  • Otitis Media

    In order to understand the pathological mechanisms underlying the OM phenotype, we studied interacting partners to NISCH along with downstream signalling molecules in the[]

  • Osteoporosis

    (H673fs)) in a 15-year-old patient whose SATB2-associated syndrome phenotype is accompanied by osteoporosis, fractures, progressive tibial bowing, and scoliosis.[] CONCLUSION: Hemizygous mutations in PLS3 may cause a monogenic form of X-linked osteoporosis presenting in childhood with a nonspecific phenotype.[] This report describes the phenotype and evaluation of mosaic pure tetrasomy 20p syndrome and compares to nonmosaic tetrasomy 20p and trisomy 20p syndromes, both of which have[]

  • Streptococcal Infection

    Children with a pediatric autoimmune neuropsychiatric disorder associated with streptococcal infections (PANDAS) phenotype may have tics or obsessive compulsive symptoms secondary[] […] during severe invasive infection, GAS destroys its own covRS two-component system, which negatively regulates many virulence factor genes, resulting in a hyper-virulent phenotype[] In this report, we describe two patients with DDD who definitely had an antecedent streptococcal infection with the phenotype of acute post-streptococcal glomerulonephritis[]

  • Sinusitis

    Sinus pneumatization did not differ according to CRS phenotype ( p 0.699).[] A diagnosis of CRS and CRS phenotype was determined from the medical record.[] Genetic polymorphisms in taste receptors contribute to variations in T1R and T2R functionality, and phenotypic differences correlate with disease status and disease severity[]

  • Adrenal Insufficiency

    […] whereas m.8344A G point mutation in tRNA is observed, in MERRF phenotype.[] Genetic defects such as NR0B1 defects are presumed based on phenotypes, while others with broad phenotypic variability, such as STAR defects, are difficult to diagnose.[] Their phenotype included congenital cataracts, hypotonia, developmental delay, and sensorineural hearing loss.[]

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