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10,913 Possible Causes for Drosophila, protein,, svb

Did you mean: Drosophila, proteus, svb

  • Influenza

    Adaptive evolution drives divergence of a hybrid inviability gene between two species of Drosophila . Nature 423 , 715–719 (2003) 12. Webster, R. G. , Bean, W.[] Influenza virus M2 protein is an integral membrane protein expressed on the infected-cell surface. Cell 40 , 627–633 (1985). 5. Zebedee, S.L. & Lamb, R.A.[] Sequence based analysis demonstrated substantial changes in the HA protein over the last decade.[]

    Missing: svb
  • Dementia

    Jeon, Young-Won Chin, Byung-Soo Koo and Kyoung Sang Cho , In Vivo Screening of Traditional Medicinal Plants for Neuroprotective Activity against Aβ42 Cytotoxicity by Using Drosophila[] The pathogenesis of AD is complex, involving specific disease-linked proteins (amyloid-beta [Aß] and tau), inflammation, and neurotransmitter dysregulation.[] After 12 months, the intervention group showed slightly higher protein intake per day (mean difference (MD) 0.11 g/kg, 95% confidence interval (CI) -0.01 to 0.23; n 78, 1[]

    Missing: svb
  • Endocrine Dysfunction

    This concerns especially the situation where the presence of M-protein is limited and the serum protein electrophoresis (sPEP) appears normal.[] Joshi , A , Reddy , SVB , Bhatia , V et al. ( 2011 ) High prevalence of low bone mineral density in patients with tropical calcific pancreatitis .[] We evaluated thyroid function, insulin-like growth factor I, insulin-like growth factor-binding protein 3, and cortisol at 1, 3, 6, and 12 months after injury, and assessed[]

    Missing: Drosophila
  • Wolbachia

    […] sequences that are stable in Drosophila lines transinfected with wRi.[] The role of recombinant Wolbachia surface protein (rWSP), one of the most abundantly expressed proteins of the endosymbiont, in modulating cell-mediated immune responses in[] In Drosophila melanogaster, however, a strong and consistent effect of Wolbachia infection has not been found.[]

    Missing: svb
  • Malignant Neoplasm

    Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome. Cell . 1996 Jun 14. 85(6):841-51. [Medline] .[] […] of the Hmga1 protein and the Brca1 gene.[] As previously introduced, SIRT1 is a stress response protein associated with DNA repair in yeast [19] , [50] and transcriptional repression [39] , and is a component, in drosophila[]

    Missing: svb
  • Amyotrophic Lateral Sclerosis 8

    Human VapB and Drosophila Vap-33-1 (Vap) are homologous type II transmembrane proteins that are localized to the ER.[] protein B.[] Abstract A familial form of Amyotrophic lateral sclerosis (ALS8) is caused by a point mutation (P56S) in the vesicle-associated membrane protein associated protein B (VapB[]

    Missing: svb
  • Bombyx

    More recently, the newly recognized B. mori receptor for Drosophila melanogaster sex peptide (DmSP) has been identified as a receptor for BmPTSP.[] In this study, we screened BmREEPa interacting protein through co-immunoprecipitation and finally identified a membrane protein, Bombyx mori patched domain containing protein[] Biosciences, Graduate School of Frontier Sciences, The University of Tokyo, Kashiwa and 2 National Institute of Agrobiological Sciences, Tsukuba, Ibaraki, Japan ABSTRACT In Drosophila[]

    Missing: svb
  • Barth Syndrome

    Next, we asked whether the tafazzin mutation has any functional phenotype in Drosophila .[] Combining those profiles with gene set enrichment analysis allows detecting significantly affected protein complexes.[] Drosophila Genetics.[]

    Missing: svb
  • Astrovirus

    Habayeb MS, Ekengren SK, Hultmark D (2006) Nora virus, a persistent virus in Drosophila, defines a new picorna-like virus family. J Gen Virol 87: 3045–3051.[] Mature HAstV contains three predominant protein species, but the mechanism for acquired infectivity upon maturation is unclear.[] Performed the experiments: SVB AM RC TAM WB MS SC. Analyzed the data: CT LK WW AT DG TAM TG CB OG WB.[]

  • Adrenal Insufficiency

    In Drosophila, Sply mutants, which lack SGPL1, displayed a phenotype reminiscent of nephrotic syndrome in nephrocytes.[] At the protein level, the two mutations determine the p.Arg188Cys variant (rs104894090) and the p.Arg193Ter variant (rs387907235), respectively.[] We performed structural analyses to examine the effect of the p.E314K variant on protein function and show that it falls in the core of the protein may disrupt cholesterol[]

    Missing: svb