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10,912 Possible Causes for Drosophila, SmD3, protein

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  • 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.[dx.doi.org] 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.[doi.org] Sequence based analysis demonstrated substantial changes in the HA protein over the last decade.[ncbi.nlm.nih.gov]

    Missing: SmD3
  • 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[doi.org] The pathogenesis of AD is complex, involving specific disease-linked proteins (amyloid-beta [Aß] and tau), inflammation, and neurotransmitter dysregulation.[doi.org] 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[ncbi.nlm.nih.gov]

    Missing: SmD3
  • Wolbachia

    […] sequences that are stable in Drosophila lines transinfected with wRi.[ncbi.nlm.nih.gov] 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[dx.doi.org] In Drosophila melanogaster, however, a strong and consistent effect of Wolbachia infection has not been found.[ncbi.nlm.nih.gov]

    Missing: SmD3
  • 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] .[emedicine.medscape.com] […] of the Hmga1 protein and the Brca1 gene.[doi.org] 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[doi.org]

    Missing: SmD3
  • Amyotrophic Lateral Sclerosis 8

    Human VapB and Drosophila Vap-33-1 (Vap) are homologous type II transmembrane proteins that are localized to the ER.[ncbi.nlm.nih.gov] protein B.[symptoma.com] 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[ncbi.nlm.nih.gov]

    Missing: SmD3
  • Bombyx

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

    Missing: SmD3
  • Spinal Muscular Atrophy Type 2

    […] proximal SMA, we performed genome-wide linkage analysis and whole-exome sequencing and found a heterozygous de novo c.320C T (p.Ser107Leu) mutation in bicaudal D homolog 2 (Drosophila[uniprot.org] , SmD3 i SmB, i les candenes del costat de l'arginina side són simètricament dimetilades a ω-N G , N G' -dimetil-arginina.[ca.wikipedia.org] The SMN protein is expressed ubiquitously and it is found associated in a multiprotein complex, termed SMN complex, in all tissues under observation.[opus.bibliothek.uni-wuerzburg.de]

  • Barth Syndrome

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

    Missing: SmD3
  • Adrenal Insufficiency

    In Drosophila, Sply mutants, which lack SGPL1, displayed a phenotype reminiscent of nephrotic syndrome in nephrocytes.[ncbi.nlm.nih.gov] At the protein level, the two mutations determine the p.Arg188Cys variant (rs104894090) and the p.Arg193Ter variant (rs387907235), respectively.[ncbi.nlm.nih.gov] 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[ncbi.nlm.nih.gov]

    Missing: SmD3
  • Autosomal Recessive Primary Microcephaly

    Adult brain sizes are reported to be normal in drosophila and infertility has been shown in mice [ 1 , 45 , 56 , 59 ] CDK5RAP2 Cnn -/- (drosophila) Centrosome dysfunction[ncbi.nlm.nih.gov] Two previously reported (8508delGA, W1326X) and four novel sequence variants (Y1712X, I1717X, Y3353X, R3244X) were detected and all were predicted to be protein truncating[ncbi.nlm.nih.gov] (PMID: 17925396) Wood JL … Chen J (The Journal of biological chemistry 2007) 2 3 22 60 Microcephalin encodes a centrosomal protein.[genecards.org]

    Missing: SmD3