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10,672 Possible Causes for Drosophila, X11L, protein

Did you mean: Drosophila, X11L, proteus

  • 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.[] Like hemagglutinin and neuraminidase, the M2 protein is an integral membrane protein of the influenza A virus 4 , 5 .[] Sequence based analysis demonstrated substantial changes in the HA protein over the last decade.[]

    Missing: X11L
  • 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: X11L
  • 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 [Aβ] and tau), inflammation, and neurotransmitter dysregulation.[] The pathogenesis of AD is complex, involving specific disease-linked proteins (amyloid-beta [Aß] and tau), inflammation, and neurotransmitter dysregulation.[]

    Missing: X11L
  • Xeroderma Pigmentosum Complementation Group F

    Fekairi S, Scaglione S, Chahwan C, Taylor ER, Tissier A, Coulon S, Dong MQ, Ruse C, Yates JR 3rd, Russell P, Fuchs RP, McGowan CH, Gaillard PH Cell July 10, 2009 Drosophila[] Endonuclease Catalytic Subunit 2 3 5 Excision Repair Cross-Complementing Rodent Repair Deficiency, Complementation Group 4 2 3 Xeroderma Pigmentosum Group F-Complementing Protein[] (Total - 28833 nos ) Alphabetic Listing: A B C D E F G H I J K L M N O P Q R S T U V W X Y Z Protein list for alphabet: X 1: X102 protein (X102) 2: X11 3: X11L (X11-Like)[]

  • 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: X11L
  • 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: X11L
  • 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: X11L
  • 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[] Two previously reported (8508delGA, W1326X) and four novel sequence variants (Y1712X, I1717X, Y3353X, R3244X) were detected and all were predicted to be protein truncating[] (PMID: 17925396) Wood JL … Chen J (The Journal of biological chemistry 2007) 2 3 22 60 Microcephalin encodes a centrosomal protein.[]

    Missing: X11L
  • Tuberculosis

    Stuart LM, Boulais J, Charriere GM, Hennessy EJ, Brunet S, et al. (2007) A systems biology analysis of the Drosophila phagosome. Nature 445: 95–101.[] In the present study, mice fed a 2% protein diet and developing protein calorie malnutrition, in contrast to well-nourished controls receiving a 20% protein diet, rapidly[] The vaccine combines two TB proteins known to stimulate strong immune responses in humans.[]

    Missing: X11L
  • Spinocerebellar Ataxia Type 1

    We applied this approach, which integrates parallel cell-based and Drosophila genetic screens, to spinocerebellar ataxia type 1 (SCA1), a disease caused by expansion of a[] Here we show that the expanded polyglutamine tract differentially affects the function of the host protein in the context of different endogenous protein complexes.[] The association of ataxin-1 with 14-3-3 is regulated by Akt phosphorylation, and in a Drosophila model of SCA1, both 14-3-3 and Akt modulate neurodegeneration.[]

    Missing: X11L