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235 Possible Causes for Drosophila, Yuri, protein

Did you mean: Drosophila, Yuri, proteus

  • Influenza

    Jinhua Dong, Mizuho Harada, Sawako Yoshida, Yuri Kato, Akiko Murakawa, Makoto Ogata, Tatsuya Kato, Taichi Usui and Enoch Y.[doi.org] 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]

  • 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] Kayo Nakata, Yuri Ito, Winnie Magadi, Audrey Bonaventure, Charles A.[doi.org]

  • 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] Park , MD; Yuri D. Fedoriw , MD The authors have no relevant financial interest in the products or companies described in this article. Reprints: Yuri D.[doi.org]

  • Circadian Rhythm

    Clock genes period and timeless were first discovered in large-scale Drosophila genetic screens developed in the 1970s.[ncbi.nlm.nih.gov] Here we show that the product of the slimb ( slmb ) gene 9 —a member of the F-box/WD40 protein family of the ubiquitin ligase SCF complex that targets phosphorylated proteins[doi.org] Tomohide Uno, Keisuke Hata, Susumu Hiragaki, Yuri Isoyama, Le Thi Dieu Trang, Yuichi Uno, Kengo Kanamaru, Hiroshi Yamagata, Masahiko Nakamura, Michihiro Takagi and Makio Takeda[doi.org]

  • Nephronophthisis 4

    Nishikawa , Tetsuji Otsuki , Tomoyasu Sugiyama , Ryotaro Irie , Ai Wakamatsu , Koji Hayashi , Hiroyuki Sato , Keiichi Nagai , Shizuko Ishii , Jun-ichi Yamamoto , Kaoru Saito , Yuri[doi.org] The cascade was discovered by analysis of Drosophila mutations ...[ncbi.nlm.nih.gov] The NPHP4 gene encodes a 1,250-amino acid protein of unknown function that we named nephrocystin-4.[ncbi.nlm.nih.gov]

  • Spinocerebellar Ataxia Type 1

    Ji Sun Kim, Ji Soo Kim, Jinyoung Youn, Dae-Won Seo, Yuri Jeong, Ji-Hoon Kang, Jeong Ho Park and Jin Whan Cho , Ocular motor characteristics of different subtypes of spinocerebellar[doi.org] 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[ncbi.nlm.nih.gov] Here we show that the expanded polyglutamine tract differentially affects the function of the host protein in the context of different endogenous protein complexes.[ncbi.nlm.nih.gov]

  • Bloom Syndrome

    L averty et al. , 1999 The Berkeley Drosophila Genome Project gene disruption project: single P -element insertions mutating 25% of vital Drosophila genes.[genetics.org] PRKAR1A and other protein kinase A (PKA) subunits were expressed in Bloom syndrome cells and their level of expression differed by subunit and cell type.[ncbi.nlm.nih.gov] Setsuo Oto, Shigeki Miyamoto, Fumiyo Kudoh, Hirosbi Horie, Naoko Kinugawa and Yuri Okimoto , Treatment for B‐cell‐type lymphoma in a girl associated with Bloom's syndrome[doi.org]

  • Sindbis Virus Infection

    Diese Daten unterstreichen die Wichtigkeit der induzierbaren Antwort in Drosophila.[depositonce.tu-berlin.de] The Dicer proteins involved in this process are phylogenetically conserved and have the same domain organization.[ncbi.nlm.nih.gov] Kotanagi, Hitoshi; Saito, Yuri; Yoshioka, Toshiaki; Koyama, Kenji // Journal of Gastroenterology;1998, Vol. 33 Issue 6, p842 Abstract: Two cancer cell lines were established[connection.ebscohost.com]

  • Kohlschütter-Tönz Syndrome

    […] small Druze village in Northern Israel, all homozygous for the same deleterious founder mutation, namely, (p.R157X) that creates a premature stop codon in ROGDI homolog (Drosophila[deepdyve.com] protein coding human cDNAs.[genecards.org] Gennery, Yuri Kawasaki, Jose Ichishima, Mitsujiro Osawa, Hiroshi Nihira, Takeshi Shiba, Takayuki Tanaka, Maya Chrabieh, Benedetta Bigio, Hong Hur, Yuval Itan, Yupu Liang,[doi.org]

  • Oculopharyngeal Muscular Dystrophy

    Case reports Oculopharyngeal muscular dystrophy or oculopharyngeal distal myopathy: case report Tais Yuri Hashimoto b Isabella Christina Oliveira Neto c Luciano Rodrigues[scielo.br] Gov't MeSH terms Animals Animals, Genetically Modified Disease Models, Animal Drosophila melanogaster/anatomy & histology Drosophila melanogaster/physiology* Humans Molecular[ncbi.nlm.nih.gov] A green fluorescence protein tag inserted at the N-terminus of both wildtype PABPN1 (ala10) and mutant PABPN1 (ala17) proteins allowed us to visualize their subcellular localization[ncbi.nlm.nih.gov]