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Journal Abstract Search

547 related items for PubMed ID: 25488668

  • 1. Impaired O-linked N-acetylglucosaminylation in the endoplasmic reticulum by mutated epidermal growth factor (EGF) domain-specific O-linked N-acetylglucosamine transferase found in Adams-Oliver syndrome.
    Ogawa M, Sawaguchi S, Kawai T, Nadano D, Matsuda T, Yagi H, Kato K, Furukawa K, Okajima T.
    J Biol Chem; 2015 Jan 23; 290(4):2137-49. PubMed ID: 25488668
    [Abstract] [Full Text] [Related]

  • 2. N-acetylglucosamine modification in the lumen of the endoplasmic reticulum.
    Ogawa M, Sawaguchi S, Furukawa K, Okajima T.
    Biochim Biophys Acta; 2015 Jun 23; 1850(6):1319-24. PubMed ID: 25791024
    [Abstract] [Full Text] [Related]

  • 3. EOGT and O-GlcNAc on secreted and membrane proteins.
    Varshney S, Stanley P.
    Biochem Soc Trans; 2017 Apr 15; 45(2):401-408. PubMed ID: 28408480
    [Abstract] [Full Text] [Related]

  • 4. N-Glycans on EGF domain-specific O-GlcNAc transferase (EOGT) facilitate EOGT maturation and peripheral endoplasmic reticulum localization.
    Alam SMD, Tsukamoto Y, Ogawa M, Senoo Y, Ikeda K, Tashima Y, Takeuchi H, Okajima T.
    J Biol Chem; 2020 Jun 19; 295(25):8560-8574. PubMed ID: 32376684
    [Abstract] [Full Text] [Related]

  • 5. Autosomal recessive Adams-Oliver syndrome caused by homozygous mutation in EOGT, encoding an EGF domain-specific O-GlcNAc transferase.
    Cohen I, Silberstein E, Perez Y, Landau D, Elbedour K, Langer Y, Kadir R, Volodarsky M, Sivan S, Narkis G, Birk OS.
    Eur J Hum Genet; 2014 Mar 19; 22(3):374-8. PubMed ID: 23860037
    [Abstract] [Full Text] [Related]

  • 6. Congenital diseases caused by defective O-glycosylation of Notch receptors.
    Tashima Y, Okajima T.
    Nagoya J Med Sci; 2018 Aug 19; 80(3):299-307. PubMed ID: 30214079
    [Abstract] [Full Text] [Related]

  • 7. O-linked-N-acetylglucosamine modification of mammalian Notch receptors by an atypical O-GlcNAc transferase Eogt1.
    Sakaidani Y, Ichiyanagi N, Saito C, Nomura T, Ito M, Nishio Y, Nadano D, Matsuda T, Furukawa K, Okajima T.
    Biochem Biophys Res Commun; 2012 Mar 02; 419(1):14-9. PubMed ID: 22310717
    [Abstract] [Full Text] [Related]

  • 8. Mutations in EOGT confirm the genetic heterogeneity of autosomal-recessive Adams-Oliver syndrome.
    Shaheen R, Aglan M, Keppler-Noreuil K, Faqeih E, Ansari S, Horton K, Ashour A, Zaki MS, Al-Zahrani F, Cueto-González AM, Abdel-Salam G, Temtamy S, Alkuraya FS.
    Am J Hum Genet; 2013 Apr 04; 92(4):598-604. PubMed ID: 23522784
    [Abstract] [Full Text] [Related]

  • 9. O-linked-N-acetylglucosamine on extracellular protein domains mediates epithelial cell-matrix interactions.
    Sakaidani Y, Nomura T, Matsuura A, Ito M, Suzuki E, Murakami K, Nadano D, Matsuda T, Furukawa K, Okajima T.
    Nat Commun; 2011 Dec 13; 2():583. PubMed ID: 22158438
    [Abstract] [Full Text] [Related]

  • 10. GTDC2 modifies O-mannosylated α-dystroglycan in the endoplasmic reticulum to generate N-acetyl glucosamine epitopes reactive with CTD110.6 antibody.
    Ogawa M, Nakamura N, Nakayama Y, Kurosaka A, Manya H, Kanagawa M, Endo T, Furukawa K, Okajima T.
    Biochem Biophys Res Commun; 2013 Oct 11; 440(1):88-93. PubMed ID: 24041696
    [Abstract] [Full Text] [Related]

  • 11. Intracellular and extracellular O-linked N-acetylglucosamine in the nervous system.
    Ogawa M, Sawaguchi S, Kamemura K, Okajima T.
    Exp Neurol; 2015 Dec 11; 274(Pt B):166-74. PubMed ID: 26278182
    [Abstract] [Full Text] [Related]

  • 12. Structure and function of extracellular O-GlcNAc.
    Ogawa M, Okajima T.
    Curr Opin Struct Biol; 2019 Jun 11; 56():72-77. PubMed ID: 30669087
    [Abstract] [Full Text] [Related]

  • 13. Extracellular O-linked β-N-acetylglucosamine: Its biology and relationship to human disease.
    Ogawa M, Furukawa K, Okajima T.
    World J Biol Chem; 2014 May 26; 5(2):224-30. PubMed ID: 24921011
    [Abstract] [Full Text] [Related]

  • 14. Antibodies that detect O-linked β-D-N-acetylglucosamine on the extracellular domain of cell surface glycoproteins.
    Tashima Y, Stanley P.
    J Biol Chem; 2014 Apr 18; 289(16):11132-11142. PubMed ID: 24573683
    [Abstract] [Full Text] [Related]

  • 15. The EGF repeat-specific O-GlcNAc-transferase Eogt interacts with notch signaling and pyrimidine metabolism pathways in Drosophila.
    Müller R, Jenny A, Stanley P.
    PLoS One; 2013 Apr 18; 8(5):e62835. PubMed ID: 23671640
    [Abstract] [Full Text] [Related]

  • 16. O-GlcNAc on NOTCH1 EGF repeats regulates ligand-induced Notch signaling and vascular development in mammals.
    Sawaguchi S, Varshney S, Ogawa M, Sakaidani Y, Yagi H, Takeshita K, Murohara T, Kato K, Sundaram S, Stanley P, Okajima T.
    Elife; 2017 Apr 11; 6():. PubMed ID: 28395734
    [Abstract] [Full Text] [Related]

  • 17. Heterozygous Loss-of-Function Mutations in DLL4 Cause Adams-Oliver Syndrome.
    Meester JA, Southgate L, Stittrich AB, Venselaar H, Beekmans SJ, den Hollander N, Bijlsma EK, Helderman-van den Enden A, Verheij JB, Glusman G, Roach JC, Lehman A, Patel MS, de Vries BB, Ruivenkamp C, Itin P, Prescott K, Clarke S, Trembath R, Zenker M, Sukalo M, Van Laer L, Loeys B, Wuyts W.
    Am J Hum Genet; 2015 Sep 03; 97(3):475-82. PubMed ID: 26299364
    [Abstract] [Full Text] [Related]

  • 18. Contribution of extracellular O-GlcNAc to the stability of folded epidermal growth factor-like domains and Notch1 trafficking.
    Ogawa M, Tashima Y, Sakaguchi Y, Takeuchi H, Okajima T.
    Biochem Biophys Res Commun; 2020 May 21; 526(1):184-190. PubMed ID: 32201074
    [Abstract] [Full Text] [Related]

  • 19. SHCBP1 interacting with EOGT enhances O-GlcNAcylation of NOTCH1 and promotes the development of pancreatic cancer.
    Yang C, Hu JF, Zhan Q, Wang ZW, Li G, Pan JJ, Huang L, Liao CY, Huang Y, Tian YF, Shen BY, Chen JZ, Wang YD, Chen S.
    Genomics; 2021 Mar 21; 113(2):827-842. PubMed ID: 33515675
    [Abstract] [Full Text] [Related]

  • 20. Cutaneous squamous cell carcinoma in an autosomal-recessive Adams-Oliver syndrome patient with a novel frameshift pathogenic variant in the EOGT gene.
    Lukas ML, Harald G, Sanz J, Trippel M, Sabina G, Jochen R.
    Am J Med Genet A; 2022 Nov 21; 188(11):3318-3323. PubMed ID: 36059114
    [Abstract] [Full Text] [Related]

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