Works matching DE "GLYCINE metabolism"


Results: 107
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    Insulin resistance and glycine metabolism in humans.

    Published in:
    Amino Acids, 2018, v. 50, n. 1, p. 11, doi. 10.1007/s00726-017-2508-0
    By:
    • Adeva-Andany, M.;
    • Souto-Adeva, G.;
    • Ameneiros-Rodríguez, E.;
    • Fernández-Fernández, C.;
    • Donapetry-García, C.;
    • Domínguez-Montero, A.
    Publication type:
    Article
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    Exploring the Role of Glycine Metabolism in Coronary Artery Disease: Insights from Human Genetics and Mouse Models.

    Published in:
    Nutrients, 2025, v. 17, n. 1, p. 198, doi. 10.3390/nu17010198
    By:
    • Biswas, Subarna;
    • Hilser, James R.;
    • Woodward, Nicholas C.;
    • Wang, Zeneng;
    • Gukasyan, Janet;
    • Nemet, Ina;
    • Schwartzman, William S.;
    • Huang, Pin;
    • Han, Yi;
    • Fouladian, Zachary;
    • Charugundla, Sarada;
    • Spencer, Neal J.;
    • Pan, Calvin;
    • Tang, W. H. Wilson;
    • Lusis, Aldons J.;
    • Hazen, Stanley L.;
    • Hartiala, Jaana A.;
    • Allayee, Hooman
    Publication type:
    Article
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    Non-ketotic hyperglycinemia.

    Published in:
    Romanian Journal of Pediatrics / Revista Romana de Pediatrie, 2011, v. 60, n. 2, p. 195
    By:
    • Oprea, Ioan;
    • Malancioiu, Camelia;
    • Martinescu, Adrian;
    • Grigore, Ioana
    Publication type:
    Article
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    HIPERGLICINEMIA NONCETONICĂ.

    Published in:
    Romanian Journal of Pediatrics / Revista Romana de Pediatrie, 2011, v. 60, n. 2, p. 192
    By:
    • Oprea, Ioan;
    • Malancioiu, Camelia;
    • Martinescu, Adrian;
    • Grigore, Ioana
    Publication type:
    Article
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    Phosphoglycerate dehydrogenase diverts glycolytic flux and contributes to oncogenesis.

    Published in:
    Nature Genetics, 2011, v. 43, n. 9, p. 869, doi. 10.1038/ng.890
    By:
    • Locasale, Jason W.;
    • Grassian, Alexandra R.;
    • Melman, Tamar;
    • Lyssiotis, Costas A.;
    • Mattaini, Katherine R.;
    • Bass, Adam J.;
    • Heffron, Gregory;
    • Metallo, Christian M.;
    • Muranen, Taru;
    • Sharfi, Hadar;
    • Sasaki, Atsuo T.;
    • Anastasiou, Dimitrios;
    • Mullarky, Edouard;
    • Vokes, Natalie I.;
    • Sasaki, Mika;
    • Beroukhim, Rameen;
    • Stephanopoulos, Gregory;
    • Ligon, Azra H.;
    • Meyerson, Matthew;
    • Richardson, Andrea L.
    Publication type:
    Article
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    Novel compound heterozygous LIAS mutations cause glycine encephalopathy.

    Published in:
    Journal of Human Genetics, 2015, v. 60, n. 10, p. 631, doi. 10.1038/jhg.2015.72
    By:
    • Tsurusaki, Yoshinori;
    • Tanaka, Ryuta;
    • Shimada, Shino;
    • Shimojima, Keiko;
    • Shiina, Masaaki;
    • Nakashima, Mitsuko;
    • Saitsu, Hirotomo;
    • Miyake, Noriko;
    • Ogata, Kazuhiro;
    • Yamamoto, Toshiyuki;
    • Matsumoto, Naomichi
    Publication type:
    Article
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    Variant non ketotic hyperglycinemia is caused by mutations in LIAS, BOLA3 and the novel gene GLRX5.

    Published in:
    Brain: A Journal of Neurology, 2014, v. 137, n. 2, p. 366, doi. 10.1093/brain/awt328
    By:
    • Baker, Peter R.;
    • Friederich, Marisa W.;
    • Swanson, Michael A.;
    • Shaikh, Tamim;
    • Bhattacharya, Kaustuv;
    • Scharer, Gunter H.;
    • Aicher, Joseph;
    • Creadon-Swindell, Geralyn;
    • Geiger, Elizabeth;
    • MacLean, Kenneth N.;
    • Lee, Wang-Tso;
    • Deshpande, Charu;
    • Freckmann, Mary-Louise;
    • Shih, Ling-Yu;
    • Wasserstein, Melissa;
    • Rasmussen, Malene B.;
    • Lund, Allan M.;
    • Procopis, Peter;
    • Cameron, Jessie M.;
    • Robinson, Brian H.
    Publication type:
    Article
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    Biochemical and molecular predictors for prognosis in nonketotic hyperglycinemia.

    Published in:
    2015
    By:
    • Swanson, Michael A.;
    • Coughlin, Curtis R.;
    • Scharer, Gunter H.;
    • Szerlong, Heather J.;
    • Bjoraker, Kendra J.;
    • Spector, Elaine B.;
    • Creadon‐Swindell, Geralyn;
    • Mahieu, Vincent;
    • Matthijs, Gert;
    • Hennermann, Julia B.;
    • Applegarth, Derek A.;
    • Toone, Jennifer R.;
    • Tong, Suhong;
    • Williams, Kristina;
    • Van Hove, Johan L. K.
    Publication type:
    journal article
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    Hypoxia Promotes the Expression of ADAM9 by Tubular Epithelial Cells, Which Enhances Transforming Growth Factor β1 Activation and Promotes Tissue Fibrosis in Patients With Lupus Nephritis.

    Published in:
    Arthritis & Rheumatology, 2025, v. 77, n. 2, p. 180, doi. 10.1002/art.42987
    By:
    • Umeda, Masataka;
    • Karino, Kohei;
    • Satyam, Abhigyan;
    • Yoshida, Nobuya;
    • Hisada, Ryo;
    • Bhargava, Rhea;
    • Vichos, Theodoros;
    • Kunzler, Ana Laura;
    • Igawa, Takashi;
    • Ichinose, Kunihiro;
    • Torigoe, Kenta;
    • Nishino, Tomoya;
    • Maeda, Takahiro;
    • Owen, Caroline A.;
    • Abdi, Reza;
    • Kawakami, Atsushi;
    • Tsokos, George C.
    Publication type:
    Article
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