Works matching DE "MITOCHONDRIAL enzymes"


Results: 215
    1

    Tratamiento de urgencia de la acidemia metilmalónica.

    Published in:
    Acta Pediatrica de Mexico, 2012, v. 33, n. 1, p. 48
    By:
    • Santillán-Aguayo, Enrique;
    • Revilla-Estivil, Nuria;
    • Belmont-Martínez, Leticia;
    • Fernández-Lainez, Q. F. B. Cynthia;
    • Guillén-López, L. N. C. P. Sara;
    • Ibarra-González, M en C. Isabel;
    • Monroy-Santoyo, Susana;
    • Rodríguez-Schmidt, L. N. Romina;
    • Vela-Amieva, Marcela
    Publication type:
    Article
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    Nematode Muscles Project in Spaceflight Experiment.

    Published in:
    Biological Sciences in Space, 2018, v. 32, p. 6, doi. 10.2187/bss.32.6
    By:
    • Surabhi Sudevan;
    • Toko Hashizume;
    • Sachiko Yano;
    • Kana Kuriyama;
    • Kenta Momma;
    • Shunsuke Harada;
    • Masumi Umehara;
    • Akira Higashibata;
    • Atsushi Higashitani
    Publication type:
    Article
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    3D gel map of Arabidopsis complex I.

    Published in:
    Frontiers in Plant Science, 2013, v. 4, p. 1, doi. 10.3389/fpls.2013.00153
    By:
    • Peters, Katrin;
    • Belt, Katharina;
    • Braun, Hans-Peter
    Publication type:
    Article
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    Targeting Glutamine Synthesis Inhibits Stem Cell Adipogenesis in Vitro.

    Published in:
    Cellular Physiology & Biochemistry (Cell Physiol Biochem Press GmbH & Co. KG), 2020, v. 54, n. 5, p. 917, doi. 10.33594/000000278
    By:
    • Velickovic, Ksenija;
    • Leija, Hilda Anaid Lugo;
    • Surrati, Amal;
    • Dong-Hyun Kim;
    • Sacks, Harold;
    • Symonds, Michael E.;
    • Sottile, Virginie
    Publication type:
    Article
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    A Japanese case of cerebellar ataxia, spastic paraparesis and deep sensory impairment associated with a novel homozygous TTC19 mutation.

    Published in:
    Journal of Human Genetics, 2015, v. 60, n. 4, p. 187, doi. 10.1038/jhg.2015.7
    By:
    • Kunii, Misako;
    • Doi, Hiroshi;
    • Higashiyama, Yuichi;
    • Kugimoto, Chiharu;
    • Ueda, Naohisa;
    • Hirata, Junichi;
    • Tomita-Katsumoto, Atsuko;
    • Kashikura-Kojima, Mari;
    • Kubota, Shun;
    • Taniguchi, Midori;
    • Murayama, Kei;
    • Nakashima, Mitsuko;
    • Tsurusaki, Yoshinori;
    • Miyake, Noriko;
    • Saitsu, Hirotomo;
    • Matsumoto, Naomichi;
    • Tanaka, Fumiaki
    Publication type:
    Article
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    Diagnostic pitfall in antenatal manifestations of CPT II deficiency.

    Published in:
    Clinical Genetics, 2016, v. 89, n. 2, p. 193, doi. 10.1111/cge.12593
    By:
    • Boemer, F.;
    • Deberg, M.;
    • Schoos, R.;
    • Caberg, J.‐H.;
    • Gaillez, S.;
    • Dugauquier, C.;
    • Delbecque, K.;
    • François, A.;
    • Maton, P.;
    • Demonceau, N.;
    • Senterre, G.;
    • Ferdinandusse, S.;
    • Debray, F.‐G.
    Publication type:
    Article
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    Dopamine.

    Published in:
    Clefs CEA (English), 2014, n. 62, p. 52
    Publication type:
    Article
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