Výsledky vyhledávání - "Electron Transport Complex I/metabolism"

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    Zdroj: The Journal of Clinical Endocrinology & Metabolism. 104:2501-2508

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    Zdroj: Wüst, R C I, Coolen, B F, Held, N M, Daal, M R R, Tazehkandi, V A, Baks‐Te Bulte, L, Wiersma, M, Kuster, D W D, Brundel, B J J M, van Weeghel, M, Strijkers, G J & Houtkooper, R H 2021, 'The antibiotic doxycycline impairs cardiac mitochondrial and contractile function', International Journal of Molecular Sciences, vol. 22, no. 8, 4100, pp. 1-19. https://doi.org/10.3390/ijms22084100

    Relation: info:eu-repo/semantics/altIdentifier/pmid/33921053; info:eu-repo/semantics/altIdentifier/hdl/https://hdl.handle.net/1871.1/a482a5ee-18e2-449f-b5ac-daaa2bf31091; info:eu-repo/semantics/altIdentifier/pissn/1422-0067

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    Zdroj: Acta Neuropathol Commun
    Acta Neuropathologica Communications, Vol 8, Iss 1, Pp 1-19 (2020)

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    Autoři: Ilka Wittig Daria Diodato Uwe Ahting a další

    Přispěvatelé: Ilka Wittig Daria Diodato Uwe Ahting a další

    Zdroj: Orphanet J Rare Dis
    Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-10 (2018)
    Orphanet journal of rare diseases 13(1), 120 (2018). doi:10.1186/s13023-018-0784-8
    Orphanet Journal of Rare Diseases, Vol. 13, no. 1, p. 120 [1-10] (2018)
    Orphanet journal of rare diseases
    Repp, B M, Mastantuono, E, Alston, C L, Schiff, M, Haack, T B, Rötig, A, Ardissone, A, Lombès, A, Catarino, C B, Diodato, D, Schottmann, G, Poulton, J, Burlina, A, Jonckheere, A, Munnich, A, Rolinski, B, Ghezzi, D, Rokicki, D, Wellesley, D, Martinelli, D, Wenhong, D, Lamantea, E, Ostergaard, E, Pronicka, E, Pierre, G, Smeets, H J M, Wittig, I, Scurr, I, de Coo, I F M, Moroni, I, Smet, J, Mayr, J A, Dai, L, de Meirleir, L, Schuelke, M, Zeviani, M, Morscher, R J, McFarland, R, Seneca, S, Klopstock, T, Meitinger, T, Wieland, T, Strom, T M, Herberg, U, Ahting, U, Sperl, W, Nassogne, M-C, Ling, H, Fang, F, Freisinger, P, Van Coster, R, Strecker, V, Taylor, R W, Häberle, J, Vockley, J, Prokisch, H & Wortmann, S 2018, ' Clinical, biochemical and genetic spectrum of 70 patients with ACAD9 deficiency : is riboflavin supplementation effective? ', Orphanet Journal of Rare Diseases, vol. 13, 120 . https://doi.org/10.1186/s13023-018-0784-8
    Orphanet J. Rare Dis. 13:120 (2018)
    ORPHANET JOURNAL OF RARE DISEASES
    Orphanet Journal of Rare Diseases

    Témata: Electron Transport Complex I/metabolism, Male, 0301 basic medicine, Mitochondrial Diseases, genetics [Mitochondrial Diseases], PHENOTYPIC SPECTRUM, Riboflavin, therapeutic use [Riboflavin], Acidosis/genetics, Heart transplantation, heart transplantation, OXIDATION, Acyl-CoA Dehydrogenase, 0302 clinical medicine, drug therapy [Muscle Weakness], Neonatal, Activities Of Daily Living, Cardiomyopathy, Complex I, Heart Transplantation, Lactic Acidosis, Mitochondrial Disorder, Prognosis, Treatment, Vitamin, Activities of Daily Living, Medicine and Health Sciences, Amino Acid Metabolism, Inborn Errors/genetics, Cardiomyopathy, Hypertrophic/genetics, ddc:610, 0303 health sciences, Muscle Weakness, genetics [Cardiomyopathy, Hypertrophic], complex I, Lactic acidosis, Activities of daily living, Mitochondrial disorder, Riboflavin/therapeutic use, ddc, 3. Good health, lactic acidosis, metabolism [Acidosis], Genetics (clinical), Pharmacology (medical), metabolism [Mitochondrial Diseases], Acidosis, Amino Acid Metabolism, Inborn Errors, Cardiomyopathy, Hypertrophic, Electron Transport Complex I, Female, Humans, genetics [Muscle Weakness], pathology [Cardiomyopathy, Hypertrophic], SKELETAL-MUSCLE, Medicine, pathology [Amino Acid Metabolism, Inborn Errors], DISORDERS, EMC OR-01, metabolism [Cardiomyopathy, Hypertrophic], pathology [Acidosis], Mitochondrial Diseases/genetics, DIAGNOSIS, metabolism [Acyl-CoA Dehydrogenase], Muscle Weakness/drug therapy, neonatal, 03 medical and health sciences, genetics [Amino Acid Metabolism, Inborn Errors], mitochondrial disorder, metabolism [Electron Transport Complex I], pathology [Muscle Weakness], Hypertrophic/genetics, MUTATIONS, deficiency [Acyl-CoA Dehydrogenase], Research, Biology and Life Sciences, metabolism [Muscle Weakness], BEZAFIBRATE, Acyl-CoA Dehydrogenase/deficiency, metabolism [Amino Acid Metabolism, Inborn Errors], PAGE, Amino Acid Metabolism, pathology [Mitochondrial Diseases], CELLS, COMPLEX-I DEFICIENCY, genetics [Acidosis], Human medicine, genetics [Acyl-CoA Dehydrogenase], cardiomyopathy, Inborn Errors/genetics

    Popis souboru: application/pdf; pdf; application/octet-stream

    Přístupová URL adresa: https://ojrd.biomedcentral.com/track/pdf/10.1186/s13023-018-0784-8
    https://pubmed.ncbi.nlm.nih.gov/30025539
    https://doaj.org/article/129e2104cafd486f9cf68aead98de16c
    https://pure.eur.nl/en/publications/94f2998b-e84c-425a-87cb-448bfb043c27
    https://doi.org/10.1186/s13023-018-0784-8
    https://epub.ub.uni-muenchen.de/62981/
    https://biblio.ugent.be/publication/8574180
    https://moh-it.pure.elsevier.com/en/publications/clinical-biochemical-and-genetic-spectrum-of-70-patients-with-aca
    https://link.springer.com/article/10.1186%2Fs13023-018-0784-8
    https://www.repository.cam.ac.uk/handle/1810/278310
    https://researchportal.vub.be/en/publications/clinical-biochemical-and-genetic-spectrum-of-70-patients-with-aca
    https://pub.dzne.de/record/140094
    https://ora.ox.ac.uk/objects/uuid:86af70da-562a-4dc4-820b-5c6a5c026974
    https://doi.org/10.1186/s13023-018-0784-8
    https://hdl.handle.net/2434/585782
    https://doi.org/10.1186/s13023-018-0784-8
    https://hdl.handle.net/10281/205487
    https://doi.org/10.1186/s13023-018-0784-8
    https://hdl.handle.net/2078.1/219940
    https://repository.uantwerpen.be/docman/irua/050c7b/152412.pdf
    https://hdl.handle.net/10067/1524120151162165141
    https://curis.ku.dk/ws/files/216562272/s13023_018_0784_8.pdf
    https://push-zb.helmholtz-muenchen.de/frontdoor.php?source_opus=53972
    https://hdl.handle.net/11577/3294657
    https://doi.org/10.1186/s13023-018-0784-8
    https://biblio.vub.ac.be/vubir/(3adb9082-292d-497d-a8ad-3f1f80d1525d).html
    https://epub.ub.uni-muenchen.de/62981/
    http://doi.org/10.1186/s13023-018-0784-8
    https://biblio.ugent.be/publication/8574180
    http://hdl.handle.net/1854/LU-8574180
    https://biblio.ugent.be/publication/8574180/file/8574184
    https://mediatum.ub.tum.de/doc/1487007/document.pdf
    https://mediatum.ub.tum.de/doc/1510482/document.pdf
    http://publikationen.ub.uni-frankfurt.de/frontdoor/index/index/docId/47166

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    Přispěvatelé: Judy R. Kersten Philip F. Pratt Danijel Pravdic a další

    Zdroj: Anesthesiology. 115:531-540

    Popis souboru: 531~40

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    Zdroj: Protein Science. 19:1445-1460

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    Zdroj: Galkin, A & Moncada, S 2007, ' S-nitrosation of mitochondrial complex I depends on its structural conformation ', Journal of Biological Chemistry, vol. 282, no. 52, pp. 37448-37453 . https://doi.org/10.1074/jbc.M707543200

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    Přispěvatelé: Nevière, Rémi Delguste, Florian Durand, Arthur a další

    Zdroj: ISSN: 1661-6596.

    Relation: info:eu-repo/semantics/altIdentifier/pmid/27973394; PUBMED: 27973394; PUBMEDCENTRAL: PMC5187875

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