The DOI matches its Crossref record; 112 of the 115 references it cites were found in a registry or an index.
Human Complex I deficiency: Clinical spectrum and involvement of oxygen free radicals in the pathogenicity of the defect
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“The second enzyme is located near the mitochondrial inner membrane. This is a SOD that binds manganese in its catalytic centre (SOD2 or Mn-SOD) [71,72].”
From Superoxide Anion Chemistry—Its Role at the Core of the Innate Immunity (2023) · cites this paper as [71]
Citations
Cites
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Research works printed but not linked: 6
- Robinson, 1994, Lacticacidemia, Biochim. Biophys. Acta, 1182, 237
- Sardanelli, 1995, Phosphorylation of an 18 kDa subunit of bovine heart complex I by a cAMP dependent kinase, FEBS Lett., 377, 470
- Chomyn, 1988, The site of synthesis of the iron–sulfur subunits of the flavoprotein and iron protein factions of human NADH dehydrogenase, J. Biol. Chem., 31, 16395, 10.1016/S0021-9258(18)37606-3 · DOI
- De Vries, 1996, Genetic and biochemical impairment of mitochondrial complex I activity in a family with Leber Hereditary Optic Neuropathy and Hereditary Spastic Dystonia, Am. J. Hum. Genet., 58, 703
- Jun, 1994, A mitochondrial DNA mutation at nucleotide pair 14 459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber Hereditary Optic Neuropathy and Dystonia, Proc. Natl. Acad. Sci. U.S.A., 91, 6206, 10.1073/pnas.91.13.6206 · DOI
- Beyer, 1991, An analysis of the role of coenzyme Q in free radical generation and as an oxidant, Biochem. Cell. Biol., 70, 343
Cited by
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Items 201–223 of 223
Genetic Discrimination of Grade 3 and Grade 4 Gliomas by Artificial Neural Network
Mekler, A. A., Schwartz, D. R., & Savelieva, O. E. (2023) · Cellular and Molecular Neurobiology · doi:10.1007/s10571-023-01448-z · Cited by 1
Pasqualotto, B. A., Tegeman, C., Frame, A. K., McPhedrain, R., Halangoda, K., Sheldon, C. A., & Rintoul, G. L. (2024) · Experimental Cell Research · doi:10.1016/j.yexcr.2024.114075 · Cited by 1
Moudgil, R., Michelakis, E. D., & Archer, S. L. (2006) · Kluwer Academic Publishers eBooks · doi:10.1007/1-4020-7858-7_9 · Cited by 1
Mitochondrial Respiratory Function Decline in Aging and Life-Span Extension by Caloric Restriction
Wu, S., Wu, Y., Wang, C., Lee, W., & Wei, Y. (2010) · Humana Press eBooks · doi:10.1007/978-1-60761-602-3_7
Opii, W. O. (2006) · UKnowledge (University of Kentucky)
Neurodegeneration caused by mitochondrial complex I dysfunction in the mouse retina
Zhang, X. (2005) · Texas ScholarWorks (Texas Digital Library)
Buettner, G. R., Oberley, L. W., Spitz, D. R., & Domann, F. E. (2003)
Aging: Is caloric restriction anti-aging?
Chatzidaki, E. E. (2010)
Mitochondrial diseases of nuclear origin
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López, J. E. D.-A., & Huesca-Hernández, F. (2007) · Anales de otorrinolaringología mexicana
Structure, Function and Pathology of Complex I
Duborjal, H., Beugnot, R., Procaccio, V., Issartel, J., & Lunardi, J. (1999) · Springer eBooks · doi:10.1007/978-3-642-59884-5_6
Rasmussen, A. K. (2001) · RUCforsk (Roskilde University)
Regulation of metabolism by the oncoprotein c-Myc
Edmunds, L. R. (2015) · D-Scholarship@Pitt (University of Pittsburgh)
The Genetics of Cardiac Electrophysiology in Humans
Pyeritz, R. E. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-383834-6.00057-4
Eshraghi, M. (2017) · uO Research (University of Ottawa) · doi:10.20381/ruor-20746
Association of heteroplasmic mutations in the mitochondrial genome with coronary heart disease
Орехова, Н. А., Sobenin, I. A., Mitrofanov, K. Y., Sazonova, M. A., Postnov, A. Y., Карагодин, В. П., & Orekhov, A. N. (2018) · Zhurnal «Patologicheskaia fiziologiia i eksperimental`naia terapiia» · doi:10.25557/0031-2991.2018.01.4-10
Mitochondrial dysfunction in reproductive and developmental toxicity
Palmeira, C. M., Machado, I. F., & Ramalho‐Santos, J. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-89773-0.00054-0
Zeviani, M., & Viscomi, C. F. (2008) · Faculty Opinions – Post-Publication Peer Review of the Biomedical Literature · doi:10.3410/f.1108057.562178
Isolated Mitochondrial Complex Deficiencies
Janssen, M. C. H., de Vries, M. C., de Boer, L., & Rodenburg, R. J. (2022) · Springer eBooks · doi:10.1007/978-3-030-67727-5_44
Unravelling the role of nutraceutical supplements in treatment of Parkinson’s Disease
Kakoty, V., Kumar, S., Parasar, S., Pamthied, S., Wardhan, Y., Vishwas, S., Gulati, M., Gupta, G., Sulakhiya, K., Dua, K., et al. (2024) · BIO Web of Conferences · doi:10.1051/bioconf/20248601045
Terada, T., Therriault, J., Kang, M. S. P., Savard, M., Pascoal, T. A., Lussier, F. Z., Tissot, C., Wang, Y.-T., Benedet, A. L., Matsudaira, T., et al. (2021) · Figshare · doi:10.6084/m9.figshare.14490235
Metadata
- Authors
- Robinson, B. H.
- Affiliations
- University of Toronto (CA)
- Corresponding author
- Robinson, Brian H
- Venue
- Biochimica et Biophysica Acta (BBA) - Bioenergetics
- Publisher
- Elsevier BV
- Published
- 1998-05
- Volume
- 1364
- Issue
- 2
- Pages
- 271-286
- ISSN
- 0005-2728 (ISSN-L)
- OpenAlex
- W2067124266
- Cited by
- 223
- References
- 115
- Citations by year
- 2025: 3 · 2024: 2 · 2023: 2 · 2022: 5 · 2021: 5 · 2020: 1 · 2019: 7 · 2018: 5 · 2017: 4 · 2016: 6 · 2015: 6 · 2014: 5 · 2013: 6 · 2012: 6
- FWCI
- 1.13
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Biochimica et Biophysica Acta (BBA) - Bioenergetics (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Heart and Stroke Foundation of Canada
- Australian Government
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Metabolism and Genetic Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Coenzyme Q10 studies and effects
- Keywords
- complex I deficiency, mitochondrial disease, clinical spectrum, oxygen free radicals, oxidative stress, lactic acidosis, optic neuropathy, exercise intolerance, mitochondrial DNA, nuclear DNA
- MeSH terms
- Free Radicals, Humans, Metabolism, Inborn Errors, NAD(P)H Dehydrogenase (Quinone)
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