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  • 1-10 ل  11 نتائج ل ""Electron Transport Complex I""

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Geographic : china
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Academic Journal

Metformin protects high glucose‑cultured cardiomyocytes from oxidative stress by promoting NDUFA13 expression and mitochondrial biogenesis via the AMPK signaling pathway.

  • Authors : Liu XD; Department of Cardiology, Tongji Hospital, School of Medicine, Tongji University, Shanghai 200065, P.R. China.; Li YG

Subjects: Electron Transport Complex I/Electron Transport Complex I/Electron Transport Complex I/*metabolism ; Metformin/Metformin/Metformin/*pharmacology ; Molecular Chaperones/Molecular Chaperones/Molecular Chaperones/*metabolism

  • Source: Molecular medicine reports [Mol Med Rep] 2020 Dec; Vol. 22 (6), pp. 5262-5270. Date of Electronic Publication: 2020 Oct 14.Publisher: D. A. Spandidos Country of Publication: Greece NLM ID: 101475259 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Mitochondrial respiratory chain enzyme assay and DNA analysis in peripheral blood leukocytes for the etiological study of Chinese children with Leigh syndrome due to complex I deficiency.

  • Authors : Ma YY; Department of Pediatrics, Peking University First Hospital , No. 1, Xi-an-men Road, Xicheng District, Beijing 100034 , P.R. China.; Wu TF

Subjects: Point Mutation*; Electron Transport Complex I/Electron Transport Complex I/Electron Transport Complex I/*genetics ; Electron Transport Complex I/Electron Transport Complex I/Electron Transport Complex I/*metabolism Mitochondrial complex I deficiency

  • Source: Mitochondrial DNA [Mitochondrial DNA] 2013 Feb; Vol. 24 (1), pp. 67-73. Date of Electronic Publication: 2012 Sep 05.Publisher: Informa Healthcare Country of Publication: England NLM ID: 101487102 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Mutations in mitochondrially encoded complex I enzyme as the second common cause in a cohort of Chinese patients with mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes.

  • Authors : Zhao D; Department of Neurology, Peking University First Hospital, Beijing, China.; Hong D

Subjects: Mutation*; DNA, Mitochondrial/DNA, Mitochondrial/DNA, Mitochondrial/*chemistry ; Electron Transport Complex I/Electron Transport Complex I/Electron Transport Complex I/*genetics

  • Source: Journal of human genetics [J Hum Genet] 2011 Nov; Vol. 56 (11), pp. 759-64. Date of Electronic Publication: 2011 Aug 18.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 9808008 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Novel mitochondrial DNA mutations associated with Chinese familial hypertrophic cardiomyopathy.

  • Authors : Wei YL; Institute of Material Medica and Department of Pharmaceutics, School of Pharmacy, Third Military Medical University, Chongqing, China.; Yu CA

Subjects: DNA, Mitochondrial* ; Mutation*; Asian People/Asian People/Asian People/*genetics

  • Source: Clinical and experimental pharmacology & physiology [Clin Exp Pharmacol Physiol] 2009 Sep; Vol. 36 (9), pp. 933-9. Date of Electronic Publication: 2009 Mar 26.Publisher: Wiley-Blackwell Country of Publication: Australia NLM ID: 0425076 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Mitochondrial NADH Dehydrogenase Subunit 3 Polymorphism Associated with an Earlier Age at Onset in Male Machado-Joseph disease Patients.

  • Authors : Chen S; Department of Neurology and Research Center of Neurology in Second Affiliated Hospital and the Collaborative Innovation Center for Brain Science, Zhejiang University School of Medicine, Hangzhou, China.; Department of Neurology and Institute of Neurology, Huashan Hospital, Shanghai Medical College, Fudan University, Shanghai, China.

Subjects: Polymorphism, Single Nucleotide*; Electron Transport Complex I/Electron Transport Complex I/Electron Transport Complex I/*genetics ; Machado-Joseph Disease/Machado-Joseph Disease/Machado-Joseph Disease/*genetics

  • Source: CNS neuroscience & therapeutics [CNS Neurosci Ther] 2016 Jan; Vol. 22 (1), pp. 38-42. Date of Electronic Publication: 2015 Sep 04.Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 101473265 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Female genetic distribution bias in mitochondrial genome observed in Parkinson's Disease patients in northern China.

  • Authors : Chu Q; School of Forensic Medicine, China Medical University, No.77 Puhe Road, Shenyang North New Area, Shenyang 110122, P.R. China.; Luo X

Subjects: Asian People/Asian People/Asian People/*genetics ; DNA, Mitochondrial/DNA, Mitochondrial/DNA, Mitochondrial/*genetics ; Parkinson Disease/Parkinson Disease/Parkinson Disease/*genetics

  • Source: Scientific reports [Sci Rep] 2015 Nov 25; Vol. 5, pp. 17170. Date of Electronic Publication: 2015 Nov 25.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN:

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Academic Journal

Phylogeographic structure of cotton pest Adelphocoris suturalis (Hemiptera: Miridae): strong subdivision in China inferred from mtDNA and rDNA ITS markers.

  • Authors : Zhang L; Department of Entomology, China Agricultural University, Beijing 100193, China.; Cotton Research Institute, Chinese Academy of Agricultural Sciences, Anyang, Henan 455000, China.

Subjects: Evolution, Molecular*; DNA, Mitochondrial/DNA, Mitochondrial/DNA, Mitochondrial/*genetics ; DNA, Ribosomal Spacer/DNA, Ribosomal Spacer/DNA, Ribosomal Spacer/*genetics

  • Source: Scientific reports [Sci Rep] 2015 Sep 21; Vol. 5, pp. 14009. Date of Electronic Publication: 2015 Sep 21.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN:

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Academic Journal

Do nuclear-encoded core subunits of mitochondrial complex I confer genetic susceptibility to schizophrenia in Han Chinese populations?

  • Authors : Li X; 1] Key Laboratory of Animal Models and Human Disease Mechanisms of the Chinese Academy of Sciences &Yunnan Province, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming 650223, China [2] Kunming College of Life Science, University of Chinese Academy of Sciences, Kunming 650223, China.; Zhang W

Subjects: Genetic Predisposition to Disease*; Electron Transport Complex I/Electron Transport Complex I/Electron Transport Complex I/*genetics ; NADH Dehydrogenase/NADH Dehydrogenase/NADH Dehydrogenase/*genetics

  • Source: Scientific reports [Sci Rep] 2015 Jun 08; Vol. 5, pp. 11076. Date of Electronic Publication: 2015 Jun 08.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN:

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Academic Journal

Novel mutations m.3959G>A and m.3995A>G in mitochondrial gene MT-ND1 associated with MELAS.

  • Authors : Lin J; Department of Neurology, Huashan Hospital .; Zhao CB

Subjects: Electron Transport Complex I/Electron Transport Complex I/Electron Transport Complex I/*metabolism ; MELAS Syndrome/MELAS Syndrome/MELAS Syndrome/*genetics ; MELAS Syndrome/MELAS Syndrome/MELAS Syndrome/*pathology

  • Source: Mitochondrial DNA [Mitochondrial DNA] 2014 Feb; Vol. 25 (1), pp. 56-62. Date of Electronic Publication: 2013 Jul 08.Publisher: Informa Healthcare Country of Publication: England NLM ID: 101487102 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

Genetic variability within and among Haemonchus contortus isolates from goats and sheep in China.

Subjects: Genetic Variation*; Goat Diseases/Goat Diseases/Goat Diseases/*parasitology ; Haemonchiasis/Haemonchiasis/Haemonchiasis/*veterinary

  • Source: Parasites & vectors [Parasit Vectors] 2013 Sep 25; Vol. 6 (1), pp. 279. Date of Electronic Publication: 2013 Sep 25.Publisher: BioMed Central Country of Publication: England NLM ID: 101462774 Publication Model: Electronic Cited Medium: Internet ISSN: 1756-3305

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  • 1-10 ل  11 نتائج ل ""Electron Transport Complex I""