Literature DB >> 3061381

Evidence for the existence of tissue specific isoenzymes of mitochondrial NADH dehydrogenase.

V J Clay1, C I Ragan.   

Abstract

Mitochondrial NADH dehydrogenase from a variety of rat tissues was isolated by immunoprecipitation with an antiserum to the bovine heart enzyme. The subunit composition of the enzyme from liver, kidney and lung differed from that present in heart, brain and skeletal muscle by the absence of an Mr 18,500 protein and the absence of an Mr 17,000 protein, suggesting the existence of tissue-specific isoenzymes.

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Year:  1988        PMID： 3061381     DOI： 10.1016/s0006-291x(88)81034-9

Source DB:  PubMed          Journal:  Biochem Biophys Res Commun        ISSN： 0006-291X            Impact factor:   3.575


  11 in total

1.  Muscle carnitine acetyltransferase and carnitine deficiency in a case of mitochondrial encephalomyopathy.

Authors:  B Melegh; L Seress; T Bedekovics; G Kispál; B Sümegi; K Trombitás; K Méhes
Journal:  J Inherit Metab Dis       Date:  1999-10       Impact factor: 4.982

2.  [3H]dihydrorotenone binding to NADH: ubiquinone reductase (complex I) of the electron transport chain: an autoradiographic study.

Authors:  D S Higgins; J T Greenamyre
Journal:  J Neurosci       Date:  1996-06-15       Impact factor: 6.167

3.  Toxicity of octanoate and decanoate in rat peripheral tissues: evidence of bioenergetic dysfunction and oxidative damage induction in liver and skeletal muscle.

Authors:  Giselli Scaini; Kellen R Simon; Anelise M Tonin; Estela N B Busanello; Alana P Moura; Gustavo C Ferreira; Moacir Wajner; Emilio L Streck; Patrícia F Schuck
Journal:  Mol Cell Biochem       Date:  2011-10-21       Impact factor: 3.396

Review 4.  Mitochondrial myopathies.

Authors:  A H Schapira
Journal:  BMJ       Date:  1989-04-29

5.  The human nuclear-encoded acyl carrier subunit (NDUFAB1) of the mitochondrial complex I in human pathology.

Authors:  R Triepels; J Smeitink; J Loeffen; R Smeets; C Buskens; F Trijbels; L van den Heuvel
Journal:  J Inherit Metab Dis       Date:  1999-04       Impact factor: 4.982

6.  A case of mitochondrial myopathy, lactic acidosis and complex I deficiency.

Authors:  L Bet; N Bresolin; M Moggio; G Meola; A Prelle; A H Schapira; T Binzoni; A Chomyn; F Fortunato; P Cerretelli
Journal:  J Neurol       Date:  1990-11       Impact factor: 4.849

7.  Evaluation of brain and kidney energy metabolism in an animal model of contrast-induced nephropathy.

Authors:  Clarissa A Roza; Giselli Scaini; Isabela C Jeremias; Gabriela K Ferreira; Natalia Rochi; Joana Benedet; Gislaine T Rezin; Francieli Vuolo; Larissa S Constantino; Fabricia C Petronilho; Felipe Dal-Pizzol; Emilio L Streck
Journal:  Metab Brain Dis       Date:  2011-03-25       Impact factor: 3.584

8.  Evidence that glycine induces lipid peroxidation and decreases glutathione concentrations in rat cerebellum.

Authors:  Alana Pimentel Moura; Mateus Grings; Gustavo Flora Marcowich; Anna Paula Bumbel; Belisa Parmeggiani; Leonardo de Moura Alvorcem; Moacir Wajner; Guilhian Leipnitz
Journal:  Mol Cell Biochem       Date:  2014-06-18       Impact factor: 3.396

9.  Fatal infantile mitochondrial cardiomyopathy and myopathy with heterogeneous tissue expression of combined respiratory chain deficiencies.

Authors:  J Müller-Höcker; H Ibel; I Paetzke; T Deufel; W Endres; B Kadenbach; J M Gokel; G Hübner
Journal:  Virchows Arch A Pathol Anat Histopathol       Date:  1991

10.  Glycine intracerebroventricular administration disrupts mitochondrial energy homeostasis in cerebral cortex and striatum of young rats.

Authors:  Alana Pimentel Moura; Mateus Grings; Belisa Dos Santos Parmeggiani; Gustavo Flora Marcowich; Anelise Miotti Tonin; Carolina Maso Viegas; Angela Zanatta; César Augusto João Ribeiro; Moacir Wajner; Guilhian Leipnitz
Journal:  Neurotox Res       Date:  2013-05-03       Impact factor: 3.911
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