paris 12 ue1 biochimie fiche de cours n°13 seances medisup (pr. loric) chaine respiratoire mitochondriale “*les notions indiquées tombent fréquemment au. Les mitochondries sont preparees par centrifugation diffe- rentielle dans un milieu structure de l’antibiotique-activite sur la chaine respiratoire mitochondriale. Le dinitrophénol (DNP) est un composé chimique aromatique de formule C6H4N 2O5. C’est un Le dinitrophénol est un découplant de la chaîne respiratoire mitochondriale. Les intoxications aux dérivés nitrés du phénol sont reconnues.

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Médecine thérapeutique

Please enter recipient e-mail address es. Human molecular genetics, 19, 10, p.

Would you also like to submit a review for miitochondriale item? The E-mail message field is required. Sequential changes in the expression of mitochondrial protein mRNA during the development of brown adipose tissue in bovine and ovine species.

Brown adipose tissue oxidative metabolism contributes to energy expenditure during acute cold exposure in humans. Unexpected evidence for active brown adipose tissue in adult humans.

Physiol Rev ; Cell metabolism, 8, 3, p. Initial download of the metrics may take a while. Reviews User-contributed reviews Add a review and share your thoughts with other readers. Voir aussi Maladie de Charcot-Marie-Tooth de type 4: Whereas the function of p28 remains unknown, p43 is a T3-dependent transcription factor of the mitochondrial genome, acting through dimeric complexes involving at least two other truncated forms of nuclear receptors, mtRXR and mtPPAR.


La Chaîne Respiratoire Flashcards & Quizzes | Brainscape

Muscle physiology in healthy men and women and those with metabolic myopathies Devries MC, Tarnopolsky MA Neurologic clinics, 26, 1, p. Your rating has been recorded. You may send this item to up to five recipients.

The E-mail Address es you entered is are not in a valid format. A PGC1-alpha-dependent myokine that drives brown-fat-like development of white fat and thermogenesis. Reversible infantile respiratory chain deficiency is a unique, genetically heterogenous mitochondrial disease Uusimaa J, Jungbluth H, Fratter C, et al. Maladie de Charcot-Marie-Tooth de type 4: Journal of physiology The,23, p.

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A homozygous mutation in the SCO2 gene causes a spinal muscular atrophy like presentation with stridor and respiratory insufficiency Pronicki M, Kowalski P, Piekutowska-Abramczuk D, et al. Advanced Search Find a Library.

Vaincre les myopathies,p. Archives of neurology, 65, 1, p. Identification of the chwine mutation m. Brown adipocyte progenitor population is modified in obese and diabetic skeletal muscle.


Brown adipose tissue activity controls triglyceride clearance. In parallel, the recent discovery of significant amounts of BAT in human adults has renewed the interest of the scientific community for this tissue.

J Clin Invest ; WorldCat is the world’s largest library catalog, helping you find library materials online.

While both white and brown adipocytes have been considered for a long time as two very close cellular types sharing a common precursor, recent data challenge these conclusions and propose the existence of a new possible type of adipocyte, the BRITE brown-in-white adipocyte. Services Articles citing this article CrossRef 6. Impaired mitochondrial respiration and decreased fatigue resistance followed by severe muscle weakness in skeletal muscle of mtDNA mutator mice Yamada T, Ivarsson N, Hernandez A, et al.

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