Výsledky vyhledávání - "Mitochondrial Membranes/chemistry"

Distribution and dynamics of quinones in the lipid bilayer mimicking the inner membrane of mitochondria

Autor: Ilpo Vattulainen, Vivek Sharma, Petri Kaurola, Amanda Vonk, Tomasz Róg

Publikováno v: Kaurola, P, Sharma, V, Vonk, A, Vattulainen, I & Róg, T 2016, ' Distribution and dynamics of quinones in the lipid bilayer mimicking the inner membrane of mitochondria ', Biochimica et Biophysica Acta-Biomembranes, vol. 1858, no. 9, pp. 2116-2122 . https://doi.org/10.1016/j.bbamem.2016.06.016

Quinone and its analogues (Q) constitute an important class of compounds that perform key electron transfer reactions in oxidative- and photo-phosphorylation. In the inner membrane of mitochondria, ubiquinone molecules undergo continuous redox transi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f12c36a24a5a1f902b6baf727fabaa10
https://pubmed.ncbi.nlm.nih.gov/27342376

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Targeting the Retinoblastoma Protein by MC007L, Gene Product of the Molluscum Contagiosum Virus: Detection of a Novel Virus-Cell Interaction by a Member of the Poxviruses

Autor: Martin Zeier, Jean-Claude Martinou, Walter Muranyi, Paola Massimi, Stefan Mohr, Stéphanie Grandemange, Lawrence Banks, Gholamreza Darai

Publikováno v: Journal of virology, Vol. 82, No 21 (2008) pp. 10625-33

The human pathogenic poxvirus molluscum contagiosum virus (MCV) is the causative agent of benign neoplasm, with worldwide incidence, characterized by intraepidermal hyperplasia and hypertrophy of cells. Here, we present evidence that the MC007L prote

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ba804ae653c2dc4b436cdea9dfa753f
https://doi.org/10.1128/jvi.01187-08

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LETM1, deleted in Wolf-Hirschhorn syndrome is required for normal mitochondrial morphology and cellular viability

Autor: Alberto Casarin, Leonardo Salviati, Kai Stefan Dimmer, Luca Scorrano, Francesca Navoni, Andreas Winterpacht, Sabine Endele, Eva Trevisson

Publikováno v: Human Molecular Genetics, Vol. 17, No 2 (2008) pp. 201-214

Wolf-Hirschhorn syndrome (WHS) is a complex congenital syndrome caused by a monoallelic deletion of the short arm of chromosome 4. Seizures in WHS have been associated with deletion of LETM1 gene. LETM1 encodes for the human homologue of yeast Mdm38p

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf8f277c72d24ab76ebcf0879920cacb
https://archive-ouverte.unige.ch/unige:19109

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