المؤلفون: Charif, Majida, Chevrollier, Arnaud, Gueguen, Naïg, Kane, Selma, Bris, Céline, Goudenège, David, Desquiret-Dumas, Valerie, Meunier, Isabelle, Mochel, Fanny, Jeanjean, Luc, Varenne, Fanny, Procaccio, Vincent, Reynier, Pascal, Bonneau, Dominique, Amati-Bonneau, Patrizia, Lenaers, Guy

المساهمون: Université Mohamed 1 Oujda MAROC, MitoVasc - Physiopathologie Cardiovasculaire et Mitochondriale (MITOVASC), Université d'Angers (UA)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre National de la Recherche Scientifique (CNRS), Centre Hospitalier Universitaire d'Angers (CHU Angers), PRES Université Nantes Angers Le Mans (UNAM), SFR UA 4208 Interactions Cellulaires et Applications Thérapeutiques (ICAT), Université d'Angers (UA), Physiologie Fonctionnelle des Organismes Marins (PFOM), Institut Français de Recherche pour l'Exploitation de la Mer (IFREMER), Laboratoire de Biologie Intégrative des Modèles Marins (LBI2M), Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Station biologique de Roscoff = Roscoff Marine Station (SBR), Sorbonne Université (SU)-Centre National de la Recherche Scientifique (CNRS)-Centre National de la Recherche Scientifique (CNRS), Centre Hospitalier Régional Universitaire Montpellier (CHRU Montpellier), Institut des Neurosciences de Montpellier (INM), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Montpellier (UM), CHU Pitié-Salpêtrière AP-HP, Assistance publique - Hôpitaux de Paris (AP-HP) (AP-HP)-Sorbonne Université (SU), Centre Hospitalier Universitaire de Nîmes (CHU Nîmes), Centre Hospitalier Universitaire de Toulouse (CHU Toulouse)

المصدر: ISSN: 2073-4425 ; Genes ; https://hal.science/hal-03861086 ; Genes, 2022, 13 (7), pp.1202. ⟨10.3390/genes13071202⟩.

مصطلحات موضوعية: Dominant optic atrophy, mitochondrial peptidase, mitochondrial dynamic, heterozygous variants, retinal ganglion cell degeneration, [SDV]Life Sciences [q-bio]

الاتاحة: https://hal.science/hal-03861086
https://hal.science/hal-03861086v1/document
https://hal.science/hal-03861086v1/file/GENEJOURNAL-S-21-00887%20%282%29.pdf
https://doi.org/10.3390/genes13071202

المؤلفون: Gispert, Suzana, Parganlija, Dajana, Klinkenberg, Michael, Droese, Stefan, Wittig, Ilka, Mittelbronn, Michel, Grzmil, Paweł, Koob, Sebastian, Hamann, Andrea, Walter, Michael, Buechel, Finja, Adler, Thure, de Angelis, Martin Hrabe, Busch, Dirk H., Zell, Andreas, Reichert, Andreas S., Brandt, Ulrich, Osiewacz, Heinz D., Jendrach, Marina, Auburger, Georg

مصطلحات موضوعية: CLPX, infertility, mitochondrial peptidase, growth retardation

Relation: http://ruj.uj.edu.pl/xmlui/handle/item/8706

الاتاحة: http://ruj.uj.edu.pl/xmlui/handle/item/8706
https://doi.org/10.1093/hmg/ddt338

المؤلفون: Paweł Grzmil, Martin Hrabé de Angelis, Michael Klinkenberg, Heinz D. Osiewacz, Suzana Gispert, Sebastian Koob, Georg Auburger, Ulrich Brandt, Dirk H. Busch, Michael A. Walter, Marina Jendrach, Andreas S. Reichert, Thure Adler, Stefan Dröse, Ilka Wittig, Andreas Zell, Finja Büchel, Michel Mittelbronn, Andrea Hamann, Dajana Parganlija

المصدر: Human Molecular Genetics, 22, 24, pp. 4871-87
Europe PubMed Central
Human Molecular Genetics, 22, 4871-87
Human Molecular Genetics
Hum. Mol. Genet. 22, 4871-4887 (2013)

مصطلحات موضوعية: Male, Mitochondrion, CLPX, Lymphocyte Activation, Mice, 0302 clinical medicine, T-Lymphocyte Subsets, Gene Order, Genetics (clinical), Growth Disorders, Genetics, Mice, Knockout, 0303 health sciences, biology, Proteolytic enzymes, Mitochondrial medicine Energy and redox metabolism [IGMD 8], General Medicine, Endopeptidase Clp, Articles, Phenotype, Cell biology, Mitochondria, medicine.anatomical_structure, Mitochondrial medicine [IGMD 8], Mitochondrial matrix, Female, Inflammation Mediators, infertility, Mitochondrial DNA, Cell Respiration, growth retardation, Motor Activity, DNA, Mitochondrial, mitochondrial peptidase, 03 medical and health sciences, Mitochondrial unfolded protein response, medicine, Animals, Gonads, Hearing Loss, Molecular Biology, 030304 developmental biology, Spermatid, Disease Models, Animal, Chaperone (protein), Infertility, Mutation, biology.protein, 030217 neurology & neurosurgery, Spleen, Molecular Chaperones

وصف الملف: application/pdf

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9aae6b27bcffda0dc96f248e269ad894
https://hdl.handle.net/2066/125623