Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Valentina Strecker"'
Autor:
Birgit M. Repp, Elisa Mastantuono, Charlotte L. Alston, Manuel Schiff, Tobias B. Haack, Agnes Rötig, Anna Ardissone, Anne Lombès, Claudia B. Catarino, Daria Diodato, Gudrun Schottmann, Joanna Poulton, Alberto Burlina, An Jonckheere, Arnold Munnich, Boris Rolinski, Daniele Ghezzi, Dariusz Rokicki, Diana Wellesley, Diego Martinelli, Ding Wenhong, Eleonora Lamantea, Elsebet Ostergaard, Ewa Pronicka, Germaine Pierre, Hubert J. M. Smeets, Ilka Wittig, Ingrid Scurr, Irenaeus F. M. de Coo, Isabella Moroni, Joél Smet, Johannes A. Mayr, Lifang Dai, Linda de Meirleir, Markus Schuelke, Massimo Zeviani, Raphael J. Morscher, Robert McFarland, Sara Seneca, Thomas Klopstock, Thomas Meitinger, Thomas Wieland, Tim M. Strom, Ulrike Herberg, Uwe Ahting, Wolfgang Sperl, Marie-Cecile Nassogne, Han Ling, Fang Fang, Peter Freisinger, Rudy Van Coster, Valentina Strecker, Robert W. Taylor, Johannes Häberle, Jerry Vockley, Holger Prokisch, Saskia Wortmann
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 13, Iss 1, Pp 1-10 (2018)
Abstract Background Mitochondrial acyl-CoA dehydrogenase family member 9 (ACAD9) is essential for the assembly of mitochondrial respiratory chain complex I. Disease causing biallelic variants in ACAD9 have been reported in individuals presenting with
Externí odkaz:
https://doaj.org/article/129e2104cafd486f9cf68aead98de16c
Autor:
Jürgen Bereiter-Hahn, August Bernd, Heike Beschmann, Irina Eberle, Stefan Kippenberger, Maila Rossberg, Valentina Strecker, Nadja Zöller
Publikováno v:
Acta Medica, Vol 57, Iss 2, Pp 41-48 (2014)
Egg-oil (Charismon©) is known for its beneficial action in wound healing and other skin irritancies and its antibacterial activity. The physiological basis for these actions has been investigated using cells in culture: HaCaT-cells (immortalized hum
Externí odkaz:
https://doaj.org/article/4e69106a1a9640b2b6e051662b60c617
Publikováno v:
PLoS ONE, Vol 11, Iss 8, p e0160258 (2016)
Mitochondrial cristae are connected to the inner boundary membrane via crista junctions which are implicated in the regulation of oxidative phosphorylation, apoptosis, and import of lipids and proteins. The MICOS complex determines formation of crist
Externí odkaz:
https://doaj.org/article/d24bfcae1c08422cacb184e941d73236
Autor:
Lore Becker, Eva Kling, Evelyn Schiller, Ramona Zeh, Anja Schrewe, Sabine M Hölter, Ilona Mossbrugger, Julia Calzada-Wack, Valentina Strecker, Ilka Wittig, Iulia Dumitru, Tina Wenz, Andreas Bender, Michaela Aichler, Dirk Janik, Frauke Neff, Axel Walch, Leticia Quintanilla-Fend, Thomas Floss, Raffi Bekeredjian, Valérie Gailus-Durner, Helmut Fuchs, Wolfgang Wurst, Thomas Meitinger, Holger Prokisch, Martin Hrabě de Angelis, Thomas Klopstock
Publikováno v:
PLoS ONE, Vol 9, Iss 12, p e114918 (2014)
Recently, mutations in the mitochondrial translation optimization factor 1 gene (MTO1) were identified as causative in children with hypertrophic cardiomyopathy, lactic acidosis and respiratory chain defect. Here, we describe an MTO1-deficient mouse
Externí odkaz:
https://doaj.org/article/5fb946e312a94325a7492aee89c6f092
Autor:
Britta Muster, Wladislaw Kohl, Ilka Wittig, Valentina Strecker, Friederike Joos, Winfried Haase, Jürgen Bereiter-Hahn, Karin Busch
Publikováno v:
PLoS ONE, Vol 5, Iss 7, p e11910 (2010)
BACKGROUND: Mitochondria, the main suppliers of cellular energy, are dynamic organelles that fuse and divide frequently. Constraining these processes impairs mitochondrial is closely linked to certain neurodegenerative diseases. It is proposed that f
Externí odkaz:
https://doaj.org/article/451a36c6b40a4624ae16649e34934d6e
Publikováno v:
Journal of Biological Chemistry. 292:5216-5226
The yeast Rcf1 protein is a member of the conserved family of proteins termed the hypoxia-induced gene (domain) 1 (Hig1 or HIGD1) family. Rcf1 interacts with components of the mitochondrial oxidative phosphorylation system, in particular the cytochro
Autor:
Christoph S. Clemen, Viktoriya Peeva, Harald Herrmann, Britta Eggers, Carolin Berwanger, Lilli Winter, Cornelia Kornblum, Wolfram S. Kunz, Katalin Barkovits, Valentina Strecker, Rolf Schröder, Ilka Wittig, Rudolf A. Kley, Juliana Heidler, Katrin Marcus, Frédéric Chevessier
Publikováno v:
Acta Neuropathologica
Secondary mitochondrial dysfunction is a feature in a wide variety of human protein aggregate diseases caused by mutations in different proteins, both in the central nervous system and in striated muscle. The functional relationship between the expre
Autor:
Juliana Heidler, Ravi K. Singhal, Christine Kruse, Klaus Zwicker, Johannes M. Herrmann, Ilka Wittig, Valentina Strecker, Lea Düsterwald, Benedikt Westermann, Doron Rapaport
Publikováno v:
Molecular Biology of the Cell
Coi1 was identified as an important assembly factor for mitochondrial complex III, complex IV, and their supercomplexes. Deletion of COI1 in yeast cells results in severe growth defect, reduced membrane potential, hampered respiration, and altered as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da42cf8f6ad7c3c4676bd48545f531fe
http://publikationen.ub.uni-frankfurt.de/frontdoor/index/index/docId/45062
http://publikationen.ub.uni-frankfurt.de/frontdoor/index/index/docId/45062
Publikováno v:
The Journal of biological chemistry. 292(13)
The yeast Rcf1 protein is a member of the conserved family of proteins termed the hypoxia-induced gene (domain) 1 (Hig1 or HIGD1) family. Rcf1 interacts with components of the mitochondrial oxidative phosphorylation system, in particular the cytochro
Autor:
Thomas Meitinger, Detlef Boehm, Eleonora Lamantea, Graziella Uziel, Boris Rolinski, Hans-Werner Mewes, Saskia Biskup, Jonathan Hoser, Massimo Zeviani, Federica Invernizzi, Arcangela Iuso, Joanna Poulton, Tobias B. Haack, Thorsten Schmidt, Holger Prokisch, Birgit Haberberger, Katharina Danhauser, Valentina Strecker, Ilka Wittig
An isolated defect of respiratory chain complex I activity is a frequent biochemical abnormality in mitochondrial disorders. Despite intensive investigation in recent years, in most instances, the molecular basis underpinning complex I defects remain
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::01684733634c50430d1fee85f550d47c
https://ora.ox.ac.uk/objects/uuid:03fdd482-6107-48b8-888b-c999ac96f82e
https://ora.ox.ac.uk/objects/uuid:03fdd482-6107-48b8-888b-c999ac96f82e