Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Lisa Myketin"'
Autor:
Daniel Poveda-Huertes, Asli Aras Taskin, Ines Dhaouadi, Lisa Myketin, Adinarayana Marada, Lukas Habernig, Sabrina Büttner, F-Nora Vögtle
Publikováno v:
PLoS Genetics, Vol 17, Iss 7, p e1009664 (2021)
Mitochondrial defects can cause a variety of human diseases and protective mechanisms exist to maintain mitochondrial functionality. Imbalances in mitochondrial proteostasis trigger a transcriptional program, termed mitochondrial unfolded protein res
Externí odkaz:
https://doaj.org/article/4bc527a29d51462a9590e7b42257a8e8
Autor:
Natalie M. Niemi, Gary M. Wilson, Katherine A. Overmyer, F.-Nora Vögtle, Lisa Myketin, Danielle C. Lohman, Kathryn L. Schueler, Alan D. Attie, Chris Meisinger, Joshua J. Coon, David J. Pagliarini
Publikováno v:
Nature Communications, Vol 10, Iss 1, Pp 1-14 (2019)
The mitochondria houses several phosphatases, but their function is not well characterized. Here, the authors show that mitochondrial phosphatase Pptc7 is important during development for proper mitochondrial function and has a role regulating protei
Externí odkaz:
https://doaj.org/article/0cc3120d036a46b9807f1cae4a084aeb
Autor:
Lisa Myketin, Sabrina Büttner, Ines Dhaouadi, F.-Nora Vögtle, A. A. Taskin, Daniel Poveda-Huertes, Lukas Habernig, Adinarayana Marada
Publikováno v:
PLoS Genetics
PLoS Genetics, Vol 17, Iss 7, p e1009664 (2021)
PLoS Genetics, Vol 17, Iss 7, p e1009664 (2021)
Mitochondrial defects can cause a variety of human diseases and protective mechanisms exist to maintain mitochondrial functionality. Imbalances in mitochondrial proteostasis trigger a transcriptional program, termed mitochondrial unfolded protein res
Autor:
Daniel Papinski, Daniel Poveda-Huertes, Chris Meisinger, Lukas Habernig, Patrycja Mulica, F.-Nora Vögtle, Lutz Hein, Oliver Kretz, Adinarayana Marada, Sergi Tosal-Castano, Claudine Kraft, Lisa Myketin, Sabrina Büttner, Ralf Gilsbach, A. A. Taskin, Cansu Kücükköse, Stanka Matic, Mariya Licheva
Publikováno v:
Molecular Cell
Summary The mitochondrial proteome is built mainly by import of nuclear-encoded precursors, which are targeted mostly by cleavable presequences. Presequence processing upon import is essential for proteostasis and survival, but the consequences of dy
Autor:
F.-Nora Vögtle, Carolyn F. Delto, Hiltrud Muhle, Nils Burger, Marisa W. Friederich, Johanna A. Jähn, Ingo Helbig, Audrey Burnett, Maie Walsh, Naomichi Matsumoto, Cansu Kücükköse, Björn Brändl, Franz-Josef Müller, Hung-Chun Yu, Andreas van Baalen, Deepali N. Shinde, Austin Larson, Susan M. White, Alice Basinger, Noriko Miyake, Oliver Keminer, Ulrich Stephani, Manuela Pendziwiat, Dirk Mossmann, Lisa Myketin, Katherine L. Helbig, Mark A. Lovell, Johan L.K. Van Hove
Publikováno v:
American Journal of Human Genetics
Mitochondrial disorders causing neurodegeneration in childhood are genetically heterogeneous, and the underlying genetic etiology remains unknown in many affected individuals. We identified biallelic variants in PMPCB in individuals of four families