Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Mitochondrial protein processing"'
Autor:
Katie Powell, Naoki Oishi, Ji Luo, Xiaoling Luo, Sean P. Martin, Hien Dang, Xiaolin Wu, Snorri S. Thorgeirsson, Qing-Hai Ye, Hu-Liang Jia, Dana A. Dominguez, Xin Wei Wang, Gary Mitchell, Rachel Bagni, Jin-Qiu Chen, Atsushi Takai, Subreen A. Khatib, Lun-Xiu Qin
Publikováno v:
Cancer Research. 79:2379-2391
Hepatocellular carcinoma (HCC) is a genetically heterogeneous disease for which a dominant actionable molecular driver has not been identified. Patients with the stem cell–like EpCAM+AFP+ HCC subtype have poor prognosis. Here, we performed a genome
Publikováno v:
FEBS lettersReferences. 595(8)
Mitochondria contain more than 1000 different proteins, including several proteolytic enzymes. These mitochondrial proteases form a complex system that performs limited and terminal proteolysis to build the mitochondrial proteome, maintain, and contr
Autor:
Chitra Prasad, Oleksandr Gakh, Jean-Pierre Desvignes, Mirna Assoum, Nicole M. Roslin, Christian R. Marshall, Nicolas Lévy, Susan Blaser, Alexis Brice, André Mégarbané, Guy A. Rouleau, Alexandra Durr, Valérie Delague, Grazia Isaya, Julian Raiman, Andrew D. Paterson, Rebekah Jobling, Stephen W. Scherer, Grace Yoon, Tara Paton, Nathalie Roeckel-Trevisiol, Emmanuel Roze, Cyril Mignot
Publikováno v:
Brain-A Journal of Neurology
Brain-A Journal of Neurology, 2015, 138 (6), pp.1505-1517. ⟨10.1093/brain/awv057⟩
Brain-A Journal of Neurology, Oxford University Press (OUP), 2015, 138 (6), pp.1505-1517. ⟨10.1093/brain/awv057⟩
Paediatrics Publications
Brain-A Journal of Neurology, 2015, 138 (6), pp.1505-1517. ⟨10.1093/brain/awv057⟩
Brain-A Journal of Neurology, Oxford University Press (OUP), 2015, 138 (6), pp.1505-1517. ⟨10.1093/brain/awv057⟩
Paediatrics Publications
International audience; Non-progressive cerebellar ataxias are a rare group of disorders that comprise approximately 10% of static infantile encephalopathies. We report the identification of mutations in PMPCA in 17 patients from four families affect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6133d4f56c814872f31298f5fa27c53d
https://hal.science/hal-01680921
https://hal.science/hal-01680921
Autor:
Patrick F. Chinnery, Rita Horvath
Publikováno v:
Brain. 138:1451-1453
This scientific commentary refers to ‘ PMPCA mutations cause abnormal mitochondrial protein processing in patients with non-progressive cerebellar ataxia’, by Jobling et al. (doi:10.1093/brain/awv057). In the not too distant past, non-progressive
Publikováno v:
Protein Science. 11:1026-1035
Most mitochondrial matrix space proteins are synthesized as a precursor protein, and the N-terminal extension of amino acids that served as the leader sequence is removed after import by the action of a metalloprotease called mitochondrial processing
Publikováno v:
Plant Molecular Biology. 38:311-338
Mitochondrial biogenesis requires a coordinated expression of both the nuclear and the organellar genomes and specific intracellular protein trafficking, processing and assembly machinery. Most mitochondrial proteins are synthesised as precursor prot
Publikováno v:
Journal of Experimental Biology. 200:321-330
A novel Saccharomyces cerevisiae mutant, unable to grow in the presence of 12.5 mmol l−1 EGTA, was isolated. The phenotype of the mutant is caused by a single amino acid change (Gly149 to Arg) in the essential yeast cell division cycle gene CDC1. T
Autor:
Alicja Omanska-Klusek, Eleonora Napoli, Dolores Garcia-Arocena, Cedrick Barrow, Christine Iwahashi, Catherine Ross-Inta, Paul J. Hagerman, Elizabeth Berry-Kravis, Randi J Hagerman, Danielle Sakaguchi, Cecilia R Giulivi, Sarah Wong
Publikováno v:
Human molecular genetics. 20(15)
Fragile X-associated tremor/ataxia syndrome (FXTAS) is a late-onset neurodegenerative disorder that affects individuals who are carriers of small CGG premutation expansions in the fragile X mental retardation 1 (FMR1) gene. Mitochondrial dysfunction
Publikováno v:
Protein Trafficking in Plant Cells ISBN: 9789401062299
Mitochondrial biogenesis requires a coordinated expression of both the nuclear and the organellar genomes and specific intracellular protein trafficking, processing and assembly machinery. Most mitochondrial proteins are synthesised as precursor prot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::320beaaccb5b4f01addbf25cf26131c9
https://doi.org/10.1007/978-94-011-5298-3_16
https://doi.org/10.1007/978-94-011-5298-3_16
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