Zobrazeno 1 - 10
of 36
pro vyhledávání: '"Kinsey Maundrell"'
Autor:
Mathias Wenes, Anouk Lepez, Vladimir Arinkin, Kinsey Maundrell, Orsolya Barabas, Federico Simonetta, Valérie Dutoit, Pedro Romero, Jean-Claude Martinou, Denis Migliorini
Publikováno v:
Molecular Therapy: Oncology, Vol 32, Iss 4, Pp 200897- (2024)
Adoptive cell transfer with chimeric antigen receptor (CAR)-expressing T cells can induce remarkable complete responses in cancer patients. Therapeutic success has been correlated with central and stem cell-like memory T cell subsets in the infusion
Externí odkaz:
https://doaj.org/article/7ba4b4c02c104d69af18e040907089f6
Autor:
Alexis A. Jourdain, Mirko Koppen, Christopher D. Rodley, Kinsey Maundrell, Naïg Gueguen, Pascal Reynier, Adela M. Guaras, José A. Enriquez, Paul Anderson, Maria Simarro, Jean-Claude Martinou
Publikováno v:
Cell Reports, Vol 10, Iss 7, Pp 1110-1121 (2015)
The mitochondrial genome relies heavily on post-transcriptional events for its proper expression, and misregulation of this process can cause mitochondrial genetic diseases in humans. Here, we report that a novel translational variant of Fas-activate
Externí odkaz:
https://doaj.org/article/b6ce38cb0ef84325becc22f3de66943b
Autor:
Alexis A. Jourdain, Erik Boehm, Jean-Claude Martinou, Kinsey Maundrell, Stéphane Thore, Sofia Zaganelli
Publikováno v:
Nucleic Acids Research
Nucleic Acids Research, Oxford University Press, 2017, 45 (10), pp.6135-6146. ⟨10.1093/nar/gkx164⟩
Nucleic acids research, vol. 45, no. 10, pp. 6135-6146
Nucleic Acids Research, Oxford University Press, 2017, 45 (10), pp.6135-6146. ⟨10.1093/nar/gkx164⟩
Nucleic acids research, vol. 45, no. 10, pp. 6135-6146
FASTK family proteins have been identified as regulators of mitochondrial RNA homeostasis linked to mitochondrial diseases, but much remains unknown about these proteins. We show that CRISPR-mediated disruption of FASTKD1 increases ND3 mRNA level, wh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e9b1928c183bf58555a235bd024046e3
https://hal.archives-ouvertes.fr/hal-02472346
https://hal.archives-ouvertes.fr/hal-02472346
Autor:
Sandra Pierredon, Robert N. Lightowlers, Zofia M.A. Chrzanowska-Lightowlers, Agata Rozanska, Michal Minczuk, Kinsey Maundrell, Sofia Zaganelli, Pedro Rebelo-Guiomar, Christopher A. Powell, Nicolas Hulo, Jean-Claude Martinou, Alexis A. Jourdain
Publikováno v:
The Journal of biological chemistry, vol. 292, no. 11, pp. 4519-4532
The Journal of Biological Chemistry
The Journal of Biological Chemistry
Mitochondrial gene expression is a fundamental process that is largely dependent on nuclear-encoded proteins. Several steps of mitochondrial RNA processing and maturation, including RNA post-transcriptional modification, appear to be spatially organi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc172c2fe97df479b878c1a07887e7e4
https://www.repository.cam.ac.uk/handle/1810/267433
https://www.repository.cam.ac.uk/handle/1810/267433
Publikováno v:
The Journal of Cell Biology
The Journal of cell biology, vol. 212, no. 6, pp. 611-614
The Journal of cell biology, vol. 212, no. 6, pp. 611-614
In mitochondria, DNA replication, gene expression, and RNA degradation machineries coexist within a common nondelimited space, raising the question of how functional compartmentalization of gene expression is achieved. Here, we discuss the recently c
Publikováno v:
European Journal of Biochemistry. 107:577-585
The 20-S globin mRNA-protein complex isolated from the post-polyribosomal supernatant of duck reticulocyte lysates was tested for its translational capacities in two different cell-free protein-synthesizing systems, one derived from wheat germ, the o
Publikováno v:
European Journal of Biochemistry. 112:617-633
Globin messenger ribonucleoprotein (mRNP) particles which have been isolated from duck erythroblast post-polyribosomal supernatant are translationally inactive in vivo and in vitro but contain translatable mRNA active after deproteinisation. They wer
Publikováno v:
The American Journal of Pathology. 165:1839-1848
The main event in the pathogenesis of prion diseases is the conversion of the cellular prion protein (PrP(C)) into the abnormal, protease-resistant prion protein (PrP(res)). PrP(C) is a GPI-anchored protein located in lipid rafts or detergent-resista
Publikováno v:
EMBO J
Prion diseases are characterized by accumulation of misfolded prion protein (PrP(Sc)), and neuronal death by apoptosis. Here we show that nanomolar concentrations of purified PrP(Sc) from mouse scrapie brain induce apoptosis of N2A neuroblastoma cell
Autor:
Evi Schyr, Rosita Accardi, Ellinor Oxelmark, Massimo Tommasino, Ilaria Malanchi, Vito De Pinto, Jean Claude Jauniaux, Antonio Marchini, Kinsey Maundrell
Publikováno v:
Yeast. 19:703-711
A novel family of small proteins, termed p14.5 or YERO57c/YJGFc, has been identified. Independent studies indicate that p14.5 family members are multifunctional proteins involved in several pathways, e.g. regulation of translation or activation of th