Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Nathalie Krusy"'
Autor:
Aviel Even, Giovanni Morelli, Silvia Turchetto, Michal Shilian, Romain Le Bail, Sophie Laguesse, Nathalie Krusy, Ariel Brisker, Alexander Brandis, Shani Inbar, Alain Chariot, Frédéric Saudou, Paula Dietrich, Ioannis Dragatsis, Bert Brone, Loïc Broix, Jean-Michel Rigo, Miguel Weil, Laurent Nguyen
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-14 (2021)
Microtubule tracks are important for the transport of molecules within axons. Here, the authors show that ATAT1, the enzyme responsible for acetylating a-tubulin, receives acetyl groups from ATP citrate lyase whose stability is regulated by Elongator
Externí odkaz:
https://doaj.org/article/56060abcde1a4c4f802c73b700424575
Autor:
Aviel Even, Giovanni Morelli, Silvia Turchetto, Michal Shilian, Romain Le Bail, Sophie Laguesse, Nathalie Krusy, Ariel Brisker, Alexander Brandis, Shani Inbar, Alain Chariot, Frédéric Saudou, Paula Dietrich, Ioannis Dragatsis, Bert Brone, Loïc Broix, Jean-Michel Rigo, Miguel Weil, Laurent Nguyen
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-1 (2021)
Externí odkaz:
https://doaj.org/article/79e79303396a442f8f0694398022f331
Autor:
Samuel Guenin, Mustapha Mouallif, Rachel Deplus, Xavier Lampe, Nathalie Krusy, Emilie Calonne, Katty Delbecque, Frederic Kridelka, François Fuks, My Mustapha Ennaji, Philippe Delvenne
Publikováno v:
PLoS ONE, Vol 7, Iss 8, p e42704 (2012)
Promoter methylation profiles are proposed as potential prognosis and/or diagnosis biomarkers in cervical cancer. Up to now, little is known about the promoter methylation profile and expression pattern of stem cell (SC) markers during tumor developm
Externí odkaz:
https://doaj.org/article/4d38725939264037b81b3a189d99caf5
Autor:
Daphne J Smits, Rachel Schot, Nathalie Krusy, Katja Wiegmann, Olaf Utermöhlen, Monique T Mulder, Sandra den Hoedt, Grace Yoon, Ashish R Deshwar, Christina Kresge, Beth Pletcher, Maura van Mook, Marta Serio Ferreira, Raymond A Poot, Johan A Slotman, Gert-Jan Kremers, Abeer Ahmad, Buthaina Albash, Laila Bastaki, Dana Marafi, Jordy Dekker, Tjakko J van Ham, Laurent Nguyen, Grazia M S Mancini
Publikováno v:
Brain.
Biallelic loss-of-function variants in SMPD4 cause a rare and severe neurodevelopmental disorder with progressive congenital microcephaly and early death. SMPD4 encodes a sphingomyelinase that hydrolyses sphingomyelin into ceramide at neutral pH and
Autor:
Alexander Brandis, Miguel Weil, Nathalie Krusy, Alain Chariot, Paula Dietrich, Giovanni Morelli, Ariel Brisker, Michal Shilian, Aviel Even, Loïc Broix, Shani Inbar, Silvia Turchetto, Sophie Laguesse, Ioannis Dragatsis, Frédéric Saudou, Romain Le Bail, Jean-Michel Rigo, Bert Brône, Laurent Nguyen
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-1 (2021)
Nature Communications
Nature Communications
Autor:
Carla G, Silva, Elise, Peyre, Mohit H, Adhikari, Sylvia, Tielens, Sebastian, Tanco, Petra, Van Damme, Lorenza, Magno, Nathalie, Krusy, Gulistan, Agirman, Maria M, Magiera, Nicoletta, Kessaris, Brigitte, Malgrange, Annie, Andrieux, Carsten, Janke, Laurent, Nguyen
Publikováno v:
Cell
Summary Interneurons navigate along multiple tangential paths to settle into appropriate cortical layers. They undergo a saltatory migration paced by intermittent nuclear jumps whose regulation relies on interplay between extracellular cues and genet
Autor:
Carla Gomes Da Silva, Nathalie Krusy, Sebastian Tanco, Carsten Janke, Elise Peyre, Mohit H. Adhikari, Maria M. Magiera, Sylvia Tielens, Annie Andrieux, Nicoletta Kessaris, Brigitte Malgrange, Lorenza Magno, Laurent Nguyen, Petra Van Damme
Publikováno v:
Frontiers in Neuroscience. 11
Autor:
Juliette D. Godin, Philippe Alix, Benjamin Grobarczyk, Elise Peyre, Philippe Lefebvre, Kevin Hanon, Audrey Purnelle, Nathalie Krusy, Vincent Seutin, Laurent Nguyen, Laurence Borgs, Pierre Maquet, Brigitte Malgrange
Publikováno v:
Scientific Reports
Scientific Reports, Nature Publishing Group, 2016, 6 (1), ⟨10.1038/srep33377⟩
Scientific Reports, Nature Publishing Group, 2016, 6 (1), ⟨10.1038/srep33377⟩
Some mutations of the LRRK2 gene underlie autosomal dominant form of Parkinson’s disease (PD). The G2019S is a common mutation that accounts for about 2% of PD cases. To understand the pathophysiology of this mutation and its possible developmental
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1bbd47dc72680c72307a9251cb34386
https://hal.archives-ouvertes.fr/hal-03373867
https://hal.archives-ouvertes.fr/hal-03373867
Autor:
Nathalie Jacobs, Pascale Hubert, Mustapha Mouallif, Moulay Mustapha Ennaji, Anaelle Duray, Samuel Guenin, Nathalie Krusy, Sven Saussez, Philippe Delvenne
Publikováno v:
Molecular Carcinogenesis. 53:667-673
Head and neck squamous cell carcinoma (HNSCC) represent the sixth most common malignancy diagnosed worldwide. Patient's survival is low due the high frequency of tumor recurrence. Inflammation promotes carcinogenesis as well as the formation of metas
Autor:
Pierre Close, Sophie Laguesse, Nathalie Krusy, Alain Chariot, Gabsang Lee, Bénédicte Franco, Guérin Duysens, Sebastian A. Leidel, Laurent Nguyen, Nicolas Thelen, Laurence Borgs, Juliette D. Godin, Pierre Paul Prévot, Brigitte Malgrange, Marc Thiry, Catherine Creppe, Sandra Huysseune, Danny D. Nedialkova
Publikováno v:
Developmental Cell
Developmental Cell, Elsevier, 2015, 35 (5), pp.553-567. ⟨10.1016/j.devcel.2015.11.005⟩
Developmental Cell, Elsevier, 2015, 35 (5), pp.553-567. ⟨10.1016/j.devcel.2015.11.005⟩
SummaryThe cerebral cortex contains layers of neurons sequentially generated by distinct lineage-related progenitors. At the onset of corticogenesis, the first-born progenitors are apical progenitors (APs), whose asymmetric division gives birth direc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3a33aee6f13a2c66cbcbbe1ecdbc6d37
https://hal.archives-ouvertes.fr/hal-03373877
https://hal.archives-ouvertes.fr/hal-03373877