Zobrazeno 1 - 10
of 50
pro vyhledávání: '"Franck, Aimond"'
Autor:
Sophie Layalle, Franck Aimond, Véronique Brugioti, Claire Guissart, Cédric Raoul, Laurent Soustelle
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-13 (2024)
Abstract Amyotrophic lateral sclerosis (ALS) is a devastating paralytic disorder caused by the death of motoneurons. Several mutations in the KIF5A gene have been identified in patients with ALS. Some mutations affect the splicing sites of exon 27 le
Externí odkaz:
https://doaj.org/article/b0fbda0c71d844aea463901fe3f792da
Autor:
Sarka Jelinkova, Aleksandra Vilotic, Jan Pribyl, Franck Aimond, Anton Salykin, Ivana Acimovic, Martin Pesl, Guido Caluori, Simon Klimovic, Tomas Urban, Hana Dobrovolna, Vladimir Soska, Petr Skladal, Alain Lacampagne, Petr Dvorak, Albano C. Meli, Vladimir Rotrekl
Publikováno v:
Frontiers in Bioengineering and Biotechnology, Vol 8 (2020)
Duchenne muscular dystrophy (DMD) is a severe genetic disorder characterized by the lack of functional dystrophin. DMD is associated with progressive dilated cardiomyopathy, eventually leading to heart failure as the main cause of death in DMD patien
Externí odkaz:
https://doaj.org/article/894acdf8147b4845b5659a63c9f195eb
Autor:
Sarka Jelinkova, Yvonne Sleiman, Petr Fojtík, Franck Aimond, Amanda Finan, Gerald Hugon, Valerie Scheuermann, Deborah Beckerová, Olivier Cazorla, Marie Vincenti, Pascal Amedro, Sylvain Richard, Josef Jaros, Petr Dvorak, Alain Lacampagne, Gilles Carnac, Vladimir Rotrekl, Albano C. Meli
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 9, p 5025 (2021)
Duchenne muscular dystrophy (DMD) is a devastating condition shortening the lifespan of young men. DMD patients suffer from age-related dilated cardiomyopathy (DCM) that leads to heart failure. Several molecular mechanisms leading to cardiomyocyte de
Externí odkaz:
https://doaj.org/article/f77b0ad1eb374f42a3c3b2ffb803ec46
Autor:
Anne Virsolvy, Aurélie Fort, Lucie Erceau, Azzouz Charrabi, Maurice Hayot, Franck Aimond, Sylvain Richard
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 5, p 2570 (2021)
Arterial smooth muscle exhibits rhythmic oscillatory contractions called vasomotion and believed to be a protective mechanism against tissue hypoperfusion or hypoxia. Oscillations of vascular tone depend on voltage and follow oscillations of the memb
Externí odkaz:
https://doaj.org/article/0ab3daac91904efebc94216e158b2f46
Publikováno v:
Cells, Vol 9, Iss 12, p 2550 (2020)
Amyotrophic lateral sclerosis (ALS) is a fatal neurological disorder characterized by the progressive degeneration of upper and lower motoneurons. Despite motoneuron death being recognized as the cardinal event of the disease, the loss of glial cells
Externí odkaz:
https://doaj.org/article/480cde706f574510a4fe2e7cc1947d00
Autor:
Karen Lambert, Adèle Faucherre, Marie Demion, Franck Aimond, Christophe Hedon, Nourdine Chakouri, Patrice Bideaux, Jean-Yves Le Guennec, Jérôme Thireau, Sylvain Richard, Cécile Cassan
Publikováno v:
Progress in Biophysics and Molecular Biology
Progress in Biophysics and Molecular Biology, Elsevier, 2021, 159, pp.105-117. ⟨10.1016/j.pbiomolbio.2020.09.006⟩
Progress in Biophysics and Molecular Biology, Elsevier, 2020, ⟨10.1016/j.pbiomolbio.2020.09.006⟩
Progress in Biophysics and Molecular Biology, 2021, 159, pp.105-117. ⟨10.1016/j.pbiomolbio.2020.09.006⟩
Progress in Biophysics and Molecular Biology, Elsevier, 2021, 159, pp.105-117. ⟨10.1016/j.pbiomolbio.2020.09.006⟩
Progress in Biophysics and Molecular Biology, Elsevier, 2020, ⟨10.1016/j.pbiomolbio.2020.09.006⟩
Progress in Biophysics and Molecular Biology, 2021, 159, pp.105-117. ⟨10.1016/j.pbiomolbio.2020.09.006⟩
International audience; The transient receptor potential Melastatin 4 (TRPM4) channel is a calcium-activated non-selective cation channel expressed widely. In the heart, using a knock-out mouse model, the TRPM4 channel has been shown to be involved i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a291490cebb5c2248a5ed0e7a6479ea4
https://doi.org/10.1016/j.pbiomolbio.2020.09.006
https://doi.org/10.1016/j.pbiomolbio.2020.09.006
Autor:
Marie Demion, Jérôme Thireau, Mélanie Gueffier, Amanda Finan, Ziad Khoueiry, Cécile Cassan, Nicolas Serafini, Franck Aimond, Mathieu Granier, Jean-Luc Pasquié, Pierre Launay, Sylvain Richard
Publikováno v:
PLoS ONE, Vol 9, Iss 12, p e115256 (2014)
RATIONALE:TRPM4 is a non-selective Ca2+-activated cation channel expressed in the heart, particularly in the atria or conduction tissue. Mutations in the Trpm4 gene were recently associated with several human conduction disorders such as Brugada synd
Externí odkaz:
https://doaj.org/article/ef1b6feb451640c3bbc80010e7f4f47d
Autor:
Alain Lacampagne, Petr Fojtík, Josef Jaroš, Pascal Amedro, Valérie Scheuermann, Marie Vincenti, Albano C. Meli, Vladimír Rotrekl, Franck Aimond, Petr Dvorak, Amanda Finan, Šárka Jelínková, Gilles Carnac, Gérald Hugon, Olivier Cazorla, Yvonne Sleiman, Deborah Beckerová, Sylvain Richard
Publikováno v:
International Journal of Molecular Sciences
International Journal of Molecular Sciences, MDPI, 2021, 22 (9), pp.5025. ⟨10.3390/ijms22095025⟩
Volume 22
Issue 9
International Journal of Molecular Sciences, Vol 22, Iss 5025, p 5025 (2021)
International Journal of Molecular Sciences, MDPI, 2021, 22 (9), pp.5025. ⟨10.3390/ijms22095025⟩
Volume 22
Issue 9
International Journal of Molecular Sciences, Vol 22, Iss 5025, p 5025 (2021)
International audience; Duchenne muscular dystrophy (DMD) is a devastating condition shortening the lifespan of young men. DMD patients suffer from age-related dilated cardiomyopathy (DCM) that leads to heart failure. Several molecular mechanisms lea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::06de4bd855df49e4b8c84bfeb7f38a80
https://hal.archives-ouvertes.fr/hal-03258363
https://hal.archives-ouvertes.fr/hal-03258363
Autor:
William Ritchie, Donovan Pineau, Sophie Muxel, Meera Augustus, Frédérique Scamps, Hugues Duffau, Safa Azar, Catherine Gozé, Valérie Rigau, Amélie Darlix, Davide Lecca, Jean-Philippe Hugnot, Franck Aimond
Publikováno v:
Cancers
Cancers, 2021, 13 (9), pp.2107. ⟨10.3390/cancers13092107⟩
Volume 13
Issue 9
Cancers, MDPI, 2021, 13 (9), pp.2107. ⟨10.3390/cancers13092107⟩
Cancers, Vol 13, Iss 2107, p 2107 (2021)
Cancers, 2021, 13 (9), pp.2107. ⟨10.3390/cancers13092107⟩
Volume 13
Issue 9
Cancers, MDPI, 2021, 13 (9), pp.2107. ⟨10.3390/cancers13092107⟩
Cancers, Vol 13, Iss 2107, p 2107 (2021)
Diffuse grade II IDH−mutant gliomas are slow−growing brain tumors that progress into high−grade gliomas. They present intratumoral cell heterogeneity, and no reliable markers are available to distinguish the different cell subtypes. The molecul
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e72468395a39fe3559656947a9a8d98a
https://hal.science/hal-03218662/document
https://hal.science/hal-03218662/document
Autor:
Meera, Augustus, Donovan, Pineau, Franck, Aimond, Safa, Azar, Davide, Lecca, Frédérique, Scamps, Sophie, Muxel, Amélie, Darlix, William, Ritchie, Catherine, Gozé, Valérie, Rigau, Hugues, Duffau, Jean-Philippe, Hugnot
Publikováno v:
Cancers
Simple Summary Diffuse grade II IDH-mutant gliomas are rare brain tumors mainly affecting young patients. These tumors are composed of different populations of tumoral cells. Little is known of these cells and how they are generated. These different
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1fc31badd94a8d8b72a6b363cee24b2a
https://pubmed.ncbi.nlm.nih.gov/33925547
https://pubmed.ncbi.nlm.nih.gov/33925547