Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Jimmy, Perrot"'
Autor:
Pierre Stephan, Jimmy Perrot, Allison Voisin, Maud Barbery, Thibault Andrieu, Maxime Grimont, Julie Caramel, Mathilde Bardou, Garance Tondeur, Edoardo Missiaglia, Philippe Gaulard, François Lemmonier, Laurence de Leval, Emmanuel Bachy, Pierre Sujobert, Laurent Genestier, Alexandra Traverse-Glehen, Yenkel Grinberg-Bleyer
Publikováno v:
Haematologica, Vol 999, Iss 1 (2024)
Whereas immunotherapies have revolutionized the treatment of different solid and hematological cancers, their efficacy in nodal peripheral T-cell lymphomas (PTCLs) is limited, due to a lack of understanding of the immune response they trigger. To ful
Externí odkaz:
https://doaj.org/article/07a54dde7d7a45488d6e41ed5e630c1d
Autor:
Jimena A. Miranda, MD, Charles Huvet, MD, Marie Donzel, MD, Anne Lazareth, MD, Jimmy Perrot, Eng, Stéphane Dalle, MD, PhD
Publikováno v:
JAAD Case Reports, Vol 40, Iss , Pp 92-95 (2023)
Externí odkaz:
https://doaj.org/article/16183c7c50354dccb354299c2285d8bc
Autor:
Jérémy Guillot, Chloé Dominici, Adrien Lucchesi, Huyen Thi Trang Nguyen, Angélique Puget, Mélanie Hocine, Martha M. Rangel-Sosa, Milesa Simic, Jérémy Nigri, Fabienne Guillaumond, Martin Bigonnet, Nelson Dusetti, Jimmy Perrot, Jonathan Lopez, Anders Etzerodt, Toby Lawrence, Pierre Pudlo, Florence Hubert, Jean-Yves Scoazec, Serge A. van de Pavert, Richard Tomasini, Sophie Chauvet, Fanny Mann
Publikováno v:
Nature Communications, Vol 13, Iss 1, Pp 1-19 (2022)
The autonomic nervous systems densely innervate the pancreas, but its contribution to pancreatic ductal adenocarcinoma (PDAC) progression is not fully understood. Here, the authors characterize the pattern of sympathetic innervation by 3D imaging in
Externí odkaz:
https://doaj.org/article/f2a238503c59462b8745c93b2bc9627d
Autor:
Gaspard Jeremie, Fabienne Allias, Alexis Trecourt, Lucie Gaillot-Durand, Pierre Adrien Bolze, Françoise Descotes, Garance Tondeur, Jimmy Perrot, Touria Hajri, Benoit You, François Golfier, Jonathan Lopez, Mojgan Devouassoux-Shisheboran
Gestational trophoblastic diseases derived from the chorionic-type intermediate trophoblast include benign placental site nodule (PSN) and malignant epithelioid trophoblastic tumor (ETT). Among PSN, the WHO classification introduced a new entity name
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6de5c6ab225f9bc663ee6b1d53c3e658
https://doi.org/10.21203/rs.3.rs-1978810/v1
https://doi.org/10.21203/rs.3.rs-1978810/v1
Autor:
Patrick Aubourg, Jean-Marie Cuisset, Philippe Latour, Kouider Beladgham, Jimmy Perrot, Lucie Guyant-Marechal, Bruno Francou, Laurent Kremer, Naziha Baaloul, Alain Verloes, Andoni Echaniz-Laguna
Publikováno v:
neurogenetics. 21:29-37
Giant axonal neuropathy (GAN) is an autosomal recessive disease caused by mutations in the GAN gene encoding gigaxonin. Patients develop a progressive sensorimotor neuropathy affecting peripheral nervous system (PNS) and central nervous system (CNS).
Publikováno v:
The Journal of Physiology. 595:6417-6428
Key points Missense mutations in the gene encoding the α1 subunit of the skeletal muscle voltage-gated Ca2+ channel induce type 1 hypokalaemic periodic paralysis, a poorly understood neuromuscular disease characterized by episodic attacks of paralys
Na leak with gating pore properties in hypokalemic periodic paralysis V876E mutant muscle Ca channel
Autor:
Pierre Charnet, Vincent Jacquemond, Bruno Allard, Christine Berthier, Jimmy Perrot, Clarisse Fuster
Publikováno v:
The Journal of General Physiology
The V876E mutation in the muscle voltage-gated Ca2+ channel induces hypokalemic periodic paralysis. Fuster et al. show that the mutation generates strong resting inward leak Na+ currents even though it is not located in the voltage sensor segments.
Publikováno v:
Les Cahiers de Myologie. :63-65
La Paralysie Periodique Hypokaliemique de type 1 (HypoPPl) est une maladie neuromusculaire caracterisee par des crises de paralysies musculaires transitoires pouvant durer de quelques heures a quelques jours et associees a une hypokaliemie. Ces paral
Autor:
Jimmy Perrot, Tanya Stojkovic, Guenaelle Piguet-Lacroix, Marion Masingue, Robert-Yves Carlier, Philippe Latour
Publikováno v:
Neurogenetics. 19(2)
Charcot-Marie-Tooth disease (CMT) refers to a group of clinically and genetically heterogeneous inherited neuropathies. Ganglioside-induced differentiation-associated protein 1 GDAP1-related CMT has been reported in an autosomal dominant or recessive
Publikováno v:
The Journal of General Physiology
Missense mutations in the gene encoding the α1 subunit of the skeletal muscle voltage-gated CaMissense mutations in the gene encoding the α1 subunit of the skeletal muscle voltage-gated Ca