Zobrazeno 1 - 10
of 427
pro vyhledávání: '"A, Lahary"'
Autor:
Zakaria Bouchouireb, Damien Olivier-Jimenez, Titouan Jaunet-Lahary, Steeve H. Thany, Jean-Yves Le Questel
Publikováno v:
Ecotoxicology and Environmental Safety, Vol 281, Iss , Pp 116582- (2024)
Molecular docking, pivotal in predicting small-molecule ligand binding modes, struggles with accurately identifying binding conformations and affinities. This is particularly true for neonicotinoids, insecticides whose impacts on ecosystems require p
Externí odkaz:
https://doaj.org/article/3766600ed36e40198113435dde7ffd68
Autor:
Bouchouireb, Zakaria, Olivier-Jimenez, Damien, Jaunet-Lahary, Titouan, Thany, Steeve H., Le Questel, Jean-Yves
Publikováno v:
In Ecotoxicology and Environmental Safety August 2024 281
Akademický článek
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Autor:
Titouan Jaunet-Lahary, Tatsuro Shimamura, Masahiro Hayashi, Norimichi Nomura, Kouta Hirasawa, Tetsuya Shimizu, Masao Yamashita, Naotaka Tsutsumi, Yuta Suehiro, Keiichi Kojima, Yuki Sudo, Takashi Tamura, Hiroko Iwanari, Takao Hamakubo, So Iwata, Kei-ichi Okazaki, Teruhisa Hirai, Atsuko Yamashita
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-15 (2023)
Abstract An oxalate-degrading bacterium in the gut microbiota absorbs food-derived oxalate to use this as a carbon and energy source, thereby reducing the risk of kidney stone formation in host animals. The bacterial oxalate transporter OxlT selectiv
Externí odkaz:
https://doaj.org/article/de2c77162a52411e8b5bf5628545b201
Autor:
Guillaume Feugray, Fiston Kasonga, Maximilien Grall, Cécile Dumesnil, Ygal Benhamou, Valery Brunel, Véronique Le Cam Duchez, Agnès Lahary, Paul Billoir
Publikováno v:
Frontiers in Cardiovascular Medicine, Vol 9 (2022)
IntroductionSickle cell disease (SCD) is an inherited hemoglobinopathy disorder. The main consequence is synthesis of hemoglobin S leading to chronic hemolysis associated with morbidity. The aim of this study was to investigate Thrombin Generation As
Externí odkaz:
https://doaj.org/article/918921fd6c24402ea25b3cf990aa478e
Autor:
Titouan Jaunet-Lahary, Tatsuro Shimamura, Masahiro Hayashi, Norimichi Nomura, Kouta Hirasawa, Tetsuya Shimizu, Masao Yamashita, Naotaka Tsutsumi, Yuta Suehiro, Keiichi Kojima, Yuki Sudo, Takashi Tamura, Hiroko Iwanari, Takao Hamakubo, So Iwata, Kei-ichi Okazaki, Teruhisa Hirai, Atsuko Yamashita
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-1 (2023)
Externí odkaz:
https://doaj.org/article/9be3c076e3ae4fe6ae061a608a4997d4
Autor:
Guillaume Feugray, Fiston Kasonga, Maximilien Grall, Ygal Benhamou, Victor Bobée-Schneider, Gérard Buchonnet, Sylvie Daliphard, Véronique Le Cam Duchez, Agnès Lahary, Paul Billoir
Publikováno v:
Frontiers in Medicine, Vol 9 (2022)
Sickle cell disease is a complex genetic disease involving cell adhesion between red blood cells, white blood cells, platelets and endothelial cells, inducing painful vaso-occlusive crisis (VOC). We assessed reticulocyte and erythrocyte parameters in
Externí odkaz:
https://doaj.org/article/3420da86291a4c36bdb8de718b544cc2
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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Autor:
null Yashaswee Yeluri, null Ashwini Dudala, null Lahary Chunchu, null Priyanka Kushwaha, null Sai Krishna Guguloth, null Sudhakar Kotlapati, null Amrutha Guguloth
Publikováno v:
International Journal of Science and Research Archive. 8:131-149
Hepatitis B and C viruses can lead to serious complications such as hepatic fibrosis, liver cirrhosis, and hepatocellular carcinoma (HCC) and are therefore responsible for a significant portion of liver cancer cases worldwide, with over 1.3 million d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b2b22f70078aba0d6e3e5906ca9954a0
https://doi.org/10.30574/ijsra.2023.8.1.0358
https://doi.org/10.30574/ijsra.2023.8.1.0358
Autor:
Alexis Caulier, Nicolas Jankovsky, Yohann Demont, Hakim Ouled-Haddou, Julien Demagny, Corinne Guitton, Lavinia Merlusca, Delphine Lebon, Pascal Vong, Aurélien Aubry, Agnès Lahary, Christian Rose, Sandrine Gréaume, Emilie Cardon, Jessica Platon, Halima Ouadid-Ahidouch, Jacques Rochette, Jean-Pierre Marolleau, Véronique Picard, Loïc Garçon
Publikováno v:
Haematologica, Vol 105, Iss 3 (2020)
Hereditary xerocytosis is a dominantly inherited red cell membrane disorder caused in most cases by gain-of-function mutations in PIEZO1, encoding a mechanosensitive ion channel that translates a mechanic stimulus into calcium influx. We found that P
Externí odkaz:
https://doaj.org/article/6806504b74624d9894dc56b0db43c8b2