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Thrombosis and Haemostasis|February 7, 2014
Treatment with Angiotensin-(1-7) reduces inflammation in carotid atherosclerotic plaquesRodrigo A Fraga-Silva, Silvia Q Savergnini, Fabrizio Montecucco, et al.
Nature|May 18, 2018
RSPO2 inhibition of RNF43 and ZNRF3 governs limb development independently of LGR4/5/6Emmanuelle Szenker-Ravi, Umut Altunoglu, Marc Leushacke, et al.
Nature|July 7, 2018
Author Correction: RSPO2 inhibition of RNF43 and ZNRF3 governs limb development independently of LGR4/5/6Emmanuelle Szenker-Ravi, Umut Altunoglu, Marc Leushacke, et al.
Plos Genetics|May 3, 2011
Loss-of-function mutations in PTPN11 cause metachondromatosis, but not Ollier disease or Maffucci syndromeMargot E Bowen, Eric D Boyden, Ingrid A Holm, et al.
American Journal of Human Genetics|October 1, 2019
Autosomal-Recessive Mutations in MESD Cause Osteogenesis ImperfectaShahida Moosa, Guilherme L Yamamoto, Lutz Garbes, et al.
Journal of Pharmacological and Toxicological Methods|May 11, 2025
Lipopolysaccharide-induced abdominal nociception behavioral model in adult zebrafish (Danio rerio)Maria Rayane C de Oliveira, Sacha Aubrey A R Santos, Gabriela A do Nascimento, et al.
American Journal of Human Genetics|January 31, 2017
Mutations in EXTL3 Cause Neuro-immuno-skeletal Dysplasia SyndromeMachteld M Oud, Paul Tuijnenburg, Maja Hempel, et al.
Frontiers in Immunology|February 11, 2025
Plasma IL-17A is increased in patients with critical MIS-C and associated to in-hospital mortalityEmmerson C F de Farias, Luciana M P P do Nascimento, Manoel J C Pavão Junior, et al.
Scientific Reports|March 6, 2024
Factors associated to mortality in children with critical COVID-19 and multisystem inflammatory syndrome in a resource-poor settingEmmerson C F de Farias, Manoel J C Pavão Junior, Susan C D de Sales, et al.
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