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Journal of Medicinal Chemistry|April 21, 2001
Development of orally active nonpeptidic inhibitors of human neutrophil elastaseK Ohmoto, T Yamamoto, M Okuma, et al.Heart (British Cardiac Society)|December 17, 2002
Catecholaminergic polymorphic ventricular tachycardia: electrocardiographic characteristics and optimal therapeutic strategies to prevent sudden deathN Sumitomo, K Harada, M Nagashima, et al.Nature Communications|March 24, 2021
NAC blocks Cystatin C amyloid complex aggregation in a cell system and in skin of HCCAA patientsMichael E March, Alvaro Gutierrez-Uzquiza, Asbjorg Osk Snorradottir, et al.Shokuhin Eiseigaku Zasshi. Journal of the Food Hygienic Society of Japan|June 1, 2001
[Estimation of daily dietary intake of aluminum]R Matsuda, K Sasaki, H Sakai, et al.The Japanese Journal of Antibiotics|April 30, 1999
[Clinical effects of combination therapy with cefozopran and tobramycin for severe infections in patients with hematologic diseases]K Toyama, M Yaguchi, Y Uchida, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 24, 2024
Novel insights into the phenotypic spectrum and pathogenesis of Hardikar syndromeAlanna Strong, Michael E March, Christopher J Cardinale, et al.Nature Medicine|July 3, 2019
ARAF recurrent mutation causes central conducting lymphatic anomaly treatable with a MEK inhibitorDong Li, Michael E March, Alvaro Gutierrez-Uzquiza, et al.Human Genetics|April 3, 2021
Pathogenic variants in CDH11 impair cell adhesion and cause Teebi hypertelorism syndromeDong Li, Michael E March, Paola Fortugno, et al.JCI Insight|May 8, 2023
Lymphatic disorders caused by mosaic, activating KRAS variants respond to MEK inhibitionSarah E Sheppard, Michael E March, Christoph Seiler, et al.European Journal of Human Genetics : EJHG|July 27, 2023
Heterozygous rare variants in NR2F2 cause a recognizable multiple congenital anomaly syndrome with developmental delaysMythily Ganapathi, Leticia S Matsuoka, Michael March, et al.Pageof 34