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Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association|July 13, 2010
Inhibitory effects of quercetin on aflatoxin B1-induced hepatic damage in miceK-C Choi, W-T Chung, J-K Kwon, et al.Pediatric Neurology|August 17, 2017
Early Detection of Tuberous Sclerosis Complex: An Opportunity for Improved Neurodevelopmental OutcomeClara W T Chung, John A Lawson, Vanessa Sarkozy, et al.Molecular Genetics & Genomic Medicine|October 1, 2024
Deep Sequencing and Phenotyping in an Australian Tuberous Sclerosis Complex "No Mutations Identified" CohortClara W T Chung, Adam M Bournazos, Lok Chi Denise Chan, et al.Osteoarthritis and Cartilage|June 16, 2015
Leptin protects rat articular chondrocytes from cytotoxicity induced by TNF-α in the presence of cyclohexamideS W Lee, J H Rho, S Y Lee, et al.Journal of Medical Genetics|July 14, 2019
<i>RASA1</i> mosaic mutations in patients with capillary malformation-arteriovenous malformationNicole Revencu, Elodie Fastre, Marie Ravoet, et al.Blood|January 27, 2023
A cell-based functional assay that accurately links genotype to phenotype in familial HLHTahereh Noori, Jesse A Rudd-Schmidt, Alisa Kane, et al.Clinical and Experimental Rheumatology|August 29, 2003
Association between HLA-DR B1 and clinical features of adult onset Still's disease in KoreaC I Joung, H S Lee, S W Lee, et al.Clinical and Experimental Rheumatology|November 2, 2004
Validation of the classification criteria commonly used in Korea and a modified set of preliminary criteria for Behçet's disease: a multi-center studyH K Chang, S S Lee, H J Bai, et al.Lupus|August 2, 2001
FcgammaRIIa/IIIa polymorphism and its association with clinical manifestations in Korean lupus patientsH R Yun, H K Koh, S S Kim, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 9, 2022
Biallelic loss-of-function variants in RABGAP1 cause a novel neurodevelopmental syndromeRachel Youjin Oh, Ashish R Deshwar, Ashish Marwaha, et al.Pageof 3