Showing results (71-80 of 172) with videos related to
Sort By:
Pageof 18
Blood|April 12, 2012
Phenotype diversity in type 1 Gaucher disease: discovering the genetic basis of Gaucher disease/hematologic malignancy phenotype by individual genome analysisSarah M Lo, Murim Choi, Jun Liu, et al.Molecular Genetics & Genomic Medicine|January 21, 2016
The dentin phosphoprotein repeat region and inherited defects of dentinJie Yang, Kazuhiko Kawasaki, Moses Lee, et al.Molecules and Cells|May 22, 2025
Effects of heterozygous SMG1 mutations on nonsense-mediated mRNA decay in human pluripotent stem cell modelChanyoung Lee, Jin Sook Lee, Yejin Kwon, et al.Journal of Pediatric Endocrinology & Metabolism : JPEM|March 19, 2025
Prader-Willi syndrome gene expression profiling of obese and non-obese patients reveals transcriptional changes in CLEC4D and ANXA3Ju Young Yoon, Choong Ho Shin, Murim Choi, et al.Journal of Cellular and Molecular Medicine|April 30, 2022
RNA-seq profiling of tubulointerstitial tissue reveals a potential therapeutic role of dual anti-phosphatase 1 in glomerulonephritisSehoon Park, Hajeong Lee, Jeongha Lee, et al.Human Mutation|July 3, 2019
Heterozygous variants in MYBPC1 are associated with an expanded neuromuscular phenotype beyond arthrogryposisVandana Shashi, Janelle Geist, Youngha Lee, et al.Journal of Medical Genetics|April 7, 2022
Transcriptome-based variant calling and aberrant mRNA discovery enhance diagnostic efficiency for neuromuscular diseasesSung Eun Hong, Jana Kneissl, Anna Cho, et al.Molecular Genetics & Genomic Medicine|January 29, 2015
Taurodontism, variations in tooth number, and misshapened crowns in Wnt10a null mice and human kindredsJie Yang, Shih-Kai Wang, Murim Choi, et al.Clinical and Molecular Hepatology|November 17, 2025
Novel Near-Infrared Probe for Monitoring Lipid Peroxidation-Mediated Viscosity Change in Ferroptotic HepatocytesLe Bich Hang Pham, Taeeung Kim, Seoyoung Kim, et al.Clinical and Molecular Hepatology|July 24, 2024
DNA methylome analysis reveals epigenetic alteration of complement genes in advanced metabolic dysfunction-associated steatotic liver diseaseAmal Magdy, Hee-Jin Kim, Hanyong Go, et al.Pageof 18