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Clinical and Molecular Hepatology|January 27, 2026
DNMT1 Facilitates the Progression of MASLD by Impeding Transcription Mediated by HNF4α and PPARαHyun Ahm Sohn, Hanyong Go, Tae Hyeon An, et al.Nature|August 24, 2010
Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformationsKaya Bilgüvar, Ali Kemal Oztürk, Angeliki Louvi, et al.Orphanet Journal of Rare Diseases|March 22, 2019
The Korean undiagnosed diseases program: lessons from a one-year pilot projectSoo Yeon Kim, Byung Chan Lim, Jin Sook Lee, et al.Nature Genetics|July 31, 2012
Exome sequencing identifies recurrent somatic RAC1 mutations in melanomaMichael Krauthammer, Yong Kong, Byung Hak Ha, et al.Frontiers in Immunology|February 13, 2023
Elevated IFNA1 and suppressed IL12p40 associated with persistent hyperinflammation in COVID-19 pneumoniaKyeongseok Jeon, Yuri Kim, Shin Kwang Kang, et al.Frontiers in Immunology|March 27, 2023
Corrigendum: Elevated IFNA1 and suppressed IL12p40 associated with persistent hyperinflammation in COVID-19 pneumoniaKyeongseok Jeon, Yuri Kim, Shin Kwang Kang, et al.The Journal of Clinical Investigation|April 28, 2026
Iron overload in steatotic hepatocytes drives systemic metabolic dysfunction via alterations in hepatokine productionHye Jin Jo, Ayoung Kim, Hyunsoo Rho, et al.Nature Genetics|December 3, 2024
Single-cell RNA sequencing of peripheral blood links cell-type-specific regulation of splicing to autoimmune and inflammatory diseasesChi Tian, Yuntian Zhang, Yihan Tong, et al.Proceedings of the National Academy of Sciences of the United States of America|January 30, 2013
Landscape of somatic single-nucleotide and copy-number mutations in uterine serous carcinomaSiming Zhao, Murim Choi, John D Overton, et al.Nature Genetics|November 11, 2008
Susceptibility loci for intracranial aneurysm in European and Japanese populationsKaya Bilguvar, Katsuhito Yasuno, Mika Niemelä, et al.Pageof 18