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Communications Biology|July 10, 2019
Erratum: Publisher Correction: Calaxin is required for cilia-driven determination of vertebrate lateralityKeita Sasaki, Kogiku Shiba, Akihiro Nakamura, et al.Human Molecular Genetics|February 8, 2022
Two ovarian candidate enhancers, identified by time series enhancer RNA analyses, harbor rare genetic variations identified in ovarian insufficiencyRyuichi Nakagawa, Kei Takasawa, Maki Gau, et al.Intestinal Research|April 4, 2025
Inflammatory bowel disease in a young female patient with a novel de novo TRAF3 frameshift variant responsive to ustekinumab: a case reportIchiro Takeuchi, Kosuke Taniguchi, Katsuhiro Arai, et al.The Journal of Allergy and Clinical Immunology|December 20, 2022
STAT6 gain-of-function variant exacerbates multiple allergic symptomsIchiro Takeuchi, Kumiko Yanagi, Shuji Takada, et al.Genetics in Medicine Open|December 13, 2024
Loss of function in <i>NSD2</i> causes DNA methylation signature similar to that in Wolf-Hirschhorn syndromeTomoko Kawai, Shiori Kinoshita, Yuka Takayama, et al.Orphanet Journal of Rare Diseases|October 30, 2014
Japanese founder duplications/triplications involving BHLHA9 are associated with split-hand/foot malformation with or without long bone deficiency and Gollop-Wolfgang complexEiko Nagata, Hiroki Kano, Fumiko Kato, et al.Science Advances|April 14, 2023
TEAD1 trapping by the Q353R-Lamin A/C causes dilated cardiomyopathyShintaro Yamada, Toshiyuki Ko, Masamichi Ito, et al.Pageof 13