Showing results (31-40 of 43) with videos related to

Sort By:
Pageof 5
International Journal of Molecular Sciences|March 14, 2026
Bovine Lactoferrin Modulates Mononuclear Cell Activity in Human Palatine TonsilsTakumi Yago, Chisane Kujirai, Hirotsugu Oda, et al.
American Journal of Human Genetics|July 5, 2014
Aicardi-Goutières syndrome is caused by IFIH1 mutationsHirotsugu Oda, Kenji Nakagawa, Junya Abe, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|September 6, 2016
Novel compound heterozygous mutations in a Japanese girl with Janus kinase 3 deficiencyTakeshi Sato, Tsubasa Okano, Mari Tanaka-Kubota, et al.
Journal of Clinical Immunology|November 30, 2016
A CD57+ CTL Degranulation Assay Effectively Identifies Familial Hemophagocytic Lymphohistiocytosis Type 3 PatientsMasayuki Hori, Takahiro Yasumi, Saeko Shimodera, et al.
Frontiers in Immunology|April 3, 2019
Second Case of HOIP Deficiency Expands Clinical Features and Defines Inflammatory Transcriptome Regulated by LUBACHirotsugu Oda, David B Beck, Hye Sun Kuehn, et al.
Arthritis & Rheumatology (Hoboken, N.J.)|October 28, 2016
Identification of a High-Frequency Somatic NLRC4 Mutation as a Cause of Autoinflammation by Pluripotent Cell-Based Phenotype DissectionYuri Kawasaki, Hirotsugu Oda, Jun Ito, et al.
European Journal of Human Genetics : EJHG|June 11, 2015
Exon skipping causes atypical phenotypes associated with a loss-of-function mutation in FLNA by restoring its protein functionHirotsugu Oda, Tatsuhiro Sato, Shinji Kunishima, et al.
Science Advances|February 1, 2021
Linkage-specific deubiquitylation by OTUD5 defines an embryonic pathway intolerant to genomic variationDavid B Beck, Mohammed A Basar, Anthony J Asmar, et al.
The New England Journal of Medicine|May 31, 2023
Variant STAT4 and Response to Ruxolitinib in an Autoinflammatory SyndromeHratch Baghdassarian, Sarah A Blackstone, Owen S Clay, et al.
Pageof 5