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Genetics|October 7, 2010
Bulk segregation mapping of mutations in closely related strains of miceYu Xia, Sungyong Won, Xin Du, et al.
Proceedings of the National Academy of Sciences of the United States of America|February 6, 2010
A mutation of Ikbkg causes immune deficiency without impairing degradation of IkappaB alphaOwen M Siggs, Michael Berger, Philippe Krebs, et al.
JCI Insight|July 22, 2025
A hypomorphic Mpi mutation unlocks an in vivo tool for studying global N-glycosylation deficiencyElisa B Lin, Steve Meregini, Zhao Zhang, et al.
The Journal of Experimental Medicine|November 19, 2003
A common dominant TLR5 stop codon polymorphism abolishes flagellin signaling and is associated with susceptibility to legionnaires' diseaseThomas R Hawn, Annelies Verbon, Kamilla D Lettinga, et al.
The Journal of Experimental Medicine|October 29, 2024
Suppression of melanoma by mice lacking MHC-II: Mechanisms and implications for cancer immunotherapyHexin Shi, Dawson Medler, Jianhui Wang, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 30, 2020
Genetic and structural studies of RABL3 reveal an essential role in lymphoid development and functionXue Zhong, Lijing Su, Yi Yang, et al.
The Journal of Experimental Medicine|January 28, 2020
Essential cell-extrinsic requirement for PDIA6 in lymphoid and myeloid developmentJin Huk Choi, Xue Zhong, Zhao Zhang, et al.
Nature Structural & Molecular Biology|February 9, 2024
Dynamic molecular architecture and substrate recruitment of cullin3-RING E3 ligase CRL3KBTBD2Yuxia Hu, Zhao Zhang, Qiyu Mao, et al.
The Journal of Experimental Medicine|September 28, 2019
Platelet-activating factor (PAF) mediates NLRP3-NEK7 inflammasome induction independently of PAFRMeng Deng, Haitao Guo, Jason W Tam, et al.
Journal of Immunology (Baltimore, Md. : 1950)|March 9, 2011
A point mutation in the amino terminus of TLR7 abolishes signaling without affecting ligand bindingCarlo Iavarone, Katrin Ramsauer, Andriy V Kubarenko, et al.
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