ӳ��ý

Publications

Rescue of hearing by adenine base editing in a humanized mouse model of Usher syndrome type 1F.

Peters CW, Hanlon KS, Ivanchenko M V, et al. Rescue of hearing by adenine base editing in a humanized mouse model of Usher syndrome type 1F. Molecular therapy : the journal of the American Society of Gene Therapy. 2023. doi:10.1016/j.ymthe.2023.06.007

An Epstein-Barr virus protein interaction map reveals NLRP3 inflammasome evasion via MAVS UFMylation.

Yiu SPT, Zerbe C, Vanderwall D, Huttlin EL, Weekes MP, Gewurz BE. An Epstein-Barr virus protein interaction map reveals NLRP3 inflammasome evasion via MAVS UFMylation. Molecular cell. 2023. doi:10.1016/j.molcel.2023.05.018

Reference-based cell type matching of in situ image-based spatial transcriptomics data on primary visual cortex of mouse brain.

Zhang Y, Miller JA, Park J, et al. Reference-based cell type matching of in situ image-based spatial transcriptomics data on primary visual cortex of mouse brain. Scientific reports. 2023;13(1):9567. doi:10.1038/s41598-023-36638-8

RNA-based amplicon sequencing is ineffective in measuring metabolic activity in environmental microbial communities.

Wang Y, Thompson KN, Yan Y, et al. RNA-based amplicon sequencing is ineffective in measuring metabolic activity in environmental microbial communities. Microbiome. 2023;11(1):131. doi:10.1186/s40168-022-01449-y

Development of an amplicon-based sequencing approach in response to the global emergence of mpox.

Chen NFG, Chaguza C, Gagne L, et al. Development of an amplicon-based sequencing approach in response to the global emergence of mpox. PLoS biology. 2023;21(6):e3002151. doi:10.1371/journal.pbio.3002151

DYRK1A promotes viral entry of highly pathogenic human coronaviruses in a kinase-independent manner.

Strine MS, Cai WL, Wei J, et al. DYRK1A promotes viral entry of highly pathogenic human coronaviruses in a kinase-independent manner. PLoS biology. 2023;21(6):e3002097. doi:10.1371/journal.pbio.3002097

Estimating Dementia Risk Using Multifactorial Prediction Models.

Kivimäki M, Livingston G, Singh-Manoux A, et al. Estimating Dementia Risk Using Multifactorial Prediction Models. JAMA network open. 2023;6(6):e2318132. doi:10.1001/jamanetworkopen.2023.18132

Rare penetrant mutations confer severe risk of common diseases.

Fiziev P, McRae J, Ulirsch JC, et al. Rare penetrant mutations confer severe risk of common diseases. medRxiv : the preprint server for health sciences. 2023. doi:10.1101/2023.05.01.23289356

Rare penetrant mutations confer severe risk of common diseases.

Fiziev P, McRae J, Ulirsch JC, et al. Rare penetrant mutations confer severe risk of common diseases. medRxiv : the preprint server for health sciences. 2023. doi:10.1101/2023.05.01.23289356

Rare penetrant mutations confer severe risk of common diseases.

Fiziev P, McRae J, Ulirsch JC, et al. Rare penetrant mutations confer severe risk of common diseases. medRxiv : the preprint server for health sciences. 2023. doi:10.1101/2023.05.01.23289356