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Journal of Genetics and Genomics = Yi Chuan Xue Bao|June 25, 2018
Collagen secretion screening in Drosophila supports a common secretory machinery and multiple Rab requirementsHongmei Ke, Zhi Feng, Min Liu, et al.
Human Molecular Genetics|October 18, 2022
The fly homolog of SUPT16H, a gene associated with neurodevelopmental disorders, is required in a cell-autonomous fashion for cell survivalMengqi Ma, Xi Zhang, Yiming Zheng, et al.
Plos Genetics|September 28, 2018
Dissection of Nidogen function in Drosophila reveals tissue-specific mechanisms of basement membrane assemblyJianli Dai, Beatriz Estrada, Sofie Jacobs, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 26, 2018
Specific recognition of two MAX effectors by integrated HMA domains in plant immune receptors involves distinct binding surfacesLiwei Guo, Stella Cesari, Karine de Guillen, et al.
Nature Communications|February 6, 2024
The synthetic NLR RGA5<sup>HMA5</sup> requires multiple interfaces within and outside the integrated domain for effector recognitionXin Zhang, Yang Liu, Guixin Yuan, et al.
Bioorganic & Medicinal Chemistry Letters|September 9, 2023
Discovery of marine phidianidine-based Nrf2 activators and their potential against oxLDL- and HG-induced injury in HUVECsJuan Zhang, Yong-Si Cai, Hua-Long Ji, et al.
Human Molecular Genetics|March 29, 2022
Novel dominant and recessive variants in human ROBO1 cause distinct neurodevelopmental defects through different mechanismsYan Huang, Mengqi Ma, Xiao Mao, et al.
Medrxiv : the Preprint Server for Health Sciences|July 28, 2023
Allelic strengths of encephalopathy-associated <i>UBA5</i> variants correlate between <i>in vivo</i> and <i>in vitro</i> assaysXueyang Pan, Albert N Alvarez, Mengqi Ma, et al.
Elife|December 11, 2023
Allelic strengths of encephalopathy-associated <i>UBA5</i> variants correlate between in vivo and in vitro assaysXueyang Pan, Albert N Alvarez, Mengqi Ma, et al.
American Journal of Human Genetics|October 7, 2022
De novo variants in FRMD5 are associated with developmental delay, intellectual disability, ataxia, and abnormalities of eye movementShenzhao Lu, Mengqi Ma, Xiao Mao, et al.
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