Zobrazeno 1 - 10
of 178
pro vyhledávání: '"Jin Yan"'
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 2, Pp n/a-n/a (2021)
Abstract Background Isolated sulfite oxidase deficiency (ISOD) is a life‐threatening rare autosomal recessive disorder caused by pathogenic variants in SUOX (OMIM 606887) gene. The aim of our study was to establish a comprehensive genetic diagnosis
Externí odkaz:
https://doaj.org/article/33acfdf6853c40c0b80e0ef71569408e
Autor:
Li Chun-yu, Deng Gui-ming, Yang Jing, Viljoen Altus, Jin Yan, Kuang Rui-bin, Zuo Cun-wu, Lv Zhi-cheng, Yang Qiao-song, Sheng Ou, Wei Yue-rong, Hu Chun-hua, Dong Tao, Yi Gan-jun
Publikováno v:
BMC Genomics, Vol 13, Iss 1, p 374 (2012)
Abstract Background Fusarium wilt, caused by the fungal pathogen Fusarium oxysporum f. sp. cubense tropical race 4 (Foc TR4), is considered the most lethal disease of Cavendish bananas in the world. The disease can be managed in the field by planting
Externí odkaz:
https://doaj.org/article/00dbf7bcda424c13adc8d17768ec6ea3
Autor:
Xin Li, San-Gang He, Wen-Rong Li, Ling-Yun Luo, Ze Yan, Dong-Xin Mo, Xing Wan, Feng-Hua Lv, Ji Yang, Ya-Xi Xu, Juan Deng, Qiang-Hui Zhu, Xing-Long Xie, Song-Song Xu, Chen-Xi Liu, Xin-Rong Peng, Bin Han, Zhong-Hui Li, Lei Chen, Jian-Lin Han, Xue-Zhi Ding, Renqing Dingkao, Yue-Feng Chu, Jin-Yan Wu, Li-Min Wang, Ping Zhou, Ming-Jun Liu, Meng-Hua Li
Publikováno v:
Genome Research. 32:1669-1684
Understanding the genetic mechanisms of phenotypic variation in hybrids between domestic animals and their wild relatives may aid germplasm innovation. Here, we report the high-quality genome assemblies of a male Pamir argali (O. ammon polii, 2n = 56
Autor:
Yu‐Kun Pang, Lan‐Li Qin, Tian‐Hao Zhang, Jin‐Yan Lei, Ya Zhang, Adam B. Roddy, Guo‐Feng Jiang
Publikováno v:
Physiologia Plantarum. 175
Autor:
Xueyang Zhao, Chuqing Sun, Menglu Jin, Jingchao Chen, Lulu Xing, Jin Yan, Hailei Wang, Zhi Liu, Wei-Hua Chen
Publikováno v:
Microbiology Spectrum.
As Lactiplantibacillus plantarum (previously known as Lactobacillus plantarum ) is increasingly used as a probiotic to treat human gut-related diseases, its bacteriophages may pose a certain threat to their further application and should be identifie
Autor:
Guanglin, Lei, Baofa, Li, Hao, Yang, Fang, Sun, Donghui, Li, Jin, Yan, Yonggang, Wang, Ruisheng, Li, Honghong, Liu, Shaogeng, Zhang, Yufeng, Li, Penghui, Yang
Publikováno v:
Human Gene Therapy. 33:309-317
Oncolytic virus therapy is a promising novel immunotherapy. In this report, we engineered a novel oncolytic influenza virus (IV) carrying an antihuman programmed cell death 1 (PD-1) monoclonal antibody utilizing reverse genetics. A reassortant chimer
Autor:
Ken Lin, Ding-Yun You, Li-Huan Zhang, Li-Juan Zhou, Jin-Yan Zu, Yang Xiao, Mei-Hua Sun, null Dong-Su, Xue Cao, Tie-Song Zhang, Jing Ma
Publikováno v:
Journal of Applied Genetics. 63:327-337
Congenital sensorineural hearing loss (CSHL) and microtia are development-related diseases, sharing some factors and affecting children's hearing. However, genetic tests only focus on CSHL. We try to identify the common molecular mechanism of CSHL an
Autor:
Hong Yang, Feng Xiong, Hai-Bin Qin, Qun-Tao Yu, Jin-Yan Sun, Hai-Wen Zhao, Dong Li, Youtong Zhou, Fu-Kun Zhang, Xiao-Wen Zhu, Tong Wu, Man Jiang, Xiangmin Xu, Youming Lu, Hong-Jie Shen, Wen-Bo Zeng, Fei Zhao, Min-Hua Luo
Publikováno v:
Molecular Neurodegeneration, Vol 17, Iss 1, Pp 1-19 (2022)
Molecular Neurodegeneration
Molecular neurodegeneration, vol 17, iss 1
Molecular Neurodegeneration
Molecular neurodegeneration, vol 17, iss 1
Background Viral tracers are important tools for mapping brain connectomes. The feature of predominant anterograde transneuronal transmission offers herpes simplex virus-1 (HSV-1) strain H129 (HSV1-H129) as a promising candidate to be developed as an
Publikováno v:
World Journal of Psychiatry
BACKGROUND Schizophrenia afflicts 1% of the world population. Clinical studies suggest that schizophrenia patients may have an imbalance of mitochondrial energy metabolism via inhibition of mitochondrial complex I activity. Moreover, recent studies h
Autor:
Leslie Burnett, John Reeves, Cindy S. Ma, Jennifer Stoddard, William A. Figgett, Helen C. Su, Jin Yan Yap, Gulbu Uzel, Huie Jing, Jane Peake, Paul Gray, Anna Sullivan, Bethany Pillay, Sarah K. Kummerfeld, Stuart G. Tangye, Dianne E. Campbell
Publikováno v:
Journal of Clinical Immunology. 42:119-129
Rare, biallelic loss-of-function mutations in DOCK8 result in a combined immune deficiency characterized by severe and recurrent cutaneous infections, eczema, allergies, and susceptibility to malignancy, as well as impaired humoral and cellular immun