Publications by authors named "Weilin Tang"

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[Cloning and expression pattern analysis of abscisic acid receptor gene McPYL4 in Mentha canadensis].
Wei-Lin Tang, Xia Wang, Qin Kang, Ke Wang, Dan-Dan Peng

Zhongguo Zhong Yao Za Zhi· March 2024

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Arabidopsis G-protein β subunit AGB1 represses abscisic acid signaling via attenuation of the MPK3-VIP1 phosphorylation cascade.
Dongbei Xu, Wensi Tang, Yanan Ma, Xia Wang, Yanzhi Yang, Weilin Tang, Yimiao Tang

J Exp Bot· February 2024

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[Identification and functional analysis of jasmonic acid signaling repressor McJAZ8 gene in Mentha canadensis].
Gui-Lin Zhang, Wei-Lin Tang, Qin Kang, Ming-Yang Shen, Jing-Tian Xu

Zhongguo Zhong Yao Za Zhi· February 2024

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Genome-Wide Identification and Expression Analysis of bZIP Family Genes in .
Mengyang Wu, Jinsong Chen, Weilin Tang, Yijie Jiang, Zhaoyong Hu

Genes (Basel)· October 2023

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Logistics hub location for high-speed rail freight transport with road-rail intermodal transport network.
Siyu Li, Maoxiang Lang, Xinghan Chen, Shiqi Li, Wenqian Liu, Weilin Tang

PLoS One· July 2023

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Efficient Toughening of DGEBA with a Bio-Based Protocatechuic Acid Derivative.
Xinxin Fang, Xin Guo, Weilin Tang, Qun Gu, Yue Wu

ACS Omega· March 2023

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Transcriptome-Wide Identification and Characterization of the Gene Family in L.
Dong-Bei Xu, Ya-Nan Ma, Teng-Fei Qin, Wei-Lin Tang, Xi-Wu Qi

Int J Mol Sci· August 2021

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[Analysis and prenatal diagnosis of FMR1 gene mutations among patients with unexplained mental retardation].
Shikun Luo, Wenbin He, Yi Liao, Weilin Tang, Xiurong Li

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· May 2021

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[Analysis of FMR1 gene CGG repeats among patients with diminished ovarian reserve].
Wenbin He, Weilin Tang, Yi Liao, Wen Li, Fei Gong

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· April 2021

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Novel inactivating mutations in the FSH receptor cause premature ovarian insufficiency with resistant ovary syndrome.
Wen-Bin He, Juan Du, Xiao-Wen Yang, Wen Li, Wei-Lin Tang

Reprod Biomed Online· March 2019

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Vibroacoustic behavior of an infinitely long cylindrical shell with periodic internal lengthwise ribs.
Yunzhe Tong, Jun Fan, Bin Wang, Weilin Tang

J Acoust Soc Am· September 2018

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[Identification of novel KIT gene mutations in two Chinese families with piebaldism].
Wen-bin He, Xiao Hu, Wei-lin Tang, Lu-yun Li, Guang-xiu Lu

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· August 2013

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A Chinese family with Oguchi's disease due to compound heterozygosity including a novel deletion in the arrestin gene.
Lingli Huang, Wen Li, Weilin Tang, Xiaohua Zhu, Pingbo Ou-Yang

Mol Vis· July 2012

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[Common mutations of congenital adrenal hyperplasia are also the hotspots for new mutations].
Qianjun Zhang, Wen Li, Shuangfei Li, Weilin Tang, Luyun Li

Nan Fang Yi Ke Da Xue Xue Bao· May 2012

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A novel AVPR2 missense mutation in a Chinese boy with severe inherited nephrogenic diabetes insipidus.
Lingli Huang, Wen Li, Weilin Tang, Guangxin Lu

J Pediatr Endocrinol Metab· January 2012

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[Mutation screening of the F VIII gene in 10 hemophilia A families].
Wen LI, Xiao HU, Bo-di GAO, Lu-yun LI, Yi LIAO, Xue-mei TANG, Wei-lin TANG

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· April 2011

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