Publications by authors named "Mingmin Gu"

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Investigating the effects of global gene knockout of MrgF on motor performance and pain sensitivity in mice.
Xuejiao Chen, Yan Chen, Runzhe Shu, Shunyuan Lu, Ming-Min Gu

Hereditas· March 2025

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[Study of the types of mutations of Thalassemia in Shanghai area].
Yanying Gu, Beiying Wu, Yiyi Lu, Mingmin Gu, Jiafei Lin

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· April 2024

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Multimodal imaging and genetic characteristics of Chinese patients with USH2A-associated nonsyndromic retinitis pigmentosa.
Chong Chen, Qiao Sun, Mingmin Gu, Tianwei Qian, Dawei Luo

Mol Genet Genomic Med· November 2020

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CMT2Q-causing mutation in the Dhtkd1 gene lead to sensory defects, mitochondrial accumulation and altered metabolism in a knock-in mouse model.
Chun-Jie Luan, Wenting Guo, Lei Chen, Xi-Wei Wei, Yimin He, Ming-Min Gu

Acta Neuropathol Commun· March 2020

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Research progress of myosin heavy chain genes in human genetic diseases.
Yi-Min He, Ming-Min Gu

Yi Chuan· October 2017

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A point mutation in Fgf9 impedes joint interzone formation leading to multiple synostoses syndrome.
Lingyun Tang, Xiaolin Wu, Hongxin Zhang, Shunyuan Lu, Min Wu, Mingmin Gu

Hum Mol Genet· April 2017

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The functional mechanisms and clinical application of read-through drugs.
Yang Fu, Zai-yue Shu, Ming-min Gu

Yi Chuan· July 2016

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[Mutation analysis for a family affected with Charcot-Marie-Tooth disease type 4C].
Zhen Yu, Jiaying Zhang, Ye Xu, Boyu Yang, Zhihong He, Mingmin Gu

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· February 2016

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A novel Cx50 (GJA8) p.H277Y mutation associated with autosomal dominant congenital cataract identified with targeted next-generation sequencing.
Chong Chen, Qiao Sun, Mingmin Gu, Kun Liu, Yong Sun

Graefes Arch Clin Exp Ophthalmol· June 2015

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[Advances in genetic studies of Charcot-Marie-Tooth disease type 4 (CMT4)].
Ye Xu, Jia-ying Zhang, Bo-yu Yang, Zhi-hong He, Mu-chen Zhang, Ming-min Gu

Yi Chuan· June 2015

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Two nonsense mutations cause protein C deficiency by nonsense-mediated mRNA decay.
Chun-jie Luan, Wei Shen, Zhen Yu, Lei Chen, Yi Gu, Ming-min Gu

Thromb Res· April 2015

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Deletion of Gpr128 results in weight loss and increased intestinal contraction frequency.
Ying-Yin Ni, Yan Chen, Shun-Yuan Lu, Bi-Ying Sun, Fang Wang, Guo-Hua Zhang, Ming-Min Gu

World J Gastroenterol· January 2014

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[Research progress in the mouse models of Charcot-Marie-Tooth disease type 2 (CMT2)].
Zhen Yu, Chunjie Luan, Mingmin Gu

Yi Chuan· January 2014

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DHTKD1 is essential for mitochondrial biogenesis and function maintenance.
Wangyang Xu, Houbao Zhu, Mingmin Gu, Qingqiong Luo, Jieying Ding

FEBS Lett· November 2013

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Dopamine receptor 3 might be an essential molecule in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-induced neurotoxicity.
Yan Chen, Ying-yin Ni, Jie Liu, Jia-wei Lu, Fang Wang, Ming-min Gu

BMC Neurosci· July 2013

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A nonsense mutation in DHTKD1 causes Charcot-Marie-Tooth disease type 2 in a large Chinese pedigree.
Wang-Yang Xu, Ming-Min Gu, Lian-Hua Sun, Wen-Ting Guo, Hou-Bao Zhu

Am J Hum Genet· December 2012

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[Nonsense-mediated mRNA decay and human monogenic disease].
Wen-Ting Guo, Wang-Yang Xu, Ming-Min Gu

Yi Chuan· August 2012

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The cytoplasmic domain of MUC1 induces hyperplasia in the mammary gland and correlates with nuclear accumulation of β-catenin.
Yuan Li, Haiying Yi, Yixin Yao, Xiaodong Liao, Yiqun Xie, Mingmin Gu

PLoS One· April 2011

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Germinal Cell Aplasia in Kif18a Mutant Male Mice Due to Impaired Chromosome Congression and Dysregulated BubR1 and CENP-E.
Xue-Song Liu, Xu-Dong Zhao, Xiaoxing Wang, Yi-Xin Yao, Liang-Liang Zhang, Ming-Min Gu

Genes Cancer· January 2010

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Target deletion of the cytoskeleton-associated protein palladin does not impair neurite outgrowth in mice.
Run-Zhe Shu, Feng Zhang, Xue-Song Liu, Chun-Liang Li, Long Wang, Ming-Min Gu

PLoS One· September 2009

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Multiple synostoses syndrome is due to a missense mutation in exon 2 of FGF9 gene.
Xiao-Lin Wu, Ming-Min Gu, Lei Huang, Xue-Song Liu, Hong-Xin Zhang, Hai-Guo Zhang, Qun Gu

Am J Hum Genet· July 2009

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Disruption of palladin leads to defects in definitive erythropoiesis by interfering with erythroblastic island formation in mouse fetal liver.
Xue-Song Liu, Xi-Hua Li, Yi Wang, Run-Zhe Shu, Long Wang, Ming-Min Gu

Blood· August 2007

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Palladin regulates cell and extracellular matrix interaction through maintaining normal actin cytoskeleton architecture and stabilizing beta1-integrin.
Xue-Song Liu, Hui-Jun Luo, Hua Yang, Long Wang, Hui Kong, Ming-Min Gu

J Cell Biochem· April 2007

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Disruption of palladin results in neural tube closure defects in mice.
Huijun Luo, Xuesong Liu, Fang Wang, Qiuhua Huang, Shuhong Shen, Guojiang Xu, Mingmin Gu

Mol Cell Neurosci· August 2005

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[Cloning and structural analysis of mouse genomic nucleophosmin gene].
You-Gui Xiang, Shun-Yuan Lu, Ming-Min Gu, Sheng-Yue Wang, Shuang-Xi Ren

Yi Chuan Xue Bao· June 2005

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