Publications by authors named "Mingyi Ma"

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Neural basis of cooperative behavior in biological and artificial intelligence systems.
Mengping Jiang, Linfan Gu, Mingyi Ma, Qin Li, Jonathan C Kao

Science· September 2025

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A Novel Heterozygous c.1024A>G Variant in BMPR1B Causes Either Isolated Brachydactyly Type A4 With Variable Expressivity or Incomplete Type A4 Overlapping Type D in a Chinese Han Pedigree.
Xinyi Yang, Xiaqing Wu, Hua Li, Runji Zhou, Kai Guo, Mingyi Ma

Am J Med Genet A· August 2025

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Enhanced cancer therapy using modified magnetic α-FeO/FeOnanorods: Dual role in curcumin delivery and ferroptosis induction.
Mingyi Ma, Zhongjun Pan, Ziye Zhu, Chen Ling, Jiahao Yuan

Colloids Surf B Biointerfaces· August 2025

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Temperature-dependent infrared dielectric function and localized surface phonon polaritons in polar AlN.
Huanhuan Zhao, Tao Cheng, Guodong Wang, Lei Zhang, Mingyi Ma

Opt Express· May 2025

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CRISPR/Cas14a integrated with DNA walker based on magnetic self-assembly for human papillomavirus type 16 oncoprotein E7 ultrasensitive detection.
Yao Yue, Min Liu, Mingyi Ma, Zhihao Xu, Haoda Zhang

Biosens Bioelectron· March 2025

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A type of self-assembled and label-free DNA-modified electrochemical biosensors based on magnetic α-FeO/FeO heterogeneous nanorods for ultra-sensitive detection of CYP2C19*3.
Sihan Zhao, Peng Deng, Mingyi Ma, Zhihao Xu, Aolin He

Bioelectrochemistry· December 2024

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Effect and mechanism of paclitaxel loaded on magnetic FeO@mSiO-NH-FA nanocomposites to MCF-7 cells.
Yun Ni, Peng Deng, Ruitong Yin, Ziye Zhu, Chen Ling, Mingyi Ma

Drug Deliv· December 2023

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Nucleic acid aptasensor with magnetically induced self-assembly for the detection of EpCAM glycoprotein.
Yao Yue, Hezhong Ouyang, Mingyi Ma, Yaping Yang, Haoda Zhang

Mikrochim Acta· December 2023

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Fabrication of magnetic-FeO/FeOheterostructure nanorods via the urea hydrolysis-calcination process and their biocompatibility with LOand HepGcells.
Ziye Zhu, Hezhong Ouyang, Chen Ling, Mingyi Ma, Jie Wang

Nanotechnology· October 2023

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Immobilization and property of penicillin G acylase on amino functionalized magnetic NiMgZnFeO nanoparticles prepared the rapid combustion process.
Mingyi Ma, Xiu Chen, Yao Yue, Jie Wang, Dawei He

Front Bioeng Biotechnol· March 2023

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The c.323 G>C mutation in LORICRIN causes new-found late-onset autosomal dominant loricrin keratoderma in a Chinese Han Pedigree.
Xiaojie Gao, Hua Li, Songhua Zhao, Xiabin Li, Jiao Zhao, Mingyi Ma

J Dermatol Sci· April 2022

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Correlation Between Brain Structure Atrophy and Plasma Amyloid-β and Phosphorylated Tau in Patients With Alzheimer's Disease and Amnestic Mild Cognitive Impairment Explored by Surface-Based Morphometry.
Kaidi Li, Hang Qu, Mingyi Ma, Chenyu Xia, Ming Cai, Qiang Ma

Front Aging Neurosci· April 2022

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A novel electrochemical DNA biosensor for transgenic soybean detection based on triple signal amplification.
Dongli Chen, Meng Zhang, Mingyi Ma, Hong Hai, Jianping Li

Anal Chim Acta· October 2019

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MicroRNA-101 reverses temozolomide resistance by inhibition of GSK3β in glioblastoma.
Tian Tian, Ma Mingyi, Xia Qiu, Yang Qiu

Oncotarget· November 2016

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Protective effect of treatment with low-dose gliclazide in a model of middle cerebral artery occlusion and reperfusion in rats.
Fang Tan, Hua Li, Mingyi Ma, Yerong Yu

Brain Res· April 2014

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Synthesis and biological evaluation of Combretastatin A-4 derivatives containing a 3'-O-substituted carbonic ether moiety as potential antitumor agents.
Mingyi Ma, Longru Sun, Hongxiang Lou, Mei Ji

Chem Cent J· December 2013

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[Analysis of PHEX gene mutation in a hypophosphatasia pedigree].
Ming-yi Ma, Hua Li, Yan-sen Cai

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· October 2013

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TARDBP gene mutations among Chinese patients with sporadic amyotrophic lateral sclerosis.
Rui Huang, Deng-Fu Fang, Ming-Yi Ma, Xiao-Yan Guo, Bi Zhao

Neurobiol Aging· May 2012

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Identification of novel mutations in Chinese Hans with autosomal dominant polycystic kidney disease.
Chaowen Yu, Yuan Yang, Lin Zou, Zhangxue Hu, Jing Li, Yongxin Ma, Mingyi Ma

BMC Med Genet· December 2011

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Some single-nucleotide polymorphisms of the TSSK2 gene may be associated with human spermatogenesis impairment.
Hao Zhang, Dan Su, Yuan Yang, Wei Zhang, Yunqiang Liu, Mingyi Ma, Yongxin Ma

J Androl· January 2011

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Evidence for a predisposing background for CAG expansion leading to HTT mutation in a Chinese population.
Mingyi Ma, Yuan Yang, Huifang Shang, Dan Su, Hao Zhang, Yongxin Ma

J Neurol Sci· November 2010

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Phenotypic expression of partial AZFc deletions is independent of the variations in DAZL and BOULE in a Han population.
Pu Chen, Mingyi Ma, Lei Li, Sizhong Zhang, Dan Su, Yongxin Ma

J Androl· June 2010

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GCH1 mutation and clinical study of Chinese patients with dopa-responsive dystonia.
Xin Liu, Shu-Shan Zhang, Deng-Fu Fang, Ming-Yi Ma, Xiao-Yan Guo

Mov Disord· March 2010

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[Copy number variation of trinucleotide repeat in dynamic mutation sites of autosomal dominant cerebellar ataxias related genes].
Pu Chen, Mingyi Ma, Huifang Shang, Dan Su, Sizhong Zhang

Zhonghua Yi Xue Yi Chuan Xue Za Zhi· December 2009

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Y chromosome haplogroups may confer susceptibility to partial AZFc deletions and deletion effect on spermatogenesis impairment.
Yuan Yang, Mingyi Ma, Lei Li, Wei Zhang, Pu Chen, Yongxin Ma

Hum Reprod· September 2008

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