Yi Zhu

Vanderbilt University — United States

Biochemistry, Genetics and Molecular Biology · Life Sciences

18h-index1.5kcitations36works4.32yr avg
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Research Topics

Mitochondrial Function and Pathology(16), Hearing, Cochlea, Tinnitus, Genetics(12), RNA and protein synthesis mechanisms(12), RNA modifications and cancer(5), Pain Mechanisms and Treatments(4)

Publications36 total

Magnetic soft robotic valve for minimally invasive therapy of gastroesophageal reflux disease
Device·2025· 1 cited
Magnetic mesoporous silica loaded with CGRP antagonist and curcumin coated with cerium oxide for the treatment of neuropathic pain
Journal of Materials Science Materials in Engineering·2025Open Access
Systematic pharmacology and experimental validation revealed the mechanism of Bupleurum chinense DC -mediated autophagy in alleviating osteoarthritis
Journal of Ethnopharmacology·2025· 3 cited
Mesoporous silica loaded with calcitonin gene-related peptide antagonist and curcumin alleviate oxidative stress and inflammation in the sciatic nerve
Frontiers in Molecular Biosciences·2025· 1 citedOpen Access
Curcumin relieves CFA-induced inflammatory pain by inhibiting the AP-1/c-Jun-CCL2-CCR2 pathway in the spinal dorsal horn
Molecular Pain·2025· 4 citedOpen Access
SPI1 facilitates microfracture-mediated cartilage regeneration in the elderly by enhancing bone marrow stromal cells stemness
Journal of Tissue Engineering·2025· 2 citedOpen Access
Systematic Pharmacology and Experimental Validation to Reveal the Alleviation of Astragalus membranaceus Regulating Ferroptosis in Osteoarthritis
Drug Design Development and Therapy·2024· 11 citedOpen Access
The Function of Necroptosis and Its Treatment Target in IBD
Mediators of Inflammation·2024· 12 citedOpen Access
Inhibition of BGT1/JAK2/STAT3 pathway activation correlates with the analgesic effects of Maresin1 in a neuropathic pain mouse model
Figshare·2023Open Access
Contribution of the tRNAIle 4317A→G mutation to the phenotypic manifestation of the deafness-associated mitochondrial 12S rRNA 1555A→G mutation
Journal of Biological Chemistry·2018· 40 citedOpen Access
Clinical Characteristics of Early Onset and Late-onset Parkinson’s Disease in Xinjiang Uygur Nationality
2018
Mitochondrial haplogroup B increases the risk for hearing loss among the Eastern Asian pedigrees carrying 12S rRNA 1555A>G mutation
Protein & Cell·2015· 13 citedOpen Access
GJB2 Mutation Spectrum and Genotype-Phenotype Correlation in 1067 Han Chinese Subjects with Non-Syndromic Hearing Loss
PLoS ONE·2015· 49 citedOpen Access
Mutation analysis of PARK2 in a Uyghur family with early-onset Parkinson's disease in Xinjiang, China
Journal of the Neurological Sciences·2014· 6 cited
Mitochondrial 12S rRNA A1555G mutation associated with nonsyn-dromic hearing loss in twenty-five Han Chinese pedigrees
Hereditas (Beijing)·2013· 4 cited
Human Mitochondrial tRNA Mutations in Maternally Inherited Deafness
Journal of Otology·2013· 1 citedOpen Access
Spectrum and frequency of mitochondrial 12S rRNA variants in the Chinese subjects with nonsynrdomic hearing loss in Zhejiang Prov-ince
Hereditas (Beijing)·2012· 3 cited
Mitochondrial tRNA Mutations Associated With Hearing Loss*
PROGRESS IN BIOCHEMISTRY AND BIOPHYSICS·2012· 2 cited
Frequency and spectrum of mitochondrial 12S rRNA variants in 440 Han Chinese hearing impaired pediatric subjects from two otology clinics
Journal of Translational Medicine·2011· 31 citedOpen Access
Maternally inherited hearing loss is associated with the novel mitochondrial tRNASer(UCN) 7505T>C mutation in a Han Chinese family
Molecular Genetics and Metabolism·2010· 40 cited
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Frequent Co-authors

Min‐Xin Guan(21), Jianxin Lü(15), Xiaowen Tang(14), Li Yang(13), Jing Zheng(10), Jindan Wang(9), Aifen Yang(8), Ronghua Li(7), Zhisu Liao(7), Bobei Chen(7), Dongmei Sun(7), Xinjian Wang(7), Yaping Qian(6), Jianyue Zhao(6), Zhihua Tao(6), Zhiyuan Li(5), Jian‐Fu Chen(5), Shuki Mizutani(4), Shigeaki Nonoyama(4), Guang-Hua Peng(4)