المؤلفون: Lihao Jin, Dingyi Gan, Wentao He, Na Wu, Shuchenlu Xiang, Yinsheng Wei, Gilbert Eriani, Yanchun Ji, Min‐Xin Guan, Meng Wang

المصدر: Advanced Science, Vol 11, Iss 41, Pp n/a-n/a (2024)

مصطلحات موضوعية: apoptosis, leber's hereditary optic neuropathy, mitochondrial tRNA mutation, mitophagy, phenotypic expression, Science

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2198-3844

URL الوصول: https://doaj.org/article/09acd8d11e7d4ff6a273c8b8f179e03b

المؤلفون: Riqiang Hu, Ting Yang, Qing Ai, Yuan Shi, Yanchun Ji, Qian Sun, Bei Tong, Jie Chen, Zhengli Wang

المصدر: Journal of Translational Medicine, Vol 22, Iss 1, Pp 1-18 (2024)

مصطلحات موضوعية: Autoinducer-2, Lactobacillus rhamnosus GG, Intestinal barrier function, Antibiotics-induced intestinal flora, Tight junctions, Butyric acid, Medicine

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1479-5876

URL الوصول: https://doaj.org/article/2cb30cbeb9b04cf0bc061002ffee16c9

المؤلفون: Jing Wang, Yanchun Ji, Cheng Ai, Jia-Rong Chen, Dingyi Gan, Juanjuan Zhang, Jun Q. Mo, Min-Xin Guan

المصدر: Journal of Biomedical Science, Vol 30, Iss 1, Pp 1-17 (2023)

مصطلحات موضوعية: Leber’s hereditary optic neuropathy, Mitochondrial DNA mutation, Complex I, Allotopic expression, Apoptosis, Mitophagy, Medicine

وصف الملف: electronic resource

Relation: https://doaj.org/toc/1423-0127

URL الوصول: https://doaj.org/article/88f101b335bf4e43ae57e28557b88262

المؤلفون: Yuanyuan Lyu, Man Xu, Jie Chen, YanChun Ji, Min-Xin Guan, Juanjuan Zhang

المصدر: Mitochondrial DNA. Part B. Resources, Vol 4, Iss 2, Pp 2266-2280 (2019)

مصطلحات موضوعية: leber’s hereditary optic neuropathy (lhon), mt-tt gene, variant, spectrum, chinese, Genetics, QH426-470

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2380-2359

URL الوصول: https://doaj.org/article/a465b536226a46368c3e49935bcdfd54

المؤلفون: Juanjuan Zhang, Xiaoling Liu, Xiaoyang Liang, Yuanyuan Lu, Ling Zhu, Runing Fu, Yanchun Ji, Wenlu Fan, Jie Chen, Bing Lin, Yimin Yuan, Pingping Jiang, Xiangtian Zhou, Min-Xin Guan

المصدر: Scientific Reports, Vol 7, Iss 1, Pp 1-13 (2017)

مصطلحات موضوعية: Medicine, Science

وصف الملف: electronic resource

Relation: https://doaj.org/toc/2045-2322

URL الوصول: https://doaj.org/article/fcfbc8471f944ec8a3d919a33f79392d

المؤلفون: Min Liang, Yanchun Ji, Liyao Zhang, Xuan Wang, Cuifang Hu, Juanjuan Zhang, Yiwei Zhu, Jun Q Mo, Min-Xin Guan

المصدر: Human Molecular Genetics. 31:3299-3312

مصطلحات موضوعية: Electron Transport Complex I, RNA, Mitochondrial, Ubiquitin-Protein Ligases, Mitophagy, Cytochromes c, RNA-Binding Proteins, Apoptosis, NADH Dehydrogenase, Optic Atrophy, Hereditary, Leber, General Medicine, DNA, Mitochondrial, Adenosine Triphosphate, Caspases, Mutation, Genetics, Homeostasis, Humans, RNA, RNA, Messenger, Annexin A5, Reactive Oxygen Species, Protein Kinases, Molecular Biology, Genetics (clinical), bcl-2-Associated X Protein

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21ddc97f7c6022dd60cbbedc3af4c5b0
https://doi.org/10.1093/hmg/ddac109

المؤلفون: Jia-Rong Chen, Chao Chen, Jie Chen, Yanchun Ji, Yanna Lian, Juanjuan Zhang, Jialing Yu, Xiang-Yao Li, Jia Qu, Min-Xin Guan

المصدر: Human molecular genetics.

مصطلحات موضوعية: Genetics, General Medicine, Molecular Biology, Genetics (clinical)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d32e1e7fc2fe6883bb3ffb799438e90b
https://pubmed.ncbi.nlm.nih.gov/36611011

المؤلفون: Feilong Meng, Zidong Jia, Jing Zheng, Yanchun Ji, Jing Wang, Yun Xiao, Yong Fu, Meng Wang, Feng Ling, Min-Xin Guan

المصدر: Nucleic acids research. 50(16)

مصطلحات موضوعية: DNA Replication, DNA-Binding Proteins, Mitochondrial Proteins, RNA, Transfer, Cys, Mutation, Genetics, Humans, Deafness, DNA, Mitochondrial, Mitochondria

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aab6a1bb2ad09fec33d44d4fe186f658
https://pubmed.ncbi.nlm.nih.gov/36039763

المؤلفون: Zidong Jia, Feilong Meng, Hui Chen, Gao Zhu, Xincheng Li, Yunfan He, Liyao Zhang, Xiao He, Huisen Zhan, Mengquan Chen, Yanchun Ji, Meng Wang, Min-Xin Guan

المصدر: Nucleic acids research. 50(16)

مصطلحات موضوعية: Mammals, RNA, Transfer, Pro, RNA, Transfer, Met, RNA, Transfer, Asn, RNA, Transfer, RNA, Transfer, Gln, Genetics, Animals, Humans, Intramolecular Transferases, RNA, Transfer, Glu, Pseudouridine, HeLa Cells

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::024bc392015bb6dbc467d673b9aa251e
https://pubmed.ncbi.nlm.nih.gov/36018806

المؤلفون: Yanqi Zhang, Jiang Liu, Hong Wei, Qing Ai, Ya Hu, Qian Sun, Yanchun Ji

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::788a00a7485a0187e1b5f083cf58b70c
https://doi.org/10.21203/rs.3.rs-1750223/v1

المؤلفون: Zhipeng Nie, Chenghui Wang, Jiarong Chen, Yanchun Ji, Hongxing Zhang, Fuxin Zhao, Xiangtian Zhou, Min-Xin Guan

المصدر: Human molecular genetics.

مصطلحات موضوعية: Genetics, General Medicine, Molecular Biology, Genetics (clinical)

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::becac2831ff0c09e5ae3484a4d3aa7fc
https://pubmed.ncbi.nlm.nih.gov/35947995

المؤلفون: Yanchun Ji, Juanjuan Zhang, Min Liang, Feilong Meng, Minglian Zhang, Jun Q. Mo, Meng Wang, Min-Xin Guan

المصدر: Mitochondrion. 65

مصطلحات موضوعية: China, RNA, Transfer, Mutation, Molecular Medicine, Humans, NADH Dehydrogenase, Cell Biology, Optic Atrophy, Hereditary, Leber, Molecular Biology, DNA, Mitochondrial, Pedigree

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b02969b03aef6293229e10bb319e0f1d
https://pubmed.ncbi.nlm.nih.gov/35623556

المؤلفون: Yanchun, Ji, Zhipeng, Nie, Feilong, Meng, Cuifang, Hu, Hui, Chen, Lihao, Jin, Mengquan, Chen, Minglian, Zhang, Juanjuan, Zhang, Min, Liang, Meng, Wang, Min-Xin, Guan

المصدر: The Journal of Biological Chemistry

مصطلحات موضوعية: autophagy, RNA, Mitochondrial, RNA Stability, PARP, poly ADP ribose polymerase, oxidative phosphorylation, Apoptosis, RNA, Transfer, Ala, LAMP1, lysosome-associated membrane glycoprotein 1, LHON, Leber’s hereditary optic neuropathy, Electron Transport, Mitochondrial Proteins, Adenosine Triphosphate, ROS, reactive oxidative species, Humans, OCR, oxygen consumption rate, RNA Processing, Post-Transcriptional, A73, adenosine at position 73, mDNA, mitochondrial DNA, Membrane Potential, Mitochondrial, mitochondrial tRNA 3’-end metabolisms, Base Sequence, OXPHOS, oxidative phosphorylation system, Mitophagy, Cytochromes c, TBE, Tris-borate-EDTA, RGC, retinal ganglion cell, Mitochondria, Mutation, Nucleic Acid Conformation, Transfer RNA Aminoacylation, Leber’s hereditary optic neuropathy, Reactive Oxygen Species, TRNT1, tRNA nucleotidyltransferase, Research Article

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::513910878a65d58108a6af53b8e3a784
https://pubmed.ncbi.nlm.nih.gov/34023389

المؤلفون: Yuanyuan, Lyu, Man, Xu, Jie, Chen, YanChun, Ji, Min-Xin, Guan, Juanjuan, Zhang

المصدر: Mitochondrial DNA. Part B, Resources
article-version (VoR) Version of Record

مصطلحات موضوعية: congenital, hereditary, and neonatal diseases and abnormalities, Chinese, genetic structures, variant, nutritional and metabolic diseases, MT-TT gene, Leber’s hereditary optic neuropathy (LHON), Mito Communications, eye diseases, Research Article, spectrum

URL الوصول: https://explore.openaire.eu/search/publication?articleId=pmid________::426dd6388295839f127517ac314bd963
https://pubmed.ncbi.nlm.nih.gov/33365504

المؤلفون: Feilong Meng, Xiaoying Luo, Yilin Tao, Tao Zhu, Weixin Cheng, Peifang Jiang, Yanchun Ji, Yinjie Ling

المصدر: Bioscience Reports

مصطلحات موضوعية: 0301 basic medicine, Biophysics, Pedigree chart, Mitochondrion, Biology, Biochemistry, Molecular Bases of Health & Disease, 03 medical and health sciences, 0302 clinical medicine, genetics, Epigenetics, Molecular Biology, Gene, Research Articles, pathophysiology, Genetics, Chinese, Phylogenetic tree, Cell Biology, Penetrance, Phenotype, 030104 developmental biology, Tourette’s disorder, Mutation, Transfer RNA, 030217 neurology & neurosurgery

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8d1729282dc02f1c2421ef8ae5249b4
https://doi.org/10.1042/bsr20201856

المؤلفون: Min-Xin Guan, Yanchun Ji, Minglian Zhang, Feilong Meng, Yuanyuan Lu, Juanjuan Zhang, Rulai Yang, Xiaoting Mao, Qiuzi Yi, Mengquan Chen, Yun Xiao, Shipeng Xie

المصدر: J Biol Chem

مصطلحات موضوعية: 0301 basic medicine, Male, Mitochondrial DNA, Non-Mendelian inheritance, congenital, hereditary, and neonatal diseases and abnormalities, Mitochondrial disease, Optic Atrophy, Hereditary, Leber, Mitochondrion, Biology, Bioenergetics, medicine.disease_cause, Biochemistry, DNA, Mitochondrial, Cell Line, 03 medical and health sciences, medicine, Humans, Point Mutation, Molecular Biology, Gene, Genetics, Mutation, 030102 biochemistry & molecular biology, Leber's hereditary optic neuropathy, NADH Dehydrogenase, Cell Biology, medicine.disease, Penetrance, eye diseases, 030104 developmental biology, Phenotype, Female

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::67b663a4856e6efad4ae96eeb7ab6221
https://pubmed.ncbi.nlm.nih.gov/32723871

المؤلفون: Min-Xin Guan, Juanjuan Zhang, Jie Chen, Yanchun Ji, Minglian Zhang, Xiaoling Liu, Bibin Wang

المصدر: Mitochondrion. 42:84-91

مصطلحات موضوعية: 0301 basic medicine, Non-Mendelian inheritance, Mitochondrial DNA, Mutation, medicine.diagnostic_test, Leber's hereditary optic neuropathy, Cell Biology, Mitochondrion, Biology, medicine.disease, medicine.disease_cause, Molecular biology, 03 medical and health sciences, 030104 developmental biology, 0302 clinical medicine, Western blot, Transfer RNA, medicine, Molecular Medicine, Northern blot, Molecular Biology, 030217 neurology & neurosurgery

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::558e0249d853183a8a3d9dd75f36ed0b
https://doi.org/10.1016/j.mito.2017.12.003

المؤلفون: Xiaoling Liu, Min-Xin Guan, Yinglong Gao, Juanjuan Zhang, Qi‑Ping Wei, Ling Zhu, Zidong Jia, Xiaoyang Liang, Yanchun Ji, Pingping Jiang, Lihua Qiao

المصدر: Molecular Medicine Reports. 16:8997-9004

مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Cancer Research, Mitochondrial DNA, Adolescent, genetic structures, DNA Mutational Analysis, Optic Atrophy, Hereditary, Leber, Biology, medicine.disease_cause, DNA, Mitochondrial, Biochemistry, Haplogroup, Optic neuropathy, 03 medical and health sciences, 0302 clinical medicine, Asian People, Genetics, medicine, Humans, Family, Genetic Predisposition to Disease, Child, Molecular Biology, Gene, Genetic Association Studies, Aged, Mutation, Base Sequence, Leber's hereditary optic neuropathy, medicine.disease, eye diseases, Pedigree, 030104 developmental biology, Oncology, Transfer RNA, 030221 ophthalmology & optometry, Molecular Medicine, Female, Age of onset

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a02d4766814f4e2877a5245c4ba4b73a
https://doi.org/10.3892/mmr.2017.7734

المؤلفون: Wenlu Fan, Ling Zhu, Bing Lin, Yanchun Ji, Runing Fu, Min-Xin Guan, Yimin Yuan, Xiangtian Zhou, Yuanyuan Lu, Pingping Jiang, Xiaoling Liu, Xiaoyang Liang, Juanjuan Zhang, Jie Chen

المصدر: Scientific Reports, Vol 7, Iss 1, Pp 1-13 (2017)
Scientific Reports

مصطلحات موضوعية: 0301 basic medicine, Mitochondrial DNA, Science, Apoptosis, Biology, Mitochondrion, medicine.disease_cause, Retinal ganglion, DNA, Mitochondrial, Article, Cell Line, GTP Phosphohydrolases, 03 medical and health sciences, 0302 clinical medicine, Asian People, Optic Atrophy, Autosomal Dominant, medicine, Humans, Genetics, Membrane Potential, Mitochondrial, Mutation, Multidisciplinary, ATP synthase, Molecular biology, eye diseases, Mitochondria, Blot, 030104 developmental biology, Cell culture, biology.protein, Medicine, Reactive Oxygen Species, 030217 neurology & neurosurgery

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::82c1a86b5e128737a3c1cfbc598e75ac
https://doaj.org/article/fcfbc8471f944ec8a3d919a33f79392d

المؤلفون: Ningning Zhao, Guanping Dong, Feilong Meng, Junfen Fu, Jinling Wang, Ke Huang, Yanchun Ji, Xiaoting Mao

المصدر: Bioscience Reports. 40

مصطلحات موضوعية: Genetics, Mutation (genetic algorithm), Biophysics, medicine, Cell Biology, Biology, Chinese family, medicine.disease, Molecular Biology, Biochemistry, Mitochondrial trna, Obesity

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::0b3b6ccb71ba7a7d9035eb46683f3d9f
https://doi.org/10.1042/bsr20200131