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المؤلفون: Dong Chen, Jiuliang Yan, Peng Huang, Lianpeng Wu, Yanzhang Tian, Shushu Lu, Yu Tong, Chenchan Hu, Tuo Shao, Jichan Shi, Jianping Huang, Andre J Jeyarajan, Feifei Su, Zhimeng Cheng, Raymond T. Chung, Jianyi Dai, Xianning Dai, Shasha Li
المصدر: Hepatology Communications
مصطلحات موضوعية: medicine.medical_specialty, Coronavirus disease 2019 (COVID-19), ACE2, Chronic liver disease, medicine.disease_cause, gamma‐glutamyltransferase, Gastroenterology, digestive system, cholangiocyte injury, SARS‐CoV‐2, Liver disease, Internal medicine, medicine, Gamma-glutamyltransferase, Case report form, Coronavirus, Hepatology, biology, business.industry, Original Articles, medicine.disease, Elevated alkaline phosphatase, biology.protein, Biomarker (medicine), Original Article, medicine.symptom, business, liver disease
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المؤلفون: Huihui Zhou, Juanjuan Zhang, Min-Xin Guan, Xianning Dai, Qi-Ping Wei, Yan-Hong Sun, Xiangtian Zhou, Bei Lin, Fuxin Zhao, Jia Qu, Hui Mi, Xiaoling Liu
المصدر: Hereditas (Beijing). 34:1031-1042
مصطلحات موضوعية: Proband, Genetics, Mitochondrial DNA, genetic structures, Leber's hereditary optic neuropathy, Pedigree chart, General Medicine, Biology, medicine.disease, Penetrance, eye diseases, Haplogroup, Polymorphism (computer science), Mutation (genetic algorithm), medicine
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::a9176d2286d6e2d256230e04ff1fbb36
https://doi.org/10.3724/sp.j.1005.2012.01031 -
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المؤلفون: Xujie Dong, Min-Xin Guan, Hao Feng, Huihui Zhou, Bing Lin, Yan Li, Xiaoling Liu, Juanjuan Zhang, Xianning Dai, Yimin Yuan
المصدر: Biochemical and Biophysical Research Communications. 419:670-675
مصطلحات موضوعية: Adult, Male, China, Mitochondrial DNA, Adolescent, Sequence analysis, Molecular Sequence Data, Biophysics, Biology, Biochemistry, GTP Phosphohydrolases, Young Adult, Exon, Atrophy, Asian People, Optic Atrophy, Autosomal Dominant, medicine, Animals, Humans, Missense mutation, Amino Acid Sequence, Molecular Biology, Gene, Conserved Sequence, Loss function, Aged, Genetics, Cell Biology, Middle Aged, medicine.disease, eye diseases, Pedigree, Mutation, Mutation (genetic algorithm), Female
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المؤلفون: Huihui Zhou, Jun Qin Mo, Pingping Jiang, Yi Tong, Juanjuan Zhang, Yaping Qian, Yanchun Ji, Min Liang, Xianning Dai, Min-Xin Guan, Fuxin Zhao, Jia Qu, Xiangtian Zhou
المصدر: Investigative ophthalmologyvisual science. 53(8)
مصطلحات موضوعية: Adult, Male, congenital, hereditary, and neonatal diseases and abnormalities, China, genetic structures, Adolescent, DNA Mutational Analysis, macromolecular substances, Optic Atrophy, Hereditary, Leber, Mitochondrion, Biology, DNA, Mitochondrial, Haplogroup, Optic neuropathy, Young Adult, medicine, Humans, Family, Genetic Predisposition to Disease, Child, Gene, Cells, Cultured, Genetics, ATP synthase, Leber's hereditary optic neuropathy, nutritional and metabolic diseases, NADH Dehydrogenase, Articles, Middle Aged, medicine.disease, Phenotype, eye diseases, Pedigree, Genes, Mitochondrial, Child, Preschool, Mutation (genetic algorithm), Mutation, biology.protein, Female, Follow-Up Studies
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1be404a120d276c8193e54fd150febce
https://pubmed.ncbi.nlm.nih.gov/22577081