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1دورية أكاديمية
المؤلفون: Xue-Jiao Yu, Yu Ding
المصدر: Mitochondrial DNA. Part B. Resources, Vol 5, Iss 3, Pp 3778-3783 (2020)
مصطلحات موضوعية: mt-trna mutations, phylogenetic analysis, pathogenic, ndm, Genetics, QH426-470
وصف الملف: electronic resource
العلاقة: https://doaj.org/toc/2380-2359Test
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المؤلفون: Yu Ding, Xue-Jiao Yu
المصدر: Mitochondrial DNA. Part B, Resources
article-version (VoR) Version of Recordمصطلحات موضوعية: 0106 biological sciences, 0301 basic medicine, Genetics, phylogenetic analysis, mt-tRNA mutations, pathogenic, NDM, Biology, 010603 evolutionary biology, 01 natural sciences, Mitochondrial trna, 03 medical and health sciences, 030104 developmental biology, Molecular Biology, Rapid Communication, Research Article
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9556464eecf9b01c83cc194189721e5Test
https://doi.org/10.1080/23802359.2020.1839364Test -
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المؤلفون: Liuchun, Yang, Qinxian, Guo, Jianhang, Leng, Keyi, Wang, Yu, Ding
المصدر: Journal of Clinical Laboratory Analysis
مصطلحات موضوعية: Adult, Male, Mitochondrial Diseases, Deafness, Middle Aged, DNA, Mitochondrial, Pedigree, mt‐tRNA mutations, Diabetes Mellitus, Type 2, RNA, Transfer, m.A5514G, MIDD, Mutation, Animals, Humans, Female, m.C12237T, Research Articles, Research Article
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::f2c0532534522b89d68c8c274161526fTest
https://pubmed.ncbi.nlm.nih.gov/34811812Test -
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المؤلفون: Rosalba Carrozzo, Helen A. L. Tuppen, Sara Seneca, Se Olpin, Fabiana Fattori, Eileen P. Treacy, Massimo Zeviani, Joanne Martindale, Robert McFarland, Salvatore DiMauro, Robert W. Taylor, Filippo M. Santorelli
المساهمون: Department of Embryology and Genetics
المصدر: Vrije Universiteit Brussel
مصطلحات موضوعية: Male, Mitochondrial Diseases, RNA, Mitochondrial, Biopsy, DNA Mutational Analysis, Mitochondrion, medicine.disease_cause, Mitochondria, Heart, homoplasmic mt tRNA mutations, Child, Cells, Cultured, Genetics (clinical), Adult, DNA, Mitochondrial, Female, Fibroblasts, Humans, Infant, Mitochondria, Muscle, Muscle, Skeletal, Polymorphism, Genetic, RNA, RNA, Transfer, Thr, Skin, Mutation, Genetics, Homoplasmy, education.field_of_study, Cultured, Heart, Skeletal, Heteroplasmy, Mitochondrial, Mitochondria, Transfer RNA, Muscle, Mitochondrial DNA, Cells, Population, Biology, Thr, Genetic, medicine, Polymorphism, education, Gene, mt disorders, DNA, Molecular biology, Transfer, mt tRNAThr gene
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87f550d06dcd909676b51fe193331b8cTest
https://biblio.vub.ac.be/vubir/further-pitfalls-in-the-diagnosis-of-mtdnaTest-mutations -homoplasmic-mttrna-mutations (7df88070-a1f9-4b04-9724-e159210f5ccb).html