Tài liệu tham khảo |
Loại |
Chi tiết |
8. Bai R. K., Wong L. J. C. (2004), “Detection and quantification of heteroplasmic mutant mitochondrial DNA by real-time amplification refractory mutation system quantitative PCR analysis: A single-step approach”, Clinical Chemistry, 50, pp. 996-1001 |
Sách, tạp chí |
Tiêu đề: |
Detection and quantification of heteroplasmic mutant mitochondrial DNA by real-time amplification refractory mutation system quantitative PCR analysis: A single-step approach”, "Clinical Chemistry |
Tác giả: |
Bai R. K., Wong L. J. C |
Năm: |
2004 |
|
11. Blasiak J., Glowacki S., Kauppinen A., Kaarniranta K. (2013), “Mitochondrial and Nuclear DNA Damage and Repair in Age-Related Macular Degeneration”, International Journal of Molecular Sciences, 14(2), pp.2996-3010 |
Sách, tạp chí |
Tiêu đề: |
Mitochondrial and Nuclear DNA Damage and Repair in Age-Related Macular Degeneration”, "International Journal of Molecular Sciences |
Tác giả: |
Blasiak J., Glowacki S., Kauppinen A., Kaarniranta K |
Năm: |
2013 |
|
12. Bornsttein B., Mas J. A., Patrono. C., Fernández-Moreno M. A., González- Vioque E., Campos. Y., Carrozzo. R., Martín. M. A., Del Hoyo . P., Santorelli. F. M., Arenas J., Garesse R. (2005), “Comparative analysis of the pathogenic mechanisms associated with the G8363A and A8296G mutations in the mitochondrial tRNA Lys gene”, Biochemical Journal, 387, pp. 773–77 |
Sách, tạp chí |
Tiêu đề: |
Comparative analysis of the pathogenic mechanisms associated with the G8363A and A8296G mutations in the mitochondrial tRNA Lys gene”, "Biochemical Journal |
Tác giả: |
Bornsttein B., Mas J. A., Patrono. C., Fernández-Moreno M. A., González- Vioque E., Campos. Y., Carrozzo. R., Martín. M. A., Del Hoyo . P., Santorelli. F. M., Arenas J., Garesse R |
Năm: |
2005 |
|
13. Boulet L., Karpati G., Shoubridge E. A. (1992) “Distribution and threshold expression of the tRNA-lys mutation in skeletal muscle of patients with myoclonic epilepsy and ragged-red fibers (MERRF)”, The American Journal of Human Genetics, 51(6), pp. 1187 - 1200 |
Sách, tạp chí |
Tiêu đề: |
Distribution and threshold expression of the tRNA-lys mutation in skeletal muscle of patients with myoclonic epilepsy and ragged-red fibers (MERRF)”, "The American Journal of Human Genetics |
|
14. Burgstaller J. P., Johnston I. G., Poulton J. (2015), “Mitochondrial DNA disease and developmental implications for reproductive strategies”, Molecular Human Reproduction, 21(1), pp.11-22 |
Sách, tạp chí |
Tiêu đề: |
Mitochondrial DNA disease and developmental implications for reproductive strategies”, "Molecular Human Reproduction |
Tác giả: |
Burgstaller J. P., Johnston I. G., Poulton J |
Năm: |
2015 |
|
15. Calabresi P. A., Silvestri G., Dimauro S., Grigga R. C. (1994), “Ekbom’s syndrome: Lipomas, ataxia, and neuropathy with MERRF”, Muscle and Nerve, 17, pp. 943-945 |
Sách, tạp chí |
Tiêu đề: |
Ekbom’s syndrome: Lipomas, ataxia, and neuropathy with MERRF”, "Muscle and Nerve |
Tác giả: |
Calabresi P. A., Silvestri G., Dimauro S., Grigga R. C |
Năm: |
1994 |
|
16. Cao Y., Ma Y., Zhang Y., Li Y., Fang F., Wang S., Bu D., Xu Y., Pei P., Li L., Xiao Y., Wua H, Yang Y., Zou L., Qi Y. (2010), “Detection of eight frequently encountered point mutations in mitochondria in Chinese patients suggestive of mitochondrial encephalomyopathies”, Mitochondrion, 10, pp.330-334 |
Sách, tạp chí |
Tiêu đề: |
Detection of eight frequently encountered point mutations in mitochondria in Chinese patients suggestive of mitochondrial encephalomyopathies”, "Mitochondrion |
Tác giả: |
Cao Y., Ma Y., Zhang Y., Li Y., Fang F., Wang S., Bu D., Xu Y., Pei P., Li L., Xiao Y., Wua H, Yang Y., Zou L., Qi Y |
Năm: |
2010 |
|
17. Chong J. W., Annuar A. A, Wong W. T., Thong M. K., Goh K. J. (2014), “Single mitochondrial DNA deletions in chronic progressive external ophthalmoplegia (CPEO) and Kearns-Sayre syndrome (KSS) patients from a multiethnic Asian population”, Neurology Asia, 19(1), pp. 27-36 |
Sách, tạp chí |
Tiêu đề: |
Single mitochondrial DNA deletions in chronic progressive external ophthalmoplegia (CPEO) and Kearns-Sayre syndrome (KSS) patients from a multiethnic Asian population”, "Neurology Asia |
Tác giả: |
Chong J. W., Annuar A. A, Wong W. T., Thong M. K., Goh K. J |
Năm: |
2014 |
|
18. Cohen H. B. (2013), “Neuromuscular and Systemic Presentations in Adults: diagnoses beyond MERRF and MELAS”, Neurotherapeutics, 10, pp. 227–242 |
Sách, tạp chí |
Tiêu đề: |
Neuromuscular and Systemic Presentations in Adults: diagnoses beyond MERRF and MELAS”, "Neurotherapeutics |
Tác giả: |
Cohen H. B |
Năm: |
2013 |
|
20. De la Mata M., Garrido-Maraver J., Cotán D., Cordero M. D., Oropesa-Ávila M., Izquierdo L. G., De Miguel M., Lorite J. B., Infante E. R., Ybot P., Jackson S., Sánchez-Alcázar J. A. (2012), “Recovery of MERRF Fibroblasts and Cybrids Pathophysiology by Coenzyme Q 10 ”, Neurotherapeutics, 9, pp. 446-463 |
Sách, tạp chí |
Tiêu đề: |
Recovery of MERRF Fibroblasts and Cybrids Pathophysiology by Coenzyme Q10”, "Neurotherapeutics |
Tác giả: |
De la Mata M., Garrido-Maraver J., Cotán D., Cordero M. D., Oropesa-Ávila M., Izquierdo L. G., De Miguel M., Lorite J. B., Infante E. R., Ybot P., Jackson S., Sánchez-Alcázar J. A |
Năm: |
2012 |
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21. Detmer S. A., Chan D. C. (2007), “Functions and dysfunctions of mitochondrial dynamics”, Nature Publishing Group, 8, pp. 870-879 |
Sách, tạp chí |
Tiêu đề: |
Functions and dysfunctions of mitochondrial dynamics”, "Nature Publishing Group |
Tác giả: |
Detmer S. A., Chan D. C |
Năm: |
2007 |
|
22. Duchen M. R. (2004), “Roles of Mitochondria in Health and Disease”, Diabetes, 53, pp. 96-102 |
Sách, tạp chí |
Tiêu đề: |
Roles of Mitochondria in Health and Disease”, "Diabetes |
Tác giả: |
Duchen M. R |
Năm: |
2004 |
|
23. Duchen M. R., Szabadkai G. (2010), “Role of mitochondria in human disease”, Essay in Biochemistry, 47, pp. 118-136 |
Sách, tạp chí |
Tiêu đề: |
Role of mitochondria in human disease”, "Essay in Biochemistry |
Tác giả: |
Duchen M. R., Szabadkai G |
Năm: |
2010 |
|
24. El-Hattab A. W., Scaglia F. (2013), “Mitochondrial DNA Depletion Syndromes: Review and Updates of Genetic Basis, Manifestations, and Therapeutic Options”, Neurotherapeutics, 10, pp. 186-198 |
Sách, tạp chí |
Tiêu đề: |
Mitochondrial DNA Depletion Syndromes: Review and Updates of Genetic Basis, Manifestations, and Therapeutic Options”, "Neurotherapeutics |
Tác giả: |
El-Hattab A. W., Scaglia F |
Năm: |
2013 |
|
28. Fukuhara N., Tokiguchi S., Shirakawa K., Tsubaki T. (1980), “Myoclonus epilepsy associated with ragged-red fibers (mitochondrial abnormalities) disease entity or a syndrome”, Journal Neurol Science, 4791, pp. 117-133 |
Sách, tạp chí |
Tiêu đề: |
Myoclonus epilepsy associated with ragged-red fibers (mitochondrial abnormalities) disease entity or a syndrome”, "Journal Neurol Science |
Tác giả: |
Fukuhara N., Tokiguchi S., Shirakawa K., Tsubaki T |
Năm: |
1980 |
|
29. Giles R. E. (1980), “Maternal inheritance of human mitochondria DNA”, Genetics, 77, pp. 6715-6719 |
Sách, tạp chí |
Tiêu đề: |
Maternal inheritance of human mitochondria DNA”, "Genetics |
Tác giả: |
Giles R. E |
Năm: |
1980 |
|
30. Graf W.D., Sumi S. M., Copass M. K., Ojemann L. M., Longstreth W. T., Shanske S., Lombes A., DiMauro S. (1993), “Phenotypic Heterogeneity in families with the Myoclonic Epilepsy and Ragged-Red Fiber Disease Point Mutation in Mitochondrial DNA”, American Neurological Association, 33, pp. 640-645 |
Sách, tạp chí |
Tiêu đề: |
Phenotypic Heterogeneity in families with the Myoclonic Epilepsy and Ragged-Red Fiber Disease Point Mutation in Mitochondrial DNA”, "American Neurological Association |
Tác giả: |
Graf W.D., Sumi S. M., Copass M. K., Ojemann L. M., Longstreth W. T., Shanske S., Lombes A., DiMauro S |
Năm: |
1993 |
|
31. Greaves L. C., Reeve A. K., Taylor R. W., Turnbull D. M. (2012) “Mitochondrial DNA and disease”, The Journal of Pathology, 226, pp. 274- 286 |
Sách, tạp chí |
Tiêu đề: |
Mitochondrial DNA and disease”, "The Journal of Pathology |
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32. Green R. D., Reed C. J. (1998), “Mitochondria and apoptosis”, Science, 281, pp. 1309 – 1311 |
Sách, tạp chí |
Tiêu đề: |
Mitochondria and apoptosis”, "Science |
Tác giả: |
Green R. D., Reed C. J |
Năm: |
1998 |
|
33. Hammans S. R., Sweeney M. G., Brockington M., Lennox G. G., Lawton N. F., Kennedy C. R., Morgan-Hughes J. A., Harding A. E. (1993), “The mitochondrial DNA transfer RNA Lys A G (8344) mutation and the syndrome of myoclonic epilepsy with ragged red fibres (MERRF): Relationship of clinical phenotype to proportion of mutant mitochondrial DNA”, Brain,116, pp. 617-632 |
Sách, tạp chí |
Tiêu đề: |
The mitochondrial DNA transfer RNALys AG(8344) mutation and the syndrome of myoclonic epilepsy with ragged red fibres (MERRF): Relationship of clinical phenotype to proportion of mutant mitochondrial DNA”, "Brain |
Tác giả: |
Hammans S. R., Sweeney M. G., Brockington M., Lennox G. G., Lawton N. F., Kennedy C. R., Morgan-Hughes J. A., Harding A. E |
Năm: |
1993 |
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