-
1دورية أكاديمية
المؤلفون: Sharon L Rowan, Karolina Rygiel, Fennigje M Purves-Smith, Nathan M Solbak, Douglas M Turnbull, Russell T Hepple
المصدر: PLoS ONE, Vol 7, Iss 1, p e29082 (2012)
وصف الملف: electronic resource
-
2دورية أكاديمية
المؤلفون: Jaakko L O Pohjoismäki, Steffi Goffart, Robert W Taylor, Douglas M Turnbull, Anu Suomalainen, Howard T Jacobs, Pekka J Karhunen
المصدر: PLoS ONE, Vol 5, Iss 5, p e10426 (2010)
وصف الملف: electronic resource
-
3
المؤلفون: Lydia Gutierrez-Gonzalez, Patrick F. Chinnery, Paul J. Tadrous, Tariq G. Fellous, Mona El-Bahrawy, Stuart McDonald, Satyajit Bhattacharya, Robert W. Taylor, Julia Burkert, Lisa Mears, Laura C. Greaves, George Elia, Christopher P. Day, Malcolm R. Alison, Adam Humphries, Hemant M. Kocher, Nemantha M.W. De‐Alwis, Douglas M. Turnbull, Nicholas A. Wright, Shahriar Islam
المصدر: Stem Cells. 27:1410-1420
مصطلحات موضوعية: Mitochondrial DNA, Cell, Biology, Cell fate determination, Outer root sheath, medicine.disease_cause, DNA, Mitochondrial, Electron Transport Complex IV, medicine, Humans, Cell Lineage, Stem Cell Niche, Progenitor cell, Genetics, Mutation, Epithelial Cells, Cell Biology, Immunohistochemistry, Clone Cells, Cell biology, medicine.anatomical_structure, Paneth cell, Molecular Medicine, Stem cell, Developmental Biology
-
4
المؤلفون: Nicholas A. Wright, Shahriar Islam, Douglas M. Turnbull, Lisa Mears, Paul J. Tadrous, Laura C. Greaves, Satyajit Bhattacharya, Tariq G. Fellous, George Elia, Patrick F. Chinnery, Robert W. Taylor, Malcolm R. Alison, Stuart McDonald, Hemant M. Kocher, Geoffery Taylor
المصدر: Hepatology. 49:1655-1663
مصطلحات موضوعية: Mitochondrial DNA, Liver cytology, DNA Mutational Analysis, Cell, Biology, DNA, Mitochondrial, law.invention, Electron Transport Complex IV, law, medicine, Humans, Cytochrome c oxidase, Cell Lineage, Stem Cell Niche, Polymerase chain reaction, Genetics, Hepatology, Cytochrome c, Immunohistochemistry, Molecular biology, medicine.anatomical_structure, Liver, Hepatocyte, Hepatocytes, biology.protein, Stem cell
-
5
المؤلفون: Don J. Mahad, Douglas M. Turnbull, Iryna Ziabreva, Hans Lassmann
المصدر: Brain
Mahad, D, Ziabreva, I, Lassmann, H & Turnbull, D 2008, ' Mitochondrial defects in acute multiple sclerosis lesions ', Brain, vol. 131, no. 7, pp. 1722-1735 . https://doi.org/10.1093/brain/awn105مصطلحات موضوعية: Male, Pathology, Mitochondrial Diseases, Respiratory chain, multiple sclerosis, Pathogenesis, PERSISTENT INHIBITION, Myelin, 0302 clinical medicine, cytochrome c oxidase, CULTURED HUMAN-CELLS, Aged, 80 and over, 0303 health sciences, Mitochondrial respiratory chain complex IV, Middle Aged, ENCODED SUBUNITS, Mitochondria, mitochondria, Oligodendroglia, Mitochondrial respiratory chain, medicine.anatomical_structure, Acute Disease, MYELIN-ASSOCIATED GLYCOPROTEIN, Female, RESPIRATORY-CHAIN, WHITE-MATTER, Adult, medicine.medical_specialty, CYTOCHROME-C-OXIDASE, Multiple Sclerosis, Pattern III lesion, Biology, COMPLEX-I, White matter, Electron Transport, Electron Transport Complex IV, Mitochondrial Proteins, 03 medical and health sciences, Mitochondrial Encephalomyopathies, medicine, Humans, 030304 developmental biology, Aged, NITRIC-OXIDE, Multiple sclerosis, Diffuse Cerebral Sclerosis of Schilder, Original Articles, medicine.disease, Axons, Astrocytes, Immunology, Neurology (clinical), NEURODEGENERATIVE DISEASES, 030217 neurology & neurosurgery
وصف الملف: application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5afc31ec1a7fa617240c152acb7bcea0
http://europepmc.org/articles/PMC2442422 -
6
المؤلفون: Patrick F. Chinnery, Douglas M. Turnbull
المصدر: The Lancet. 354:S17-S21
مصطلحات موضوعية: Chromosome Aberrations, Gene Rearrangement, Genetics, Mitochondrial DNA, business.industry, Point mutation, Genetic Diseases, Inborn, Chromosome Disorders, General Medicine, Gene rearrangement, Disease, Biology, MT-RNR1, DNA, Mitochondrial, Human mitochondrial genetics, Genetic determinism, chemistry.chemical_compound, chemistry, Internal Medicine, Humans, Point Mutation, Apoptosis-inducing factor, Medicine, business, DNA
-
7
المؤلفون: Anu Suomalainen, Kari Majamaa, Patrick F. Chinnery, Michael G. Hanna, Douglas M. Turnbull, Valerio Carelli, Saskia Koene, Laurence A. Bindoff, Patrick Yu-Wai-Man, Robert McFarland, Rita Horvath, Michio Hirano, Jan A.M. Smeitink, Massimo Zeviani, Vamsi K. Mootha, Thomas Klopstock, Gerald Pfeffer
المساهمون: G. Pfeffer, R. Horvath, T. Klopstock, V. K. Mootha, A. Suomalainen, S. Koene, M. Hirano, M. Zeviani, L. A. Bindoff, P. Y. Wai-Man, M. Hanna, V. Carelli, R. McFarland, K. Majamaa, D. M. Turnbull, J. Smeitink, P. F. Chinnery
المصدر: Nature Reviews. Neurology, 9, 474-81
Nature Reviews Neurology; Vol 9
Nature Reviews. Neurology, 9, 8, pp. 474-81مصطلحات موضوعية: medicine.medical_specialty, Pathology, Mitochondrial Diseases, Mitochondrial disease, Alternative medicine, MEDLINE, Article, Bias (Epidemiology), Humans, Mitochondrial Disease, 03 medical and health sciences, Cellular and Molecular Neuroscience, 0302 clinical medicine, Bias, medicine, Humans, Clinical significance, Intensive care medicine, 030304 developmental biology, 0303 health sciences, business.industry, Reproducibility of Results, Mitochondrial medicine Energy and redox metabolism [IGMD 8], Publication bias, medicine.disease, 3. Good health, Multisystem disease, Mitochondrial medicine [IGMD 8], epidemiology/therapy, Reproducibility of Results, Biomarker (medicine), Neurology (clinical), business, 030217 neurology & neurosurgery
وصف الملف: STAMPA
-
8
المؤلفون: Sharon L. Rowan, Douglas M. Turnbull, Karolina A. Rygiel, Fennigje M. Purves-Smith, Nathan M. Solbak, Russell T. Hepple
المصدر: PLoS ONE
PLoS ONE, Vol 7, Iss 1, p e29082 (2012)مصطلحات موضوعية: Male, Aging, Anatomy and Physiology, Muscle Fibers, Skeletal, lcsh:Medicine, Muscle Proteins, Cell Count, Sodium Channels, NAV1.5 Voltage-Gated Sodium Channel, Tripartite Motif Proteins, 0302 clinical medicine, Myosin, Myocyte, lcsh:Science, Musculoskeletal System, Denervation, Motor Neurons, 0303 health sciences, Multidisciplinary, Organ Size, Muscle atrophy, medicine.anatomical_structure, Spinal Cord, Muscle, Medicine, Female, medicine.symptom, Research Article, Nervous System Physiology, medicine.medical_specialty, Proteasome Endopeptidase Complex, Ubiquitin-Protein Ligases, Biology, Neurological System, Muscle Types, 03 medical and health sciences, Gastrocnemius muscle, Atrophy, Internal medicine, medicine, Animals, 030304 developmental biology, Motor Systems, SKP Cullin F-Box Protein Ligases, Myosin Heavy Chains, lcsh:R, Skeletal muscle, Spinal cord, medicine.disease, Rats, Endocrinology, Gene Expression Regulation, Proteolysis, lcsh:Q, Physiological Processes, 030217 neurology & neurosurgery
-
9
المؤلفون: Kim J. Krishnan, Yevgenya Kraytsberg, Douglas M. Turnbull, Yuriy L. Orlov, Konstantin Popadin, Konstantin Khrapko, Gábor Zsurka, Wolfram S. Kunz, Natalya Markuzon, Xinhong Guo
المصدر: Trends in genetics : TIG. 26(8)
مصطلحات موضوعية: Genetics, Mitochondrial DNA, MtDNA deletions, Extramural, media_common.quotation_subject, Breakpoint, Longevity, Biology, Genome, DNA, Mitochondrial, Article, chemistry.chemical_compound, chemistry, Genome, Mitochondrial, Direct repeat, Animals, Humans, DNA, Gene Deletion, media_common, Repetitive Sequences, Nucleic Acid
-
10
المؤلفون: Pekka J. Karhunen, Howard T. Jacobs, Jaakko L. O. Pohjoismäki, Steffi Goffart, Douglas M. Turnbull, Anu Suomalainen, Robert W. Taylor
المساهمون: University of Tampere, Research Programs Unit, Research Programme for Molecular Neurology, Department of Neurosciences
المصدر: PLoS ONE
PLoS ONE, Vol 5, Iss 5, p e10426 (2010)مصطلحات موضوعية: ALPERS-SYNDROME, Male, Mitochondrial Diseases, lcsh:Medicine, Mitochondrion, medicine.disease_cause, Mice, 0302 clinical medicine, Lääketieteen bioteknologia - Medical biotechnology, FAILURE, lcsh:Science, Child, Genetics, Aged, 80 and over, Recombination, Genetic, 0303 health sciences, Mutation, Multidisciplinary, Cardiac muscle, Middle Aged, Phenotype, 3. Good health, medicine.anatomical_structure, MULTIPLE MTDNA DELETIONS, Child, Preschool, Cardiovascular Disorders/Myopathies, Female, Cardiovascular Disorders/Myocardial Infarction, PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA, Research Article, Adult, DNA Replication, Mitochondrial DNA, Adolescent, DNA Copy Number Variations, Heart Diseases, Mitochondrial disease, Heart Ventricles, education, Biology, DNA, Mitochondrial, Mitochondrial Proteins, 03 medical and health sciences, medicine, Animals, Humans, 030304 developmental biology, Molecular Biology/DNA Replication, Aged, TRANSCRIPTION FACTOR-A, Molecular Biology/Recombination, Molecular Biology/DNA Repair, MUTATIONS, HUMAN-CELLS, Point mutation, Myocardium, lcsh:R, DNA replication, DNA Helicases, Infant, Newborn, Infant, Developmental Biology/Aging, medicine.disease, DNA Polymerase I, HUMAN HEART, Case-Control Studies, HELICASE TWINKLE, lcsh:Q, AUTOSOMAL-DOMINANT, 030217 neurology & neurosurgery
وصف الملف: fulltext
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::af1f87e324379a826cde143730081198
https://trepo.tuni.fi/handle/10024/65917