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Wyszukujesz frazę ""DNA, Mitochondrial genetics"" wg kryterium: Temat


Tytuł :
Family Phenotypic Heterogeneity Caused by Mitochondrial DNA Mutation A3243G
Autorzy :
Daniela Alves
Maria Eufémia Calmeiro
Carmo Macário
Rosa Silva
Pokaż więcej
Temat :
Child
Deafness/genetics
Diabetes Mellitus/genetics
DNA, Mitochondrial/genetics
Mutation
Medicine
Medicine (General)
R5-920
Źródło :
Acta Médica Portuguesa, Vol 30, Iss 7-8, Pp 581-585 (2017)
Opis pliku :
electronic resource
Relacje :
http://actamedicaportuguesa.com/revista/index.php/amp/article/view/8638; https://doaj.org/toc/0870-399X; https://doaj.org/toc/1646-0758
Dostęp URL :
https://doaj.org/article/9f8f1653d6694d698d3a3f1f1871f8f6
Czasopismo naukowe
Tytuł :
Letter to the Editor: Maternally Inherited Diabetes and Deafness is Not Only Biorgan but Multiorgan
Autorzy :
Josef Finsterer
Sinda Zarrouk-Mahjoub
Pokaż więcej
Temat :
Child
Deafness/genetics
Diabetes Mellitus/genetics
DNA, Mitochondrial/genetics
Mutation
Medicine
Medicine (General)
R5-920
Źródło :
Acta Médica Portuguesa, Vol 30, Iss 9, Pp 665-666 (2017)
Opis pliku :
electronic resource
Relacje :
http://actamedicaportuguesa.com/revista/index.php/amp/article/view/9716; https://doaj.org/toc/0870-399X; https://doaj.org/toc/1646-0758
Dostęp URL :
https://doaj.org/article/72f93549ec384caf87be8a696bb7d332
Czasopismo naukowe
Tytuł :
DNA repair in plant mitochondria - a complete base excision repair pathway in potato tuber mitochondria
Autorzy :
Ferrando, Beatriz
de Matos Furlanetto, Ana Luiza Dorigan
Gredilla, Ricardo
Havelund, Jesper F
Hebelstrup, Kim H
Møller, Ian Max
Stevnsner, Tinna
Pokaż więcej
Temat :
food and beverages
DNA-(Apurinic or Apyrimidinic Site) Lyase/genetics
Reactive Oxygen Species/metabolism
DNA Glycosylases/genetics
DNA, Mitochondrial/genetics
fungi
Mitochondria/genetics
DNA, Plant/genetics
DNA Repair/genetics
Solanum tuberosum/genetics
DNA-Directed DNA Polymerase/genetics
Źródło :
Ferrando, B, de Matos Furlanetto, A L D, Gredilla, R, Havelund, J F, Hebelstrup, K H, Møller, I M & Stevnsner, T 2019, ' DNA repair in plant mitochondria - A complete base excision repair pathway in potato tuber mitochondria ', Physiologia Plantarum, vol. 166, no. 2, pp. 494-512 . https://doi.org/10.1111/ppl.12801
Ferrando, B, Furlanetto, A L D M, Gredilla, R, Havelund, J F, Hebelstrup, K H, Møller, I M & Stevnsner, T 2019, ' DNA repair in plant mitochondria - a complete base excision repair pathway in potato tuber mitochondria ', Physiologia Plantarum, vol. 166, no. 2, pp. 494-512 . https://doi.org/10.1111/ppl.12801
Opis pliku :
application/pdf
Tytuł :
Germline selection shapes human mitochondrial DNA diversity
Autorzy :
Wei, Wei
Tuna, Salih
Smith, Katherine R.
Beales, Phil L.
Bennett, David L.
Gale, Daniel P.
Brennan, Paul
Elliott, Perry
Floto, R. Andres
Houlden, Henry
Koziell, Ania
Maher, Eamonn R.
Markus, Hugh S.
Morrell, Nicholas W.
Newman, William G.
Sayer, John A.
Smith, Kenneth G. C.
Taylor, Jenny C.
Watkins, Hugh
Webster, Andrew R.
Wilkie, Andrew O. M.
Penkett, Christopher J.
Stirrups, Kathleen E.
Rendon, Augusto
Bradley, John R.
Turro, Ernest
Chinnery, Patrick F.
Keogh, Michael J.
Aitman, Timothy J.
Bitner-Glindzicz, Maria A. K.
Black, Graeme C.
Flinter, Frances A.
Irving, Melita
Roberts, Irene
Williamson, Catherine
Ashford, Sofie
Ouwehand, Willem H.
Raymond, F. Lucy
Caulfield, Mark
Pokaż więcej
Temat :
HETEROPLASMY
TRANSCRIPTION
ASSOCIATION
Multidisciplinary Sciences
Maternal Inheritance
100,000 Genomes Project–Rare Diseases Pilot
General
MUTATIONS
DNA, Mitochondrial/genetics
LEIGH-DISEASE
Science & Technology - Other Topics
Selection, Genetic
Female
REPLICATION
NIHR BioResource–Rare Diseases
MD Multidisciplinary
MTDNA
yes
Genetic Variation
GENOME
SEQUENCE
Science & Technology
General Science & Technology
Genome, Mitochondrial
Ovum/growth & development
REPLACEMENT
Humans
Źródło :
NIHR BioResource–Rare Diseases, 100,000 Genomes Project–Rare Diseases Pilot & Daniels, M J 2019, ' Germline selection shapes human mitochondrial DNA diversity ', Science (New York, N.Y.), vol. 364, no. 6442 . https://doi.org/10.1126/science.aau6520
Science, 364(6442). American Association for the Advancement of Science
Tomlinson, I 2019, ' Germline selection shapes human mitochondrial DNA diversity ', Science, vol. 364, no. 6442, pp. 749-+ . https://doi.org/10.1126/science.aau6520
Opis pliku :
application/pdf
Tytuł :
ImtRDB: a database and software for mitochondrial imperfect interspersed repeats annotation
Autorzy :
Shamanskiy, Viktor N.
Timonina, Valeria N.
Popadin, Konstantin Yu.
Gunbin, Konstantin V.
Pokaż więcej
Temat :
Database
Algorithms
DNA, Circular/genetics
DNA, Mitochondrial/genetics
Databases, Genetic
Repetitive Sequences, Nucleic Acid
Software
Imperfect repeats
Selection on dinucleotides
mtDNA
Biotechnology
QH426-470
Genetics
TP248.13-248.65
Źródło :
BMC genomics, vol. 20, no. Suppl 3, pp. 295
BMC Genomics, Vol 20, Iss S3, Pp 1-17 (2019)
Opis pliku :
application/pdf
Tytuł :
TK2-related Myopathic Mitochondrial Depletion Syndrome
Autorzy :
Finsterer, Josef
Zarrouk-Mahjoub, Sinda
Pokaż więcej
Temat :
education
MESH: Muscle, Skeletal
embryonic structures
health care economics and organizations
MESH: Humans
animal structures
integumentary system
MESH: DNA, Mitochondrial/genetics
MESH: Mutation
[SDV.MHEP]Life Sciences [q-bio]/Human health and pathology
Źródło :
Pediatric and developmental pathology
Pediatric and developmental pathology, Springer Verlag, 2018, 21 (5), pp.507-508. ⟨10.1177/1093526617743906⟩
Tytuł :
Phylogeography of Aegean green toads (Bufo viridis subgroup): continental hybrid swarm vs. insular diversification with discovery of a new island endemic
Autorzy :
Stöck, Matthias
Dufresnes, Christophe
Lymberakis, Petros
Kornilios, Panagiotis
Savary, Romain
Perrin, Nicolas
Pokaż więcej
Temat :
Animals
Base Sequence
Biodiversity
Bufonidae/classification
Cell Nucleus/genetics
DNA, Mitochondrial/genetics
Gene Flow
Genetic Drift
Genetics, Population
Genome
Greece
Islands
Likelihood Functions
Mitochondria/genetics
Phylogeny
Phylogeography
Reproductive Isolation
Sequence Analysis, DNA
Evolution
QH359-425
Research
Źródło :
BMC Evolutionary Biology, Vol 18, Iss 1, Pp 1-12 (2018)
BMC evolutionary biology, vol. 18, no. 1, pp. 67
Opis pliku :
application/pdf
Tytuł :
Profound genetic divergence and asymmetric parental genome contributions as hallmarks of hybrid speciation in polyploid toads.
Autorzy :
Perrin, Nicolas
Stöck, Matthias
Betto-Colliard, Caroline
Hofmann, Sylvia
Sermier, Roberto
Pokaż więcej
Temat :
food and beverages
Research Article
Bufo viridis subgroup
Amphibian Proteins/genetics
Amphibian Proteins/metabolism
Animals
Bufonidae/genetics
Cell Nucleus/genetics
DNA, Mitochondrial/genetics
Genetic Speciation
Genetic Variation
Genome
Hybridization, Genetic
Multilocus Sequence Typing
Phylogeny
Polyploidy
Sequence Analysis, DNA
directional asymmetry
divergence
hybridization
multi-locus phylogeny
polyploidy
Evolution
Źródło :
Proceedings of the Royal Society B: Biological Sciences
Proceedings. Biological sciences, vol. 285, no. 1872, pp. 20172667
Opis pliku :
application/pdf
Tytuł :
Kinship structures create persistent channels for language transmission
Autorzy :
Bhattacharya, Tanmoy
Cox, Murray P.
Lansing, J. Stephen
Abundo, Cheryl
Jacobs, Guy S.
Guillot, E.
Thurner, Stefan
Downey, Sean S.
Chew, Lock Yue
Chung, Ning Ning
Sudoyo, Herawati
Pokaż więcej
Temat :
population genetics
Anthropology
Social Sciences
coevolution
kinship
language
DNA, Mitochondrial/genetics
Family
Female
Genetic Variation
Human Migration
Humans
Indonesia
Islands
Language
Linguistics
Male
Phylogeny
Sequence Analysis, DNA
cultural evolution
Źródło :
Proceedings of the National Academy of Sciences of the United States of America, vol. 114, no. 49, pp. 12910-12915
Proceedings of the National Academy of Sciences of the United States of America
Opis pliku :
text; application/pdf
Tytuł :
Mitochondrial DNA double-strand breaks in oligodendrocytes cause demyelination, axonal injury, and CNS inflammation
Autorzy :
Madsen, Pernille M.
Pinto, Milena
Patel, Shreyans
McCarthy, Stephanie
Gao, Han
Taherian, Mehran
Karmally, Shaffiat
Pereira, Claudia V.
Dvoriantchikova, Galina
Ivanov, Dmitry
Tanaka, Kenji F.
Moraes, Carlos T.
Brambilla, Roberta
Pokaż więcej
Temat :
Locomotion/physiology
Mitochondria
Multiple sclerosis
DNA Breaks, Double-Stranded
Mice
Oxidative phosphorylation
Encephalomyelitis, Autoimmune, Experimental/genetics
Mice, Inbred C57BL
Mice, Transgenic
Demyelinating Diseases/genetics
DNA, Mitochondrial/genetics
Demyelination
Oligodendroglia/pathology
Central Nervous System/pathology
Inflammation/genetics
Nerve Degeneration/genetics
Research Articles
Animals
Animal model
Female
Axons/pathology
Male
Remyelination
Źródło :
Madsen, P M, Pinto, M, Patel, S, McCarthy, S, Gao, H, Taherian, M, Karmally, S, Pereira, C V, Dvoriantchikova, G, Ivanov, D, Tanaka, K F, Moraes, C T & Brambilla, R 2017, ' Mitochondrial DNA double-strand breaks in oligodendrocytes cause demyelination, axonal injury, and CNS inflammation ', Journal of Neuroscience, vol. 37, no. 42, pp. 10185-10199 . https://doi.org/10.1523/JNEUROSCI.1378-17.2017
Opis pliku :
application/pdf
Tytuł :
Dysregulated mitophagy and mitochondrial organization in optic atrophy due to OPA1 mutations
Autorzy :
Liao, Chunyan
Ashley, Neil
Diot, Alan
Morten, Karl
Phadwal, Kanchan
Williams, Andrew
Fearnley, Ian
Rosser, Lyndon
Lowndes, Jo
Fratter, Carl
Ferguson, David J P
Vay, Laura
Quaghebeur, Gerardine
Moroni, Isabella
Bianchi, Stefania
Lamperti, Costanza
Downes, Susan M
Sitarz, Kamil S
Flannery, Padraig J
Carver, Janet
Dombi, Eszter
East, Daniel
Laura, Matilde
Reilly, Mary M
Mortiboys, Heather
Prevo, Remko
Campanella, Michelangelo
Daniels, Matthew J
Zeviani, Massimo
Yu-Wai-Man, Patrick
Simon, Anna Katharina
Votruba, Marcela
Poulton, Joanna
Pokaż więcej
Temat :
Antioxidants/pharmacology
Cells, Cultured
Cognition Disorders/etiology
DNA Mutational Analysis
DNA, Mitochondrial/genetics
Family Health
Female
Fibroblasts/drug effects
GTP Phosphohydrolases/genetics
Humans
Male
Membrane Potential, Mitochondrial/genetics
Mitochondrial Proteins/genetics
Mitophagy/genetics
Mutation/genetics
Optic Atrophy/complications
Pedigree
Protein Kinases/genetics
RNA, Small Interfering/genetics
Transfection
Ubiquinone/analogs & derivatives
Ubiquitin-Protein Ligases/genetics
Źródło :
Liao, C, Ashley, N, Diot, A, Morten, K, Phadwal, K, Williams, A, Fearnley, I, Rosser, L, Lowndes, J, Fratter, C, Ferguson, D J P, Vay, L, Quaghebeur, G, Moroni, I, Bianchi, S, Lamperti, C, Downes, S M, Sitarz, K S, Flannery, P J, Carver, J, Dombi, E, East, D, Laura, M, Reilly, M M, Mortiboys, H, Prevo, R, Campanella, M, Daniels, M J, Zeviani, M, Yu-Wai-Man, P, Simon, A K, Votruba, M & Poulton, J 2017, ' Dysregulated mitophagy and mitochondrial organization in optic atrophy due to OPA1 mutations ', Neurology, vol. 88, no. 2, pp. 131-142 . https://doi.org/10.1212/WNL.0000000000003491
Opis pliku :
application/pdf

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