Suchergebnisse - "Mitochondria pathology"

Timed topical dexamethasone eye drops improve mitochondrial function to prevent severe retinopathy of prematurity

Autoren: Yagi, Hitomi Boeck, Myriam Petrishka-Lozenska, Mariya et al.

Quelle: Angiogenesis

Schlagwörter: Male, Original Paper, Administration, Topical, Infant, Newborn, Infant, Newborn [MeSH], Mice, Inbred C57BL [MeSH], Neovascularization, Retinopathy of Prematurity/pathology [MeSH], Oxygen-induced retinopathy, Mitochondria/pathology [MeSH], Ophthalmic Solutions/administration, Mitochondrial function, Male [MeSH], Dexamethasone, Retinal Neovascularization/metabolism [MeSH], Dexamethasone/administration, Retinopathy of Prematurity/drug therapy [MeSH], Ophthalmic Solutions/pharmacology [MeSH], Administration, Topical [MeSH], Retinal Neovascularization/drug therapy [MeSH], Disease Models, Animal [MeSH], Retinal Neovascularization/pathology [MeSH], Female [MeSH], Mitochondria/metabolism [MeSH], Humans [MeSH], Animals [MeSH], Mice [MeSH], Eye drops, Mitochondria/drug effects [MeSH], Retinopathy of prematurity, Retinopathy of Prematurity/prevention, Dexamethasone/pharmacology [MeSH], Retinal Neovascularization/prevention, Retinal Neovascularization, Mitochondria, Mice, Inbred C57BL, Mice, Disease Models, Animal, Animals, Humans, Retinopathy of Prematurity, Female, Ophthalmic Solutions

Dateibeschreibung: pdf

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/39287727
https://repository.publisso.de/resource/frl:6492366

AI-driven immunology, quantum bioenergetics, bioelectromagnetic modulation, immunometabolism, epigenetic immunomodulation, precision immunotherapy, immune recalibration, quantum computing in biology, personalized medicine

Autoren: Mohamed, Anwar

Schlagwörter: Epigenomics, AI Immunology, Immune Cell Metabolism, RNA, Mitochondrial, CRISPR-Associated Proteins, Quantum Biology, Autoimmunity, Adaptive Immunity/immunology, Mitochondria/chemistry, Adaptive Immunity, Mitochondrial ADP, ATP Translocases/genetics, Epigenesis, Genetic, Redox Signaling, Inflammation/genetics, Immune Engineering, Systems Biology, Inflammation/metabolism, Longevity/genetics, Cytokine Storm, Histone Modification, Innate Immunity, Mitochondria, Quantum Immunology, Immune System Diseases, CRISPR, Autoimmunity/genetics, Mitochondria/pathology, Inflammation/therapy, Epigenetics, Inflammation Mediators, Epigenomics/education, Immune System/innervation, Mitochondrial ADP, ATP Translocases/immunology, Epigenetic Memory/immunology, Innate Immunity Recognition/immunology, Longevity, Innate Immunity Recognition/genetics, Bioenergetics, DNA, Mitochondrial, Immunity, Innate/immunology, Mitochondria/metabolism, Bioelectric Medicine, miRNA, Inflammation, Immunometabolism, Immune Reprogramming, Systems Biology/trends, Frequency Medicine, Innate Immunity Recognition, Immunity, Innate, ATP, Longevity/immunology, Adaptive Immunity/genetics, Immune system, Immune Aging, Immune System, Mitochondria/genetics, Immunity, Innate/genetics, Immune System/immunology, Mitochondrial ADP, ATP Translocases/metabolism, Epigenetic Memory, Epigenomics/trends, Inflammation/pathology

Maternal lactoferrin supplementation prevents mitochondrial and redox homeostasis dysfunction, and improves antioxidant defenses through Nrf2 and UCP2 signaling after neonatal hypoxia-ischemia

Autoren: Carvalho, Andrey Vinicios S Farias Sanches, Eduardo Ribeiro, Rafael T et al.

Quelle: ISSN: 0891-5849 ; Free radical biology & medicine, vol. 231 (2025) p. 68-79.

Schlagwörter: info:eu-repo/classification/ddc/618, Antioxidants, Bovine lactoferrin, Mitochondria, Neonatal hypoxia-ischemia, Neuroprotection, Oxidative stress, Animals, Lactoferrin / administration & dosage, Lactoferrin / pharmacology, NF-E2-Related Factor 2 / metabolism, NF-E2-Related Factor 2 / genetics, Female, Mitochondria / drug effects, Mitochondria / metabolism, Mitochondria / pathology, Uncoupling Protein 2 / metabolism, Uncoupling Protein 2 / genetics, Rats, Hypoxia-Ischemia, Brain / metabolism, Brain / pathology, Brain / drug therapy, Brain / diet therapy, Pregnancy, Oxidative Stress / drug effects, Wistar, Signal Transduction / drug effects, Newborn, Male

Relation: info:eu-repo/semantics/altIdentifier/pmid/40010517; unige:188896

Verfügbarkeit: https://archive-ouverte.unige.ch/unige:188896

α-Synuclein pathology disrupts mitochondrial function in dopaminergic and cholinergic neurons at-risk in Parkinson’s disease

Autoren: Fanni F. Geibl Martin T. Henrich Zhong Xie et al.

Quelle: Mol Neurodegener
Molecular Neurodegeneration, Vol 19, Iss 1, Pp 1-19 (2024)

Schlagwörter: Dopaminergic, Dopaminergic Neurons, RC952-954.6, Parkinson Disease, Cholinergic Neurons, Mitochondria, Alpha-synuclein, Substantia Nigra, Pedunculopontine nucleus, Mice, Inbred C57BL, Mice, Geriatrics, Parkinson Disease/metabolism [MeSH], Dopaminergic Neurons/metabolism [MeSH], Mice, Inbred C57BL [MeSH], Mitochondria/metabolism [MeSH], Bioenergetics, Cholinergic Neurons/pathology [MeSH], Lewy pathology, Cholinergic Neurons/metabolism [MeSH], Animals [MeSH], Mitochondria/pathology [MeSH], Mice [MeSH], Dopaminergic Neurons/pathology [MeSH], Transcriptome, Electrophysiology, alpha-Synuclein/metabolism [MeSH], Parkinson Disease/pathology [MeSH], Research Article, Parkinson's disease, alpha-Synuclein, Animals, Neurology. Diseases of the nervous system, RC346-429

Zugangs-URL: https://pubmed.ncbi.nlm.nih.gov/39379975
https://doaj.org/article/265447b0a3f045d6bd80bc0702c9544d
https://repository.publisso.de/resource/frl:6493898

Mitochondrial Dysfunction in Systemic Lupus Erythematosus with a Focus on Lupus Nephritis.

Autoren: Halfon, M. Tankeu, A.T. Ribi, C.

Quelle: International journal of molecular sciences, vol. 25, no. 11

Schlagwörter: Humans, Lupus Nephritis/metabolism, Lupus Nephritis/pathology, Lupus Nephritis/immunology, Lupus Nephritis/etiology, Mitochondria/metabolism, Mitochondria/pathology, Lupus Erythematosus, Systemic/metabolism, Systemic/pathology, Systemic/immunology, DNA, Mitochondrial/metabolism, Animals, Biomarkers, Mitophagy, interferon, kidney, lupus, lupus nephritis, mitochondria, mitochondrial DNA

Dateibeschreibung: application/pdf

Relation: info:eu-repo/semantics/altIdentifier/pmid/38892349; info:eu-repo/semantics/altIdentifier/eissn/1422-0067; info:eu-repo/semantics/altIdentifier/urn/urn:nbn:ch:serval-BIB_53E45C4DF3094; https://serval.unil.ch/notice/serval:BIB_53E45C4DF309; https://serval.unil.ch/resource/serval:BIB_53E45C4DF309.P001/REF.pdf

Verfügbarkeit: https://serval.unil.ch/notice/serval:BIB_53E45C4DF309
https://doi.org/10.3390/ijms25116162
https://serval.unil.ch/resource/serval:BIB_53E45C4DF309.P001/REF.pdf
http://nbn-resolving.org/urn/resolver.pl?urn=urn:nbn:ch:serval-BIB_53E45C4DF3094

Chronic maternal exposure to low-dose PM2.5 impacts cognitive outcomes in a sex-dependent manner

Autoren: Oliver, Brian G Huang, Xiaomin Yarak, Rochelle et al.

Quelle: Oliver, B G, Huang, X, Yarak, R, Bai, X, Wang, Q, Zakarya, R, Reddy, K D, Donovan, C, Kim, R Y, Morkaya, J, Wang, B, Lung Chan, Y, Saad, S, Faiz, A, Reyk, D V, Verkhratsky, A, Yi, C & Chen, H 2024, 'Chronic maternal exposure to low-dose PM2.5 impacts cognitive outcomes in a sex-dependent manner', Environment International, vol. 191, pp. 108971. https://doi.org/10.1016/j.envint.2024.108971

Schlagwörter: Air Pollution, Animals, Mice, Inbred BALB C, Particulate Matter/toxicity, Male, Female, Sex Characteristics, Neurons/cytology, Memory, Maternal Exposure, Brain/pathology, Mitochondria/pathology, Gene Expression, Newborn, Histone Demethylases/genetics, Cells, Cultured

Verfügbarkeit: https://research.manchester.ac.uk/en/publications/597d6b1c-0976-47d5-b33e-3cb625842673
https://doi.org/10.1016/j.envint.2024.108971

Magnetic resonance reveals mitochondrial dysfunction and muscle remodelling in spinal muscular atrophy

Autoren: Laura E Habets Bart Bartels Fay-Lynn Asselman et al.

Weitere Verfasser: Laura E Habets Bart Bartels Fay-Lynn Asselman et al.

Quelle: Brain

Schlagwörter: Magnetic Resonance Spectroscopy, muscle, Muscular Atrophy, Spinal/diagnostic imaging, Phosphates, magnetic resonance, Muscular Atrophy, Spinal, 03 medical and health sciences, Adenosine Triphosphate, 0302 clinical medicine, Journal Article, Humans, Muscle, Skeletal, spinal muscular atrophy, Muscle Weakness, exercise, Magnetic Resonance Imaging, Atrophy/pathology, Mitochondria, Muscular Atrophy, Muscle, Skeletal/pathology, Mitochondria/pathology, Lactates, Original Article, Muscular Atrophy/pathology, Atrophy, metabolism

Dateibeschreibung: application/pdf

Zugangs-URL: https://academic.oup.com/brain/advance-article-pdf/doi/10.1093/brain/awab411/41132931/awab411.pdf
https://pubmed.ncbi.nlm.nih.gov/34788410
https://www.ncbi.nlm.nih.gov/pubmed/34788410
https://dspace.library.uu.nl/handle/1874/444414
https://pure.amsterdamumc.nl/en/publications/9e987d6f-e038-4658-b74f-41dc9b37357d
https://doi.org/10.1093/brain/awab411

Sarcopenia and Muscle Aging: A Brief Overview

Autoren: Dao, Tam Green, Alexander E. Kim, Yun A et al.

Quelle: Endocrinol Metab (Seoul)
Endocrinology and Metabolism, Vol 35, Iss 4, Pp 716-732 (2020)

Schlagwörter: 0301 basic medicine, Aging, Sarcopenia, urolithin, Sarcopenia / pathology, nad+, Skeletal muscle, Review Article, Diseases of the endocrine glands. Clinical endocrinology, sarcopenia, 03 medical and health sciences, Coumarins, NAD+, Animals, Humans, Aging / metabolism, skeletal muscle, Muscle, Skeletal, Exercise, Gastrointestinal microbiome, NAD / metabolism, gastrointestinal microbiome, Aged, exercise, aging, Mitochondria / metabolism, Mitophagy, Mitochondria / pathology, Muscle, Skeletal / metabolism, Sarcopenia / therapy, RC648-665, NAD, Gastrointestinal Microbiome / physiology, Gastrointestinal Microbiome, Mitochondria, 3. Good health, Urolithin, mitochondria, Coumarins / metabolism, Mitophagy / physiology, mitophagy, Muscle, Skeletal / pathology, Aging / pathology, Sarcopenia / metabolism

Dateibeschreibung: application/pdf

Zugangs-URL: https://www.e-enm.org/upload/pdf/enm-2020-405.pdf
https://pubmed.ncbi.nlm.nih.gov/33397034
https://doaj.org/article/d612c77d85d14fc98572de8da22d4336
https://www.kci.go.kr/kciportal/ci/sereArticleSearch/ciSereArtiView.kci?sereArticleSearchBean.artiId=ART002661655
https://pubmed.ncbi.nlm.nih.gov/33397034/
https://www.e-enm.org/journal/view.php?number=2102
https://www.e-enm.org/upload/pdf/enm-2020-405.pdf
https://kmbase.medric.or.kr/KMID/1141520200350040716
https://europepmc.org/article/PMC/PMC7803599
https://archive-ouverte.unige.ch/unige:169230
https://doi.org/10.3803/enm.2020.405

The Impact of Mitochondrial Dysfunction on Dopaminergic Neurons in the Olfactory Bulb and Odor Detection

Autoren: Rudolf J. Wiesner Markus Rothermel Sandra Blaess et al.

Quelle: Mol Neurobiol
Molecular neurobiology 57(9), 3646-3657 (2020). doi:10.1007/s12035-020-01947-w

Schlagwörter: 0301 basic medicine, Time Factors, PAX6 Transcription Factor, Tyrosine 3-Monooxygenase, Cell Count, Article, Electron Transport, Odorants [MeSH], Substantia Nigra/metabolism [MeSH], Mice, Inbred C57BL [MeSH], Neostriatum/metabolism [MeSH], High Mobility Group Proteins/metabolism [MeSH], Stem Cells/metabolism [MeSH], Mitochondrial dysfunction, Animals [MeSH], Mesencephalon/pathology [MeSH], Time Factors [MeSH], PAX6 Transcription Factor/metabolism [MeSH], DNA-Binding Proteins/metabolism [MeSH], Olfactory bulb, Mitochondria/pathology [MeSH], Tyrosine 3-Monooxygenase/metabolism [MeSH], Dopaminergic Neurons/pathology [MeSH], Electron Transport [MeSH], Olfactory Bulb/pathology [MeSH], Neurogenesis, Nerve Degeneration/pathology [MeSH], Cell Count [MeSH], Parkinson's disease, 03 medical and health sciences, Mesencephalon, Animals, 2. Zero hunger, 0303 health sciences, Dopaminergic Neurons, Stem Cells, High Mobility Group Proteins, Olfactory Bulb, Mitochondria, DNA-Binding Proteins, Mice, Inbred C57BL, Neostriatum, Substantia Nigra, Nerve Degeneration, Odorants

Zugangs-URL: https://link.springer.com/content/pdf/10.1007/s12035-020-01947-w.pdf
https://pubmed.ncbi.nlm.nih.gov/32564285
https://pubmed.ncbi.nlm.nih.gov/32564285/
https://link.springer.com/content/pdf/10.1007/s12035-020-01947-w.pdf
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7398899
https://link.springer.com/article/10.1007/s12035-020-01947-w
https://repository.publisso.de/resource/frl:6471720
https://publications.rwth-aachen.de/record/794352

Axonal response of mitochondria to demyelination and complex IV activity within demyelinated axons in experimental models of multiple sclerosis

Autoren: Licht-Mayer, Simon Campbell, Graham R. Mehta, Arpan R et al.

Quelle: Licht-Mayer, S, Campbell, G R, Mehta, A R, McGill, K, Symonds, A, Al-Azki, S, Pryce, G, Zandee, S, Zhao, C, Kipp, M, Smith, K J, Baker, D, Altmann, D, Anderton, S M, Kap, Y S, Laman, J D, 't Hart, B A, Rodriguez, M, Franklin, R J M, Chandran, S, Lassmann, H, Trapp, B D & Mahad, D J 2023, 'Axonal response of mitochondria to demyelination and complex IV activity within demyelinated axons in experimental models of multiple sclerosis', Neuropathology and Applied Neurobiology, vol. 49, no. 1, pp. e12851. https://doi.org/10.1111/nan.12851

Schlagwörter: Animals, Multiple Sclerosis/pathology, Axons/pathology, Encephalomyelitis, Autoimmune, Experimental/pathology, Neurons/pathology, Mitochondria/pathology

Dateibeschreibung: application/pdf

Relation: info:eu-repo/semantics/altIdentifier/pmid/36181265; info:eu-repo/semantics/altIdentifier/pissn/0305-1846; info:eu-repo/semantics/altIdentifier/eissn/1365-2990

Verfügbarkeit: https://discovery.dundee.ac.uk/en/publications/afe917db-ee9b-408e-9624-b0243511ca70
https://doi.org/10.1111/nan.12851
https://discovery.dundee.ac.uk/ws/files/121716484/Neuropathology_Appl_Neurobio_-_2022_-_Licht_Mayer_-_Axonal_response_of_mitochondria_to_demyelination_and_complex_IV.pdf

Mitochondria-Endoplasmic Reticulum Contact Sites Dynamics and Calcium Homeostasis Are Differentially Disrupted in PINK1-PD or PRKN-PD Neurons.

Autoren: Grossmann, Dajana Malburg, Nina Grünewald, Anne et al.

Quelle: Movement disorders 38(10), 1822 - 1836 (2023). doi:10.1002/mds.29525

Schlagwörter: info:eu-repo/classification/ddc/610, Humans, Parkinson Disease: pathology, Calcium: metabolism, Thapsigargin: metabolism, Mitochondria: pathology, Dopaminergic Neurons: metabolism, Protein Kinases: genetics, Ubiquitin-Protein Ligases: genetics, Endoplasmic Reticulum: metabolism, Homeostasis, PINK1, Parkin, Parkinson's disease, calcium, mitochondria-ER contact sites, Thapsigargin, Protein Kinases, Ubiquitin-Protein Ligases

Geographisches Schlagwort: DE

Relation: info:eu-repo/semantics/altIdentifier/pmid/pmid:37449534; info:eu-repo/semantics/altIdentifier/issn/1531-8257; info:eu-repo/semantics/altIdentifier/issn/0885-3185; https://pub.dzne.de/record/265796

Verfügbarkeit: https://pub.dzne.de/record/265796
https://pub.dzne.de/search?p=id:%22DZNE-2023-01040%22

Inflammatory myopathy in a patient with Aicardi-Goutières syndrome.

Autoren: Tumienė, B. Voisin, N. Preikšaitienė, E. et al.

Schlagwörter: Autoimmune Diseases of the Nervous System/genetics, Autoimmune Diseases of the Nervous System/pathology, Base Sequence, Child, DNA, Mitochondrial/genetics, Exodeoxyribonucleases/genetics, Female, Genetic Predisposition to Disease, Humans, Interferon Type I/immunology, Mitochondria/genetics, Mitochondria/pathology, Myositis/pathology, Nervous System Malformations/genetics, Nervous System Malformations/pathology, Phosphoproteins/genetics, Sequence Analysis

Relation: European Journal of Medical Genetics; https://iris.unil.ch/handle/iris/99448; serval:BIB_0DE163527E7F; 000398068600002

Verfügbarkeit: https://iris.unil.ch/handle/iris/99448
https://doi.org/10.1016/j.ejmg.2016.12.004

Association of N-acetylaspartate and cerebrospinal fluid Aβ42 in dementia.

Autoren: Jessen, F. Lewczuk, P. Gür, O. et al.

Schlagwörter: Aged, Alzheimer Disease/cerebrospinal fluid, Alzheimer Disease/diagnosis, Amyloid beta-Peptides/cerebrospinal fluid, Aspartic Acid/analogs & derivatives, Aspartic Acid/metabolism, Biological Markers/cerebrospinal fluid, Biological Markers/metabolism, Dementia/cerebrospinal fluid, Dementia/diagnosis, Female, Humans, Male, Middle Aged, Mild Cognitive Impairment/cerebrospinal fluid, Mild Cognitive Impairment/diagnosis, Mitochondria/metabolism, Mitochondria/pathology, Neurons/metabolism, Neurons/pathology, Peptide Fragments/cerebrospinal fluid

Dateibeschreibung: application/pdf

Relation: Journal of Alzheimer's Disease; https://iris.unil.ch/handle/iris/92925; serval:BIB_049C4F0B7D4F; 000297215900015

Verfügbarkeit: https://iris.unil.ch/handle/iris/92925
https://doi.org/10.3233/JAD-2011-110398

E1 empty set E4 protein of human papillomavirus type 16 associates with mitochondria.

Autoren: Raj, K. Berguerand, S. Southern, S. et al.

Schlagwörter: Amino Acid Sequence, Apoptosis, Cell Line, Hela Cells, Humans, Leucine, Membrane Potentials/drug effects, Mitochondria/metabolism, Mitochondria/pathology, Mutation, Oncogene Proteins, Fusion/chemistry, Fusion/genetics, Papillomaviridae/genetics, Papillomaviridae/metabolism, Transfection, Viral Proteins/chemistry, Viral Proteins/genetics

Relation: Journal of Virology; https://iris.unil.ch/handle/iris/77205; serval:BIB_31407; 000222153800052

Verfügbarkeit: https://iris.unil.ch/handle/iris/77205
https://doi.org/10.1128/JVI.78.13.7199-7207.2004

Inhibition of the c-Jun N-terminal kinase-mediated mitochondrial cell death pathway restores auditory function in sound-exposed animals

Autoren: Wang, J. Ruel, J. Ladrech, S. et al.

Schlagwörter: Animals Apoptosis/*drug effects Carrier Proteins/metabolism Caspases/physiology Cytochromes c/secretion Guinea Pigs Hair Cells/pathology/ultrastructure Hearing Loss, Noise-Induced/*drug therapy/pathology JNK Mitogen-Activated Protein Kinases/*antagonists & inhibitors/physiology MAP Kinase Signaling System/drug effects Microfilament Proteins/metabolism Mitochondria/*pathology Necrosis Peptides/*administration & dosage/pharmacology Phosphorylation Protein Transport Proto-Oncogene Proteins c-jun/metabolism Round Window/drug effects bcl-2-Associated X Protein/metabolism

Relation: Molecular Pharmacology; https://iris.unil.ch/handle/iris/68543; serval:BIB_5CB9D0177083; 000244290400004

Verfügbarkeit: https://iris.unil.ch/handle/iris/68543
https://doi.org/10.1124/mol.106.028936

Synaptic dysfunction, memory deficits and hippocampal atrophy due to ablation of mitochondrial fission in adult forebrain neurons.

Autoren: Oettinghaus, B. Schulz, J.M. Restelli, L.M. et al.

Schlagwörter: Animals, Antioxidants/administration & dosage, Atrophy/genetics, Atrophy/metabolism, Dynamins/biosynthesis, Dynamins/genetics, Hippocampus/growth & development, Hippocampus/metabolism, Memory Disorders/genetics, Memory Disorders/pathology, Mice, Mitochondria/metabolism, Mitochondria/pathology, Mitochondrial Dynamics/genetics, Nerve Degeneration/genetics, Nerve Degeneration/metabolism, Nervous System/growth & development, Nervous System/pathology, Neurons/metabolism, Neurons/pathology, Prosencephalon/growth & development, Prosencephalon/metabolism

Dateibeschreibung: application/pdf

Relation: Cell Death & Differentiation; https://iris.unil.ch/handle/iris/166607; serval:BIB_BDF780D8E819; 000368062000010

Verfügbarkeit: https://iris.unil.ch/handle/iris/166607
https://doi.org/10.1038/cdd.2015.39

TMX2 Is a Crucial Regulator of Cellular Redox State, and Its Dysfunction Causes Severe Brain Developmental Abnormalities

Autoren: Javad Akhondian Amal Al Hashem Juliann M. Savatt et al.

Weitere Verfasser: Javad Akhondian Amal Al Hashem Juliann M. Savatt et al.

Quelle: The American Journal of Human Genetics. 105:1126-1147

Schlagwörter: Male, 0301 basic medicine, Developmental Disabilities, Brain / abnormalities, calnexin, epilepsy, hydrogen peroxide, microcephaly, mitochondria-associated membrane, PDI, polymicrogyria, redox, SERCA2, TMX2, Fibroblasts / metabolism, Cohort Studies, Developmental Disabilities / metabolism, Skin / metabolism, Genetics(clinical), Child, EMC MGC-02-96-01, Skin, Brain Diseases, 0303 health sciences, Mitochondria / metabolism, Brain, Prognosis, Membrane Proteins / metabolism, Brain Diseases / metabolism, Mitochondria, Thioredoxins / genetics, Developmental Disabilities / genetics, Child, Preschool, Female, Oxidation-Reduction, Adult, Brain Diseases / genetics, Fibroblasts / pathology, Adolescent, 03 medical and health sciences, Brain Diseases / pathology, Genetics, Humans, Developmental Disabilities / pathology, Thioredoxins / metabolism, Membrane Proteins / genetics, Skin / pathology, Infant, Newborn, Infant, Membrane Proteins, EMC MM-03-24-01, Fibroblasts, Mitochondria / pathology, Hydrogen peroxide, Polymicrogyria, EMC MGC-01-12-03, Transcriptome, Follow-Up Studies

Dateibeschreibung: application/pdf

Zugangs-URL: http://www.cell.com/article/S0002929719303970/pdf
https://pubmed.ncbi.nlm.nih.gov/31735293
https://orca.cardiff.ac.uk/id/eprint/126968/1/Vandervore_TMX2_final_draft.pdf
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6904804/
https://www.sciencedirect.com/science/article/abs/pii/S0002929719303970
https://repozitorij.mef.unizg.hr/islandora/object/mef%3A2663
https://dabar.srce.hr/en/islandora/object/mef%3A2663
https://pubmed.ncbi.nlm.nih.gov/31735293/
https://repub.eur.nl/pub/121983
https://dspace.library.uu.nl/handle/1874/439080
https://biblio.vub.ac.be/vubir/tmx2-is-a-crucial-regulator-of-cellular-redox-state-and-its-dysfunction-causes-severe-brain-developmental-abnormalities(1f06fab7-13e5-4758-9e0b-8faeb95094cd).html
https://urn.nsk.hr/urn:nbn:hr:105:093095
https://doi.org/10.1016/j.ajhg.2019.10.009
https://discovery-pp.ucl.ac.uk/id/eprint/10087996/

Cardiolipin acyl chain compostion tailors the conformation of mammalian ATP synthase dimers

Autoren: Makowski, Marcin orcid:0000-0001-6929- Almendro Vedia, Victor G. et al.

Weitere Verfasser: Makowski, Marcin orcid:0000-0001-6929- Almendro Vedia, Victor G. et al.

Schlagwörter: Mitochondria/pathology, Mitochondria/ultrastructure, Cardiolipins/chemistry, Cardiolipins/ultrastructure, Barth Syndrome, ATP Synthetase Complexes/deficiency

Relation: https://zenodo.org/records/14732771; oai:zenodo.org:14732771; https://doi.org/10.5281/zenodo.14732771

Verfügbarkeit: https://doi.org/10.5281/zenodo.14732771
https://zenodo.org/records/14732771

Magnetic resonance reveals mitochondrial dysfunction and muscle remodelling in spinal muscular atrophy

Autoren: Habets, Laura E Bartels, Bart Asselman, Fay-Lynn et al.

Weitere Verfasser: Habets, Laura E Bartels, Bart Asselman, Fay-Lynn et al.

Schlagwörter: Adenosine Triphosphate, Atrophy/pathology, Humans, Lactates, Magnetic Resonance Imaging, Magnetic Resonance Spectroscopy, Mitochondria/pathology, Muscle Weakness, Muscle, Skeletal/pathology, Muscular Atrophy, Spinal/diagnostic imaging, Muscular Atrophy/pathology, Phosphates, exercise, magnetic resonance, metabolism, spinal muscular atrophy, Journal Article

Dateibeschreibung: application/pdf

Relation: https://dspace.library.uu.nl/handle/1874/444414

Verfügbarkeit: https://dspace.library.uu.nl/handle/1874/444414

Reductive Stress-Induced Mitochondrial Dysfunction and Cardiomyopathy

Autoren: Ma, Wei-Xing Li, Chun-Yan Tao, Ran et al.

Quelle: Oxidative Medicine and Cellular Longevity

Schlagwörter: Animals, Cardiomyopathies / pathology, Cardiomyopathies / physiopathology, Humans, Mitochondria / pathology, Oxidation-Reduction, Oxidative Stress, Reactive Oxygen Species / metabolism, Signal Transduction

Dateibeschreibung: application/pdf

Relation: https://doi.org/10.1155/2020/5136957; https://hdl.handle.net/20.500.12503/31569; 2020

Verfügbarkeit: https://hdl.handle.net/20.500.12503/31569