المؤلفون: C Vandenbogert, P Muus, Mjm Vangalen, Pa Bolhuis, Hl Dekker, Marijke Holtrop, H Devries, Jw Taanman

المصدر: Biochimica et Biophysica Acta (BBA) - Bioenergetics. 1144:177-183

مصطلحات موضوعية: Cell Nucleus, DNA Replication, Mitochondrial DNA, Oxidase test, Cytochrome, Biophysics, Cell Biology, Biology, Biochemistry, Mitochondria, Electron Transport Complex IV, Gene Expression Regulation, Mitochondrial biogenesis, Transcription (biology), Gene expression, biology.protein, Humans, Cytochrome c oxidase, RNA, Messenger, Gene

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1308cc3bfc93d7c938ec772d53791b67
https://doi.org/10.1016/0005-2728(93)90170-k

المؤلفون: H. de Vries, J Bijl, Peter Reuvekamp, Jw Taanman, E Agsteribbe, C Schrage, Marijke Hartog

المصدر: Gene, 102(2), 237-244. Elsevier

مصطلحات موضوعية: animal structures, RESPIRATORY CHAIN, LIVER, CYP3A, Pseudogene, Molecular Sequence Data, Restriction Mapping, Respiratory chain, ORGANIZATION, Biology, Homology (biology), RECOMBINANT DNA, Electron Transport Complex IV, ALU REPETITIVE ELEMENT, Molecular evolution, Complementary DNA, NUCLEOTIDE-SEQUENCE, Genetics, Humans, Amino Acid Sequence, NUCLEAR GENE, NUCLEOTIDE SEQUENCE ANALYSIS, Gene, IV GENE, MITOCHONDRIAL PROTEIN, Base Sequence, General Medicine, DNA, Biological Evolution, Molecular biology, FAMILY, MITOCHONDRIAL GENOME, PROCESSED PSEUDOGENE, Multigene Family, HEART, Human genome, MESSENGER-RNA, Pseudogenes

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3768c9a52248f9a2bbfe94ebb42a3ae9
https://doi.org/10.1016/0378-1119(91)90083-N

المؤلفون: H Devries, Nh Herzberg, Jw Taanman, C Vandenbogert, Pa Bolhuis

المصدر: Biochimica et biophysica acta. 1139(1-2)

مصطلحات موضوعية: Gene isoform, Adult, Male, Cytochrome, Transcription, Genetic, Protein subunit, Electron Transport Complex IV, RNA, Ribosomal, 16S, Cytochrome c oxidase, Humans, Northern blot, RNA, Messenger, Molecular Biology, Cells, Cultured, Adenosine Triphosphatases, biology, ATP synthase, Myogenesis, Muscles, Molecular biology, Mitochondria, Muscle, Isoenzymes, biology.protein, Molecular Medicine, Female, sense organs, ATP synthase alpha/beta subunits

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbb409451e8174fef97ba0f10a9169f6
https://pubmed.ncbi.nlm.nih.gov/1319212

المؤلفون: H Devries, Jw Taanman, C Schrage, Ay Vanderveen, Chcm Buys

المصدر: Human genetics. 87(3)

مصطلحات موضوعية: Oxidase test, Genomic Library, animal structures, Nuclear gene, Protein subunit, Biotin, Chromosome Mapping, Nucleic Acid Hybridization, Biology, Molecular biology, Fluorescence, Electron Transport Complex IV, Exon, genomic DNA, Blotting, Southern, Gene mapping, Genetics, biology.protein, Cytochrome c oxidase, Humans, Gene, Chromosomes, Human, Pair 19, Genetics (clinical), Cells, Cultured

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bb1577979d641ec9ed67eed665aaab1a
https://pubmed.ncbi.nlm.nih.gov/1650756

المؤلفون: Peter Reuvekamp, E Agsteribbe, E Bokma, C Schrage, H Devries, Jw Taanman

المصدر: Biochimica et biophysica acta, 1089(2), 283-285

مصطلحات موضوعية: (HUMAN), GENOMIC DNA SEQUENCE, Protein subunit, Molecular Sequence Data, Biophysics, Biology, Biochemistry, DNA, Mitochondrial, DNA sequencing, CLONING, Electron Transport Complex IV, Exon, ALU REPETITIVE ELEMENT, Structural Biology, Genetics, Cytochrome c oxidase, Humans, Amino Acid Sequence, Gene, Peptide sequence, Oxidase test, MITOCHONDRIAL PROTEIN, Base Sequence, CYTOCHROME-C OXIDASE, Nucleic acid sequence, Exons, Molecular biology, biology.protein, VECTORS

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f4951e0626641146a9c65bec94d9d79e
https://pubmed.ncbi.nlm.nih.gov/1647217

المؤلفون: Jw Taanman, C Schrage, H Devries, N Ponne, E Agsteribbe, Pa Bolhuis

المصدر: Nucleic Acids Research, 17(4), 1766-1766. Oxford University Press

مصطلحات موضوعية: Genetics, Oxidase test, biology, Base Sequence, Macromolecular Substances, Protein subunit, Molecular Sequence Data, Nucleic acid sequence, Electron Transport Complex IV, DNA, Molecular biology, Mitochondria, Genes, Complementary DNA, Sequence Homology, Nucleic Acid, biology.protein, Cytochrome c oxidase, Animals, Humans, Cattle, Amino Acid Sequence, Peptide sequence, Gene

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e81814a17be66bbcca8f14fc36fd2c35
https://doi.org/10.1093/nar/17.4.1766

المؤلفون: Neueder A; Department of Neurology, Ulm University, 89081 Ulm, Germany., Kojer K; Department of Neurology, Ulm University, 89081 Ulm, Germany., Gu Z; Division of Nutritional Sciences, Cornell University, Ithaca, NY 14853, USA., Wang Y; Division of Nutritional Sciences, Cornell University, Ithaca, NY 14853, USA., Hering T; Department of Neurology, Ulm University, 89081 Ulm, Germany., Tabrizi S; UCL Huntington's Disease Centre, UCL Queen Square Institute of Neurology and National Hospital for Neurology and Neurosurgery, London WC1N 3BG, UK.; Dementia Research Institute at UCL, London WC1N 3BG, UK., Taanman JW; Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, London NW3 2PF, UK., Orth M; Department of Neurology, Ulm University, 89081 Ulm, Germany.; Swiss Huntington Centre, Siloah AG, 3073 Gümligen, Switzerland.; University Hospital of Old Age Psychiatry and Psychotherapy, Bern University, CH-3000 Bern 60, Switzerland.

المصدر: Brain : a journal of neurology [Brain] 2024 Jun 03; Vol. 147 (6), pp. 2009-2022.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Oxford University Press Country of Publication: England NLM ID: 0372537 Publication Model: Print Cited Medium: Internet ISSN: 1460-2156 (Electronic) Linking ISSN: 00068950 NLM ISO Abbreviation: Brain Subsets: MEDLINE

مواضيع طبية MeSH: Huntington Disease*/genetics , Huntington Disease*/metabolism , Huntington Disease*/pathology , DNA, Mitochondrial*/genetics , Mutation* , Huntingtin Protein*/genetics , Huntingtin Protein*/metabolism , Mitochondrial Dynamics*/genetics, Humans ; Male ; Muscle, Skeletal/metabolism ; Muscle, Skeletal/pathology ; Female ; Oxidative Phosphorylation ; Middle Aged ; Mitochondria/metabolism ; Mitochondria/genetics ; Adult ; Mitophagy/genetics

المؤلفون: Caon E; Regenerative Medicine and Fibrosis Group, Institute for Liver and Digestive Health, University College London, Royal Free Campus, London, UK., Martins M; Regenerative Medicine and Fibrosis Group, Institute for Liver and Digestive Health, University College London, Royal Free Campus, London, UK., Hodgetts H; Regenerative Medicine and Fibrosis Group, Institute for Liver and Digestive Health, University College London, Royal Free Campus, London, UK., Blanken L; Regenerative Medicine and Fibrosis Group, Institute for Liver and Digestive Health, University College London, Royal Free Campus, London, UK., Vilia MG; Regenerative Medicine and Fibrosis Group, Institute for Liver and Digestive Health, University College London, Royal Free Campus, London, UK., Levi A; Regenerative Medicine and Fibrosis Group, Institute for Liver and Digestive Health, University College London, Royal Free Campus, London, UK., Thanapirom K; Regenerative Medicine and Fibrosis Group, Institute for Liver and Digestive Health, University College London, Royal Free Campus, London, UK., Al-Akkad W; Regenerative Medicine and Fibrosis Group, Institute for Liver and Digestive Health, University College London, Royal Free Campus, London, UK., Abu-Hanna J; Research Department of Surgical Biotechnology, Division of Surgery and Interventional Science, University College London, London, UK., Baselli G; Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Milan, Italy., Hall AR; Sheila Sherlock Liver Centre, Royal Free London NHS Foundation Trust, London, UK; Department of Cellular Pathology, Royal Free London NHS Foundation Trust, London, UK., Luong TV; Sheila Sherlock Liver Centre, Royal Free London NHS Foundation Trust, London, UK; Department of Cellular Pathology, Royal Free London NHS Foundation Trust, London, UK., Taanman JW; Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, University College London, London UK., Vacca M; Laboratory of Hepatic Metabolism and NAFLD, Roger Williams Institute of Hepatology, London, UK; Clinica Medica 'Frugoni', Interdisciplinary Department of Medicine, University of Bari 'Aldo Moro', Bari, Italy., Valenti L; Department of Pathophysiology and Transplantation, Università degli Studi di Milano, Milan, Italy; Precision Medicine, Biological Resource Center, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy., Romeo S; Department of Molecular and Clinical Medicine, Institute of Medicine, Sahlgrenska Academy, Wallenberg Laboratory, University of Gothenburg, Gothenburg, Sweden., Mazza G; Regenerative Medicine and Fibrosis Group, Institute for Liver and Digestive Health, University College London, Royal Free Campus, London, UK., Pinzani M; Regenerative Medicine and Fibrosis Group, Institute for Liver and Digestive Health, University College London, Royal Free Campus, London, UK., Rombouts K; Regenerative Medicine and Fibrosis Group, Institute for Liver and Digestive Health, University College London, Royal Free Campus, London, UK. Electronic address: k.rombouts@ucl.ac.uk.

المصدر: Journal of hepatology [J Hepatol] 2024 Jun; Vol. 80 (6), pp. 941-956. Date of Electronic Publication: 2024 Feb 15.

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Elsevier Country of Publication: Netherlands NLM ID: 8503886 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1600-0641 (Electronic) Linking ISSN: 01688278 NLM ISO Abbreviation: J Hepatol Subsets: MEDLINE

مواضيع طبية MeSH: Hepatic Stellate Cells*/metabolism , Hepatic Stellate Cells*/pathology , Membrane Proteins*/genetics , Membrane Proteins*/metabolism , Extracellular Matrix*/metabolism , Extracellular Matrix*/genetics , Lipase*/genetics , Lipase*/metabolism , Liver Cirrhosis*/genetics , Liver Cirrhosis*/pathology , Liver Cirrhosis*/metabolism , Transforming Growth Factor beta1*/metabolism , Transforming Growth Factor beta1*/genetics, Humans ; Cells, Cultured ; Liver/pathology ; Liver/metabolism ; Signal Transduction/genetics ; Obesity/genetics ; Obesity/metabolism ; Male ; Acyltransferases ; Phospholipases A2, Calcium-Independent

المؤلفون: Manzoni E; Department of Medical and Surgical Sciences, Alma Mater Studiorum University of Bologna, Bologna 40138, Italy.; IRCCS Istituto delle Scienze Neurologiche, UO Neuropsichiatria dell'età Pediatrica di Bologna, Bologna 40124, Italy., Carli S; Department of Medical and Surgical Sciences, Alma Mater Studiorum University of Bologna, Bologna 40138, Italy., Gaignard P; Department of Biochemistry, Bicêtre Hospital, Reference Center for Mitochondrial Disease, University of Paris-Saclay, Assistance Publique-Hôpitaux de Paris, Paris 94275, France., Schlieben LD; School of Medicine, Institute of Human Genetics, Technical University of Munich, Munich, 80333  Germany.; Institute of Neurogenomics, Computational Health Center, Helmholtz Zentrum München, Neuherberg 80333, Germany., Hirano M; H. Houston Merritt Neuromuscular Research Center, Department of Neurology, Columbia University Irving Medical Center, New York, NY 10033, USA., Ronchi D; Dino Ferrari Center, Department of Pathophysiology and Transplantation, University of Milan, Milan 20122, Italy., Gonzales E; Pediatric Hepatology and Pediatric Liver Transplantation Unit, Bicêtre Hospital, Reference Center for Mitochondrial Disease, University of Paris-Saclay, Assistance Publique-Hôpitaux de Paris, Paris 94270, France., Shimura M; Center for Medical Genetics, Department of Metabolism, Chiba Children's Hospital, Chiba 260-0842, Japan., Murayama K; Center for Medical Genetics, Department of Metabolism, Chiba Children's Hospital, Chiba 260-0842, Japan.; Diagnostics and Therapeutic of Intractable Diseases, Intractable Disease Research Center, Graduate School of Medicine, Juntendo University, Tokyo 113-8421, Japan., Okazaki Y; Diagnostics and Therapeutic of Intractable Diseases, Intractable Disease Research Center, Graduate School of Medicine, Juntendo University, Tokyo 113-8421, Japan., Barić I; Department of Pediatrics, University Hospital Centre Zagreb and University of Zagreb, School of Medicine, Zagreb 10000, Croatia., Petkovic Ramadza D; Department of Pediatrics, University Hospital Centre Zagreb and University of Zagreb, School of Medicine, Zagreb 10000, Croatia., Karall D; Clinic for Pediatrics, Division of Inherited Metabolic Disorders, Medical University of Innsbruck, 6020 Innsbruck, Austria., Mayr J; University Children's Hospital, Paracelsus Medical University (PMU), 5020 Salzburg, Austria., Martinelli D; Division of Metabolism, Bambino Gesù Children's Hospital IRCCS, Rome 00165, Italy., La Morgia C; Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna 40123, Italy.; IRCCS Istituto di Scienze Neurologiche di Bologna, Programma di Neurogenetica, Bologna 40124, Italy., Primiano G; Dipartimento di Neuroscienze, Organi di Senso e Torace -Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome 00136, Italy.; Dipartimento Di Neuroscienze, Università Cattolica del Sacro Cuore, Rome 00168, Italy., Santer R; Department of Pediatrics, University Medical Center Eppendorf, Hamburg 20246, Germany., Servidei S; Dipartimento di Neuroscienze, Organi di Senso e Torace -Fondazione Policlinico Universitario Agostino Gemelli IRCCS, Rome 00136, Italy.; Dipartimento Di Neuroscienze, Università Cattolica del Sacro Cuore, Rome 00168, Italy., Bris C; University Angers, Angers Hospital, INSERM, CNRS, MITOVASC, SFR ICAT, Angers F-49000, France., Cano A; Centre de référence des maladies héréditaires du métabolisme, CHU la Timone Enfants, Marseille 13005, France., Furlan F; Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Regional Clinical Center for Expanded Newborn Screening, Milan 20122, Italy., Gasperini S; Department of Pediatrics, Fondazione IRCCS San Gerardo dei Tintori, 20900 Monza, Italy., Laborde N; Unité de Gastroentérologie, Hépatologie, Nutrition et Maladies Héréditaires du Métabolisme, Hôpital des Enfants, CHU de Toulouse, Toulouse 31300, France., Lamperti C; Division of Medical Genetics and Neurogenetics, Fondazione IRCCS Neurological Institute 'C. Besta', Milan 20133, Italy., Lenz D; Division of Neuropaediatrics and Paediatric Metabolic Medicine, Center for Paediatric and Adolescent Medicine, University Hospital Heidelberg, Heidelberg 69120, Germany., Mancuso M; Department of Clinical and Experimental Medicine, Neurological Institute, University of Pisa & AOUP, Pisa 56126, Italy., Montano V; Department of Clinical and Experimental Medicine, Neurological Institute, University of Pisa & AOUP, Pisa 56126, Italy., Menni F; Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Regional Clinical Center for Expanded Newborn Screening, Milan 20122, Italy., Musumeci O; Unit of Neurology and Neuromuscular Disorders, Department of Clinical and Experimental Medicine, University of Messina, Messina 98125, Italy., Nesbitt V; Department of Paediatrics, Medical Sciences Division, Oxford University, Oxford OX3 9DU, UK., Procopio E; Metabolic Unit, Meyer Children's Hospital IRCCS, Florence 50139, Italy., Rouzier C; Centre de référence des Maladies Mitochondriales, Service de Génétique Médicale, CHU de Nice, Université Côte d'Azur, CNRS, INSERM, IRCAN, Nice 06000, France., Staufner C; Division of Neuropaediatrics and Paediatric Metabolic Medicine, Center for Paediatric and Adolescent Medicine, University Hospital Heidelberg, Heidelberg 69120, Germany., Taanman JW; Department of Clinical and Movement Neurosciences, UCL Queen Square Institute of Neurology, University College London, London WC1N 3BG, UK., Tal G; Metabolic Clinic, Ruth Rappaport Children's Hospital, Rambam Health Care Campus, Haifa 3109601, Israel.; The Ruth and Bruce Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa 3109601, Israel., Ticci C; Metabolic Unit, Meyer Children's Hospital IRCCS, Florence 50139, Italy., Cordelli DM; Department of Medical and Surgical Sciences, Alma Mater Studiorum University of Bologna, Bologna 40138, Italy.; IRCCS Istituto delle Scienze Neurologiche, UO Neuropsichiatria dell'età Pediatrica di Bologna, Bologna 40124, Italy., Carelli V; Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna 40123, Italy.; IRCCS Istituto di Scienze Neurologiche di Bologna, Programma di Neurogenetica, Bologna 40124, Italy., Procaccio V; University Angers, Angers Hospital, INSERM, CNRS, MITOVASC, SFR ICAT, Angers F-49000, France., Prokisch H; School of Medicine, Institute of Human Genetics, Technical University of Munich, Munich, 80333  Germany.; Institute of Neurogenomics, Computational Health Center, Helmholtz Zentrum München, Neuherberg 80333, Germany., Garone C; Department of Medical and Surgical Sciences, Alma Mater Studiorum University of Bologna, Bologna 40138, Italy.; IRCCS Istituto delle Scienze Neurologiche, UO Neuropsichiatria dell'età Pediatrica di Bologna, Bologna 40124, Italy.

المصدر: Brain communications [Brain Commun] 2024 May 06; Vol. 6 (3), pp. fcae160. Date of Electronic Publication: 2024 May 06 (Print Publication: 2024).

نوع المنشور: Journal Article

بيانات الدورية: Publisher: Oxford University Press Country of Publication: England NLM ID: 101755125 Publication Model: eCollection Cited Medium: Internet ISSN: 2632-1297 (Electronic) Linking ISSN: 26321297 NLM ISO Abbreviation: Brain Commun Subsets: PubMed not MEDLINE

المؤلفون: Abu-Hanna J; Centre for Cardiovascular Physiology and Pharmacology, Institute of Cardiovascular Science, University College London, London, United Kingdom; Centre for Rheumatology, Division of Medicine, University College London, London, United Kingdom., Anastasakis E; Centre for Cardiovascular Physiology and Pharmacology, Institute of Cardiovascular Science, University College London, London, United Kingdom; Centre for Rheumatology, Division of Medicine, University College London, London, United Kingdom., Patel JA; Centre for Cardiovascular Physiology and Pharmacology, Institute of Cardiovascular Science, University College London, London, United Kingdom., Eddama MMR; Department of Surgical Biotechnology, Division of Surgery and Interventional Science, University College London, London, United Kingdom., Denton CP; Centre for Rheumatology, Division of Medicine, University College London, London, United Kingdom., Taanman JW; Department of Clinical and Movement Neurosciences, Queen Square Institute of Neurology, University College London, London, United Kingdom., Abraham D; Centre for Rheumatology, Division of Medicine, University College London, London, United Kingdom., Clapp LH; Centre for Cardiovascular Physiology and Pharmacology, Institute of Cardiovascular Science, University College London, London, United Kingdom. Electronic address: l.clapp@ucl.ac.uk.

المصدر: Vascular pharmacology [Vascul Pharmacol] 2023 Aug; Vol. 151, pp. 107194. Date of Electronic Publication: 2023 Jul 11.

نوع المنشور: Journal Article; Research Support, Non-U.S. Gov't

بيانات الدورية: Publisher: Elsevier Science Country of Publication: United States NLM ID: 101130615 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1879-3649 (Electronic) Linking ISSN: 15371891 NLM ISO Abbreviation: Vascul Pharmacol Subsets: MEDLINE

مواضيع طبية MeSH: Pulmonary Arterial Hypertension*/metabolism, Humans ; Cell Proliferation ; Dynamins/metabolism ; Dynamins/pharmacology ; Pulmonary Artery/metabolism ; Mitochondrial Dynamics