EUROMIT 2023 - International Meeting on Mitochondrial Pathology

A list of all persons who contribute to the sessions of this conference. Please select a letter below to list all persons with the corresponding surname. Select the presentation in the right-hand column to access session and presentation details.

Author(s)	Organization(s)	Contribution Title
Yahata, Naoki	Fujita Health University School of Medicine, Japan	Development of mutant mtDNA-targeted TALENs and their application to iPSC-based mitochondrial disease model. Presenter
Yamada, Yuma	Faculty of Pharmaceutical Sciences, Hokkaido University, Sapporo, Japan; FOREST Program, Japan Science and Technology Agency Japan, Saitama, Japan; Fusion Oriented REsearch for disruptive Science and Technology (FOREST) Program, Japan Science and Technology Agency (JST) Japan, Saitama, Japan	Innovative technology for regulating mitochondrial function in host cells Presenter Myocardial regeneration therapy using human cardiosphere-derived cells with activated mitochondria The use of a coenzyme Q10 encapsulated mitochondrial targeting lipid nanoparticle formulation has therapeutic effects on a drug-induced liver injury. Validation of drug delivery and functional activation to mitochondria in skeletal muscle cell
Yamamoto, Masamichi	National Cerebral and Cardiovascular Center, Japan	Visualizing ATP dynamics in living mice Presenter
Yamamoto, Naoko	DOJINDO LABORATORIES	Analysis of mitochondrial function using novel detection reagents
Yan, Jingyi	Karolinska Institutet, Sweden	Mitochondrial dysfunction promotes liver fibrosis through the ACOT2-MCT6-OXCT1 axis.
Yang, Jason	Department of Biology, MIT, Cambridge, MA, USA; Whitehead Institute for Biomedical Research, Cambridge, MA, USA	SLC25A38 is Necessary for Mitochondrial Pyridoxal 5’-Phosphate (PLP) Accumulation
Yang, Ming	CECAD Research Center, Germany; Institute for Mitochondrial Diseases and Aging, Medical Faculty, University of Cologne	Tissue-specific adaptation of stress responses upon COX10 deficiency
Yarosz, Emily	University of Michigan, United States of America	Iron homeostasis in mitochondria is critical for the survival of T cells
Yee, Chenxian	University of Michigan, United States of America	Iron homeostasis in mitochondria is critical for the survival of T cells
Yee, Irene	Mitochondrial Medicine, Department of Clinical Sciences, Lund University, Lund, Sweden	Quinone compounds in primary mitochondrial disease: acute metabolic effects in human-derived cells in vitro Succinate does not increase reactive oxygen species generation in phosphorylating human mitochondria Presenter
Yépez, Vicente A.	Institute of Human Genetics, School of Medicine, Technical University of Munich, Munich, Germany	Contribution of RNA-seq to diagnosis and determination of functional impact of candidate variants in 45 patients suspected of mitochondrial disease.
Yépez, Vincente	Institute of Human Genetics, School of Medicine, Technical University Munich, München, Germany.; Department of Informatics, Technical University of Munich, Garching, Germany.	Novel genetic discoveries detected using diagnostic OMICSs in patients suspected to suffer from multiple acyl-CoA dehydrogenation deficiency
Yessenbekova, Arailym	Department of Biophysics, Biomedicine and Neuroscience, Al-Farabi Kazakh National University, Almaty, Kazakhstan	Inflammatory conditions, redox status and c-miRNAs as potential predictors of vascular damage in type 2 diabetes mellitus patients.
Ygberg, Sofia	Centre of inherited metabolic diseases, Karolinska University Hospital, Stockholm, Sweden; Neuropediatric Unit, Dept of Women’s, and Children's Health, Karolinska Institutet, Stockholm, Sweden	Novel atypical variants causing pyruvate dehydrogenase complex deficiency
Yin, Yajie	Department of Pathology, Stanford University, Stanford, CA 94305, USA	Single-cell multi-omics reveals dynamics of purifying selection of pathogenic mitochondrial DNA across human immune cells
Ylikallio, Emil	Stem Cells and Metabolism Research Program, Faculty of Medicine, University of Helsinki; Clinical Neurosciences, Neurology, Helsinki University Hospital	Proteotoxicity induced mitochondrial integrated stress response in CHCHD10-linked adult-onset spinal muscular atrophy
Ylla-Català, Maria	Research Group on Neuromuscular and Mitochondrial Diseases, Vall d’Hebron Research Institute, Universitat Autònoma de Barcelona, Spain; Biomedical Network Research Centre on Rare Diseases (CIBERER), Instituto de Salud Carlos III, Madrid, Spain	Preclinical studies of efficacy and genetic safety of deoxyribonucleosides as a therapy for mitochondrial DNA maintenance defects
Yokota, Takafumi	Department of Hematology and Oncology, Graduate School of Medicine, Osaka University, Osaka, Japan.; Department of Hematology, Osaka International Cancer Institute, Osaka, Japan.	A novel therapeutic strategy for mitochondrial Leigh Syndrome
Yoshihara, Toshitada	Gunma University	Analysis of mitochondrial function using novel detection reagents
Yoshimi, Ayami	Department of Paediatrics and Adolescent Medicine, Division of Paediatric Haematology and Oncology, Medical Center, Faculty of Medicine, University of Freiburg, Germany	Natural history of Pearson syndrome: various clinical courses with changes in clinical phenotypes Presenter
Young, Anthony	University of Pennsylvania, United States of America	[18F]ROStrace PET as a biomarker of mitochondria-induced neuroinflammation in the prodromal phase of Parkinson’s disease mouse models
Youssef, Lina	Biomedical Network Research Centre on Rare Diseases (CIBERER), Instituto de Salud Carlos III, 28029 Madrid, Spain; BCNatal—Barcelona Centre for Maternal-Foetal and Neonatal Medicine (Hospital Clínic and Hospital Sant Joan de Déu), IDIBAPS, University of Barcelona, 08036 Barcelona, Spain	The mitokine GDF15 correlates with differentially dietary fat intake in pregnancies with intrauterine growth restriction
Yu-Wai-Man, Patrick	Cambridge Centre for Brain Repair and MRC Mitochondrial Biology Unit, Department of Clinical Neurosciences, University of Cambridge, Cambridge, UK; Moorfields Eye Hospital NHS Foundation Trust, London, UK; Institute of Ophthalmology, University College London, London, UK; Cambridge Eye Unit, Addenbrooke’s Hospital, Cambridge University Hospitals, Cambridge, UK	Indirect comparison of lenadogene nolparvovec gene therapy versus natural history in m.11778G>A MT-ND4 Leber hereditary optic neuropathy patients Indirect comparison of lenadogene nolparvovec gene therapy versus natural history in m.11778G>A MT-ND4 Leber hereditary optic neuropathy patients Known genes, new genes and new phenotypes in inherited mitochondrial eye diseases Long-term efficacy of idebenone in patients with LHON in the LEROS study: Analyzing change in visual acuity categories according to mitochondrial DNA mutation and disease phase Long-term efficacy of idebenone in patients with LHON in the LEROS study: Analyzing change in visual acuity over time according to mitochondrial DNA mutation and disease phase Long-term efficacy of idebenone in patients with LHON in the LEROS study: Analyzing the impact of idebenone on rates of recovery and worsening of vision according to disease phase Long-term efficacy of idebenone in patients with LHON in the LEROS study: Analyzing the impact of idebenone on rates of recovery and worsening of vision according to primary mitochondrial DNA mutation
Yu-Wai-Man, Patrick	University of Cambridge, United Kingdom	Retinal pathophysiology characterisation of the novel mitochondrial heteroplasmy mouse model
Yu-Wai-Man, Patrick	University of Cambridge, Cambridge, UK; Moorfields Eye Hospital and UCL Institute of Ophthalmology, London, UK	The European landscape of mitogenomes from LHON patients carrying the m.14484T>C/MT-ND6 pathogenic variant Treatment with lenadogene nolparvovec gene therapy results in sustained visual improvement in m.11778G>A MT-ND4-LHON patients: the RESTORE study Presenter Use of lenadogene nolparvovec gene therapy for Leber hereditary optic neuropathy in early access programs Use of lenadogene nolparvovec gene therapy for Leber hereditary optic neuropathy in early access programs
Yuan, Taolin	Department of Medical Biochemistry and Biophysics, Karolinska Institutet, Sweden	Inhibition of mtDNA transcription in liver reverses diet-induced obesity and hepatosteatosis in the mouse
Yue, Xiao	Department of Pediatrics, Graduate School of Medicine, Gifu University Hospital, Gifu, Japan.	Novel genetic discoveries detected using diagnostic OMICSs in patients suspected to suffer from multiple acyl-CoA dehydrogenation deficiency

Index of Authors