Related references
Note: Only part of the references are listed.Illuminating NAD(+) Metabolism in Live Cells and In Vivo Using a Genetically Encoded Fluorescent Sensor
Yejun Zou et al.
DEVELOPMENTAL CELL (2020)
Mitocellular communication: Shaping health and disease
Adrienne Mottis et al.
SCIENCE (2019)
Mitochondrial DNA mutation m.3243A>G is associated with altered mitochondrial function in peripheral blood mononuclear cells, with heteroplasmy levels and with clinical phenotypes
X. Geng et al.
DIABETIC MEDICINE (2019)
Mitochondrial genome mutations in mesenchymal stem cells derived from human dental induced pluripotent stem cells
Jumi Park et al.
BMB REPORTS (2019)
Mitochondrial diseases: the contribution of organelle stress responses to pathology
Anu Suomalainen et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2018)
The mitochondrial UPR: mechanisms, physiological functions and implications in ageing
Tomer Shpilka et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2018)
mtDNA heteroplasmy level and copy number indicate disease burden in m.3243A>G mitochondrial disease
John P. Grady et al.
EMBO MOLECULAR MEDICINE (2018)
Human urine-derived stem cells play a novel role in the treatment of STZ-induced diabetic mice
Tianxue Zhao et al.
JOURNAL OF MOLECULAR HISTOLOGY (2018)
Mitochondrial Point Mutation m.3243A>G Associates With Lower Bone Mineral Density, Thinner Cortices, and Reduced Bone Strength: A Case-Control Study
Jakob Hogild Langdahl et al.
JOURNAL OF BONE AND MINERAL RESEARCH (2017)
Homeostatic Responses Regulate Selfish Mitochondrial Genome Dynamics in C. elegans
Bryan L. Gitschlag et al.
CELL METABOLISM (2016)
The Transcription Factor ATF5 Mediates a Mammalian Mitochondrial UPR
Christopher J. Fiorese et al.
CURRENT BIOLOGY (2016)
Mitochondrial and nuclear DNA matching shapes metabolism and healthy ageing
Ana Latorre-Pellicer et al.
NATURE (2016)
Maintenance and propagation of a deleterious mitochondrial genome by the mitochondrial unfolded protein response
Yi-Fan Lin et al.
NATURE (2016)
Mitonuclear communication in homeostasis and stress
Pedro M. Quiros et al.
NATURE REVIEWS MOLECULAR CELL BIOLOGY (2016)
Exosomes secreted by human urine-derived stem cells could prevent kidney complications from type I diabetes in rats
Zhen-zhen Jiang et al.
STEM CELL RESEARCH & THERAPY (2016)
Mitochondrial diseases
Grainne S. Gorman et al.
NATURE REVIEWS DISEASE PRIMERS (2016)
Human urine-derived stem cells can be induced into osteogenic lineage by silicate bioceramics via activation of the Wnt/β-catenin signaling pathway
Junjie Guan et al.
BIOMATERIALS (2015)
The mitochondrial unfolded protein response - synchronizing genomes
Virginija Jovaisaite et al.
CURRENT OPINION IN CELL BIOLOGY (2015)
Mitochondrial and Nuclear Accumulation of the Transcription Factor ATFS-1 Promotes OXPHOS Recovery during the UPRmt
Amrita M. Nargund et al.
MOLECULAR CELL (2015)
Mutations causing mitochondrial disease: What is new and what challenges remain?
Robert N. Lightowlers et al.
SCIENCE (2015)
Silver nanoparticles promote osteogenic differentiation of human urine-derived stem cells at noncytotoxic concentrations
Hui Qin et al.
INTERNATIONAL JOURNAL OF NANOMEDICINE (2014)
The mitochondrial unfolded protein response, a conserved stress response pathway with implications in health and disease
Virginija Jovaisaite et al.
JOURNAL OF EXPERIMENTAL BIOLOGY (2014)
Pyrosequencing Is an Accurate and Reliable Method for the Analysis of Heteroplasmy of the A3243G Mutation in Patients with Mitochondrial Diabetes
Jing-bin Yan et al.
JOURNAL OF MOLECULAR DIAGNOSTICS (2014)
Progressive increase in mtDNA 3243A>G heteroplasmy causes abrupt transcriptional reprogramming
Martin Picard et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2014)
Biological Characteristics of Human-Urine-Derived Stem Cells: Potential for Cell-Based Therapy in Neurology
Jun-Jie Guan et al.
TISSUE ENGINEERING PART A (2014)
Cytoplasmic hybrid (cybrid) cell lines as a practical model for mitochondriopathies
Heather M. Wilkins et al.
REDOX BIOLOGY (2014)
Urine-derived stem cells: A novel and versatile progenitor source for cell-based therapy and regenerative medicine
Deying Zhang et al.
GENES & DISEASES (2014)
The NAD+/Sirtuin Pathway Modulates Longevity through Activation of Mitochondrial UPR and FOXO Signaling
Laurent Mouchiroud et al.
CELL (2013)
A mitochondrial bioenergetic etiology of disease
Douglas C. Wallace
JOURNAL OF CLINICAL INVESTIGATION (2013)
Mitonuclear protein imbalance as a conserved longevity mechanism
Riekelt H. Houtkooper et al.
NATURE (2013)
Tissue- and cell-type-specific manifestations of heteroplasmic mtDNA 3243A>G mutation in human induced pluripotent stem cell-derived disease model
Riikka H. Hamalainen et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2013)
Induced pluripotent stem cells generated from diabetic patients with mitochondrial DNA A3243G mutation
J. Fujikura et al.
DIABETOLOGIA (2012)
Human Mitochondrial tRNAs: Biogenesis, Function, Structural Aspects, and Diseases
Tsutomu Suzuki et al.
ANNUAL REVIEW OF GENETICS, VOL 45 (2011)
Somatic coding mutations in human induced pluripotent stem cells
Athurva Gore et al.
NATURE (2011)
Altered mitochondrial membrane potential, mass, and morphology in the mononuclear cells of humans with type 2 diabetes
Michael E. Widlansky et al.
TRANSLATIONAL RESEARCH (2010)
Mitochondrial tRNA mutations and disease
John W. Yarham et al.
WILEY INTERDISCIPLINARY REVIEWS-RNA (2010)
Molecular mechanisms of angiotensin II-mediated mitochondrial dysfunction - Linking mitochondrial oxidative damage and vascular endothelial dysfunction
Abdulrahman K. Doughan et al.
CIRCULATION RESEARCH (2008)
Clinical features, diagnosis and management of maternally inherited diabetes and deafness (MIDD) associated with the 3243A > G mitochondrial point mutation
R. Murphy et al.
DIABETIC MEDICINE (2008)
The pathogenic A3243G mutation in human mitochondrial tRNALeu(UUR) decreases the efficiency of aminoacylation
H Park et al.
BIOCHEMISTRY (2003)
Assessment of equine sperm mitochondrial function using JC-1
CG Gravance et al.
THERIOGENOLOGY (2000)
Decreased aminoacylation of mutant tRNAs in MELAS but not in MERRF patients
GV Börner et al.
HUMAN MOLECULAR GENETICS (2000)
Modification defect at anticodon wobble nucleotide of mitochondrial tRNAsLeu(UUR) with pathogenic mutations of mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes
T Yasukawa et al.
JOURNAL OF BIOLOGICAL CHEMISTRY (2000)