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Circulating cell-free mitochondrial DNA levels in Parkinson's disease are influenced by treatment

Molecular neurodegeneration, 2020-02, Vol.15 (1), p.10-10, Article 10

2020

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Segregation of mitochondrial DNA heteroplasmy through a developmental genetic bottleneck in human embryos

Nature cell biology, 2018-02, Vol.20 (2), p.144-151

2018

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Nanobiopsy investigation of the subcellular mtDNA heteroplasmy in human tissues

Scientific reports, 2024-06, Vol.14 (1), p.13789-12

2024

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Somatic mtDNA variation is an important component of Parkinson's disease

Neurobiology of aging, 2016-02, Vol.38, p.217.e1-217.e6

2016

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Use of whole-exome sequencing to determine the genetic basis of multiple mitochondrial respiratory chain complex deficiencies

JAMA : the journal of the American Medical Association, 2014-07, Vol.312 (1), p.68

2014

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Exome sequencing in undiagnosed inherited and sporadic ataxias

Brain (London, England : 1878), 2015-02, Vol.138 (2), p.276-283

2015

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Reduced cerebrospinal fluid mitochondrial DNA is a biomarker for early-stage Parkinson's disease

Annals of neurology, 2015-12, Vol.78 (6), p.1000-1004

2015

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Defective mitochondrial protease LonP1 can cause classical mitochondrial disease

Human molecular genetics, 2018-05, Vol.27 (10), p.1743-1753

2018

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metabolic profiling of Parkinson's disease and mild cognitive impairment

Movement disorders, 2017-06, Vol.32 (6), p.927-932

2017

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Mitochondrial DNA changes in pedunculopontine cholinergic neurons in Parkinson disease

Annals of neurology, 2017-12, Vol.82 (6), p.1016-1021

2017

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Metabolic effects of bezafibrate in mitochondrial disease

EMBO molecular medicine, 2020-03, Vol.12 (3), p.e11589-n/a

2020

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Variant load of mitochondrial DNA in single human mesenchymal stem cells

Scientific reports, 2024-09, Vol.14 (1), p.20989-10, Article 20989

2024

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A Continuum of Play-Based Learning: The Role of the Teacher in Play-Based Pedagogy and the Fear of Hijacking Play

Early education and development, 2017-04, Vol.28 (3), p.274-289

2017

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Planned Change: Drivers of High Implementation for a Pedagogical Self-Regulated Learning Intervention

Frontiers in education (Lausanne), 2021-01, Vol.5

2021

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Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain Deficiencies

American journal of human genetics, 2016-05, Vol.98 (5), p.993-1000

2016

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Extreme-Depth Re-sequencing of Mitochondrial DNA Finds No Evidence of Paternal Transmission in Humans

PLoS genetics, 2015-05, Vol.11 (5), p.e1005040-e1005040

2015

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Synaptotagmin 2 Mutations Cause an Autosomal-Dominant Form of Lambert-Eaton Myasthenic Syndrome and Nonprogressive Motor Neuropathy

American journal of human genetics, 2014-09, Vol.95 (3), p.332-339

2014

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Heteroplasmic mitochondrial DNA variants in cardiovascular diseases

PLoS genetics, 2022-04, Vol.18 (4), p.e1010068-e1010068

2022

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Kindergarten teachers' facilitation of social and emotional learning in classroom play contexts

Education Inquiry, 2023-03, Vol.ahead-of-print (ahead-of-print), p.1-22

2023

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Effects of thyroid hormone on mitochondria and metabolism of human preimplantation embryos

Stem cells (Dayton, Ohio), 2020-03, Vol.38 (3), p.369-381

2020

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Exposure of Monocytic Cells to Lipopolysaccharide Induces Coordinated Endotoxin Tolerance, Mitochondrial Biogenesis, Mitophagy, and Antioxidant Defenses

Frontiers in immunology, 2018-09, Vol.9, p.2217-2217

2018

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ANO10 mutations cause ataxia and coenzyme Q10 deficiency

Journal of neurology, 2014-11, Vol.261 (11), p.2192-2198

2014

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Altered 2-thiouridylation impairs mitochondrial translation in reversible infantile respiratory chain deficiency

Human molecular genetics, 2013-11, Vol.22 (22), p.4602-4615

2013

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Instability of the mitochondrial alanyl-tRNA synthetase underlies fatal infantile-onset cardiomyopathy

Human molecular genetics, 2019-01, Vol.28 (2), p.258-268

2019

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Fall in circulating mononuclear cell mitochondrial DNA content in human sepsis

Intensive care medicine, 2010-06, Vol.36 (6), p.956-962

2010

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Circulating cell-free mitochondrial DNA levels in Parkinson's disease are influenced by treatment

Segregation of mitochondrial DNA heteroplasmy through a developmental genetic bottleneck in human embryos

Nanobiopsy investigation of the subcellular mtDNA heteroplasmy in human tissues

Somatic mtDNA variation is an important component of Parkinson's disease

Use of whole-exome sequencing to determine the genetic basis of multiple mitochondrial respiratory chain complex deficiencies

Exome sequencing in undiagnosed inherited and sporadic ataxias

Reduced cerebrospinal fluid mitochondrial DNA is a biomarker for early-stage Parkinson's disease

Defective mitochondrial protease LonP1 can cause classical mitochondrial disease

metabolic profiling of Parkinson's disease and mild cognitive impairment

Mitochondrial DNA changes in pedunculopontine cholinergic neurons in Parkinson disease

Metabolic effects of bezafibrate in mitochondrial disease

Variant load of mitochondrial DNA in single human mesenchymal stem cells

A Continuum of Play-Based Learning: The Role of the Teacher in Play-Based Pedagogy and the Fear of Hijacking Play

Planned Change: Drivers of High Implementation for a Pedagogical Self-Regulated Learning Intervention

Recessive Mutations in TRMT10C Cause Defects in Mitochondrial RNA Processing and Multiple Respiratory Chain Deficiencies

Extreme-Depth Re-sequencing of Mitochondrial DNA Finds No Evidence of Paternal Transmission in Humans

Synaptotagmin 2 Mutations Cause an Autosomal-Dominant Form of Lambert-Eaton Myasthenic Syndrome and Nonprogressive Motor Neuropathy

Heteroplasmic mitochondrial DNA variants in cardiovascular diseases

Kindergarten teachers' facilitation of social and emotional learning in classroom play contexts

Effects of thyroid hormone on mitochondria and metabolism of human preimplantation embryos

Exposure of Monocytic Cells to Lipopolysaccharide Induces Coordinated Endotoxin Tolerance, Mitochondrial Biogenesis, Mitophagy, and Antioxidant Defenses

ANO10 mutations cause ataxia and coenzyme Q10 deficiency

Altered 2-thiouridylation impairs mitochondrial translation in reversible infantile respiratory chain deficiency

Instability of the mitochondrial alanyl-tRNA synthetase underlies fatal infantile-onset cardiomyopathy

Fall in circulating mononuclear cell mitochondrial DNA content in human sepsis

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