UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

The effect of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) severity on cellular bioenergetic function

PloS one, 2020-04, Vol.15 (4), p.e0231136-e0231136

2020

Volltextzugriff (PDF)

Strong purifying selection in transmission of mammalian mitochondrial DNA

PLoS biology, 2008-01, Vol.6 (1), p.e10-e10

2008

Volltextzugriff (PDF)

Mitochondrial DNA population variation is not associated with Alzheimer’s in the Japanese population: A consistent finding across global populations

PloS one, 2022-10, Vol.17 (10), p.e0276169-e0276169

2022

Volltextzugriff (PDF)

Clonal expansion of early to mid-life mitochondrial DNA point mutations drives mitochondrial dysfunction during human ageing

PLoS genetics, 2014-09, Vol.10 (9), p.e1004620-e1004620

2014

Volltextzugriff (PDF)

A comparative analysis approach to determining the pathogenicity of mitochondrial tRNA mutations

Human mutation, 2011-11, Vol.32 (11), p.1319-1325

2011

Volltextzugriff (PDF)

Mitochondrial DNA changes in pedunculopontine cholinergic neurons in Parkinson disease

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

2017

Volltextzugriff (PDF)

Deep-brain stimulation associates with improved microvascular integrity in the subthalamic nucleus in Parkinson's disease

Neurobiology of disease, 2015-02, Vol.74, p.392-405

2015

Volltextzugriff (PDF)

Mitochondrial DNA sequence context in the penetrance of mitochondrial t-RNA mutations: A study across multiple lineages with diagnostic implications

PloS one, 2017-11, Vol.12 (11), p.e0187862-e0187862

2017

Volltextzugriff (PDF)

Our current understanding of the toxicity of altered mito-ribosomal fidelity during mitochondrial protein synthesis: What can it tell us about human disease?

Frontiers in physiology, 2023-06, Vol.14, p.1082953-1082953

2023

Volltextzugriff (PDF)

A broad comparative genomics approach to understanding the pathogenicity of Complex I mutations

Scientific reports, 2021-10, Vol.11 (1), p.19578-12, Article 19578

2021

Volltextzugriff (PDF)

Structural analysis of mitochondrial rRNA gene variants identified in patients with deafness

Frontiers in physiology, 2023-06, Vol.14, p.1163496-1163496

2023

Volltextzugriff (PDF)

Purifying selection of mtDNA and its implications for understanding evolution and mitochondrial disease

Nature reviews. Genetics, 2008-09, Vol.9 (9), p.657-662

2008

Volltextzugriff (PDF)

Mitochondrial tRNA mutations and disease

Wiley interdisciplinary reviews. RNA, 2010-09, Vol.1 (2), p.304-324

2010

Volltextzugriff (PDF)

What can a comparative genomics approach tell us about the pathogenicity of mtDNA mutations in human populations?

Evolutionary applications, 2019-12, Vol.12 (10), p.1912-1930

2019

Volltextzugriff (PDF)

Mitochondrial complex activity in permeabilised cells of chronic fatigue syndrome patients using two cell types

PeerJ (San Francisco, CA), 2019-03, Vol.7, p.e6500-e6500, Article e6500

2019

Volltextzugriff (PDF)

Mitochondrial DNA variation in Parkinson’s disease: Analysis of “out-of-place” population variants as a risk factor

Frontiers in aging neuroscience, 2022-07, Vol.14, p.921412-921412

2022

Volltextzugriff (PDF)

Comparison of mitochondrial mutation spectra in ageing human colonic epithelium and disease: absence of evidence for purifying selection in somatic mitochondrial DNA point mutations

PLoS genetics, 2012-11, Vol.8 (11), p.e1003082-e1003082

2012

Volltextzugriff (PDF)

Correction: Cellular bioenergetics is impaired in patients with chronic fatigue syndrome

PloS one, 2018-02, Vol.13 (2), p.e0192817-e0192817

2018

Volltextzugriff (PDF)

Cellular bioenergetics is impaired in patients with chronic fatigue syndrome

PloS one, 2017-10, Vol.12 (10), p.e0186802-e0186802

2017

Volltextzugriff (PDF)

Nature of Mitochondrial DNA Deletions in Substantia Nigra Neurons

American journal of human genetics, 2008-01, Vol.82 (1), p.228-235

2008

Volltextzugriff (PDF)

New mtDNA Association Model, MutPred Variant Load, Suggests Individuals With Multiple Mildly Deleterious mtDNA Variants Are More Likely to Suffer From Atherosclerosis

Frontiers in genetics, 2019-01, Vol.9, p.702-702

2019

Volltextzugriff (PDF)

Reduced-Median-Network Analysis of Complete Mitochondrial DNA Coding-Region Sequences for the Major African, Asian, and European Haplogroups

American journal of human genetics, 2002-05, Vol.70 (5), p.1152-1171

2002

Volltextzugriff (PDF)

Habitual physical activity in mitochondrial disease

PloS one, 2011-07, Vol.6 (7), p.e22294-e22294

2011

Volltextzugriff (PDF)

Mitochondrial DNA and survival after sepsis: a prospective study

The Lancet (British edition), 2005-12, Vol.366 (9503), p.2118-2121

2005

Volltextzugriff (PDF)

mtDNA mutations and common neurodegenerative disorders

Trends in genetics, 2005-11, Vol.21 (11), p.583-586

2005

Volltextzugriff (PDF)

1 – 25 von 172

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(168)
Mit Volltextzugriff
(147)

Publikationsform

Artikel
(172)

Sprache

Englisch
(171)

Erscheinungsjahr

n.n

Thema

Science & Technology
(145)
Humans
(122)
Life Sciences & Biomedicine
(116)
Female
(55)
Genomes
(53)
Genetics & Heredity
(51)
Male
(51)
Genome-Wide Association Study
(41)
Biomedical And Life Sciences
(40)
Mitochondrial Dna
(39)
631/208/205/2138
(36)
Neurosciences
(36)
Multidisciplinary Sciences
(35)
Mutation
(35)
Science & Technology - Other Topics
(35)
Dna, Mitochondrial - Genetics
(34)
Adult
(31)
Biomedicine
(31)
Neurosciences & Neurology
(29)
45/43
(28)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

The effect of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) severity on cellular bioenergetic function

Strong purifying selection in transmission of mammalian mitochondrial DNA

Mitochondrial DNA population variation is not associated with Alzheimer’s in the Japanese population: A consistent finding across global populations

Clonal expansion of early to mid-life mitochondrial DNA point mutations drives mitochondrial dysfunction during human ageing

A comparative analysis approach to determining the pathogenicity of mitochondrial tRNA mutations

Mitochondrial DNA changes in pedunculopontine cholinergic neurons in Parkinson disease

Deep-brain stimulation associates with improved microvascular integrity in the subthalamic nucleus in Parkinson's disease

Mitochondrial DNA sequence context in the penetrance of mitochondrial t-RNA mutations: A study across multiple lineages with diagnostic implications

Our current understanding of the toxicity of altered mito-ribosomal fidelity during mitochondrial protein synthesis: What can it tell us about human disease?

A broad comparative genomics approach to understanding the pathogenicity of Complex I mutations

Structural analysis of mitochondrial rRNA gene variants identified in patients with deafness

Purifying selection of mtDNA and its implications for understanding evolution and mitochondrial disease

Mitochondrial tRNA mutations and disease

What can a comparative genomics approach tell us about the pathogenicity of mtDNA mutations in human populations?

Mitochondrial complex activity in permeabilised cells of chronic fatigue syndrome patients using two cell types

Mitochondrial DNA variation in Parkinson’s disease: Analysis of “out-of-place” population variants as a risk factor

Comparison of mitochondrial mutation spectra in ageing human colonic epithelium and disease: absence of evidence for purifying selection in somatic mitochondrial DNA point mutations

Correction: Cellular bioenergetics is impaired in patients with chronic fatigue syndrome

Cellular bioenergetics is impaired in patients with chronic fatigue syndrome

Nature of Mitochondrial DNA Deletions in Substantia Nigra Neurons

New mtDNA Association Model, MutPred Variant Load, Suggests Individuals With Multiple Mildly Deleterious mtDNA Variants Are More Likely to Suffer From Atherosclerosis

Reduced-Median-Network Analysis of Complete Mitochondrial DNA Coding-Region Sequences for the Major African, Asian, and European Haplogroups

Habitual physical activity in mitochondrial disease

Mitochondrial DNA and survival after sepsis: a prospective study

mtDNA mutations and common neurodegenerative disorders

Suchergebnisse filtern