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...

Mitochondrial impairment and synaptic dysfunction are associated with neurological defects in iPSCs-derived cortical neurons of MERRF patients

Journal of biomedical science, 2023-08, Vol.30 (1), p.1-70, Article 70

2023

Volltextzugriff (PDF)

Profiling of cardiolipins and their hydroperoxides in HepG2 cells by LC/MS

Analytical and bioanalytical chemistry, 2017-09, Vol.409 (24), p.5735-5745

2017

Volltextzugriff (PDF)

Response to the increase of oxidative stress and mutation of mitochondrial DNA in aging

Biochimica et biophysica acta, 2009-10, Vol.1790 (10), p.1021-1029

2009

Volltextzugriff (PDF)

Oxidative Stress-related Alteration of the Copy Number of Mitochondrial DNA in Human Leukocytes

Free radical research, 2003-12, Vol.37 (12), p.1307-1317

2003

Volltextzugriff (PDF)

The protective roles of phosphorylated heat shock protein 27 in human cells harboring myoclonus epilepsy with ragged‐red fibers A8344G mtDNA mutation

The FEBS journal, 2012-08, Vol.279 (16), p.2987-3001

2012

Volltextzugriff (PDF)

Depletion of Sirt3 leads to the impairment of adipogenic differentiation and insulin resistance via interfering mitochondrial function of adipose-derived human mesenchymal stem cells

Free radical research, 2018-12, Vol.52 (11-12), p.1398-1415

2018

Volltextzugriff (PDF)

Promoter analysis and transcriptional regulation of human carbonic anhydrase VIII gene in a MERRF disease cell model

Archives of biochemistry and biophysics, 2018-03, Vol.641, p.50-61

2018

Volltextzugriff (PDF)

High glucose modulates antiproliferative effect and cytotoxicity of 5-fluorouracil in human colon cancer cells

DNA and cell biology, 2014-02, Vol.33 (2), p.64-72

2014

Volltextzugriff (PDF)

Increases of Mitochondrial Mass and Mitochondrial Genome in Association with Enhanced Oxidative Stress in Human Cells Harboring 4,977 BP-Deleted Mitochondrial DNA

Annals of the New York Academy of Sciences, 2001-04, Vol.928 (1), p.97-112

2001

Volltextzugriff (PDF)

Mitochondrial DNA Mutation-Elicited Oxidative Stress, Oxidative Damage, and Altered Gene Expression in Cultured Cells of Patients with MERRF Syndrome

Molecular neurobiology, 2010-06, Vol.41 (2-3), p.256-266

2010

Volltextzugriff (PDF)

Effects of Tolerance-Induced Preconditioning on Mitochondrial Biogenesis in Undifferentiated and Differentiated Neuronal Cells

Frontiers in bioscience (Landmark. Print), 2022-04, Vol.27 (4), p.115-115

2022

Volltextzugriff (PDF)

Effects of carbonic anhydrase-related protein VIII on human cells harbouring an A8344G mitochondrial DNA mutation

Biochemical journal, 2014-04, Vol.459 (1), p.149-160

2014

Volltextzugriff (PDF)

MtDNA mutations, functional decline and turnover of mitochondria in aging

Frontiers in bioscience, 2008-05, Vol.13 (13), p.3661

2008

Volltextzugriff (PDF)

Decreased heat shock protein 27 expression and altered autophagy in human cells harboring A8344G mitochondrial DNA mutation

Mitochondrion, 2011-09, Vol.11 (5), p.739-749

2011

Volltextzugriff (PDF)

Oxidative Damage and Mutation to Mitochondrial DNA and Age-dependent Decline of Mitochondrial Respiratory Function

Annals of the New York Academy of Sciences, 1998-11, Vol.854 (1), p.155-170

1998

Volltextzugriff (PDF)

Oxidative Stress in Human Aging and Mitochondrial Disease-Consequences of Defective Mitochondrial Respiration and Impaired Antioxidant Enzyme System

Chinese journal of physiology, 2001-03, Vol.44 (1), p.1-11

2001

Volltextzugriff (PDF)

Upregulation of Matrix Metalloproteinase 1 and Disruption of Mitochondrial Network in Skin Fibroblasts of Patients with MERRF Syndrome

Annals of the New York Academy of Sciences, 2005-05, Vol.1042 (1), p.55-63

2005

Volltextzugriff (PDF)

High prevalence of the COII/tRNA(Lys) intergenic 9-bp deletion in mitochondrial DNA of Taiwanese patients with MELAS or MERRF syndrome

Annals of the New York Academy of Sciences, 2005-05, Vol.1042, p.82-87

2005

Volltextzugriff (PDF)

Oculopharyngeal somatic myopathy in a patient with a novel large-scale 3399 bp deletion and a homoplasmic T5814C transition of the mitochondrial DNA

Clinical neurology and neurosurgery, 2006-06, Vol.108 (4), p.407-410

2006

Volltextzugriff (PDF)

Clinical phenotype, prognosis and mitochondrial DNA mutation load in mitochondrial encephalomyopathies

Journal of biomedical science, 2002-01, Vol.9 (6 Pt 1), p.527-533

2002

Volltextzugriff (PDF)

Respiratory function decline and DNA mutation in mitochondria, oxidative stress and altered gene expression during aging

Chang Gung medical journal, 2009-03, Vol.32 (2), p.113-132

2009

Volltextzugriff (PDF)

Mitochondrial DNA mutations and oxidative damage in skeletal muscle of patients with chronic uremia

Journal of biomedical science, 2002-01, Vol.9 (6 Pt 1), p.549-560

2002

Volltextzugriff (PDF)

The protective roles of phosphorylated heat shock protein27 in human cells harboring myoclonus epilepsy with ragged-red fibers A8344G mtDNA mutation

The FEBS journal, 2012-08, Vol.279 (16), p.2987

2012

Volltextzugriff (PDF)

Oxidative Stress and its Biochemical Consequences in Mitochondrial DNA Mutation‐Associated Diseases: Implications of Redox Therapy for Mitochondrial Diseases

Oxidative Stress in Vertebrates and Invertebrates, 2011, p.33-49

2011

Volltextzugriff (PDF)

Oculopharyngeal somatic myopathy in a patient with a novel large-scale 3,399 bp deletion and a homoplasmic T5814C transition of the mitochondrial DNA

Clinical neurology and neurosurgery, 2006-06, Vol.108 (4), p.407-410

2006

Volltextzugriff (PDF)

1 – 25 von 43

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(37)
Mit Volltextzugriff
(40)

Publikationsform

Sprache

Englisch
(43)
Japanisch
(6)

Erscheinungsjahr

n.n

Thema

Science & Technology
(28)
Humans
(23)
Life Sciences & Biomedicine
(22)
Dna, Mitochondrial - Genetics
(15)
Biochemistry & Molecular Biology
(12)
Mutation
(12)
Cell Biology
(11)
Mitochondrial Dna
(11)
Oxidative Stress
(11)
Animals
(9)
Merrf Syndrome - Genetics
(7)
Mitochondria
(7)
Female
(6)
Gene Expression
(6)
Mitochondria - Metabolism
(6)
Aging
(5)
Dna Damage
(5)
Mice
(5)
Multidisciplinary Sciences
(5)
Reactive Oxygen Species - Metabolism
(5)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Mitochondrial impairment and synaptic dysfunction are associated with neurological defects in iPSCs-derived cortical neurons of MERRF patients

Profiling of cardiolipins and their hydroperoxides in HepG2 cells by LC/MS

Response to the increase of oxidative stress and mutation of mitochondrial DNA in aging

Oxidative Stress-related Alteration of the Copy Number of Mitochondrial DNA in Human Leukocytes

The protective roles of phosphorylated heat shock protein 27 in human cells harboring myoclonus epilepsy with ragged‐red fibers A8344G mtDNA mutation

Depletion of Sirt3 leads to the impairment of adipogenic differentiation and insulin resistance via interfering mitochondrial function of adipose-derived human mesenchymal stem cells

Promoter analysis and transcriptional regulation of human carbonic anhydrase VIII gene in a MERRF disease cell model

High glucose modulates antiproliferative effect and cytotoxicity of 5-fluorouracil in human colon cancer cells

Increases of Mitochondrial Mass and Mitochondrial Genome in Association with Enhanced Oxidative Stress in Human Cells Harboring 4,977 BP-Deleted Mitochondrial DNA

Mitochondrial DNA Mutation-Elicited Oxidative Stress, Oxidative Damage, and Altered Gene Expression in Cultured Cells of Patients with MERRF Syndrome

Effects of Tolerance-Induced Preconditioning on Mitochondrial Biogenesis in Undifferentiated and Differentiated Neuronal Cells

Effects of carbonic anhydrase-related protein VIII on human cells harbouring an A8344G mitochondrial DNA mutation

MtDNA mutations, functional decline and turnover of mitochondria in aging

Decreased heat shock protein 27 expression and altered autophagy in human cells harboring A8344G mitochondrial DNA mutation

Oxidative Damage and Mutation to Mitochondrial DNA and Age-dependent Decline of Mitochondrial Respiratory Function

Oxidative Stress in Human Aging and Mitochondrial Disease-Consequences of Defective Mitochondrial Respiration and Impaired Antioxidant Enzyme System

Upregulation of Matrix Metalloproteinase 1 and Disruption of Mitochondrial Network in Skin Fibroblasts of Patients with MERRF Syndrome

High prevalence of the COII/tRNA(Lys) intergenic 9-bp deletion in mitochondrial DNA of Taiwanese patients with MELAS or MERRF syndrome

Oculopharyngeal somatic myopathy in a patient with a novel large-scale 3399 bp deletion and a homoplasmic T5814C transition of the mitochondrial DNA

Clinical phenotype, prognosis and mitochondrial DNA mutation load in mitochondrial encephalomyopathies

Respiratory function decline and DNA mutation in mitochondria, oxidative stress and altered gene expression during aging

Mitochondrial DNA mutations and oxidative damage in skeletal muscle of patients with chronic uremia

The protective roles of phosphorylated heat shock protein27 in human cells harboring myoclonus epilepsy with ragged-red fibers A8344G mtDNA mutation

Oxidative Stress and its Biochemical Consequences in Mitochondrial DNA Mutation‐Associated Diseases: Implications of Redox Therapy for Mitochondrial Diseases

Oculopharyngeal somatic myopathy in a patient with a novel large-scale 3,399 bp deletion and a homoplasmic T5814C transition of the mitochondrial DNA

Suchergebnisse filtern