UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 49

Sortiert nach

Bioenergetic profiling of zebrafish embryonic development

PloS one, 2011-09, Vol.6 (9), p.e25652-e25652

2011

Volltextzugriff (PDF)

Opa1 is required for proper mitochondrial metabolism in early development

PloS one, 2013-03, Vol.8 (3), p.e59218-e59218

2013

Volltextzugriff (PDF)

Urinary mitochondrial DNA is a biomarker of mitochondrial disruption and renal dysfunction in acute kidney injury

Kidney international, 2015-12, Vol.88 (6), p.1336-1344

2015

Volltextzugriff (PDF)

Loss of the Mia40a oxidoreductase leads to hepato-pancreatic insufficiency in zebrafish

PLoS genetics, 2018-11, Vol.14 (11), p.e1007743-e1007743

2018

Volltextzugriff (PDF)

Correction: Loss of the Mia40a oxidoreductase leads to hepato-pancreatic insufficiency in zebrafish

PLoS genetics, 2019-01, Vol.15 (1), p.e1007972-e1007972

2019

Volltextzugriff (PDF)

Design of Hydrazide-Bearing HDACIs Based on Panobinostat and Their p53 and FLT3-ITD Dependency in Antileukemia Activity

Journal of medicinal chemistry, 2020-05, Vol.63 (10), p.5501-5525

2020

Volltextzugriff (PDF)

High-Throughput Tissue Bioenergetics Analysis Reveals Identical Metabolic Allometric Scaling for Teleost Hearts and Whole Organisms

PloS one, 2015-09, Vol.10 (9), p.e0137710

2015

Volltextzugriff (PDF)

Mitochondrial protein quality control: the mechanisms guarding mitochondrial health

Antioxidants & redox signaling, 2015-04, Vol.22 (12), p.977

2015

Volltextzugriff (PDF)

Disease Mutations in the Human Mitochondrial DNA Polymerase Thumb Subdomain Impart Severe Defects in Mitochondrial DNA Replication

The Journal of biological chemistry, 2009-07, Vol.284 (29), p.19501-19510

2009

Volltextzugriff (PDF)

Molecular diagnosis of Alpers syndrome

Journal of hepatology, 2006-07, Vol.45 (1), p.108-116

2006

Volltextzugriff (PDF)

Induced Torpor as a Countermeasure for Low Dose Radiation Exposure in a Zebrafish Model

Cells (Basel, Switzerland), 2021-04, Vol.10 (4), p.906

2021

Volltextzugriff (PDF)

Modulation of the W748S mutation in DNA polymerase γ by the E1143G polymorphismin mitochondrial disorders

Human molecular genetics, 2006-12, Vol.15 (23), p.3473-3483

2006

Volltextzugriff (PDF)

Decreased mtDNA, oxidative stress, cardiomyopathy, and death from transgenic cardiac targeted human mutant polymerase γ

Laboratory investigation, 2007-04, Vol.87 (4), p.326-335

2007

Volltextzugriff (PDF)

Inherited mitochondrial genomic instability and chemical exposures

Toxicology (Amsterdam), 2017-11, Vol.391, p.75-83

Chan, Sherine S.L.

2017

Volltextzugriff (PDF)

Sources, mechanisms, and consequences of chemical-induced mitochondrial toxicity

Toxicology (Amsterdam), 2017-11, Vol.391, p.2-4

2017

Volltextzugriff (PDF)

The Common A467T Mutation in the Human Mitochondrial DNA Polymerase (POLG) Compromises Catalytic Efficiency and Interaction with the Accessory Subunit

The Journal of biological chemistry, 2005-09, Vol.280 (36), p.31341-31346

2005

Volltextzugriff (PDF)

Elesclomol restores mitochondrial function in genetic models of copper deficiency

Proceedings of the National Academy of Sciences - PNAS, 2018-08, Vol.115 (32), p.8161-8166

2018

Volltextzugriff (PDF)

DNA polymerase gamma and mitochondrial disease: Understanding the consequence of POLG mutations

Biochimica et biophysica acta, 2009-05, Vol.1787 (5), p.312-319

2009

Volltextzugriff (PDF)

Copper supplementation restores cytochrome c oxidase assembly defect in a mitochondrial disease model of COA6 deficiency

Human molecular genetics, 2014-07, Vol.23 (13), p.3596-3606

2014

Volltextzugriff (PDF)

Mitochondrial disorders of DNA polymerase γ dysfunction: from anatomic to molecular pathology diagnosis

Archives of pathology & laboratory medicine (1976), 2011-07, Vol.135 (7), p.925-934

2011

Volltextzugriff (PDF)

Discovery of the First Vitamin K Analogue as a Potential Treatment of Pharmacoresistant Seizures

Journal of medicinal chemistry, 2020-06, Vol.63 (11), p.5865-5878

2020

Volltextzugriff (PDF)

Metalloprotease OMA1 Fine-tunes Mitochondrial Bioenergetic Function and Respiratory Supercomplex Stability

Scientific reports, 2015-09, Vol.5 (1), p.13989-13989, Article 13989

2015

Volltextzugriff (PDF)

The cellular and molecular progression of mitochondrial dysfunction induced by 2,4-dinitrophenol in developing zebrafish embryos

Differentiation (London), 2015-03, Vol.89 (3-4), p.51-69

2015

Volltextzugriff (PDF)

Zebrafish lacking functional DNA polymerase gamma survive to juvenile stage, despite rapid and sustained mitochondrial DNA depletion, altered energetics and growth

Nucleic acids research, 2015-12, Vol.43 (21), p.10338

2015

Volltextzugriff (PDF)

De novo mutation in POLG leads to haplotype insufficiency and Alpers syndrome

Mitochondrion, 2009-09, Vol.9 (5), p.340-345

2009

Volltextzugriff (PDF)

1 – 25 von 49

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(47)
Mit Volltextzugriff
(46)

Publikationsform

Artikel
(48)
Buchkapitel
(1)

Sprache

Englisch
(49)
Japanisch
(7)

Erscheinungsjahr

n.n

Thema

Science & Technology
(36)
Life Sciences & Biomedicine
(28)
Humans
(20)
Animals
(18)
Mutation
(14)
Dna Polymerase Gamma
(12)
Mitochondria
(12)
Dna-Directed Dna Polymerase - Genetics
(11)
Zebrafish
(11)
Biochemistry & Molecular Biology
(10)
Dna, Mitochondrial - Genetics
(10)
Mitochondria - Metabolism
(10)
Mitochondrial Dna
(8)
Danio Rerio
(7)
Dna-Directed Dna Polymerase - Metabolism
(7)
Male
(7)
Mitochondrial Diseases - Genetics
(7)
Cell Biology
(6)
Deoxyribonucleic Acid
(6)
Diffuse Cerebral Sclerosis Of Schilder - Genetics
(6)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Bioenergetic profiling of zebrafish embryonic development

Opa1 is required for proper mitochondrial metabolism in early development

Urinary mitochondrial DNA is a biomarker of mitochondrial disruption and renal dysfunction in acute kidney injury

Loss of the Mia40a oxidoreductase leads to hepato-pancreatic insufficiency in zebrafish

Correction: Loss of the Mia40a oxidoreductase leads to hepato-pancreatic insufficiency in zebrafish

Design of Hydrazide-Bearing HDACIs Based on Panobinostat and Their p53 and FLT3-ITD Dependency in Antileukemia Activity

High-Throughput Tissue Bioenergetics Analysis Reveals Identical Metabolic Allometric Scaling for Teleost Hearts and Whole Organisms

Mitochondrial protein quality control: the mechanisms guarding mitochondrial health

Disease Mutations in the Human Mitochondrial DNA Polymerase Thumb Subdomain Impart Severe Defects in Mitochondrial DNA Replication

Molecular diagnosis of Alpers syndrome

Induced Torpor as a Countermeasure for Low Dose Radiation Exposure in a Zebrafish Model

Modulation of the W748S mutation in DNA polymerase γ by the E1143G polymorphismin mitochondrial disorders

Decreased mtDNA, oxidative stress, cardiomyopathy, and death from transgenic cardiac targeted human mutant polymerase γ

Inherited mitochondrial genomic instability and chemical exposures

Sources, mechanisms, and consequences of chemical-induced mitochondrial toxicity

The Common A467T Mutation in the Human Mitochondrial DNA Polymerase (POLG) Compromises Catalytic Efficiency and Interaction with the Accessory Subunit

Elesclomol restores mitochondrial function in genetic models of copper deficiency

DNA polymerase gamma and mitochondrial disease: Understanding the consequence of POLG mutations

Copper supplementation restores cytochrome c oxidase assembly defect in a mitochondrial disease model of COA6 deficiency

Mitochondrial disorders of DNA polymerase γ dysfunction: from anatomic to molecular pathology diagnosis

Discovery of the First Vitamin K Analogue as a Potential Treatment of Pharmacoresistant Seizures

Metalloprotease OMA1 Fine-tunes Mitochondrial Bioenergetic Function and Respiratory Supercomplex Stability

The cellular and molecular progression of mitochondrial dysfunction induced by 2,4-dinitrophenol in developing zebrafish embryos

Zebrafish lacking functional DNA polymerase gamma survive to juvenile stage, despite rapid and sustained mitochondrial DNA depletion, altered energetics and growth

De novo mutation in POLG leads to haplotype insufficiency and Alpers syndrome

Suchergebnisse filtern