Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Holger Prokisch
Molecular Diagnosis in Mitochondrial Complex I Deficiency Using Exome Sequencing
Journal of Medical Genetics
Genetics
VARS2andTARS2Mutations in Patients With Mitochondrial Encephalomyopathies
Human Mutation
Genetics
Neuromelanin, Neurotransmitter Status and Brainstem Location Determine the Differential Vulnerability of Catecholaminergic Neurons to Mitochondrial DNA Deletions
Molecular Brain
Molecular Neuroscience
Molecular Biology
Cellular
Fatal Neonatal Encephalopathy and Lactic Acidosis Caused by a Homozygous Loss-Of-Function Variant in COQ9
European Journal of Human Genetics
Genetics
ncRNAs: New Players in Mitochondrial Health and Disease?
Frontiers in Genetics
Genetics
Molecular Medicine
Sengers Syndrome: Six Novel AGK Mutations in Seven New Families and Review of the Phenotypic and Mutational Spectrum of 29 Patients
Orphanet Journal of Rare Diseases
Medicine
Genetics
Pharmacology
A Mutation Screening of Oncogenes, Tumor Suppressor Gene TP53 and Nuclear Encoded Mitochondrial Complex I Genes in Oncocytic Thyroid Tumors
BMC Cancer
Cancer Research
Oncology
Genetics
OCR-Stats: Robust Estimation and Statistical Testing of Mitochondrial Respiration Activities Using Seahorse XF Analyzer
PLoS ONE
Multidisciplinary
DNA Methylation Signatures of Chronic Low-Grade Inflammation Are Associated With Complex Diseases
Genome Biology
Adaptive Mitochondrial Regulation of the Proteasome
‹
1
2
3
›
