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Journal Article
Clinical & Experimental Immunology, ISSN 0009-9104, 04/2014, Volume 176, Issue 1, pp. 66 - 77
Summary We measured plasma levels of the oxidative DNA damage marker 8‐hydroxy‐2′‐deoxyguanosine (8‐OHdG) and leucocyte mRNA expression levels of the genes... 
8‐hydroxy‐2′‐deoxyguanosine (8‐OHdG) | anti‐oxidants | systemic lupus erythematosus (SLE) | mitochondrial biogenesis | glycolysis | Anti-oxidants | Glycolysis | 8-hydroxy-2′-deoxyguanosine (8-OHdG) | Systemic lupus erythematosus (SLE) | Mitochondrial biogenesis | CRITERIA | APOPTOSIS | CELLS | ACTIVATION | CLASSIFICATION | IMMUNOLOGY | METABOLISM | PATHWAY | RITUXIMAB | anti-oxidants | COPY NUMBER | STRESS | 8-hydroxy-2 '-deoxyguanosine (8-OHdG) | Deoxyguanosine - blood | Leukocytes - pathology | Superoxide Dismutase - genetics | Oxidative Stress | Humans | Middle Aged | Lupus Erythematosus, Systemic - metabolism | Male | Mitochondrial Proteins - genetics | DNA Repair - genetics | RNA, Messenger - metabolism | DNA-Binding Proteins - metabolism | Glycolysis - genetics | DNA, Mitochondrial - genetics | Mitochondria - genetics | Mitochondrial Proteins - metabolism | Lupus Erythematosus, Systemic - drug therapy | Adult | Female | DNA Glycosylases - metabolism | Deoxyguanosine - analogs & derivatives | Superoxide Dismutase - metabolism | Antirheumatic Agents - therapeutic use | Severity of Illness Index | Glutathione Peroxidase - metabolism | RNA, Messenger - genetics | DNA Glycosylases - genetics | Rituximab | Gene Dosage | Mitochondria - metabolism | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Glutathione Peroxidase - genetics | Gene Expression Regulation, Enzymologic | Transcription Factors - metabolism | Lupus Erythematosus, Systemic - genetics | Leukocytes - drug effects | DNA Damage | Leukocytes - metabolism | Antibodies, Monoclonal, Murine-Derived - therapeutic use | Original
Journal Article
Journal Article
Nature, ISSN 0028-0836, 03/2012, Volume 483, Issue 7391, pp. 598 - 602
Generation of induced pluripotent stem cells (iPSCs) by somatic cell reprogramming involves global epigenetic remodelling(1). Whereas several proteins are... 
CELLS | LEUKEMIA | PRC2 | HISTONE METHYLATION | MULTIDISCIPLINARY SCIENCES | PLURIPOTENT | Chromatin - metabolism | Homeodomain Proteins - metabolism | Humans | Methyltransferases - metabolism | Methyltransferases - genetics | Methyltransferases - biosynthesis | YY1 Transcription Factor - metabolism | Repressor Proteins - antagonists & inhibitors | DNA-Binding Proteins - metabolism | Kruppel-Like Transcription Factors - metabolism | YY1 Transcription Factor - antagonists & inhibitors | Induced Pluripotent Stem Cells - cytology | Cellular Reprogramming - genetics | Repressor Proteins - metabolism | Fibroblasts - metabolism | Induced Pluripotent Stem Cells - metabolism | DNA-Binding Proteins - antagonists & inhibitors | Nanog Homeobox Protein | Transcription Factors - antagonists & inhibitors | DNA Methylation - genetics | Polycomb-Group Proteins | Proto-Oncogene Proteins c-myc - metabolism | Enhancer of Zeste Homolog 2 Protein | Transcription Factors - metabolism | Polycomb Repressive Complex 2 | Methyltransferases - antagonists & inhibitors | Fibroblasts - cytology | RNA, Small Interfering | Histones - metabolism | Methylation | Chromatin - genetics | RNA-Binding Proteins - metabolism | Physiological aspects | Chromatin | Genetic aspects | Research | Methyltransferases | Embryonic stem cells | Enzymes | Efficiency | Stem cells | Epigenetics | Kinases | Gene expression | Apoptosis
Journal Article
Autophagy, ISSN 1554-8627, 04/2015, Volume 11, Issue 4, pp. 595 - 606
The selective degradation of mitochondria by the process of autophagy, termed mitophagy, is one of the major mechanisms of mitochondrial quality control. The... 
USP35 | l-USP35, long form of ubiquitin specific peptidase 35 | s-USP35, short form of ubiquitin specific peptidase 35 | TOMM20, translocase of outer mitochondrial membrane 20 homolog (yeast) | USP, ubiquitin specific peptidase | MTS | PARK2 | SYNJ2BP, synaptojanin 2 binding protein | DUB | neurodegenerative diseases | CCCP | Cer, cerulean | PARK2, parkin RBR E3 ubiquitin protein ligase | USP30 | MFN2, mitofusin 2 | OMM, outer mitochondrial membrane | GFP, green fluorescent protein | autophagy | DsRed, Discosoma sp. red fluorescent protein | deubiquitinating enzyme | PINK1, PTEN-induced putative kinase 1 | deubiquitinating enzymes | carbonyl cyanide m-chlorophenylhydrazone | ubiquitin | mitochondrial dynamics | mitophagy | DMSO, dimethyl sulfoxide | GAPDH, glyceraldehyde 3-phosphate dehydrogenase | HA, human influenza hemagglutinin | mitochondrial targeting sequence | Deubiquitinating enzymes | Neurodegenerative diseases | Mitochondrial dynamics | Mitophagy | Autophagy | Ubiqui tin | FUSION | P62/SQSTM1 | RECEPTOR | MITOCHONDRIAL FISSION | CELL BIOLOGY | PARKIN | DEGRADATION | PROMOTES | Endopeptidases - metabolism | Mitochondrial Proteins - metabolism | Humans | Ubiquitin - metabolism | Ubiquitin-Protein Ligases - metabolism | Cytosol - metabolism | Autophagy - physiology | Mitochondria - metabolism | Thiolester Hydrolases - metabolism | Ubiquitination - physiology | Mitochondrial Degradation - physiology
Journal Article
Journal Article
ChemBioChem, ISSN 1439-4227, 04/2019, Volume 20, Issue 8, pp. 1019 - 1022
Polyphosphate kinases (PPKs) are involved in many metabolic processes; enzymes of the second family (PPK2) are responsible for nucleotide synthesis fuelled by... 
adenosine 5′-polyphosphates | enzyme catalysis | nucleotides | phosphorylation | polyphosphate kinases 2 | Enzymes | Adenosine | Nucleotides | Catalysis | Chromatography | Phosphorylation | Nuclear magnetic resonance--NMR | Kinases | Polyphosphates | Regeneration | Organic chemistry | Polyphosphate kinase | Diphosphates | Chemical synthesis | ATP
Journal Article
Journal Article
Current Medicinal Chemistry, ISSN 0929-8673, 05/2007, Volume 14, Issue 12, pp. 1291 - 1324
Journal Article