D. Krainc
Molecular Biology · 2002–2021
A researcher in the Science corpus: 12 papers; trusts 5 researchers and is trusted by 0 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 128 citations into it
- Neurology — 88 citations into it
- Physiology — 58 citations into it
- Cell Biology — 26 citations into it
- Clinical Biochemistry — 10 citations into it
Whom D. Krainc trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Papers from D. Krainc's perspective
Ordered by how strongly the researchers D. Krainc trusts endorse each paper. Same corpus, a different order for every researcher.
- Common Structure of Soluble Amyloid Oligomers Implies Common Mechanism of Pathogenesis (Science)
- Inhibition of mTOR induces autophagy and reduces toxicity of polyglutamine expansions in fly and mouse models of Huntington disease (Nature Genetics)
- Chaperone Suppression of α-Synuclein Toxicity in a Drosophila Model for Parkinson's Disease (Science)
- A Hydrophobic Stretch of 12 Amino Acid Residues in the Middle of α-Synuclein Is Essential for Filament Assembly* (Journal of Biological Chemistry)
- Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase (Nature Genetics)
- Suppression of basal autophagy in neural cells causes neurodegenerative disease in mice (Nature)
- Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease. (Brain : a journal of neurology)
- Inclusion body formation reduces levels of mutant huntingtin and the risk of neuronal death (Nature)
- Autophagy: assays and artifacts (Journal of Pathology)
- Multi-center analysis of glucocerebrosidase mutations in Parkinson disease (New England Journal of Medicine)
Their papers
- A call for transparent reporting to optimize the predictive value of preclinical research (2012) — 1,158 citations
- Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1 (2021) — 3,841 citations
- Human iPSC-based Modeling of Late-Onset Disease via Progerin-induced Aging (2013) — 750 citations
- Thermoregulatory and metabolic defects in Huntington's disease transgenic mice implicate PGC-1alpha in Huntington's disease neurodegeneration. (2006) — 605 citations
- Sp1 and TAFII130 Transcriptional Activity Disrupted in Early Huntington's Disease (2002) — 715 citations
- Mitochondria-lysosome contacts regulate mitochondrial fission via Rab7 GTP hydrolysis (2018) — 777 citations
- Inhibition of PIP4Kγ ameliorates the pathological effects of mutant huntingtin protein (2017) — 54 citations
- Dopamine oxidation mediates mitochondrial and lysosomal dysfunction in Parkinson’s disease (2017) — 766 citations
- α-synuclein toxicity in neurodegeneration: mechanism and therapeutic strategies (2017) — 770 citations
- Editorial :Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition). DOI: 10.1080/15548627.2015.1100356;WOS:000373595400001; 2-s2.0-85013763791&;PMID: 26799652 (2016) — 1,523 citations
- Gaucher’s Disease Glucocerebrosidase and -synuclein form a bidirectional pathogenic loop in synucleinopathies (2011) — 1,296 citations
- Neuroprotective role of SIRT1 in mammalian models of Huntington’s disease through activation of multiple SIRT1 targets (2011) — 343 citations