16 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2018 Langston RG, Rudenko IN, Kumaran R, Hauser DN, Kaganovich A, Ponce LB, Mamais A, Ndukwe K, Dillman AA, Al-Saif AM, Beilina A, Cookson MR. Differences in Stability, Activity and Mutation Effects Between Human and Mouse Leucine-Rich Repeat Kinase 2. Neurochemical Research. PMID 30291536 DOI: 10.1007/S11064-018-2650-4  0.76
2018 Pellegrini L, Hauser DN, Li Y, Mamais A, Beilina A, Kumaran R, Wetzel A, Heaton G, Rudenko I, Alkaslasi M, Ivanina N, Melrose HL, Cookson MR, Harvey K. Proteomic analysis reveals co-ordinated alterations in protein synthesis and degradation pathways in LRRK2 knockout mice. Human Molecular Genetics. PMID 29917075 DOI: 10.1093/Hmg/Ddy232  0.76
2017 Hauser DN, Mamais A, Conti MM, Primiani CT, Kumaran R, Dillman AA, Langston RG, Beilina A, Garcia JH, Diaz-Ruiz A, Bernier M, Fiesel FC, Hou X, Springer W, Li Y, et al. Hexokinases link DJ-1 to the PINK1/parkin pathway. Molecular Neurodegeneration. 12: 70. PMID 28962651 DOI: 10.1186/S13024-017-0212-X  0.76
2016 Hauser DN, Primiani CT, Cookson MR. The effects of variants in the PARK2 (parkin), PINK1, and PARK7 (DJ-1) genes along with evidence for their pathogenicity. Current Protein & Peptide Science. PMID 26965687 DOI: 10.2174/1389203717666160311121954  0.76
2015 Hauser DN, Primiani CT, Langston RG, Kumaran R, Cookson MR. The Polg Mutator Phenotype Does Not Cause Dopaminergic Neurodegeneration in DJ-1-Deficient Mice. Eneuro. 2. PMID 26464968 DOI: 10.1523/ENEURO.0075-14.2015  0.76
2014 Mamais A, Chia R, Beilina A, Hauser DN, Hall C, Lewis PA, Cookson MR, Bandopadhyay R. Arsenite stress down-regulates phosphorylation and 14-3-3 binding of leucine-rich repeat kinase 2 (LRRK2), promoting self-association and cellular redistribution. The Journal of Biological Chemistry. 289: 21386-400. PMID 24942733 DOI: 10.1074/Jbc.M113.528463  0.96
2014 Prahlad J, Hauser DN, Milkovic NM, Cookson MR, Wilson MA. Use of cysteine-reactive cross-linkers to probe conformational flexibility of human DJ-1 demonstrates that Glu18 mutations are dimers. Journal of Neurochemistry. 130: 839-53. PMID 24832775 DOI: 10.1111/Jnc.12763  0.96
2014 Hauser DN, Dillman AA, Ding J, Li Y, Cookson MR. Post-translational decrease in respiratory chain proteins in the Polg mutator mouse brain. Plos One. 9: e94646. PMID 24722488 DOI: 10.1371/Journal.Pone.0094646  0.96
2014 Beilina A, Rudenko IN, Kaganovich A, Civiero L, Chau H, Kalia SK, Kalia LV, Lobbestael E, Chia R, Ndukwe K, Ding J, Nalls MA, Olszewski M, ... Hauser DN, et al. Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease. Proceedings of the National Academy of Sciences of the United States of America. 111: 2626-31. PMID 24510904 DOI: 10.1073/Pnas.1318306111  0.96
2013 Hauser DN, Dukes AA, Mortimer AD, Hastings TG. Dopamine quinone modifies and decreases the abundance of the mitochondrial selenoprotein glutathione peroxidase 4. Free Radical Biology & Medicine. 65: 419-27. PMID 23816523 DOI: 10.1016/j.freeradbiomed.2013.06.030  0.96
2013 Dillman AA, Hauser DN, Gibbs JR, Nalls MA, McCoy MK, Rudenko IN, Galter D, Cookson MR. mRNA expression, splicing and editing in the embryonic and adult mouse cerebral cortex. Nature Neuroscience. 16: 499-506. PMID 23416452 DOI: 10.1038/Nn.3332  0.96
2013 Hauser DN, Hastings TG. Mitochondrial dysfunction and oxidative stress in Parkinson's disease and monogenic parkinsonism Neurobiology of Disease. 51: 35-42. PMID 23064436 DOI: 10.1016/j.nbd.2012.10.011  0.96
2013 Hauser DN, Dukes AA, Mortimer AD, Hastings TG. Dopamine quinone modifies and decreases the abundance of the mitochondrial selenoprotein glutathione peroxidase 4 Free Radical Biology and Medicine. 65: 419-427. DOI: 10.1016/j.freeradbiomed.2013.06.030  0.96
2013 Hastings TG, Mortimer A, Hauser D. Dopamine Oxidation and Quinone Modification of Proteins: Mechanisms of Toxicity and Implications for Parkinson's Disease Catecholamine Research in the 21st Century: Abstracts and Graphical Abstracts, 10th International Catecholamine Symposium, 2012. 122. DOI: 10.1016/B978-0-12-800044-1.00105-7  0.96
2012 Rudenko IN, Kaganovich A, Hauser DN, Beylina A, Chia R, Ding J, Maric D, Jaffe H, Cookson MR. The G2385R variant of leucine-rich repeat kinase 2 associated with Parkinson's disease is a partial loss-of-function mutation. The Biochemical Journal. 446: 99-111. PMID 22612223 DOI: 10.1042/Bj20120637  0.96
2011 Hauser DN, Cookson MR. Astrocytes in Parkinson's disease and DJ-1. Journal of Neurochemistry. 117: 357-8. PMID 21413989 DOI: 10.1111/J.1471-4159.2011.07217.X  0.96
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