| Year |
Citation |
Score |
| 2019 |
McAvoy K, Kawamata H. Glial mitochondrial function and dysfunction in health and neurodegeneration. Molecular and Cellular Neurosciences. 101: 103417. PMID 31678567 DOI: 10.1016/J.Mcn.2019.103417 |
0.433 |
|
| 2019 |
Hayes LR, Asress SA, Li Y, Galkin A, Stepanova A, Kawamata H, Manfredi G, Glass JD. Distal denervation in the SOD1 knockout mouse correlates with loss of mitochondria at the motor nerve terminal. Experimental Neurology. PMID 31082391 DOI: 10.1016/J.Expneurol.2019.05.008 |
0.353 |
|
| 2019 |
Anderson CJ, Bredvik K, Burstein SR, Davis C, Meadows SM, Dash J, Case L, Milner TA, Kawamata H, Zuberi A, Piersigilli A, Lutz C, Manfredi G. ALS/FTD mutant CHCHD10 mice reveal a tissue-specific toxic gain-of-function and mitochondrial stress response. Acta Neuropathologica. PMID 30877432 DOI: 10.1007/S00401-019-01989-Y |
0.428 |
|
| 2018 |
Palomo GM, Granatiero V, Kawamata H, Konrad C, Kim M, Arreguin AJ, Zhao D, Milner TA, Manfredi G. Parkin is a disease modifier in the mutant SOD1 mouse model of ALS. Embo Molecular Medicine. PMID 30126943 DOI: 10.15252/Emmm.201808888 |
0.434 |
|
| 2018 |
Kawamata H, Manfredi G. Correction: Proteinopathies and OXPHOS dysfunction in neurodegenerative diseases. The Journal of Cell Biology. 217: 429. PMID 29269424 DOI: 10.1083/Jcb.20170917212192017C |
0.322 |
|
| 2017 |
Kawamata H, Manfredi G. Proteinopathies and OXPHOS dysfunction in neurodegenerative diseases. The Journal of Cell Biology. 216: 3917-3929. PMID 29167179 DOI: 10.1083/Jcb.201709172 |
0.447 |
|
| 2017 |
Burstein SR, Valsecchi F, Kawamata H, Bourens M, Zeng R, Zuberi A, Milner TA, Cloonan SM, Lutz C, Barrientos A, Manfredi G. In vitro and in vivo studies of the ALS-FTLD protein CHCHD10 reveal novel mitochondrial topology and protein interactions. Human Molecular Genetics. PMID 29112723 DOI: 10.1093/Hmg/Ddx397 |
0.485 |
|
| 2017 |
Kawamata H, Peixoto P, Konrad C, Palomo G, Bredvik K, Gerges M, Valsecchi F, Petrucelli L, Ravits JM, Starkov A, Manfredi G. Mutant TDP-43 does not impair mitochondrial bioenergetics in vitro and in vivo. Molecular Neurodegeneration. 12: 37. PMID 28482850 DOI: 10.1186/S13024-017-0180-1 |
0.421 |
|
| 2016 |
Doczi J, Torocsik B, Echaniz-Laguna A, Mousson de Camaret B, Starkov A, Starkova N, Gál A, Molnár MJ, Kawamata H, Manfredi G, Adam-Vizi V, Chinopoulos C. Alterations in voltage-sensing of the mitochondrial permeability transition pore in ANT1-deficient cells. Scientific Reports. 6: 26700. PMID 27221760 DOI: 10.1038/Srep26700 |
0.364 |
|
| 2016 |
Manfredi G, Kawamata H. Mitochondria and endoplasmic reticulum crosstalk in amyotrophic lateral sclerosis. Neurobiology of Disease. 90: 35-42. PMID 26282323 DOI: 10.1016/J.Nbd.2015.08.004 |
0.435 |
|
| 2014 |
Kirk K, Gennings C, Hupf JC, Tadesse S, D'Aurelio M, Kawamata H, Valsecchi F, Mitsumoto H, Manfredi G. Bioenergetic markers in skin fibroblasts of sporadic amyotrophic lateral sclerosis and progressive lateral sclerosis patients. Annals of Neurology. 76: 620-4. PMID 25090982 DOI: 10.1002/Ana.24244 |
0.374 |
|
| 2014 |
Chinopoulos C, Kiss G, Kawamata H, Starkov AA. Measurement of ADP-ATP exchange in relation to mitochondrial transmembrane potential and oxygen consumption. Methods in Enzymology. 542: 333-48. PMID 24862274 DOI: 10.1016/B978-0-12-416618-9.00017-0 |
0.319 |
|
| 2014 |
Kawamata H, Ng SK, Diaz N, Burstein S, Morel L, Osgood A, Sider B, Higashimori H, Haydon PG, Manfredi G, Yang Y. Abnormal intracellular calcium signaling and SNARE-dependent exocytosis contributes to SOD1G93A astrocyte-mediated toxicity in amyotrophic lateral sclerosis. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 34: 2331-48. PMID 24501372 DOI: 10.1523/Jneurosci.2689-13.2014 |
0.303 |
|
| 2013 |
Kiss G, Konrad C, Doczi J, Starkov AA, Kawamata H, Manfredi G, Zhang SF, Gibson GE, Beal MF, Adam-Vizi V, Chinopoulos C. The negative impact of α-ketoglutarate dehydrogenase complex deficiency on matrix substrate-level phosphorylation. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 27: 2392-406. PMID 23475850 DOI: 10.1096/Fj.12-220202 |
0.337 |
|
| 2011 |
Kawamata H, Tiranti V, Magrané J, Chinopoulos C, Manfredi G. adPEO mutations in ANT1 impair ADP-ATP translocation in muscle mitochondria. Human Molecular Genetics. 20: 2964-74. PMID 21586654 DOI: 10.1093/Hmg/Ddr200 |
0.404 |
|
| 2010 |
Kawamata H, Starkov AA, Manfredi G, Chinopoulos C. A kinetic assay of mitochondrial ADP-ATP exchange rate in permeabilized cells. Analytical Biochemistry. 407: 52-7. PMID 20691655 DOI: 10.1016/J.Ab.2010.07.031 |
0.325 |
|
| 2010 |
Kawamata H, Manfredi G. Mitochondrial dysfunction and intracellular calcium dysregulation in ALS. Mechanisms of Ageing and Development. 131: 517-26. PMID 20493207 DOI: 10.1016/J.Mad.2010.05.003 |
0.386 |
|
| 2010 |
Kawamata H, Manfredi G. Import, maturation, and function of SOD1 and its copper chaperone CCS in the mitochondrial intermembrane space. Antioxidants & Redox Signaling. 13: 1375-84. PMID 20367259 DOI: 10.1089/Ars.2010.3212 |
0.421 |
|
| 2009 |
Magrané J, Hervias I, Henning MS, Damiano M, Kawamata H, Manfredi G. Mutant SOD1 in neuronal mitochondria causes toxicity and mitochondrial dynamics abnormalities. Human Molecular Genetics. 18: 4552-64. PMID 19779023 DOI: 10.1093/Hmg/Ddp421 |
0.444 |
|
| 2008 |
Kawamata H, Magrané J, Kunst C, King MP, Manfredi G. Lysyl-tRNA synthetase is a target for mutant SOD1 toxicity in mitochondria. The Journal of Biological Chemistry. 283: 28321-8. PMID 18715867 DOI: 10.1074/Jbc.M805599200 |
0.457 |
|
| 2008 |
Kawamata H, Manfredi G. Different regulation of wild-type and mutant Cu,Zn superoxide dismutase localization in mammalian mitochondria. Human Molecular Genetics. 17: 3303-17. PMID 18703498 DOI: 10.1093/Hmg/Ddn226 |
0.397 |
|
| 2007 |
Son M, Puttaparthi K, Kawamata H, Rajendran B, Boyer PJ, Manfredi G, Elliott JL. Overexpression of CCS in G93A-SOD1 mice leads to accelerated neurological deficits with severe mitochondrial pathology. Proceedings of the National Academy of Sciences of the United States of America. 104: 6072-7. PMID 17389365 DOI: 10.1073/Pnas.0610923104 |
0.31 |
|
| 2006 |
Kawamata H, Hervias I, Kiaei M, King M, Kunst C, Manfredi G. Lysyl-tRNA synthetase: A target for mutant SOD1 toxicity in mitochondria Mitochondrion. 6: 271-272. DOI: 10.1016/J.Mito.2006.08.021 |
0.33 |
|
| 2005 |
Son JH, Kawamata H, Yoo MS, Kim DJ, Lee YK, Kim S, Dawson TM, Zhang H, Sulzer D, Yang L, Beal MF, Degiorgio LA, Chun HS, Baker H, Peng C. Neurotoxicity and behavioral deficits associated with Septin 5 accumulation in dopaminergic neurons. Journal of Neurochemistry. 94: 1040-53. PMID 16092945 DOI: 10.1111/J.1471-4159.2005.03257.X |
0.372 |
|
| 2004 |
Yoo MS, Kawamata H, Kim DJ, Chun HS, Son JH. Experimental strategy to identify genes susceptible to oxidative stress in nigral dopaminergic neurons Neurochemical Research. 29: 1223-1234. PMID 15176479 DOI: 10.1023/B:Nere.0000023609.08038.C3 |
0.317 |
|
| 2003 |
Barberi T, Klivenyi P, Calingasan NY, Lee H, Kawamata H, Loonam K, Perrier AL, Bruses J, Rubio ME, Topf N, Tabar V, Harrison NL, Beal MF, Moore MA, Studer L. Neural subtype specification of fertilization and nuclear transfer embryonic stem cells and application in parkinsonian mice. Nature Biotechnology. 21: 1200-7. PMID 14502203 DOI: 10.1038/Nbt870 |
0.307 |
|
| 2002 |
McLean PJ, Kawamata H, Shariff S, Hewett J, Sharma N, Ueda K, Breakefield XO, Hyman BT. TorsinA and heat shock proteins act as molecular chaperones: suppression of alpha-synuclein aggregation. Journal of Neurochemistry. 83: 846-54. PMID 12421356 DOI: 10.1046/J.1471-4159.2002.01190.X |
0.61 |
|
| 2001 |
Sharma N, McLean PJ, Kawamata H, Irizarry MC, Hyman BT. Alpha-synuclein has an altered conformation and shows a tight intermolecular interaction with ubiquitin in Lewy bodies. Acta Neuropathologica. 102: 329-34. PMID 11603807 DOI: 10.1007/S004010100369 |
0.638 |
|
| 2001 |
McLean PJ, Kawamata H, Hyman BT. Alpha-synuclein-enhanced green fluorescent protein fusion proteins form proteasome sensitive inclusions in primary neurons. Neuroscience. 104: 901-12. PMID 11440819 DOI: 10.1016/S0306-4522(01)00113-0 |
0.652 |
|
| 2001 |
Kawamata H, McLean PJ, Sharma N, Hyman BT. Interaction of alpha-synuclein and synphilin-1: effect of Parkinson's disease-associated mutations. Journal of Neurochemistry. 77: 929-34. PMID 11331421 DOI: 10.1046/J.1471-4159.2001.00301.X |
0.647 |
|
| 2000 |
McLean PJ, Kawamata H, Ribich S, Hyman BT. Membrane association and protein conformation of alpha-synuclein in intact neurons. Effect of Parkinson's disease-linked mutations. The Journal of Biological Chemistry. 275: 8812-6. PMID 10722726 DOI: 10.1074/Jbc.275.12.8812 |
0.654 |
|
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