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Inhibition of mitochondrial fusion by α-synuclein is rescued by PINK1, Parkin and DJ-1
Kamp, Frits, Exner, Nicole, Lutz, Anne Kathrin, Wender, Nora, Hegermann, Jan, Brunner, Bettina, Nuscher, Brigitte, Bartels, Tim, Giese, Armin, Beyer, Klaus, Eimer, Stefan, Winklhofer, Konstanze F, Haass, Christian
Published in The EMBO journal (20.10.2010)
Published in The EMBO journal (20.10.2010)
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PINK1/Parkin mitophagy and neurodegeneration—what do we really know in vivo?
Whitworth, Alexander J, Pallanck, Leo J
Published in Current opinion in genetics & development (01.06.2017)
Published in Current opinion in genetics & development (01.06.2017)
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Mitochondrial damage-associated inflammation highlights biomarkers in PRKN/PINK1 parkinsonism
Borsche, Max, König, Inke R, Delcambre, Sylvie, Petrucci, Simona, Balck, Alexander, Brüggemann, Norbert, Zimprich, Alexander, Wasner, Kobi, Pereira, Sandro L, Avenali, Micol, Deuschle, Christian, Badanjak, Katja, Ghelfi, Jenny, Gasser, Thomas, Kasten, Meike, Rosenstiel, Philip, Lohmann, Katja, Brockmann, Kathrin, Valente, Enza Maria, Youle, Richard J, Grünewald, Anne, Klein, Christine
Published in Brain (London, England : 1878) (01.10.2020)
Published in Brain (London, England : 1878) (01.10.2020)
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Comprehensive assessment of PINK1 variants in Parkinson's disease
Krohn, Lynne, Grenn, Francis P., Makarious, Mary B., Kim, Jonggeol Jeffrey, Bandres-Ciga, Sara, Roosen, Dorien A., Gan-Or, Ziv, Nalls, Mike A., Singleton, Andrew B., Blauwendraat, Cornelis
Published in Neurobiology of aging (01.07.2020)
Published in Neurobiology of aging (01.07.2020)
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Heterozygous PINK1 p.G411S increases risk of Parkinson’s disease via a dominant-negative mechanism
Puschmann, Andreas, Fiesel, Fabienne C., Caulfield, Thomas R., Hudec, Roman, Ando, Maya, Truban, Dominika, Hou, Xu, Ogaki, Kotaro, Heckman, Michael G., James, Elle D., Swanberg, Maria, Jimenez-Ferrer, Itzia, Hansson, Oskar, Opala, Grzegorz, Siuda, Joanna, Boczarska-Jedynak, Magdalena, Friedman, Andrzej, Koziorowski, Dariusz, Aasly, Jan O., Lynch, Timothy, Mellick, George D., Mohan, Megha, Silburn, Peter A., Sanotsky, Yanosh, Vilariño-Güell, Carles, Farrer, Matthew J., Chen, Li, Dawson, Valina L., Dawson, Ted M., Wszolek, Zbigniew K., Ross, Owen A., Springer, Wolfdieter
Published in Brain (London, England : 1878) (01.01.2017)
Published in Brain (London, England : 1878) (01.01.2017)
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Hidden phenotypes of PINK1/Parkin knockout mice
Paul, Swagatika, Pickrell, Alicia M.
Published in Biochimica et biophysica acta. General subjects (01.06.2021)
Published in Biochimica et biophysica acta. General subjects (01.06.2021)
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LRRK2 impairs PINK1/Parkin-dependent mitophagy via its kinase activity: pathologic insights into Parkinson's disease
Bonello, Fiona, Hassoun, Sidi-Mohamed, Mouton-Liger, François, Shin, Yea Seul, Muscat, Adeline, Tesson, Christelle, Lesage, Suzanne, Beart, Philip M, Brice, Alexis, Krupp, Johannes, Corvol, Jean-Christophe, Corti, Olga
Published in Human molecular genetics (15.05.2019)
Published in Human molecular genetics (15.05.2019)
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Resveratrol alleviates acute lung injury in mice by promoting Pink1/Parkin-related mitophagy and inhibiting NLRP3 inflammasome activation
Wu, Dongdong, Zhang, Hui, Li, Fang, Liu, Shuai, Wang, Yang, Zhang, Zhao, Wang, Jiannan, Wu, Qiuge
Published in Biochimica et biophysica acta. General subjects (01.07.2024)
Published in Biochimica et biophysica acta. General subjects (01.07.2024)
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Cytosolic cleaved PINK1 represses Parkin translocation to mitochondria and mitophagy
Fedorowicz, Maja A., de Vries-Schneider, Rosa L. A., Rüb, Cornelia, Becker, Dorothea, Huang, Yong, Zhou, Chun, Alessi Wolken, Dana M., Voos, Wolfgang, Liu, Yuhui, Przedborski, Serge
Published in EMBO reports (01.01.2014)
Published in EMBO reports (01.01.2014)
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Phosphoproteomic screening identifies Rab GTPases as novel downstream targets of PINK1
Lai, Yu-Chiang, Kondapalli, Chandana, Lehneck, Ronny, Procter, James B, Dill, Brian D, Woodroof, Helen I, Gourlay, Robert, Peggie, Mark, Macartney, Thomas J, Corti, Olga, Corvol, Jean-Christophe, Campbell, David G, Itzen, Aymelt, Trost, Matthias, Muqit, Miratul MK
Published in The EMBO journal (12.11.2015)
Published in The EMBO journal (12.11.2015)
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Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy
Lesage, Suzanne, Deramecourt, Vincent, Jacoupy, Maxime, Hassoun, Sidi Mohamed, Pujol, Claire, Maurage, Claude-Alain, Sahbatou, Mourad, Liebau, Stefan, Bilgic, Basar, Emre, Murat, Erginel-Unaltuna, Nihan, Guven, Gamze, Tison, François, Tranchant, Christine, Corvol, Jean-Christophe, Krack, Paul, Hernandez, Dena G., Gibbs, J. Raphael, Hardy, John, Wood, Nicholas W., Durr, Alexandra, Deleuze, Jean-François, Tazir, Meriem, Destée, Alain, Lohmann, Ebba, Corti, Olga, Brice, Alexis, Lesage, Suzanne, Tison, François, Vidailhet, Marie, Corvol, Jean-Christophe, Agid, Yves, Anheim, Mathieu, Bonnet, Anne-Marie, Borg, Michel, Broussolle, Emmanuel, Durif, Franck, Krack, Paul, Klebe, Stephan, Lohmann, Ebba, Vérin, Marc, Viallet, François, Brice, Alexis, Majounie, Elisa, Corvol, Jean Christophe, Ben-Shlomo, Yoav, Berg, Daniela, Bhatia, Kailash, Bochdanovits, Zoltan, Bonin, Michael, Bras, Jose M., Brockmann, Kathrin, Burn, David J., Chen, Honglei, Clarke, Carl E., Cookson, Mark R., Counsell, Carl, van Dijk, Karin D., Dong, Jing, Escott-Price, Valentina, Evans, Jonathan R., Gray, Emma, Guerreiro, Rita, van Hilten, Jacobus J., Hollenbeck, Albert, Holmans, Peter, Hu, Michèle, Hudson, Gavin, Hunt, Sarah E., Kilarski, Laura L., Jansen, Iris E., Langford, Cordelia, Lees, Andrew, Lorenz, Delia, Lubbe, Steven, Lungu, Codrin, Martinez, María, Mätzler, Walter, McNeill, Alisdair, Moorby, Catriona, O’Sullivan, Sean S., Pearson, Justin, Ravina, Bernard, Rivadeneira, Fernando, Ryten, Mina, Schapira, Anthony, Sharma, Manu, Sheerin, Una-Marie, Sidransky, Ellen, Spencer, Chris C.A., Stefánsson, Kári, Strange, Amy, Talbot, Kevin, Trabzuni, Daniah, Uitterlinden, André G., van de Warrenburg, Bart, Williams-Gray, Caroline H., Winder-Rhodes, Sophie, Hardy, John, Wood, Nicholas W.
Published in American journal of human genetics (03.03.2016)
Published in American journal of human genetics (03.03.2016)
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Brain mitochondrial impairment in early‐onset Parkinson's disease with or without PINK1 mutation
Rango, Mario, Dossi, Gabriele, Squarcina, Letizia, Bonifati, Cristiana
Published in Movement disorders (01.03.2020)
Published in Movement disorders (01.03.2020)
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A heterozygous effect for PINK1 mutations in Parkinson's disease?
Abou-Sleiman, Patrick M., Muqit, Miratul M. K., McDonald, Neil Q., Yang, Yan Xiang, Gandhi, Sonia, Healy, Daniel G., Harvey, Kirsten, Harvey, Robert J., Deas, Emma, Bhatia, Kailash, Quinn, Niall, Lees, Andrew, Latchman, David S., Wood, Nicholas W.
Published in Annals of neurology (01.10.2006)
Published in Annals of neurology (01.10.2006)
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Systematic Review and UK-Based Study of PARK2 (parkin), PINK1, PARK7 (DJ-1) and LRRK2 in early-onset Parkinson's disease
Kilarski, Laura L., Pearson, Justin P., Newsway, Victoria, Majounie, Elisa, Knipe, M. Duleeka W., Misbahuddin, Anjum, Chinnery, Patrick F., Burn, David J., Clarke, Carl E., Marion, Marie-Helene, Lewthwaite, Alistair J., Nicholl, David J., Wood, Nicholas W., Morrison, Karen E., Williams-Gray, Caroline H., Evans, Jonathan R., Sawcer, Stephen J., Barker, Roger A., Wickremaratchi, Mirdhu M., Ben-Shlomo, Yoav, Williams, Nigel M., Morris, Huw R.
Published in Movement disorders (01.10.2012)
Published in Movement disorders (01.10.2012)
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PINK1 mutations are associated with sporadic early-onset parkinsonism
Valente, Enza Maria, Salvi, Sergio, Ialongo, Tamara, Marongiu, Roberta, Elia, Antonio Emanuele, Caputo, Viviana, Romito, Luigi, Albanese, Alberto, Dallapiccola, Bruno, Bentivoglio, Anna Rita
Published in Annals of neurology (01.09.2004)
Published in Annals of neurology (01.09.2004)
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Early-onset Parkinson's disease due to PINK1 p.Q456X mutation – Clinical and functional study
Siuda, Joanna, Jasinska-Myga, Barbara, Boczarska-Jedynak, Magdalena, Opala, Grzegorz, Fiesel, Fabienne C., Moussaud-Lamodière, Elisabeth L., Scarffe, Leslie A., Dawson, Valina L., Ross, Owen A., Springer, Wolfdieter, Dawson, Ted M., Wszolek, Zbigniew K.
Published in Parkinsonism & related disorders (01.11.2014)
Published in Parkinsonism & related disorders (01.11.2014)
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Abnormal premotor–motor interaction in heterozygous Parkin- and Pink1 mutation carriers
Weissbach, Anne, Bäumer, Tobias, Pramstaller, Peter P., Brüggemann, Norbert, Tadic, Vera, Chen, Robert, Klein, Christine, Münchau, Alexander
Published in Clinical neurophysiology (01.01.2017)
Published in Clinical neurophysiology (01.01.2017)
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PINK1 mutations and parkinsonism
Ishihara-Paul, L, Hulihan, M M, Kachergus, J, Upmanyu, R, Warren, L, Amouri, R, Elango, R, Prinjha, R K, Soto, A, Kefi, M, Zouari, M, Sassi, S B, Yahmed, S B, El Euch-Fayeche, G, Matthews, P M, Middleton, L T, Gibson, R A, Hentati, F, Farrer, M J
Published in Neurology (16.09.2008)
Published in Neurology (16.09.2008)
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Establishing Equivalent Aerobic Exercise Parameters Between Early-Stage Parkinson’s Disease and Pink1 Knockout Rats
Salvatore, Michael F., Soto, Isabel, Kasanga, Ella A., James, Rachael, Shifflet, Marla K., Doshier, Kirby, Little, Joel T., John, Joshia, Alphonso, Helene M., Cunningham, J. Thomas, Nejtek, Vicki A.
Published in Journal of Parkinson's disease (01.01.2022)
Published in Journal of Parkinson's disease (01.01.2022)
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