Zobrazeno 1 - 9
of 9
pro vyhledávání: '"metabolism [Neostriatum]"'
Autor:
Matthew J. Betts, Lieke de Boer, Ivayla Apostolova, Holger Amthauer, Marc Guitart-Masip, Gabriel Ziegler, Coraline D. Metzger, Valentina Perosa, Ralph Buchert, Emrah Düzel
Publikováno v:
Cerebral Cortex
Cerebral cortex 30(5), 3340-3351 (2020). doi:10.1093/cercor/bhz313
Cerebral cortex 30(5), 3340-3351 (2020). doi:10.1093/cercor/bhz313
Pavlovian biases influence instrumental learning by coupling reward seeking with action invigoration and punishment avoidance with action suppression. Using a probabilistic go/no-go task designed to orthogonalize action (go/no-go) and valence (reward
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a745caaf91178c0bda9e6d3abac827c0
https://hdl.handle.net/21.11116/0000-0006-6963-5
https://hdl.handle.net/21.11116/0000-0006-6963-5
Publikováno v:
Scientific reports 9(1), 4857 (2019). doi:10.1038/s41598-019-41091-7
Scientific Reports
Scientific Reports, Vol 9, Iss 1, Pp 1-14 (2019)
Scientific Reports
Scientific Reports, Vol 9, Iss 1, Pp 1-14 (2019)
Dopamine (DA) release in striatum is functionally segregated across a dorsolateral/ventromedial axis. Interestingly, nigrostriatal DA signaling disruption in Parkinson’s disease (PD) preferentially affects the dorsolateral striatum. The relationshi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da83bd0ca67d4fefa1c3da2359e0f5f2
https://pub.dzne.de/record/140572
https://pub.dzne.de/record/140572
Autor:
Klaus Unsicker, Björn Spittau, Lioudmila Bogatyreva, Venissa Machado, Kerstin Krieglstein, Ralf Gilsbach, Richa Das, Andreas Schober, Dieter Hauschke
Publikováno v:
Cell & tissue research 365(2), 209-223 (2016). doi:10.1007/s00441-016-2406-x
Growth/differentiation factor−15 (Gdf-15) is a member of the transforming growth factor-β (Tgf-β) superfamily and has been shown to be a potent neurotrophic factor for midbrain dopaminergic (DAergic) neurons both in vitro and in vivo. Gdf-15 has
Publikováno v:
Trends in pharmacological sciences 38(6), 541-555 (2017). doi:10.1016/j.tips.2017.03.010
The neurotoxicant 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) causes a Parkinson's disease (PD)-like syndrome by inducing degeneration of nigrostriatal dopaminergic neurons. Studies of the MPTP model have revealed the pathomechanisms underlyi
Autor:
Grothe, Michel J, Barthel, Henryk, Aisen, Paul, Romirowsky, Aliza, deToledo-Morrell, Leyla, Shah, Raj C, Duara, Ranjan, Varon, Daniel, Roberts, Peggy, Albert, Marilyn, Onyike, Chiadi, Kielb, Stephanie, Rusinek, Henry, Petersen, Ronald, de Leon, Mony J, Glodzik, Lidia, De Santi, Susan, Doraiswamy, P Murali, Petrella, Jeffrey R, Coleman, R Edward, Arnold, Steven E, Karlawish, Jason H, Wolk, David, Smith, Charles D, Jack, Clifford R, Jicha, Greg, Hardy, Peter, Lopez, Oscar L, Oakley, MaryAnn, Simpson, Donna M, Porsteinsson, Anton P, Goldstein, Bonnie S, Martin, Kim, Makino, Kelly M, Ismail, M Saleem, Jagust, William, Brand, Connie, Mulnard, Ruth A, Thai, Gaby, Mc-Adams-Ortiz, Catherine, Womack, Kyle, Mathews, Dana, Quiceno, Mary, Diaz-Arrastia, Ramon, King, Richard, Weiner, Myron, Trojanowki, John Q, Martin-Cook, Kristen, DeVous, Michael, Levey, Allan I, Lah, James J, Cellar, Janet S, Burns, Jeffrey M, Anderson, Heather S, Swerdlow, Russell H, Apostolova, Liana, Lu, Po H, Toga, Arthur W, Bartzokis, George, Silverman, Daniel H S, Parfitt, Francine, Johnson, Heather, Farlow, Martin R, Hake, Ann Marie, Matthews, Brandy R, Herring, Scott, van Dyck, Christopher H, Carson, Richard E, Beckett, Laurel, MacAvoy, Martha G, Chertkow, Howard, Bergman, Howard, Hosein, Chris, Black, Sandra, Stefanovic, Bojana, Caldwell, Curtis, Robin Hsiung, Ging-Yuek, Feldman, Howard, Mudge, Benita, Green, Robert C, Assaly, Michele, Kertesz, Andrew, Rogers, John, Trost, Dick, Bernick, Charles, Munic, Donna, Kerwin, Diana, Mesulam, Marek-Marsel, Lipowski, Kristina, Wu, Chuang-Kuo, Saykin, Andrew J, Johnson, Nancy, Sadowsky, Carl, Martinez, Walter, Villena, Teresa, Turner, Raymond Scott, Johnson, Kathleen, Reynolds, Brigid, Sperling, Reisa A, Johnson, Keith A, Marshall, Gad, Morris, John, Frey, Meghan, Yesavage, Jerome, Taylor, Joy L, Lane, Barton, Rosen, Allyson, Tinklenberg, Jared, Sabbagh, Marwan, Belden, Christine, Jacobson, Sandra, Kowall, Neil, Sepulcre, Jorge, Liu, Enchi, Killiany, Ronald, Budson, Andrew E, Norbash, Alexander, Johnson, Patricia Lynn, Obisesan, Thomas O, Wolday, Saba, Bwayo, Salome K, Lerner, Alan, Hudson, Leon, Ogrocki, Paula, Fletcher, Evan, Carmichael, Owen, Olichney, John, DeCarli, Charles, Kittur, Smita, Borrie, Michael, Lee, T-Y, Bartha, Rob, Johnson, Sterling, Asthana, Sanjay, Montine, Tom, Carlsson, Cynthia M, Potkin, Steven G, Preda, Adrian, Nguyen, Dana, Tariot, Pierre, Fleisher, Adam, Reeder, Stephanie, Bates, Vernice, Capote, Horacio, Rainka, Michelle, Scharre, Douglas W, Kataki, Maria, Zimmerman, Earl A, Celmins, Dzintra, Brown, Alice D, Pearlson, Godfrey D, Blank, Karen, Anderson, Karen, Santulli, Robert B, Schwartz, Eben S, Sink, Kaycee M, Williamson, Jeff D, Garg, Pradeep, Watkins, Franklin, Ott, Brian R, Querfurth, Henry, Tremont, Geoffrey, Salloway, Stephen, Malloy, Paul, Gamst, Anthony, Correia, Stephen, Rosen, Howard J, Miller, Bruce L, Mintzer, Jacobo, Longmire, Crystal Flynn, Spicer, Kenneth, Finger, Elizabether, Rachinsky, Irina, Thomas, Ronald G, Drost, Dick, Pomara, Nunzio, Hernando, Raymundo, Sarrael, Antero, Schultz, Susan K, Boles Ponto, Laura L, Shim, Hyungsub, Smith, Karen Elizabeth, Relkin, Norman, Chaing, Gloria, Donohue, Michael, Raudin, Lisa, Smith, Amanda, Fargher, Kristin, Raj, Balebail Ashok, Walter, Sarah, Gessert, Devon, Dyrba, Martin, Sather, Tamie, Harvey, Danielle, Kornak, John, Dale, Anders, Bernstein, Matthew, Felmlee, Joel, Sabri, Osama, Fox, Nick, Thompson, Paul, Schuff, Norbert, Alexander, Gene, Bandy, Dan, Koeppe, Robert A, Foster, Norm, Reiman, Eric M, Teipel, Stefan J, Chen, Kewei, Mathis, Chet, Cairns, Nigel J, Taylor-Reinwald, Lisa, Trojanowki, J. Q., Shaw, Les, Lee, Virginia M Y, Korecka, Magdalena, Initiative, Alzheimer's Disease Neuroimaging, Crawford, Karen, Neu, Scott, Foroud, Tatiana M, Potkin, Steven, Shen, Li, Kachaturian, Zaven, Frank, Richard, Snyder, Peter J, Molchan, Susan, Weiner, Michael, Kaye, Jeffrey, Quinn, Joseph, Lind, Betty, Dolen, Sara, Schneider, Lon S, Pawluczyk, Sonia, Spann, Bryan M, Brewer, James, Vanderswag, Helen, Heidebrink, Judith L, Lord, Joanne L, Johnson, Kris, Doody, Rachelle S, Villanueva-Meyer, Javier, Chowdhury, Munir, Stern, Yaakov, Honig, Lawrence S, Bell, Karen L, Morris, John C, Ances, Beau, Carroll, Maria, Leon, Sue, Mintun, Mark A, Schneider, Stacy, Marson, Daniel, Griffith, Randall, Clark, David, Grossman, Hillel, Mitsis, Effie
Publikováno v:
Neurology
Neurology 89(20), 2031-2038 (2017). doi:10.1212/WNL.0000000000004643
Neurology 89(20), 2031-2038 (2017). doi:10.1212/WNL.0000000000004643
Objectives:To estimate a regional progression pattern of amyloid deposition from cross-sectional amyloid-sensitive PET data and evaluate its potential for in vivo staging of an individual's amyloid pathology.Methods:Multiregional analysis of florbeta
Autor:
Natalja Funk, Mattia Volta, Matthew J. Farrer, Chenoa Mah, Jaskaran Khinda, Rick Kornelsen, Kimberley Co, Sabrina Bergeron, Katrina Yu, Saskia Biskup, Patrick Chou, Thomas Ott, A. Jon Stoessl, Vesna Sossi, Katherine Dinelle, Lise N. Munsie, Olaf Riess, Austen J. Milnerwood, Matthew D. Walker, Marta Mroczek, Stefano Cataldi, Li Ping Cao, Dayne Beccano-Kelly, Dagmar Galter
Publikováno v:
Journal of Parkinson's Disease 4(3), 483-498 (2014). doi:10.3233/JPD-140344
BACKGROUND A major risk-factor for developing Parkinson's disease (PD) is genetic variability in leucine-rich repeat kinase 2 (LRRK2), most notably the p.G2019S mutation. Examination of the effects of this mutation is necessary to determine the etiol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bd02b05ebe9314828bf5440bff46f644
Autor:
Arjun V. Raman, Frederick P. Bellinger, Donato A. Di Monte, Vivian P. Chou, Jennifer Atienza-Duyanen, Amy B. Manning-Boğ
Publikováno v:
FEBS letters 587(10), 1562-1570 (2013). doi:10.1016/j.febslet.2013.04.001
Loss of DJ-1 function contributes to pathogenesis in Parkinson’s disease. Here, we investigate the impact of aging and DJ-1 deficiency in transgenic mice. Ventral midbrain from young DJ-1-deficient mice revealed no change in 4-hydroxy-2-nonenal (4-
Publikováno v:
Neuroscience 250, 557-564 (2013). doi:10.1016/j.neuroscience.2013.06.060
Neuroscience
Neuroscience
Motor learning requires protein synthesis within the primary motor cortex (M1). Here, we show that the immediate early gene Arc/Arg3.1 is specifically induced in M1 by learning a motor skill. Arc mRNA was quantified using a fluorescent in situ hybrid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3758e6bed48ef6228bf96a1c5a66f157
https://pub.dzne.de/record/137050
https://pub.dzne.de/record/137050
Autor:
C. Globas, Wilfred F. A. den Dunnen, Till Karsten Hauser, Kay Seidel, Ewout R. Brunt, Katrin Bürk, Kathrin Brockmann, Matthias Reimold, Ludger Schöls, Horst-Werner Korf, Udo Rüb, Gerald Reischl, Georg Auburger
Publikováno v:
Brain, 138. Oxford University Press
Brain 138(11), 3316-3326 (2015). doi:10.1093/brain/awv255
Brain 138(11), 3316-3326 (2015). doi:10.1093/brain/awv255
See Klockgether (doi:10.1093/awv253) for a scientific commentary on this article.The spinocerebellar ataxias types 2 (SCA2) and 3 (SCA3) are autosomal dominantly inherited cerebellar ataxias which are caused by CAG trinucleotide repeat expansions in