Zobrazeno 1 - 3
of 3
pro vyhledávání: '"deficiency [Dopamine]"'
Autor:
Sigrid C. Schwarz, Mareike Fauser, Johannes Schwarz, Francisco Pan-Montojo, Andreas Hermann, Philipp J. Kahle, Christian Richter, Alexander Storch
Publikováno v:
Cells, Vol 10, Iss 775, p 775 (2021)
Cells 10(4), 775-(2021). doi:10.3390/cells10040775
Cells
Volume 10
Issue 4
Cells 10(4), 775-(2021). doi:10.3390/cells10040775
Cells
Volume 10
Issue 4
Background: Consecutive adult neurogenesis is a well-known phenomenon in the ventricular–subventricular zone of the lateral wall of the lateral ventricles (V–SVZ) and has been controversially discussed in so-called “non-neurogenic” brain area
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6cf572df2e281fae610d33b0527451be
https://www.mdpi.com/2073-4409/10/4/775
https://www.mdpi.com/2073-4409/10/4/775
Publikováno v:
Cells, Vol 9, Iss 2441, p 2441 (2020)
Cells
Cells 9(11), 2441-(2020). doi:10.3390/cells9112441
Volume 9
Issue 11
Cells : open access journal 9(11), 2441 (2020). doi:10.3390/cells9112441
Cells
Cells 9(11), 2441-(2020). doi:10.3390/cells9112441
Volume 9
Issue 11
Cells : open access journal 9(11), 2441 (2020). doi:10.3390/cells9112441
The classical motor symptoms of Parkinson&rsquo
s disease (PD) are caused by degeneration of dopaminergic neurons in the substantia nigra, which is followed by secondary dendritic pruning and spine loss at striatal medium spiny neurons (MSN). We
s disease (PD) are caused by degeneration of dopaminergic neurons in the substantia nigra, which is followed by secondary dendritic pruning and spine loss at striatal medium spiny neurons (MSN). We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de4ca74a61635d26e0d7f13c9d7ec63c
https://www.mdpi.com/2073-4409/9/11/2441
https://www.mdpi.com/2073-4409/9/11/2441
Autor:
Philipp J. Kahle, Zacharias Kohl, Stephan von Hörsten, Leanie Koch, Thirumalaisamy P. Velavan, Oscar Arias-Carrión, Jana Boy, Carsten Calaminus, Huu P. Nguyen, Markus Fendt, Jacqueline Schneider, Olaf Riess, Rolf Dermietzel, Rejko Krüger, Silke Nuber, Peter Teismann, Elisabeth Petrasch-Parwez, Anna Samarina
Publikováno v:
Neurobiology of disease 44(2), 192-204 (2011). doi:10.1016/j.nbd.2011.06.017
Neurobiology of Disease, Vol 44, Iss 2, Pp 192-204 (2011)
Neurobiology of Disease, Vol 44, Iss 2, Pp 192-204 (2011)
Mutations in the N-terminus of the gene encoding α-synuclein (α-syn) are linked to autosomal dominantly inherited Parkinson's disease (PD). The vast majority of PD patients develop neuropsychiatric symptoms preceding motor impairments. During this
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::53b0bdc057263934165c4b72382eb865
