Zobrazeno 1 - 10
of 16
pro vyhledávání: '"physiology [Motor Neurons]"'
Autor:
Mudassar N. Khan, Pitchaiah Cherukuri, Francesco Negro, Ashish Rajput, Piotr Fabrowski, Vikas Bansal, Camille Lancelin, Tsung-I Lee, Yehan Bian, William P. Mayer, Turgay Akay, Daniel Müller, Stefan Bonn, Dario Farina, Till Marquardt
Publikováno v:
PLoS biology 20(12), e3001923 (2022). doi:10.1371/journal.pbio.3001923
PLoS biology 20(12), 1-34 (2022). doi:10.1371/journal.pbio.3001923 special issue: "Coloring coral larvae allows tracking of local dispersal and settlement"
PLoS biology 20(12), 1-34 (2022). doi:10.1371/journal.pbio.3001923 special issue: "Coloring coral larvae allows tracking of local dispersal and settlement"
PLoS biology 20(12), 1-34 (2022). doi:10.1371/journal.pbio.3001923 special issue: "Coloring coral larvae allows tracking of local dispersal and settlement"
Published by PLoS, Lawrence, KS
Published by PLoS, Lawrence, KS
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40297ac613bd0b98dabbb8d52e3978df
https://hdl.handle.net/11379/572005
https://hdl.handle.net/11379/572005
Autor:
José Ricardo, Vieira, Bhavin, Shah, Sebastian, Dupraz, Isidora, Paredes, Patricia, Himmels, Géza, Schermann, Heike, Adler, Alessia, Motta, Lea, Gärtner, Ariadna, Navarro-Aragall, Elena, Ioannou, Elena, Dyukova, Remy, Bonnavion, Andreas, Fischer, Dario, Bonanomi, Frank, Bradke, Christiana, Ruhrberg, Carmen, Ruiz de Almodóvar
Publikováno v:
Neuron 110(24), 4074-4089.e6 (2022). doi:10.1016/j.neuron.2022.12.005
How the vascular and neural compartment cooperate to achieve such a complex and highly specialized structure as the central nervous system is still unclear. Here, we reveal a crosstalk between motor neurons (MNs) and endothelial cells (ECs), necessar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c5097d00d3d38d8643651efba19a1ce7
https://doi.org/10.1016/j.neuron.2022.12.005
https://doi.org/10.1016/j.neuron.2022.12.005
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 2422, p 2422 (2021)
International journal of molecular sciences 22(5), 2422-(2021). doi:10.3390/ijms22052422
International Journal of Molecular Sciences
Volume 22
Issue 5
International journal of molecular sciences 22(5), 2422-(2021). doi:10.3390/ijms22052422
International Journal of Molecular Sciences
Volume 22
Issue 5
Deficient intracellular transport is a common pathological hallmark of many neurodegenerative diseases, including amyotrophic lateral sclerosis (ALS). Mutations in the fused-in-sarcoma (FUS) gene are one of the most common genetic causes for familial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::ef91019ea3d39d68003d57630d8e5536
https://www.mdpi.com/1422-0067/22/5/2422
https://www.mdpi.com/1422-0067/22/5/2422
Autor:
Phillip C. Wong, Diana Wiesner, Francesco Roselli, Tobias M. Boeckers, Deniz Yilmazer-Hanke, Barbara Commisso, Linyun Tang, Albert C. Ludolph, Jochen H. Weishaupt, Najwa Ouali Alami, Luc Dupuis, David Bayer, Bernd Baumann, Thomas Wirth
Publikováno v:
Life science alliance 3(11), e201900571 (2020). doi:10.26508/lsa.201900571
Life Science Alliance
Life Science Alliance, Life Science Alliance LLC, 2020, 3 (11), pp.e201900571. ⟨10.26508/lsa.201900571⟩
Life Science Alliance, 2020, 3 (11), pp.e201900571. ⟨10.26508/lsa.201900571⟩
Life Science Alliance
Life Science Alliance, Life Science Alliance LLC, 2020, 3 (11), pp.e201900571. ⟨10.26508/lsa.201900571⟩
Life Science Alliance, 2020, 3 (11), pp.e201900571. ⟨10.26508/lsa.201900571⟩
Chemogenetic motoneuron excitation and astrocyte GPCR-Gi signaling restore blood–spinal cord barrier, disrupted in four ALS mouse models, revealing its role in disease progression but not initiation.
Blood–spinal cord barrier (BSCB) disrupti
Blood–spinal cord barrier (BSCB) disrupti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93218dfe1100975b7bc1fb24ea761df4
https://pub.dzne.de/record/164314
https://pub.dzne.de/record/164314
Autor:
Ronny Sczech, Nicole Kreiter, Julia Japtok, Andreas Hermann, Hannes Glaß, Arun Pal, Marcel Naumann
Publikováno v:
Scientific data 5(1), 180241 (2018). doi:10.1038/sdata.2018.241
Scientific Data
Scientific Data
Neurodegenerative diseases pose a complex field with various neuronal subtypes and distinct differentially affected intra-neuronal compartments. Modelling of neurodegeneration requires faithful in vitro separation of axons and dendrites, their distal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e666a102b8007dd8ec287c9a0db815a
https://doi.org/10.1038/sdata.2018.241
https://doi.org/10.1038/sdata.2018.241
Autor:
Marta Zlatic, Avinash Khandelwal, Ibrahim Tastekin, Nico D Fessner, James W Truman, David Tadres, Albert Cardona, Matthieu Louis
Publikováno v:
Recercat. Dipósit de la Recerca de Catalunya
instname
eLife, Vol 7 (2018)
instname
eLife, Vol 7 (2018)
Sensory navigation results from coordinated transitions between distinct behavioral programs. During chemotaxis in the Drosophila melanogaster larva, the detection of positive odor gradients extends runs while negative gradients promote stops and tur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ddb8e4cef967e7086d60efd23168050
http://hdl.handle.net/10230/42838
http://hdl.handle.net/10230/42838
Autor:
Albert C. Ludolph, Tobias M. Boeckers, Stefan Liebau, Moritz Klingenstein, Julia Japtok, Stefan Putz, Xenia Lojewski, Marcel Naumann, Alexander Storch, Jared Sterneckert, Peter Reinhardt, Andreas Hermann, Maria Demestre
Publikováno v:
Neurobiology of Disease, Vol 82, Iss, Pp 420-429 (2015)
Neurobiology of disease 82, 420-429 (2015). doi:10.1016/j.nbd.2015.07.017
Neurobiology of disease 82, 420-429 (2015). doi:10.1016/j.nbd.2015.07.017
Autosomal-dominant mutations within the gene FUS (fused in sarcoma) are responsible for 5% of familial cases of amyotrophic lateral sclerosis (ALS). The FUS protein is physiologically mainly located in the nucleus, while cytoplasmic FUS aggregates ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6df30cb25e4b5550e91a70d2f177333f
http://www.sciencedirect.com/science/article/pii/S0969996115300218
http://www.sciencedirect.com/science/article/pii/S0969996115300218
Autor:
Johannes Dorst, Gabriele Nagel, Frank Hanisch, Verena Wais, Jochen H. Weishaupt, Johannes Brettschneider, Jan Kassubek, Albert C. Ludolph, Stephan Zierz, Angela Rosenbohm, Alexander Storch, Katja Kollewe, Susanne Petri, Andreas Hermann, Patrick Weydt
Publikováno v:
Acta neurologica Scandinavica 136(3), 204-211 (2016). doi:10.1111/ane.12713
Objectives Primary lateral sclerosis (PLS) is commonly considered as a motor neuron disease (MND) variant which almost exclusively affects upper motor neurons (UMN). There is still no consensus whether PLS should be regarded as an independent disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5331d076696f5417bdfbb2223ba3639
https://pubmed.ncbi.nlm.nih.gov/27858953
https://pubmed.ncbi.nlm.nih.gov/27858953
Deficiency in the mRNA export mediator Gle1 impairs Schwann cell development in the zebrafish embryo
Autor:
Basil Sharrack, H.R. Kim, Ke Ning, N.I. Alsomali, Jonathan D. Wood, Tennore Ramesh, Chiara F. Valori, A. Seytanoglu, Alan T McGown, Mimoun Azzouz
Publikováno v:
Neuroscience 322, 287-297 (2016). doi:10.1016/j.neuroscience.2016.02.039
GLE1 mutations cause lethal congenital contracture syndrome 1 (LCCS1), a severe autosomal recessive fetal motor neuron disease, and more recently have been associated with amyotrophic lateral sclerosis (ALS). The gene encodes a highly conserved prote
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::33e3ba3bbd9a53a989c0c5a753a43f3b
https://pubmed.ncbi.nlm.nih.gov/26921650
https://pubmed.ncbi.nlm.nih.gov/26921650
Autor:
Ovsepian, Saak V, Ovespian, Saak V, Bodeker, MacDara, O'Leary, Valerie B, Lawrence, Gary W, Oliver Dolly, J.
Publikováno v:
Brain structure & function 220(3), 1825-1838 (2015). doi:10.1007/s00429-015-1004-0
The prominent tropism of tetanus toxin (TeTx) towards peripheral nerves with retrograde transport and transfer to central neurons render it an invaluable probe for exploring fundamental neuronal processes such as endocytosis, retrograde trafficking a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38b43cca9a3498b5543e5f0dded563bb
https://pub.dzne.de/record/137904
https://pub.dzne.de/record/137904