Zobrazeno 1 - 7 of 7 pro vyhledávání: '"Doychin T. Stanchev"'
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Akademický článek
Restraint of presynaptic protein levels by Wnd/DLK signaling mediates synaptic defects associated with the kinesin-3 motor Unc-104
Autor: Jiaxing Li, Yao V Zhang, Elham Asghari Adib, Doychin T Stanchev, Xin Xiong, Susan Klinedinst, Pushpanjali Soppina, Thomas Robert Jahn, Richard I Hume, Tobias M Rasse, Catherine A Collins
Publikováno v: eLife, Vol 6 (2017)
The kinesin-3 family member Unc-104/KIF1A is required for axonal transport of many presynaptic components to synapses, and mutation of this gene results in synaptic dysfunction in mice, flies and worms. Our studies at the Drosophila neuromuscular jun
Externí odkaz: https://doaj.org/article/79619f4a1fa4450f97a7863533408fc2
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Restraint of presynaptic protein levels by Wnd/DLK signaling mediates synaptic defects associated with the kinesin-3 motor Unc-104
Autor: Doychin T. Stanchev, Jiaxing Li, Pushpanjali Soppina, Susan Klinedinst, Richard I. Hume, Yao V. Zhang, Tobias M. Rasse, Catherine A. Collins, Elham Asghari Adib, Xin Xiong, Thomas R. Jahn
Publikováno v: eLife
eLife, Vol 6 (2017)
The kinesin-3 family member Unc-104/KIF1A is required for axonal transport of many presynaptic components to synapses, and mutation of this gene results in synaptic dysfunction in mice, flies and worms. Our studies at the Drosophila neuromuscular jun
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b49d276e0b91d068f2b7426049cf4885
https://doi.org/10.7554/elife.24271
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5
The KIF1A homolog Unc-104 is important for spontaneous release, postsynaptic density maturation and perisynaptic scaffold organization
Autor: Yao V. Zhang, Jeannine V. Kern, Doychin T. Stanchev, Tobias M. Rasse, Thomas R. Jahn, Baran Koc, Shabab B. Hannan
Publikováno v: Scientific Reports
Nature
The kinesin-3 family member KIF1A has been shown to be important for experience dependent neuroplasticity. In Drosophila, amorphic mutations in the KIF1A homolog unc-104 disrupt the formation of mature boutons. Disease associated KIF1A mutations have
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1555b2565d514776367ae9c3e1b35a5
https://pubmed.ncbi.nlm.nih.gov/28344334
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7
Spastic paraplegia mutation N256S in the neuronal microtubule motor KIF5A disrupts axonal transport in a Drosophila HSP model
Autor: Petra Füger, Kathrin N. Karle, Doychin T. Stanchev, Carola D. Schneider, Matthias Flötenmeyer, Jeannine V. Kern, Vrinda Sreekumar, Katharina J. Daub, Vera K. Siegert, Rebecca Schüle, Tobias M. Rasse, Ludger Schöls, Heinz Schwarz
Publikováno v: PLoS Genetics
PLoS Genetics, Vol 8, Iss 11, p e1003066 (2012)
PLoS Genetics 8(11), e1003066 (2012). doi:10.1371/journal.pgen.1003066
Hereditary spastic paraplegias (HSPs) comprise a group of genetically heterogeneous neurodegenerative disorders characterized by spastic weakness of the lower extremities. We have generated a Drosophila model for HSP type 10 (SPG10), caused by mutati
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e98242ad78e8afd6297ab0e2066f6ad
https://pubmed.ncbi.nlm.nih.gov/23209432
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