Zobrazeno 1 - 10
of 103
pro vyhledávání: '"Kazuhiko Namikawa"'
Autor:
Alessandro Dorigo, Komali Valishetti, Florian Hetsch, Hideaki Matsui, Jochen C. Meier, Kazuhiko Namikawa, Reinhard W. Köster
Publikováno v:
Frontiers in Molecular Neuroscience, Vol 16 (2023)
IntroductionThe cerebellum is organized into functional regions each dedicated to process different motor or sensory inputs for controlling different locomotor behaviors. This functional regionalization is prominent in the evolutionary conserved sing
Externí odkaz:
https://doaj.org/article/a8fff6a6dafc47dcbb827ac3139fe5f1
Autor:
Stavrini Papadaki, Xinyue Wang, Yangdong Wang, Hanbin Zhang, Su Jia, Shuhong Liu, Minghan Yang, Dongdong Zhang, Jie-Min Jia, Reinhard W. Köster, Kazuhiko Namikawa, Kiryl D. Piatkevich
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-16 (2022)
Abstract Spectrally diverse fluorescent proteins (FPs) provide straightforward means for multiplexed imaging of biological systems. Among FPs fitting standard color channels, blue FPs (BFPs) are characterized by lower brightness compared to other spe
Externí odkaz:
https://doaj.org/article/424325b1b37d46fca78bea2f765dbd88
Publikováno v:
Journal of Experimental Neuroscience, Vol 13 (2019)
The cerebellum integrates sensory information and motor actions. Increasing experimental evidence has revealed that these functions as well as the cerebellar cytoarchitecture are highly conserved in zebrafish compared with mammals. However, the poten
Externí odkaz:
https://doaj.org/article/b25db3964b8344048b7833784149063a
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 14, p 7351 (2021)
Dominant spinocerebellar ataxias (SCAs) are progredient neurodegenerative diseases commonly affecting the survival of Purkinje cells (PCs) in the human cerebellum. Spinocerebellar ataxia type 1 (SCA1) is caused by the mutated ataxin1 (Atx1) gene prod
Externí odkaz:
https://doaj.org/article/8bba3fc790904aaa918413d63cf4d34f
Publikováno v:
Cell Reports, Vol 26, Iss 7, Pp 1727-1733.e6 (2019)
Summary: Parkinson’s disease (PD) is a neurodegenerative disease characterized by α-synuclein-positive inclusion bodies and loss of neurons, including dopaminergic neurons. Difficulty in replicating PD phenotypes using animal models partly limits
Externí odkaz:
https://doaj.org/article/20df400249d74d3cb3f474faa23c5a4f
Autor:
Siranush Babakhanova, Erica E. Jung, Kazuhiko Namikawa, Hanbin Zhang, Yangdong Wang, Oksana M. Subach, Dmitry A. Korzhenevskiy, Tatiana V. Rakitina, Xian Xiao, Wenjing Wang, Jing Shi, Mikhail Drobizhev, Demian Park, Lea Eisenhard, Hongyun Tang, Reinhard W. Köster, Fedor V. Subach, Edward S. Boyden, Kiryl D. Piatkevich
Publikováno v:
Protein Science. 31:728-751
In vivoimaging of model organisms is heavily reliant on fluorescent proteins with high intracellular brightness. Here we describe a practical method for rapid optimization of fluorescent proteins via directed molecular evolution in cultured mammalian
Autor:
Dorigo, Alessandro, Valishetti, Komali, Hetsch, Florian, Hideaki Matsui, Meier, Jochen C., Kazuhiko Namikawa, Köster, Reinhard W.
Publikováno v:
Frontiers in Molecular Neuroscience; 2023, p01-12, 12p
Autor:
Xinyue Wang, Lianfeng Wu, Luxia Yao, Stavrini Papadaki, Hanbin Zhang, Reinhard W. Köster, Xiaoting Sun, Kazuhiko Namikawa, Kiryl D. Piatkevich
Recent progress in fluorescent protein development has generated a large diversity of near-infrared fluorescent proteins, which are rapidly becoming popular probes for a variety of imaging applications. To assist end-users with a selection of the rig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::72119e07266d5c9baac0957c546f8eeb
https://doi.org/10.21203/rs.3.rs-797586/v1
https://doi.org/10.21203/rs.3.rs-797586/v1
Autor:
Wenjing Wang, Jing Shi, Y. Wang, S. Babakhanova, Demian Park, Fedor V. Subach, Oksana M. Subach, Reinhard W. Köster, Erica Jung, Xian Xiao, Mikhail Drobizhev, Kazuhiko Namikawa, Hongyun Tang, Lea Eisenhard, D.A. Korzhenevskiy, Kiryl D. Piatkevich, Tatiana V. Rakitina, Hanbin Zhang, Edward S. Boyden
In vivo imaging of model organisms is heavily reliant on fluorescent proteins with high intracellular brightness. Here we describe a practical method for rapid optimization of fluorescent proteins via directed molecular evolution in cultured mammalia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eef5f0427bbafbe18c0b902a9b754ef3
https://doi.org/10.21203/rs.3.rs-776185/v1
https://doi.org/10.21203/rs.3.rs-776185/v1
Publikováno v:
International Journal of Molecular Sciences
Volume 22
Issue 14
International Journal of Molecular Sciences, Vol 22, Iss 7351, p 7351 (2021)
International Journal of Molecular Sciences, 2021, 22(14), 7351; https://doi.org/10.3390/ijms22147351--Int J Mol Sci--http://www.bibliothek.uni-regensburg.de/ezeit/?2019364--https://www.mdpi.com/journal/ijms--https://www.ncbi.nlm.nih.gov/pmc/journals/808--1661-6596
Volume 22
Issue 14
International Journal of Molecular Sciences, Vol 22, Iss 7351, p 7351 (2021)
International Journal of Molecular Sciences, 2021, 22(14), 7351; https://doi.org/10.3390/ijms22147351--Int J Mol Sci--http://www.bibliothek.uni-regensburg.de/ezeit/?2019364--https://www.mdpi.com/journal/ijms--https://www.ncbi.nlm.nih.gov/pmc/journals/808--1661-6596
Dominant spinocerebellar ataxias (SCAs) are progredient neurodegenerative diseases commonly affecting the survival of Purkinje cells (PCs) in the human cerebellum. Spinocerebellar ataxia type 1 (SCA1) is caused by the mutated ataxin1 (Atx1) gene prod