Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Isabella, Palazzo"'
Autor:
Pin Lyu, Maria Iribarne, Dmitri Serjanov, Yijie Zhai, Thanh Hoang, Leah J. Campbell, Patrick Boyd, Isabella Palazzo, Mikiko Nagashima, Nicholas J. Silva, Peter F. Hitchcock, Jiang Qian, David R. Hyde, Seth Blackshaw
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-21 (2023)
Abstract Following acute retinal damage, zebrafish possess the ability to regenerate all neuronal subtypes through Müller glia (MG) reprogramming and asymmetric cell division that produces a multipotent Müller glia-derived neuronal progenitor cell
Externí odkaz:
https://doaj.org/article/71690f1b09a744288c5a191665a5f721
Autor:
Levi Todd, Isabella Palazzo, Lilianna Suarez, Xiaoyu Liu, Leo Volkov, Thanh V. Hoang, Warren A. Campbell, Seth Blackshaw, Ning Quan, Andy J. Fischer
Publikováno v:
Journal of Neuroinflammation, Vol 16, Iss 1, Pp 1-19 (2019)
Abstract Background Microglia and inflammation have context-specific impacts upon neuronal survival in different models of central nervous system (CNS) disease. Herein, we investigate how inflammatory mediators, including microglia, interleukin 1 bet
Externí odkaz:
https://doaj.org/article/6ec390cb647a4ea68a86e0194b3aa2c9
Autor:
Maura Schwartz, Alex Campbell, Joseph Caporale, Megan Baird, Isabella Palazzo, Shibi Likhite, Andrew Fischer, Kathrin Meyer
Publikováno v:
Proceedings, Vol 71, Iss 1, p 5 (2020)
Batten Disease is a fatal lysosomal storage disorder characterized by cognitive and [...]
Externí odkaz:
https://doaj.org/article/5232a16d91ed4005a9ad94e87c7e1d51
Autor:
Isabella Palazzo
Publikováno v:
Journal of Nuclear Cardiology
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::103de4fd9135998aceca49e7fa3c427f
https://doi.org/10.1007/s12350-021-02760-1
https://doi.org/10.1007/s12350-021-02760-1
Müller glia are a cellular source for neuronal regeneration in vertebrate retinas. However, the capacity for retinal regeneration varies widely across species. Understanding the mechanisms that regulate the reprogramming of Müller glia into progeni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0894b5d755c0289feaaa0cbc9a3c210b
https://doi.org/10.1101/2022.08.16.504164
https://doi.org/10.1101/2022.08.16.504164
Autor:
Warren A. Campbell, Seth Blackshaw, Amanda Fritsch-Kelleher, Andy J. Fischer, Isabella Palazzo, Thanh Hoang
Publikováno v:
Glia. 69:1515-1539
Recent studies suggest midkine (MDK) is involved in the development and regeneration of the zebrafish retina. We investigate the expression patterns of MDK and related factors, roles in neuronal survival, and influence upon the formation of Muller gl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::170aeaeab7378df96050519ac3435def
https://doi.org/10.1002/glia.23976
https://doi.org/10.1002/glia.23976
Autor:
Isabella Palazzo, Levi J. Todd, Thanh V. Hoang, Thomas A. Reh, Seth Blackshaw, Andy J. Fischer
Publikováno v:
Glia. 70
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::da09998e9a8dcd53c76ecc12e2124197
https://doi.org/10.1002/glia.24187
https://doi.org/10.1002/glia.24187
Autor:
Isabella Palazzo, Levi J. Todd, Thanh V. Hoang, Thomas A. Reh, Seth Blackshaw, Andy J. Fischer
Publikováno v:
Glia
Müller glia (MG) in mammalian retinas are incapable of regenerating neurons after damage, whereas the MG in lower vertebrates regenerate functional neurons. Identification of cell signaling pathways and gene regulatory networks that regulate MG-medi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::624dca02a7ee073ed910654bf3ef717e
https://pubmed.ncbi.nlm.nih.gov/35388544
https://pubmed.ncbi.nlm.nih.gov/35388544
Müller glia (MG) in mammalian retinas are incapable of regenerating neurons after damage, whereas the MG in lower vertebrates regenerate functional neurons. Identification networks that regulate MG-mediated regeneration is key to harnessing the rege
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::74b709ca496de8636392cef6a910ae37
https://doi.org/10.1101/2021.10.05.463152
https://doi.org/10.1101/2021.10.05.463152
Autor:
Maura Schwartz, Alex Campbell, Joseph Caporale, Megan Baird, Isabella Palazzo, Shibi Likhite, Andrew Fischer, Kathrin Meyer
Publikováno v:
Proceedings, Vol 71, Iss 5, p 5 (2021)
NEDAMSS is a newly discovered neurodevelopmental disorder with regression, abnormal movements, loss of speech and seizures. The disease is caused by heterozygous mutations in the Interferon Regulatory Factor 2 Binding Protein-Like (IRF2BPL) gene. IRF
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7297c288608e32049c231fa360ae6f3e
https://www.mdpi.com/2504-3900/71/1/5
https://www.mdpi.com/2504-3900/71/1/5