Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Sabrina I Jarrah"'
Autor:
David Mengel, Isabel G. Wellik, Kristen H. Schuster, Sabrina I. Jarrah, Madeleine Wacker, Naila S. Ashraf, Gülin Öz, Matthis Synofzik, Maria do Carmo Costa, Hayley S. McLoughlin
Publikováno v:
Disease Models & Mechanisms, Vol 16, Iss 9 (2023)
Externí odkaz:
https://doaj.org/article/e92c614177774bf6a45cbca2558c9111
Autor:
Kristen H. Schuster, Danielle M. DiFranco, Alexandra F. Putka, Juan P. Mato, Sabrina I. Jarrah, Nicholas R. Stec, Vikram O. Sundararajan, Hayley S. McLoughlin
Publikováno v:
Frontiers in Neuroscience, Vol 17 (2023)
Spinocerebellar ataxia type 3 (SCA3) is a neurodegenerative disease caused by a CAG repeat expansion in the ATXN3 gene. Though the ATXN3 protein is expressed ubiquitously throughout the CNS, regional pathology in SCA3 patients is observed within sele
Externí odkaz:
https://doaj.org/article/6737c8cc4b5e49f8befd2d154d84aac9
Autor:
Ryan Jarrah, Karim Rizwan Nathani, Shaan Bhandarkar, Chibuze S. Ezeudu, Ryan T Nguyen, Abrham Amare, Usama A Aljameey, Sabrina I Jarrah, Archis R Bhandarkar, Brian Fiani
Publikováno v:
Regenerative Medicine. 18:413-423
Among the greatest general challenges in bioengineering is to mimic human physiology. Advanced efforts in tissue engineering have led to sophisticated ‘brain-on-chip’ (BoC) microfluidic devices that can mimic structural and functional aspects of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aed5010da9d63f5a345185b1a6247094
https://doi.org/10.2217/rme-2022-0212
https://doi.org/10.2217/rme-2022-0212
Autor:
Luke C. Bartelt, Pawel M. Switonski, Grażyna Adamek, Juliana Carvalho, Lisa A. Duvick, Sabrina I. Jarrah, Hayley S. McLoughlin, Daniel R. Scoles, Stefan M. Pulst, Harry T. Orr, Court Hull, Craig B. Lowe, Albert R. La Spada
Spinocerebellar ataxia type 7 (SCA7) is an inherited neurodegenerative disorder caused by a CAG-polyglutamine repeat expansion. SCA7 patients display a striking loss of Purkinje cell (PC) neurons with disease progression; however, PCs are rare, makin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fdf061341f2af70bae8c4e4c79d1355b
https://doi.org/10.1101/2023.03.19.533345
https://doi.org/10.1101/2023.03.19.533345
Autor:
David Mengel, Isabel G. Wellik, Kristen H. Schuster, Sabrina I. Jarrah, Madeleine Wacker, Naila S. Ashraf, Gülin Öz, Matthis Synofzik, Maria do Carmo Costa, Hayley S. McLoughlin
Increased neurofilament light (NfL) protein in biofluids is reflective of neurodegeneration and has gained interest as a biomarker across neurodegenerative diseases. In spinocerebellar ataxia type 3 (SCA3), the most common dominantly inherited ataxia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a44df91b6b48104e6e202e27b3ebe63b
https://doi.org/10.1101/2023.02.28.530463
https://doi.org/10.1101/2023.02.28.530463