Zobrazeno 1 - 10
of 583
pro vyhledávání: '"A H Schuster"'
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
Publikováno v:
Cells, Vol 11, Iss 16, p 2615 (2022)
Emerging evidence has implicated non-neuronal cells, particularly oligodendrocytes, in the pathophysiology of many neurodegenerative diseases, including Alzheimer’s disease, Parkinson’s disease, amyotrophic lateral sclerosis, Huntington’s disea
Externí odkaz:
https://doaj.org/article/122c89bea9924dfda1ce58cefe476693
Autor:
Hayley S. McLoughlin, Katherine Gundry, Orion Rainwater, Kristen H. Schuster, Isabel G. Wellik, Annie J. Zalon, Michael A. Benneyworth, Lynn E. Eberly, Gülin Öz
Publikováno v:
Annals of Neurology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f1063716b1d3b4df40777f90d6cc3b14
https://doi.org/10.1002/ana.26713
https://doi.org/10.1002/ana.26713
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
Autor:
Kristen H. Schuster, Annie J. Zalon, Hongjiu Zhang, Danielle M. DiFranco, Nicholas R. Stec, Zaid Haque, Kate G. Blumenstein, Amanda M. Pierce, Yuanfang Guan, Henry L. Paulson, Hayley S. McLoughlin
Publikováno v:
J Neurosci
Spinocerebellar ataxia Type 3 (SCA3), the most common dominantly inherited ataxia, is a polyglutamine neurodegenerative disease for which there is no disease-modifying therapy. The polyglutamine-encoding CAG repeat expansion in theATXN3gene results i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::292876747fad3ec07c37933f99219098
https://doi.org/10.1523/jneurosci.1954-20.2021
https://doi.org/10.1523/jneurosci.1954-20.2021
Autor:
Kristen H. Schuster, Annie J. Zalon, Danielle M. DiFranco, Alexandra F. Putka, Nicholas Stec, Sabrina Jarrah, Arsal Naeem, Zaid Haque, Hongjiu Zhang, Yuanfang Guan, Hayley S. McLoughlin
Spinocerebellar ataxia type 3 (SCA3) is the most common dominantly inherited ataxia. Currently, no preventative or disease-modifying treatments exist for this progressive neurodegenerative disorder, although efforts using gene silencing approaches ar
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4c572e0f051424895909d2b7bfe4c0af
https://doi.org/10.1101/2022.07.18.500473
https://doi.org/10.1101/2022.07.18.500473
Autor:
M. Baz, V. Gondran-Teiller, B. Bressac, O. Cabaret, A. Fievet, M. Dimaria, V. Goldbarg, C. Colas, M. N. Bonnet-Dupeyron, J. Tinat, M. Lebrun, V. Mari, J. M. Limacher, C. Corsini, E. Ginglinger, J. C. Saurin, A. Brahimi, C. Rouzier, S. Giraud, H. Schuster, A. Hollebecque, V. Boige, E. Cauchin, D. Malka, O. Caron, E. Rouleau
Publikováno v:
Digestive diseases and sciences.
Germline DNA alterations affecting homologous recombination pathway genes have been associated with pancreatic cancer (PC) risk. BRCA2 is the most studied gene and affects the management of PC patients and their families. Even though recent reports h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15b8d5d1d5c3713cb16e5c621b1599dc
https://pubmed.ncbi.nlm.nih.gov/36315333
https://pubmed.ncbi.nlm.nih.gov/36315333
Publikováno v:
Verbandsmanagement ISBN: 9783791053943
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4aebff255257eaf08a996146d7c003e6
https://doi.org/10.34156/9783791053943-361
https://doi.org/10.34156/9783791053943-361
Autor:
S. Missel, S. Bunk, M. Hofmann, G. Pszolla, M. Hutt, F. Schwoebel, F. Unverdorben, C. Wagner, M. Jaworski, H. Schuster, F. Schwoerer, C. Schraeder, O. Schoor, T. Weinschenk, D. Maurer, C. Reinhardt
Publikováno v:
Annals of Oncology. 33:S888
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::58cd7a4d79883cc994ed27b53c635b45
https://doi.org/10.1016/j.annonc.2022.07.879
https://doi.org/10.1016/j.annonc.2022.07.879