Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Taylor A. Intihar"'
Autor:
Rachel H. Mansky, Erin A. Greguske, Dahyun Yu, Nicole Zarate, Taylor A. Intihar, Wei Tsai, Taylor G. Brown, Mackenzie N. Thayer, Kompal Kumar, Rocio Gomez-Pastor
Publikováno v:
Cell Reports, Vol 42, Iss 3, Pp 112198- (2023)
Summary: p53 and HSF1 are two major transcription factors involved in cell proliferation and apoptosis, whose dysregulation contributes to cancer and neurodegeneration. Contrary to most cancers, p53 is increased in Huntington’s disease (HD) and oth
Externí odkaz:
https://doaj.org/article/949e550daa104647992a5fe317ef7c0c
Autor:
Nicole Zarate, Taylor A. Intihar, Dahyun Yu, Jacob Sawyer, Wei Tsai, Maha Syed, Luke Carlson, Rocio Gomez-Pastor
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 23, p 13113 (2021)
PSD-95 (Dlg4) is an ionotropic glutamate receptor scaffolding protein essential in synapse stability and neurotransmission. PSD-95 levels are reduced during aging and in neurodegenerative diseases like Huntington’s disease (HD), and it is believed
Externí odkaz:
https://doaj.org/article/746e4ef875de411c8758364a71d84668
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 13 (2019)
Huntington’s disease (HD) is a neurodegenerative disease caused by an expanded CAG repeat in the huntingtin (HTT) gene, causing the protein to misfold and aggregate. HD progression is characterized by motor impairment and cognitive decline associat
Externí odkaz:
https://doaj.org/article/ce352fa374454a3594287755c972f7b3
Autor:
Melissa P Knauert, Camilla S Powierza, Margaret M Doyle, Katherine Wasden, Taylor A Intihar, Amy S Korwin, Shyoko Honiden
Publikováno v:
BMJ Open Respiratory Research, Vol 11, Iss 1 (2024)
Introduction Early enteral nutrition (EN) in critically ill adult patients is thought to improve mortality and morbidity; expert guidelines recommend early initiation of EN in critically ill adults. However, the ideal schedule and dose of EN remain u
Externí odkaz:
https://doaj.org/article/750215645c19406cba28357c5c863aa4
Autor:
Rachel H. Mansky, Erin A. Greguske, Dahyun Yu, Nicole Zarate, Taylor A. Intihar, Wei Tsai, Taylor G. Brown, Mackenzie Thayer, Kompal Kumar, Rocio Gomez-Pastor
Publikováno v:
SSRN Electronic Journal.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa1dfd8af3edfcfdfb76925ed9ba6059
https://doi.org/10.2139/ssrn.4119001
https://doi.org/10.2139/ssrn.4119001
Autor:
Jacob Sawyer, Rocío Gómez-Pastor, Taylor A. Intihar, Nicole Zarate, Luke Carlson, Maha Syed, Wei Tsai, Dahyun Yu
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 13113, p 13113 (2021)
International Journal of Molecular Sciences; Volume 22; Issue 23; Pages: 13113
International Journal of Molecular Sciences
International Journal of Molecular Sciences; Volume 22; Issue 23; Pages: 13113
International Journal of Molecular Sciences
PSD-95 (Dlg4) is an ionotropic glutamate receptor scaffolding protein essential in synapse stability and neurotransmission. PSD-95 levels are reduced during aging and in neurodegenerative diseases like Huntington’s disease (HD), and it is believed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::210cdb89a58eaa2f4485cc3ab98411fd
https://www.mdpi.com/1422-0067/22/23/13113
https://www.mdpi.com/1422-0067/22/23/13113
Publikováno v:
Chest. 162:A1479
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eed6be0d640ff6994bdc9d4950fb9aba
https://doi.org/10.1016/j.chest.2022.08.1246
https://doi.org/10.1016/j.chest.2022.08.1246
Publikováno v:
Frontiers in Cellular Neuroscience, Vol 13 (2019)
Frontiers in Cellular Neuroscience
Frontiers in Cellular Neuroscience
Huntington’s disease (HD) is a neurodegenerative disease caused by an expanded CAG repeat in the huntingtin (HTT) gene, causing the protein to misfold and aggregate. HD progression is characterized by motor impairment and cognitive decline associat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::25cf4db1081bf8b3ba7a2139b7ea521b
https://doi.org/10.3389/fncel.2019.00103
https://doi.org/10.3389/fncel.2019.00103