Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Elizabeth Alcala"'
Autor:
Won-Seok Lee, Ismael Al-Ramahi, Hyun-Hwan Jeong, Youjin Jang, Tao Lin, Carolyn J. Adamski, Laura A. Lavery, Smruti Rath, Ronald Richman, Vitaliy V. Bondar, Elizabeth Alcala, Jean-Pierre Revelli, Harry T. Orr, Zhandong Liu, Juan Botas, Huda Y. Zoghbi
Publikováno v:
The Journal of Clinical Investigation, Vol 132, Iss 9 (2022)
Many neurodegenerative disorders are caused by abnormal accumulation of misfolded proteins. In spinocerebellar ataxia type 1 (SCA1), accumulation of polyglutamine-expanded (polyQ-expanded) ataxin-1 (ATXN1) causes neuronal toxicity. Lowering total ATX
Externí odkaz:
https://doaj.org/article/15989ff1be9a4c33b23b168062a26a21
Autor:
Vineetha M. Zacharia, Yein Ra, Catherine Sue, Elizabeth Alcala, Jewel N. Reaso, Steven E. Ruzin, Matthew F. Traxler
Publikováno v:
mBio, Vol 12, Iss 3 (2021)
Streptomyces coelicolorS. coelicolor
Externí odkaz:
https://doaj.org/article/c73fb240c2a547fdb758de6b41320929
Modulation of ATXN1 S776 phosphorylation reveals the importance of allele-specific targeting in SCA1
Autor:
Larissa Nitschke, Stephanie L. Coffin, Eder Xhako, Dany B. El-Najjar, James P. Orengo, Elizabeth Alcala, Yanwan Dai, Ying-Wooi Wan, Zhandong Liu, Harry T. Orr, Huda Y. Zoghbi
Publikováno v:
JCI Insight, Vol 6, Iss 3 (2021)
Spinocerebellar ataxia type 1 (SCA1) is an adult-onset neurodegenerative disorder characterized by motor incoordination, mild cognitive decline, respiratory dysfunction, and early lethality. It is caused by the expansion of the polyglutamine (polyQ)
Externí odkaz:
https://doaj.org/article/44cca890ba554a68a49c6326c4747b78
Autor:
Jewel N Reaso, Vineetha M. Zacharia, Yein Ra, Catherine Sue, Matthew F. Traxler, Elizabeth Alcala, Steven E. Ruzin
Publikováno v:
mBio, vol 12, iss 3
mBio, Vol 12, Iss 3 (2021)
mBio
mBio, Vol 12, Iss 3 (2021)
mBio
A number of bacteria are known to differentiate into cells with distinct phenotypic traits during processes such as biofilm formation or the development of reproductive structures. These cell types, by virtue of their specialized functions, embody a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec2bdee99115053a7ad309bbcb2fd974
https://escholarship.org/uc/item/9dk5m2jf
https://escholarship.org/uc/item/9dk5m2jf
Modulation of ATXN1 S776 phosphorylation reveals the importance of allele-specific targeting in SCA1
Autor:
James P. Orengo, Eder Xhako, Larissa Nitschke, Harry T. Orr, Zhandong Liu, Yanwan Dai, Dany B. El-Najjar, Stephanie L. Coffin, Elizabeth Alcala, Huda Y. Zoghbi, Ying Wooi Wan
Publikováno v:
JCI Insight, Vol 6, Iss 3 (2021)
JCI Insight
JCI Insight
Spinocerebellar ataxia type 1 (SCA1) is an adult-onset neurodegenerative disorder characterized by motor incoordination, mild cognitive decline, respiratory dysfunction, and early lethality. It is caused by the expansion of the polyglutamine (polyQ)
Autor:
Magaña, Pavel Loeza, Solis, Iván Giovani Valdez, Carapia, Delia Daniela Fernández, Morales, Lezly Elizabeth Alcalá, Vázquez, Pedro Iván Arias, González, Héctor Ricardo Quezada
Publikováno v:
In Apunts Sports Medicine April-June 2023 58(218)