Zobrazeno 1 - 10
of 118
pro vyhledávání: '"Ying HS"'
Autor:
Ella J. Gehrke, Jacob Thompson, Emily Kalmanek, Sarah T. Stanley, Joseph Laird, Sajag Bhattarai, Brianna Lobeck, Sara Mayer, Angela Mahoney, Salma Hassan, Ying Hsu, Arlene Drack
Publikováno v:
Frontiers in Medicine, Vol 11 (2024)
IntroductionX-linked retinoschisis (XLRS) is a vitreoretinal dystrophy caused by RS1 gene mutations which disrupt retinoschisin-1 (RS1) function. Vital for retinal architecture, the absence of functional RS1 leads to the development of intraretinal c
Externí odkaz:
https://doaj.org/article/97956e756020459d94d1cdf5dba195c3
Autor:
Deng-Fu Guo, Ronald A. Merrill, Lan Qian, Ying Hsu, Qihong Zhang, Zhihong Lin, Daniel R. Thedens, Yuriy M. Usachev, Isabella Grumbach, Val C. Sheffield, Stefan Strack, Kamal Rahmouni
Publikováno v:
Molecular Metabolism, Vol 90, Iss , Pp 102038- (2024)
Externí odkaz:
https://doaj.org/article/a5863d78d79f4d7793bc4c8b5114c71c
Autor:
Ella J. Gehrke, Araniko Pandey, Jacob Thompson, Sajag Bhattarai, Prajwal Gurung, Ying Hsu, Arlene V. Drack
Publikováno v:
Frontiers in Medicine, Vol 11 (2024)
PurposePrevious studies have reported Caspase-1 (Casp1) is upregulated in mouse models of Juvenile X-linked Retinoschisis (XLRS), however no functional role for Casp1 in disease progression has been identified. We performed electroretinogram (ERG) an
Externí odkaz:
https://doaj.org/article/679fb165ad7c4d5093161d3b6add5eeb
Autor:
Salma Hassan, Ying Hsu, Jacob M. Thompson, Emily Kalmanek, Joel A. VandeLune, Sarah Stanley, Arlene V. Drack
Publikováno v:
Frontiers in Medicine, Vol 11 (2024)
PurposeX-linked retinoschisis (XLRS), due to loss-of-function mutations in the retinoschisin (RS1) gene, is characterized by a modest to severe decrease in visual acuity. Clinical trials for XLRS utilizing intravitreal (IVT) gene therapy showed ocula
Externí odkaz:
https://doaj.org/article/58df4dcdba794269ba2e10086642ed43
Autor:
Ying Hsu, Sajag Bhattarai, Jacob M. Thompson, Angela Mahoney, Jacintha Thomas, Sara K. Mayer, Poppy Datta, Janelle Garrison, Charles C. Searby, Luk H. Vandenberghe, Seongjin Seo, Val C. Sheffield, Arlene V. Drack
Publikováno v:
Molecular Therapy: Nucleic Acids, Vol 31, Iss , Pp 164-181 (2023)
Blindness in Bardet-Biedl syndrome (BBS) is caused by dysfunction and loss of photoreceptor cells in the retina. BBS10, mutations of which account for approximately 21% of all BBS cases, encodes a chaperonin protein indispensable for the assembly of
Externí odkaz:
https://doaj.org/article/595390ab39c54dacacc20bd00b9764d5
Autor:
Nicole A. Zelenski, MD, Nichole A. Joslyn, MD, Ying Hsuan Lee, MD, David Chwei-Chin Chuang, MD, Johnny Chuieng-Yi Lu, MD, MSCI, Tommy Nai-Jen Chang, MD, Robert J. Spinner, MD, Allen T. Bishop, MD, Alexander Y. Shin, MD
Publikováno v:
Plastic and Reconstructive Surgery, Global Open, Vol 11, Iss 6, p e5073 (2023)
Background:. Complete brachial plexus injuries are devastating injuries. A viable C5 spinal nerve can offer additional sources of axons and alter surgical treatment. We aimed to determine factors that portend C5 nerve root avulsion. Methods:. A retro
Externí odkaz:
https://doaj.org/article/37cdf941b8ab43469b744c755df9f4d7
Autor:
Deng-Fu Guo, Ronald A. Merrill, Lan Qian, Ying Hsu, Qihong Zhang, Zhihong Lin, Daniel R. Thedens, Yuriy M. Usachev, Isabella Grumbach, Val C. Sheffield, Stefan Strack, Kamal Rahmouni
Publikováno v:
Molecular Metabolism, Vol 67, Iss , Pp 101654- (2023)
Objective: The essential role of mitochondria in regulation of metabolic function and other physiological processes has garnered enormous interest in understanding the mechanisms controlling the function of this organelle. We assessed the role of the
Externí odkaz:
https://doaj.org/article/c91427f8083d47369d04de65198a6184
Autor:
Sara K. Mayer, Jacintha Thomas, Megan Helms, Aishwarya Kothapalli, Ioana Cherascu, Adisa Salesevic, Elliot Stalter, Kai Wang, Poppy Datta, Charles Searby, Seongjin Seo, Ying Hsu, Sajag Bhattarai, Val C. Sheffield, Arlene V. Drack
Publikováno v:
Disease Models & Mechanisms, Vol 15, Iss 9 (2022)
Externí odkaz:
https://doaj.org/article/ecd106037a8048798c7d1472715529f4
Autor:
Thomas K Pak, Calvin S Carter, Qihong Zhang, Sunny C Huang, Charles Searby, Ying Hsu, Rebecca J Taugher, Tim Vogel, Christopher C Cychosz, Rachel Genova, Nina N Moreira, Hanna Stevens, John A Wemmie, Andrew A Pieper, Kai Wang, Val C Sheffield
Publikováno v:
PLoS Genetics, Vol 17, Iss 4, p e1009484 (2021)
Primary cilia are microtubule-based organelles present on most cells that regulate many physiological processes, ranging from maintaining energy homeostasis to renal function. However, the role of these structures in the regulation of behavior remain
Externí odkaz:
https://doaj.org/article/18af8c36aad74454a8590f50cbaad918
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