Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Weihan Huai"'
Autor:
Chakraborty, Anirban, Sreenivasmurthy, Sravan Gopalkrishnashetty, Miller, Wyatt, Weihan Huai, Biswas, Tapan, Mandal, Santi Mohan, Boscá, Lisardo, Krishnan, Balaji, Ghosh, Gourisankar, Hazra, Tapas
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America; 9/24/2024, Vol. 121 Issue 39, p1-10, 24p
Autor:
Tetsuo Ashizawa, Partha S. Sarkar, Velmarini Vasquez, Xu Chen, Patrícia Maciel, Weihan Huai, Anirban Chakraborty, Muralidhar L. Hegde, Tatiana Venkova, Altaf H. Sarker, Sara Duarte-Silva, Nisha Tapryal, Gourisankar Ghosh, Tapas K. Hazra, Joy Mitra
Publikováno v:
Proc Natl Acad Sci U S A
Spinocerebellar ataxia type 3 (SCA3) is a dominantly inherited neurodegenerative disease caused by CAG (encoding glutamine) repeat expansion in the Ataxin-3 (ATXN3) gene. We have shown previously that ATXN3-depleted or pathogenic ATXN3-expressing cel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2697b602a8a066ce8ec4c239fe6501a2
https://pubmed.ncbi.nlm.nih.gov/32205441
https://pubmed.ncbi.nlm.nih.gov/32205441
Autor:
Chakraborty, Anirban, Tapryal, Nisha, Venkova, Tatiana, Mitra, Joy, Vasquez, Velmarini, Sarker, Altaf H., Duarte-Silva, Sara, Weihan Huai, Ashizawa, Tetsuo, Ghosh, Gourisankar, Maciel, Patricia, Sarkar, Partha S., Hegde, Muralidhar L., Xu Chen, Hazra, Tapas K.
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America; 4/7/2020, Vol. 117 Issue 14, p8154-8165, 12p