Zobrazeno 1 - 10
of 72
pro vyhledávání: '"Venkatraman, Anandalakshmi"'
Autor:
Jia Yi Kimberly Low, Xiangyan Shi, Venkatraman Anandalakshmi, Dawn Neo, Gary Swee Lim Peh, Siew Kwan Koh, Lei Zhou, M. K. Abdul Rahim, Ketti Boo, JiaXuan Lee, Harini Mohanram, Reema Alag, Yuguang Mu, Jodhbir S. Mehta, Konstantin Pervushin
Publikováno v:
Communications Biology, Vol 6, Iss 1, Pp 1-12 (2023)
ATP-independent amyloid-β chaperone L-PGDS disaggregates corneal amyloids in surgically excised human cornea of TGFBI-related corneal dystrophy patients by recognizing and releasing structurally frustrated regions.
Externí odkaz:
https://doaj.org/article/28fdb71f9bbb4ac495fc11425d4791b0
Publikováno v:
In Journal of Advanced Research February 2022 36:113-132
Autor:
Deshmukh, Mihir, Liu, Yu-Chi, Rim, Tyler Hyungtaek, Venkatraman, Anandalakshmi, Davidson, Matthew, Yu, Marco, Kim, Hong Seok, Lee, Geunyoung, Jun, Ikhyun, Mehta, Jodhbir S., Kim, Eung Kweon
Publikováno v:
In Computers in Biology and Medicine October 2021 137
Autor:
Venkatraman, Anandalakshmi, Duong-Thi, Minh-Dao, Pervushin, Konstantin, Ohlson, Sten, Mehta, Jodhbir Singh
Publikováno v:
In Journal of Advanced Research July 2020 24:529-543
Autor:
Venkatraman Anandalakshmi, Guillaume Hochart, David Bonnel, Jonathan Stauber, Shigeto Shimmura, Rajamani Lakshminarayanan, Konstantin Pervushin, Jodhbir S. Mehta
Publikováno v:
Separations, Vol 8, Iss 7, p 97 (2021)
Stromal corneal dystrophies are a group of hereditary disorders caused by mutations in the TGFBI gene. The mutant TGFBIp is prone to protein aggregation and the mutant protein gets deposited in the cornea, leading to severe visual impairment. The mut
Externí odkaz:
https://doaj.org/article/0f77b15411354f43ae933b20320b7a8d
Akademický článek
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Autor:
Lakshminarayanan, R., Chaurasia, Shyam S., Murugan, Elavazhagan, Venkatraman, Anandalakshmi, Chai, Shu-Ming, Vithana, Eranga N., Beuerman, Roger W., Mehta, Jodhbir S.
Publikováno v:
In The Ocular Surface January 2015 13(1):9-25
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
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Publikováno v:
International Journal of Molecular Sciences
Volume 22
Issue 3
International Journal of Molecular Sciences, Vol 22, Iss 1230, p 1230 (2021)
Volume 22
Issue 3
International Journal of Molecular Sciences, Vol 22, Iss 1230, p 1230 (2021)
Background: To evaluate the distribution of the transforming growth factor-beta induced (TGFBI) corneal dystrophies in a multi-ethnic population in Singapore, and to present the different phenotypes with the same genotype. Methods: This study include
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::40cc373b1d5c347cff709663f980c961
Autor:
David Bonnel, Jonathan Stauber, Rajamani Lakshminarayanan, Shigeto Shimmura, Guillaume Hochart, Jodhbir S. Mehta, Konstantin Pervushin, Venkatraman Anandalakshmi
Publikováno v:
Separations
Volume 8
Issue 7
Separations, Vol 8, Iss 97, p 97 (2021)
Volume 8
Issue 7
Separations, Vol 8, Iss 97, p 97 (2021)
Stromal corneal dystrophies are a group of hereditary disorders caused by mutations in the TGFBI gene. The mutant TGFBIp is prone to protein aggregation and the mutant protein gets deposited in the cornea, leading to severe visual impairment. The mut
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1191aea2a3d9bd7840a1a27ca8d17f4c
https://doi.org/10.3390/separations8070097
https://doi.org/10.3390/separations8070097