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pro vyhledávání: '"Nair, Gopinathan"'
Autor:
Nair, Gopinathan Raj.
Publikováno v:
View the Table of Contents & Abstract..
Thesis (Ph. D.)--University of Hong Kong, 1997.
Includes bibliographical references (leaves 246-271).
Includes bibliographical references (leaves 246-271).
Externí odkaz:
http://sunzi.lib.hku.hk/hkuto/record.jsp?B19672548
Autor:
Nair, Gopinathan K P
Several sugars and amino acids
Externí odkaz:
http://hdl.handle.net/2009/1337
Publikováno v:
Journal of Ophthalmic & Vision Research, Vol 13, Iss 4, Pp 397-402 (2018)
Purpose: To investigate the association of FOXE3-p.Ala170Ala (rs34082359) and PITX3-p.Ile95Ile (rs2281983) polymorphisms with congenital cataract and microphthalmia in a western Indian population. Methods: FOXE3-p.Ala170Ala (c.510C>T) and PITX3-p.Ile
Externí odkaz:
https://doaj.org/article/ad3b27e5c4954d3985d720728fa40112
Autor:
Sankaranarayanan, Rajkumar1,2 (AUTHOR) srajkumar31@gmail.com, Vidya, Nair Gopinathan1 (AUTHOR), Vasavada, Abhay Raghukant3 (AUTHOR)
Publikováno v:
Ophthalmic Genetics. Apr2019, Vol. 40 Issue 2, p99-109. 11p.
Genetic investigation of ocular developmental genes in 52 patients with anophthalmia/microphthalmia.
Autor:
Vidya, Nair Gopinathan1,2, Rajkumar, Sankaranarayanan1 srajkumar31@gmail.com, Vasavada, Abhay R.3
Publikováno v:
Ophthalmic Genetics. Jun2018, Vol. 39 Issue 3, p344-352. 9p.
Publikováno v:
Ophthalmic Genetics. 39:344-352
Background Mutation in eye developmental genes has been reported to cause anophthalmia and microphthalmia. However, in India, especially in the Western Indian population, such reports are scarce. Hence, the present study aims to investigate mutations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::de940ba5267c9099ab762610fbdabdac
https://doi.org/10.1080/13816810.2018.1436184
https://doi.org/10.1080/13816810.2018.1436184
Publikováno v:
Journal of Ophthalmic & Vision Research
Journal of Ophthalmic & Vision Research, Vol 13, Iss 4, Pp 397-402 (2018)
Journal of Ophthalmic & Vision Research, Vol 13, Iss 4, Pp 397-402 (2018)
Purpose: To investigate the association of FOXE3 -p.Ala170Ala (rs34082359) and PITX3 -p.Ile95Ile (rs2281983) polymorphisms with congenital cataract and microphthalmia in a western Indian population. Methods: FOXE3 -p.Ala170Ala (c.510C>T) and PITX3 -p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8631b2f1c62a1de33076e35d225d5551
http://europepmc.org/articles/PMC6210873
http://europepmc.org/articles/PMC6210873
Background: Age-related cataract (ARC) is profoundly associated with oxidative stress. Iron plays a pivotal role in generating oxidative stress and promoting deleterious irreversible damage to the macromolecules. Divalent metal transporter 1 (DMT1) m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9d8bc56139e65ebd50f987186db4eef7