Nutrigenomics tools to address the emerging issues in marine fish larviculture

Autor: Iyyapparaja Narasimapallavan. G, Sanal Ebeneezar, Vijayagopal, P, Linga Prabu, D, Sajina, K.A., Krupesha Sharma, S.R., Sumithra, T.G., Tamilmani, G., Saktivel, M., Anikuttan, K.K., Gopalakrishnan, A.

It is of note that the capture fisheries are under stress for many targeted species. To reduce the pressure on the wild, research on mariculture had been practicing for decades. Even though technologies for captive breeding are standardized, the grow

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf89843cebd5f5bda908a2ec628531bd

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Recessive Mutations in SLC38A8 Cause Foveal Hypoplasia and Optic Nerve Misrouting without Albinism

Autor: Eamonn Sheridan, Chris F. Inglehearn, Murugan Saktivel, Phillis Lakeman, Rohit Shetty, Anandula Venkataramana, Manir Ali, Sabrina Carrella, Bishwanath Pal, Ian M. Carr, Alex W. Hewitt, James A. Poulter, Maria M. van Genderen, Musallam Al-Araimi, Govindasamy Kumaramanickavel, Vedam L. Ramprasad, Mike Shires, David A. Mackey, David A. Parry, Carmel Toomes, Kamron N. Khan, Andrew R. Webster, Panagiotis I. Sergouniotis, Anthony T. Moore, Sandro Banfi, Moin Mohamed, Alex Tai Loong Tan, Ivan Conte, John Bradbury

Publikováno v: American journal of human genetics, 93(6), 1143-1150. Cell Press
Poulter, J A, Al-Araimi, M, Conte, I, van Genderen, M M, Sheridan, E, Carr, I M, Parry, D A, Shires, M, Carrella, S, Bradbury, J, Khan, K, Lakeman, P, Sergouniotis, P I, Webster, A R, Moore, A T, Pal, B, Mohamed, M D, Venkataramana, A, Ramprasad, V, Shetty, R, Saktivel, M, Kumaramanickavel, G, Tan, A, Mackey, D A, Hewitt, A W, Banfi, S, Ali, M, Inglehearn, C F & Toomes, C 2013, ' Recessive Mutations in SLC38A8 Cause Foveal Hypoplasia and Optic Nerve Misrouting without Albinism ', American journal of human genetics, vol. 93, no. 6, pp. 1143-1150 . https://doi.org/10.1016/j.ajhg.2013.11.002
American journal of human genetics, vol 93, iss 6

Foveal hypoplasia and optic nerve misrouting are developmental defects of the visual pathway and only co-occur in connection with albinism; to date, they have only been associated with defects in the melanin-biosynthesis pathway. Here, we report that

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4adbd3ab2052210013ccbaede5c6b0c
https://doi.org/10.1016/j.ajhg.2013.11.002