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Investigative Ophthalmology & Visual Science|April 19, 2017
Homozygosity Mapping and Genetic Analysis of Autosomal Recessive Retinal Dystrophies in 144 Consanguineous Pakistani FamiliesLin Li, Yabin Chen, Xiaodong Jiao, et al.
Proceedings of the National Academy of Sciences of the United States of America|October 7, 2009
Common variants on chromosome 2 and risk of primary open-angle glaucoma in the Afro-Caribbean population of BarbadosXiaodong Jiao, Zhenglin Yang, Xian Yang, et al.
Human Genetics|January 3, 2021
A missense allele of PEX5 is responsible for the defective import of PTS2 cargo proteins into peroxisomesMuhammad Ali, Shahid Y Khan, Tony A Rodrigues, et al.
Physical Review Letters|January 22, 2002
L-H transition in the mega-amp spherical tokamakR J Akers, G F Counsell, A Sykes, et al.
Plos Genetics|August 30, 2018
Mutation in the intracellular chloride channel CLCC1 associated with autosomal recessive retinitis pigmentosaLin Li, Xiaodong Jiao, Ilaria D'Atri, et al.
Science (New York, N.Y.)|December 18, 2015
Geomorphic and geologic controls of geohazards induced by Nepal's 2015 Gorkha earthquakeJ S Kargel, G J Leonard, D H Shugar, et al.
Autophagy|February 26, 2021
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)<sup>1</sup>Daniel J Klionsky, Amal Kamal Abdel-Aziz, Sara Abdelfatah, et al.
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