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J FIELDING

Showing results (331-340 of 420) with videos related to

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Molecular Vision|April 9, 2026
Insight into genes responsible for cornea plana, megalocornea, keratoconus and brittle cornea syndromeDi Zhu, Yuxi Zheng, Yi Jiang, et al.
Brain : a Journal of Neurology|October 18, 2024
Clinical and genetic landscape of optic atrophy in 826 families: insights from 50 nuclear genesYuxi Zheng, Panfeng Wang, Shiqiang Li, et al.
AJNR. American Journal of Neuroradiology|February 5, 2022
Lesion Volume in Relapsing Multiple Sclerosis is Associated with Perivascular Space Enlargement at the Level of the Basal GangliaS C Kolbe, L M Garcia, N Yu, et al.
Vaccine|January 7, 2021
Constructing an ethical framework for priority allocation of pandemic vaccinesJ Fielding, S G Sullivan, F Beard, et al.
American Journal of Human Genetics|June 4, 2011
Mutations in FYCO1 cause autosomal-recessive congenital cataractsJianjun Chen, Zhiwei Ma, Xiaodong Jiao, et al.
Molecular Vision|April 3, 2010
Autosomal recessive congenital cataract linked to EPHA2 in a consanguineous Pakistani familyHaiba Kaul, S Amer Riazuddin, Mariam Shahid, et al.
Investigative Ophthalmology & Visual Science|March 13, 2026
βA4-Crystallin Mutations Disrupt Structural Stability and Crystallin Interactions in Congenital Cataract PathogenesisXiaoshan Lin, Shasha Deng, Wenqian Li, et al.
Genes, Brain, and Behavior|February 14, 2014
Symbolic sequence learning is associated with cognitive-affective profiles in female FMR1 premutation carriersC M Kraan, D R Hocking, J L Bradshaw, et al.
National Science Review|June 13, 2025
Spin-regulated Fe-N-C catalyst enabled by adjusting coordination nitrogen species for robust oxygen reductionNing Wang, Chao Meng, Bin Wang, et al.
Molecular Vision|November 27, 2025
Phenotype-genotype correlation of patients with congenital cataracts and hair anomaliesQiwei Wang, Xiaoshan Lin, Dongni Wang, et al.
Pageof 42

Showing results (331-340 of 420) with videos related to

Sort By:
Pageof 42
Molecular Vision|April 9, 2026
Insight into genes responsible for cornea plana, megalocornea, keratoconus and brittle cornea syndromeDi Zhu, Yuxi Zheng, Yi Jiang, et al.
Brain : a Journal of Neurology|October 18, 2024
Clinical and genetic landscape of optic atrophy in 826 families: insights from 50 nuclear genesYuxi Zheng, Panfeng Wang, Shiqiang Li, et al.
AJNR. American Journal of Neuroradiology|February 5, 2022
Lesion Volume in Relapsing Multiple Sclerosis is Associated with Perivascular Space Enlargement at the Level of the Basal GangliaS C Kolbe, L M Garcia, N Yu, et al.
Vaccine|January 7, 2021
Constructing an ethical framework for priority allocation of pandemic vaccinesJ Fielding, S G Sullivan, F Beard, et al.
American Journal of Human Genetics|June 4, 2011
Mutations in FYCO1 cause autosomal-recessive congenital cataractsJianjun Chen, Zhiwei Ma, Xiaodong Jiao, et al.
Molecular Vision|April 3, 2010
Autosomal recessive congenital cataract linked to EPHA2 in a consanguineous Pakistani familyHaiba Kaul, S Amer Riazuddin, Mariam Shahid, et al.
Investigative Ophthalmology & Visual Science|March 13, 2026
βA4-Crystallin Mutations Disrupt Structural Stability and Crystallin Interactions in Congenital Cataract PathogenesisXiaoshan Lin, Shasha Deng, Wenqian Li, et al.
Genes, Brain, and Behavior|February 14, 2014
Symbolic sequence learning is associated with cognitive-affective profiles in female FMR1 premutation carriersC M Kraan, D R Hocking, J L Bradshaw, et al.
National Science Review|June 13, 2025
Spin-regulated Fe-N-C catalyst enabled by adjusting coordination nitrogen species for robust oxygen reductionNing Wang, Chao Meng, Bin Wang, et al.
Molecular Vision|November 27, 2025
Phenotype-genotype correlation of patients with congenital cataracts and hair anomaliesQiwei Wang, Xiaoshan Lin, Dongni Wang, et al.
Pageof 42