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J Fielding

Showing results (401-410 of 493) with videos related to

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Molecular Vision|July 21, 2012
Spatial expression patterns of autophagy genes in the eye lens and induction of autophagy in lens cellsLisa Ann Brennan, Wanda Lee Kantorow, Daniel Chauss, et al.
European Journal of Surgical Oncology : the Journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology|May 12, 2004
A phase II study of G17DT in gastric carcinomaA D Gilliam, S A Watson, M Henwood, et al.
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.
Pageof 50

Showing results (401-410 of 493) with videos related to

Sort By:
Pageof 50
Molecular Vision|July 21, 2012
Spatial expression patterns of autophagy genes in the eye lens and induction of autophagy in lens cellsLisa Ann Brennan, Wanda Lee Kantorow, Daniel Chauss, et al.
European Journal of Surgical Oncology : the Journal of the European Society of Surgical Oncology and the British Association of Surgical Oncology|May 12, 2004
A phase II study of G17DT in gastric carcinomaA D Gilliam, S A Watson, M Henwood, et al.
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.
Pageof 50