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J Fielding

Showing results (311-320 of 493) with videos related to

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Investigative Ophthalmology & Visual Science|July 28, 2004
A homozygous splice mutation in the HSF4 gene is associated with an autosomal recessive congenital cataractNizar Smaoui, Omar Beltaief, Sonia BenHamed, et al.
Molecular Vision|May 28, 2009
Novel SIL1 mutations in consanguineous Pakistani families mapping to chromosomes 5q31S Amer Riazuddin, Laleh Amiri-Kordestani, Haiba Kaul, et al.
Molecular Genetics and Genomics : MGG|April 22, 2021
Pathogenicity evaluation and the genotype-phenotype analysis of OPA1 variantsXingyu Xu, Panfeng Wang, Xiaoyun Jia, et al.
Archives of Physical Medicine and Rehabilitation|February 12, 2005
Alendronate in the treatment of low bone mass in steroid-treated boys with Duchennes muscular dystrophyGillian A Hawker, Rowena Ridout, Vivien A Harris, et al.
Annals of the New York Academy of Sciences|February 22, 2000
A framework for evidenced-based reviews of interventions for supportive social environmentsL Anderson, M Fullilove, S Scrimshaw, et al.
Human Genetics|February 28, 2003
Genetic linkage of Francois-Neetens fleck (mouchetée) corneal dystrophy to chromosome 2q35Xiaodong Jiao, Francis L Munier, Daniel F Schorderet, et al.
Plos One|July 18, 2014
A novel MIP gene mutation analysis in a Chinese family affected with congenital progressive punctate cataractXuchen Ding, Nan Zhou, Hui Lin, et al.
Retina (Philadelphia, Pa.)|February 2, 2023
CHARACTERIZATION OF MACULAR NEOVASCULARIZATION IN BIETTI CRYSTALLINE DYSTROPHY USING MULTIMODAL IMAGING MODALITIESQian Li, Shengjuan Zhang, Lihua Kang, et al.
Plos Genetics|June 23, 2020
Thyroid hormone receptor beta mutations alter photoreceptor development and function in Danio rerio (zebrafish)Ciana Deveau, Xiaodong Jiao, Sachihiro C Suzuki, et al.
Journal of the American Chemical Society|February 14, 2013
Enzymatic single-molecule kinetic isotope effectsChristopher R Pudney, Richard S K Lane, Alistair J Fielding, et al.
Pageof 50

Showing results (311-320 of 493) with videos related to

Sort By:
Pageof 50
Investigative Ophthalmology & Visual Science|July 28, 2004
A homozygous splice mutation in the HSF4 gene is associated with an autosomal recessive congenital cataractNizar Smaoui, Omar Beltaief, Sonia BenHamed, et al.
Molecular Vision|May 28, 2009
Novel SIL1 mutations in consanguineous Pakistani families mapping to chromosomes 5q31S Amer Riazuddin, Laleh Amiri-Kordestani, Haiba Kaul, et al.
Molecular Genetics and Genomics : MGG|April 22, 2021
Pathogenicity evaluation and the genotype-phenotype analysis of OPA1 variantsXingyu Xu, Panfeng Wang, Xiaoyun Jia, et al.
Archives of Physical Medicine and Rehabilitation|February 12, 2005
Alendronate in the treatment of low bone mass in steroid-treated boys with Duchennes muscular dystrophyGillian A Hawker, Rowena Ridout, Vivien A Harris, et al.
Annals of the New York Academy of Sciences|February 22, 2000
A framework for evidenced-based reviews of interventions for supportive social environmentsL Anderson, M Fullilove, S Scrimshaw, et al.
Human Genetics|February 28, 2003
Genetic linkage of Francois-Neetens fleck (mouchetée) corneal dystrophy to chromosome 2q35Xiaodong Jiao, Francis L Munier, Daniel F Schorderet, et al.
Plos One|July 18, 2014
A novel MIP gene mutation analysis in a Chinese family affected with congenital progressive punctate cataractXuchen Ding, Nan Zhou, Hui Lin, et al.
Retina (Philadelphia, Pa.)|February 2, 2023
CHARACTERIZATION OF MACULAR NEOVASCULARIZATION IN BIETTI CRYSTALLINE DYSTROPHY USING MULTIMODAL IMAGING MODALITIESQian Li, Shengjuan Zhang, Lihua Kang, et al.
Plos Genetics|June 23, 2020
Thyroid hormone receptor beta mutations alter photoreceptor development and function in Danio rerio (zebrafish)Ciana Deveau, Xiaodong Jiao, Sachihiro C Suzuki, et al.
Journal of the American Chemical Society|February 14, 2013
Enzymatic single-molecule kinetic isotope effectsChristopher R Pudney, Richard S K Lane, Alistair J Fielding, et al.
Pageof 50