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Ian J Jackson

Showing results (31-40 of 88) with videos related to

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Journal of Cell Science|September 4, 2008
Diphthamide modification of eEF2 requires a J-domain protein and is essential for normal developmentTom R Webb, Sally H Cross, Lisa McKie, et al.
Neuropharmacology|July 15, 2009
GABAergic amacrine cells and visual function are reduced in PAC1 transgenic miceBing Lang, Lei Zhao, Li Cai, et al.
Disease Models & Mechanisms|August 9, 2021
A mouse model of brittle cornea syndrome caused by mutation in Zfp469Chloe M Stanton, Amy S Findlay, Camilla Drake, et al.
Nature Communications|December 12, 2018
Genome-wide study of hair colour in UK Biobank explains most of the SNP heritabilityMichael D Morgan, Erola Pairo-Castineira, Konrad Rawlik, et al.
The Journal of Investigative Dermatology|July 9, 2013
A conditional zebrafish MITF mutation reveals MITF levels are critical for melanoma promotion vs. regression in vivoJames A Lister, Amy Capper, Zhiqiang Zeng, et al.
Zebrafish|January 13, 2009
mc1r Pathway regulation of zebrafish melanosome dispersionJennifer Richardson, Pia Rengtved Lundegaard, Natalie L Reynolds, et al.
Human Molecular Genetics|July 11, 2006
Cardiac malformations and midline skeletal defects in mice lacking filamin AAlan W Hart, Joanne E Morgan, Jürgen Schneider, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 16, 2004
Wa5 is a novel ENU-induced antimorphic allele of the epidermal growth factor receptorDaekee Lee, Sally H Cross, Karen E Strunk, et al.
Investigative Ophthalmology & Visual Science|May 2, 2013
A CNS-specific hypomorphic Pdgfr-beta mutant model of diabetic retinopathyShalini Jadeja, Richard L Mort, Margaret Keighren, et al.
Open Biology|June 12, 2015
Warburg Micro syndrome is caused by RAB18 deficiency or dysregulationMark T Handley, Sarah M Carpanini, Girish R Mali, et al.
Pageof 9

Showing results (31-40 of 88) with videos related to

Sort By:
Pageof 9
Journal of Cell Science|September 4, 2008
Diphthamide modification of eEF2 requires a J-domain protein and is essential for normal developmentTom R Webb, Sally H Cross, Lisa McKie, et al.
Neuropharmacology|July 15, 2009
GABAergic amacrine cells and visual function are reduced in PAC1 transgenic miceBing Lang, Lei Zhao, Li Cai, et al.
Disease Models & Mechanisms|August 9, 2021
A mouse model of brittle cornea syndrome caused by mutation in Zfp469Chloe M Stanton, Amy S Findlay, Camilla Drake, et al.
Nature Communications|December 12, 2018
Genome-wide study of hair colour in UK Biobank explains most of the SNP heritabilityMichael D Morgan, Erola Pairo-Castineira, Konrad Rawlik, et al.
The Journal of Investigative Dermatology|July 9, 2013
A conditional zebrafish MITF mutation reveals MITF levels are critical for melanoma promotion vs. regression in vivoJames A Lister, Amy Capper, Zhiqiang Zeng, et al.
Zebrafish|January 13, 2009
mc1r Pathway regulation of zebrafish melanosome dispersionJennifer Richardson, Pia Rengtved Lundegaard, Natalie L Reynolds, et al.
Human Molecular Genetics|July 11, 2006
Cardiac malformations and midline skeletal defects in mice lacking filamin AAlan W Hart, Joanne E Morgan, Jürgen Schneider, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|September 16, 2004
Wa5 is a novel ENU-induced antimorphic allele of the epidermal growth factor receptorDaekee Lee, Sally H Cross, Karen E Strunk, et al.
Investigative Ophthalmology & Visual Science|May 2, 2013
A CNS-specific hypomorphic Pdgfr-beta mutant model of diabetic retinopathyShalini Jadeja, Richard L Mort, Margaret Keighren, et al.
Open Biology|June 12, 2015
Warburg Micro syndrome is caused by RAB18 deficiency or dysregulationMark T Handley, Sarah M Carpanini, Girish R Mali, et al.
Pageof 9