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Patsy M Nishina

Showing results (21-30 of 80) with videos related to

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Physiological Genomics|May 5, 2005
Type 2 diabetes mouse model TallyHo carries an obesity gene on chromosome 6 that exaggerates dietary obesityJung Han Kim, Taryn P Stewart, Weidong Zhang, et al.
Investigative Ophthalmology & Visual Science|January 17, 2012
Meckelin is necessary for photoreceptor intraciliary transport and outer segment morphogenesisGayle B Collin, Jungyeon Won, Wanda L Hicks, et al.
The Journal of Nutrition|May 6, 2003
New leptin receptor mutations in mice: Lepr(db-rtnd), Lepr(db-dmpg) and Lepr(db-rlpy)Jung Han Kim, Paul N Taylor, Dawn Young, et al.
Nature Genetics|April 2, 2002
Microtubule-associated protein 1A is a modifier of tubby hearing (moth1)Akihiro Ikeda, Qing Yin Zheng, Aamir R Zuberi, et al.
Investigative Ophthalmology & Visual Science|March 26, 2011
An ENU-induced mutation in the Mertk gene (Mertknmf12) leads to a slow form of retinal degenerationDennis M Maddox, Wanda L Hicks, Douglas Vollrath, et al.
Investigative Ophthalmology & Visual Science|February 11, 2012
An allele of microtubule-associated protein 1A (Mtap1a) reduces photoreceptor degeneration in Tulp1 and Tub Mutant MiceDennis M Maddox, Sakae Ikeda, Akihiro Ikeda, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|February 21, 2008
Mapping of genetic modifiers of Nr2e3 rd7/rd7 that suppress retinal degeneration and restore blue cone cells to normal quantityNeena B Haider, Weidong Zhang, Ron Hurd, et al.
Human Molecular Genetics|June 28, 2018
An FRMD4B variant suppresses dysplastic photoreceptor lesions in models of enhanced S-cone syndrome and of Nrl deficiencyYang Kong, Lihong Zhao, Jeremy R Charette, et al.
Physiological Genomics|July 20, 2006
Defective carbohydrate metabolism in mice homozygous for the tubby mutationYun Wang, Kevin Seburn, Lawrence Bechtel, et al.
Investigative Ophthalmology & Visual Science|December 19, 2013
Correction of the Crb1rd8 allele and retinal phenotype in C57BL/6N mice via TALEN-mediated homology-directed repairBenjamin E Low, Mark P Krebs, J Keith Joung, et al.
Pageof 8

Showing results (21-30 of 80) with videos related to

Sort By:
Pageof 8
Physiological Genomics|May 5, 2005
Type 2 diabetes mouse model TallyHo carries an obesity gene on chromosome 6 that exaggerates dietary obesityJung Han Kim, Taryn P Stewart, Weidong Zhang, et al.
Investigative Ophthalmology & Visual Science|January 17, 2012
Meckelin is necessary for photoreceptor intraciliary transport and outer segment morphogenesisGayle B Collin, Jungyeon Won, Wanda L Hicks, et al.
The Journal of Nutrition|May 6, 2003
New leptin receptor mutations in mice: Lepr(db-rtnd), Lepr(db-dmpg) and Lepr(db-rlpy)Jung Han Kim, Paul N Taylor, Dawn Young, et al.
Nature Genetics|April 2, 2002
Microtubule-associated protein 1A is a modifier of tubby hearing (moth1)Akihiro Ikeda, Qing Yin Zheng, Aamir R Zuberi, et al.
Investigative Ophthalmology & Visual Science|March 26, 2011
An ENU-induced mutation in the Mertk gene (Mertknmf12) leads to a slow form of retinal degenerationDennis M Maddox, Wanda L Hicks, Douglas Vollrath, et al.
Investigative Ophthalmology & Visual Science|February 11, 2012
An allele of microtubule-associated protein 1A (Mtap1a) reduces photoreceptor degeneration in Tulp1 and Tub Mutant MiceDennis M Maddox, Sakae Ikeda, Akihiro Ikeda, et al.
Mammalian Genome : Official Journal of the International Mammalian Genome Society|February 21, 2008
Mapping of genetic modifiers of Nr2e3 rd7/rd7 that suppress retinal degeneration and restore blue cone cells to normal quantityNeena B Haider, Weidong Zhang, Ron Hurd, et al.
Human Molecular Genetics|June 28, 2018
An FRMD4B variant suppresses dysplastic photoreceptor lesions in models of enhanced S-cone syndrome and of Nrl deficiencyYang Kong, Lihong Zhao, Jeremy R Charette, et al.
Physiological Genomics|July 20, 2006
Defective carbohydrate metabolism in mice homozygous for the tubby mutationYun Wang, Kevin Seburn, Lawrence Bechtel, et al.
Investigative Ophthalmology & Visual Science|December 19, 2013
Correction of the Crb1rd8 allele and retinal phenotype in C57BL/6N mice via TALEN-mediated homology-directed repairBenjamin E Low, Mark P Krebs, J Keith Joung, et al.
Pageof 8