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Alisdair R Philp

Showing results (1-10 of 11) with videos related to

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Vision Research|September 11, 2007
Visual function testing: a quantifiable visually guided behavior in miceStewart Thompson, Alisdair R Philp, Edwin M Stone
Investigative Ophthalmology & Visual Science|June 3, 2008
Divergent phenotypes of vision and accessory visual function in mice with visual cycle dysfunction (Rpe65 rd12) or retinal degeneration (rd/rd)Stewart Thompson, Robert F Mullins, Alisdair R Philp, et al.
Brain Research. Molecular Brain Research|December 19, 2002
Zebrafish melanopsin: isolation, tissue localisation and phylogenetic positionJames Bellingham, David Whitmore, Alisdair R Philp, et al.
Molecular Vision|January 7, 2005
Genetic analysis of oculocutaneous albinism type 1 (OCA1) in Indian families: two novel frameshift mutations in the TYR GenePeriasamy Sundaresan, Asim Kumar Sil, Alisdair R Philp, et al.
Human Mutation|February 2, 2010
Bardet-Biedl syndrome in Denmark--report of 13 novel sequence variations in six genesTina Duelund Hjortshøj, Karen Grønskov, Alisdair R Philp, et al.
American Journal of Medical Genetics. Part A|January 19, 2008
Novel mutations in BBS5 highlight the importance of this gene in non-Caucasian Bardet-Biedl syndrome patientsTina Duelund Hjortshøj, Karen Grønskov, Alisdair R Philp, et al.
Genomics|August 30, 2006
Identical mutation in a novel retinal gene causes progressive rod-cone degeneration in dogs and retinitis pigmentosa in humansBarbara Zangerl, Orly Goldstein, Alisdair R Philp, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 20, 2006
Regulation of gene expression in the mammalian eye and its relevance to eye diseaseTodd E Scheetz, Kwang-Youn A Kim, Ruth E Swiderski, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 23, 2009
Visual impairment in the absence of dystroglycanJakob S Satz, Alisdair R Philp, Huy Nguyen, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 23, 2007
A knockin mouse model of the Bardet-Biedl syndrome 1 M390R mutation has cilia defects, ventriculomegaly, retinopathy, and obesityRoger E Davis, Ruth E Swiderski, Kamal Rahmouni, et al.
Pageof 2

Showing results (1-10 of 11) with videos related to

Sort By:
Pageof 2
Vision Research|September 11, 2007
Visual function testing: a quantifiable visually guided behavior in miceStewart Thompson, Alisdair R Philp, Edwin M Stone
Investigative Ophthalmology & Visual Science|June 3, 2008
Divergent phenotypes of vision and accessory visual function in mice with visual cycle dysfunction (Rpe65 rd12) or retinal degeneration (rd/rd)Stewart Thompson, Robert F Mullins, Alisdair R Philp, et al.
Brain Research. Molecular Brain Research|December 19, 2002
Zebrafish melanopsin: isolation, tissue localisation and phylogenetic positionJames Bellingham, David Whitmore, Alisdair R Philp, et al.
Molecular Vision|January 7, 2005
Genetic analysis of oculocutaneous albinism type 1 (OCA1) in Indian families: two novel frameshift mutations in the TYR GenePeriasamy Sundaresan, Asim Kumar Sil, Alisdair R Philp, et al.
Human Mutation|February 2, 2010
Bardet-Biedl syndrome in Denmark--report of 13 novel sequence variations in six genesTina Duelund Hjortshøj, Karen Grønskov, Alisdair R Philp, et al.
American Journal of Medical Genetics. Part A|January 19, 2008
Novel mutations in BBS5 highlight the importance of this gene in non-Caucasian Bardet-Biedl syndrome patientsTina Duelund Hjortshøj, Karen Grønskov, Alisdair R Philp, et al.
Genomics|August 30, 2006
Identical mutation in a novel retinal gene causes progressive rod-cone degeneration in dogs and retinitis pigmentosa in humansBarbara Zangerl, Orly Goldstein, Alisdair R Philp, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 20, 2006
Regulation of gene expression in the mammalian eye and its relevance to eye diseaseTodd E Scheetz, Kwang-Youn A Kim, Ruth E Swiderski, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|October 23, 2009
Visual impairment in the absence of dystroglycanJakob S Satz, Alisdair R Philp, Huy Nguyen, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 23, 2007
A knockin mouse model of the Bardet-Biedl syndrome 1 M390R mutation has cilia defects, ventriculomegaly, retinopathy, and obesityRoger E Davis, Ruth E Swiderski, Kamal Rahmouni, et al.
Pageof 2