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P Kenna

Showing results (41-50 of 80) with videos related to

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Human Molecular Genetics|June 17, 1999
Structural and functional rescue of murine rod photoreceptors by human rhodopsin transgeneN McNally, P Kenna, M M Humphries, et al.
American Journal of Human Genetics|April 1, 1989
Autosomal dominant retinitis pigmentosa: exclusion of the gene from the short arm of chromosome 1 including the region surrounding the rhesus locusD G Bradley, G J Farrar, E M Sharp, et al.
Genomics|December 1, 1991
Autosomal dominant retinitis pigmentosa: a mutation in codon 178 of the rhodopsin gene in two families of Celtic originG J Farrar, P Kenna, R Redmond, et al.
American Journal of Human Genetics|December 1, 1990
Autosomal dominant retinitis pigmentosa: absence of the rhodopsin proline----histidine substitution (codon 23) in pedigrees from EuropeG J Farrar, P Kenna, R Redmond, et al.
Genomics|July 1, 1990
Epidermolysis bullosa: evidence for linkage to genetic markers on chromosome 1 in a family with the autosomal dominant simplex formM M Humphries, D Sheils, M Lawler, et al.
Genomics|October 1, 1989
Autosomal dominant retinitis pigmentosa (ADRP): localization of an ADRP gene to the long arm of chromosome 3P McWilliam, G J Farrar, P Kenna, et al.
Genomics|September 1, 1990
Autosomal dominant retinitis pigmentosa: linkage to rhodopsin and evidence for genetic heterogeneityG J Farrar, P McWilliam, D G Bradley, et al.
Nature Genetics|May 1, 1993
Localization of an autosomal dominant retinitis pigmentosa gene to chromosome 7qS A Jordan, G J Farrar, P Kenna, et al.
Journal of Medical Genetics|July 25, 2013
Delineating the genetic heterogeneity of ALS using targeted high-throughput sequencingKevin P Kenna, Russell L McLaughlin, Susan Byrne, et al.
Visual Neuroscience|August 11, 2001
Comparative structural and functional analysis of photoreceptor neurons of Rho-/- mice reveal increased survival on C57BL/6J in comparison to 129Sv genetic backgroundM M Humphries, S Kiang, N McNally, et al.
Pageof 8

Showing results (41-50 of 80) with videos related to

Sort By:
Pageof 8
Human Molecular Genetics|June 17, 1999
Structural and functional rescue of murine rod photoreceptors by human rhodopsin transgeneN McNally, P Kenna, M M Humphries, et al.
American Journal of Human Genetics|April 1, 1989
Autosomal dominant retinitis pigmentosa: exclusion of the gene from the short arm of chromosome 1 including the region surrounding the rhesus locusD G Bradley, G J Farrar, E M Sharp, et al.
Genomics|December 1, 1991
Autosomal dominant retinitis pigmentosa: a mutation in codon 178 of the rhodopsin gene in two families of Celtic originG J Farrar, P Kenna, R Redmond, et al.
American Journal of Human Genetics|December 1, 1990
Autosomal dominant retinitis pigmentosa: absence of the rhodopsin proline----histidine substitution (codon 23) in pedigrees from EuropeG J Farrar, P Kenna, R Redmond, et al.
Genomics|July 1, 1990
Epidermolysis bullosa: evidence for linkage to genetic markers on chromosome 1 in a family with the autosomal dominant simplex formM M Humphries, D Sheils, M Lawler, et al.
Genomics|October 1, 1989
Autosomal dominant retinitis pigmentosa (ADRP): localization of an ADRP gene to the long arm of chromosome 3P McWilliam, G J Farrar, P Kenna, et al.
Genomics|September 1, 1990
Autosomal dominant retinitis pigmentosa: linkage to rhodopsin and evidence for genetic heterogeneityG J Farrar, P McWilliam, D G Bradley, et al.
Nature Genetics|May 1, 1993
Localization of an autosomal dominant retinitis pigmentosa gene to chromosome 7qS A Jordan, G J Farrar, P Kenna, et al.
Journal of Medical Genetics|July 25, 2013
Delineating the genetic heterogeneity of ALS using targeted high-throughput sequencingKevin P Kenna, Russell L McLaughlin, Susan Byrne, et al.
Visual Neuroscience|August 11, 2001
Comparative structural and functional analysis of photoreceptor neurons of Rho-/- mice reveal increased survival on C57BL/6J in comparison to 129Sv genetic backgroundM M Humphries, S Kiang, N McNally, et al.
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