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P Kenna

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

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Nucleic Acids Research|December 25, 1991
A sequence polymorphism in the human peripherin/RDS geneG J Farrar, P Kenna, S A Jordan, et al.
Lancet (London, England)|November 29, 1975
Letter: Escherichia coli K1C J Bacon, A P Kenna, H R Ingham, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 1, 1991
Ocular findings associated with a rhodopsin gene codon 58 transversion mutation in autosomal dominant retinitis pigmentosaG A Fishman, E M Stone, L D Gilbert, et al.
Human Molecular Genetics|July 1, 1993
Exclusion of the involvement of all known retinitis pigmentosa loci in the disease present in a family of Irish origin provides evidence for a sixth autosomal dominant locus (RP8)R Kumar-Singh, G J Farrar, F Mansergh, et al.
Human Molecular Genetics|December 1, 1992
Autosomal dominant retinitis pigmentosa: a novel mutation in the rhodopsin gene in the original 3q linked familyG J Farrar, J B Findlay, R Kumar-Singh, et al.
Human Molecular Genetics|September 1, 1992
Autosomal dominant retinitis pigmentosa (adRP): exclusion of a gene from three mapped loci provides evidence for the existence of a fourth locusS A Jordan, T del Rio, N Soriano, et al.
The British Journal of Ophthalmology|March 1, 1997
Clinical and molecular genetic characterisation of a family segregating autosomal dominant retinitis pigmentosa and sensorineural deafnessP Kenna, F Mansergh, S Millington-Ward, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 4, 2018
Transcription factor Pebbled/RREB1 regulates injury-induced axon degenerationJonathan E Farley, Thomas C Burdett, Romina Barria, et al.
Current Opinion in Neurology|August 3, 2021
Advances in the genetic classification of amyotrophic lateral sclerosisJohnathan Cooper-Knock, Calum Harvey, Sai Zhang, et al.
Genomics|February 1, 1993
Autosomal dominant retinitis pigmentosa: a novel mutation at the peripherin/RDS locus in the original 6p-linked pedigreeG J Farrar, P Kenna, S A Jordan, et al.
Pageof 8

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

Sort By:
Pageof 8
Nucleic Acids Research|December 25, 1991
A sequence polymorphism in the human peripherin/RDS geneG J Farrar, P Kenna, S A Jordan, et al.
Lancet (London, England)|November 29, 1975
Letter: Escherichia coli K1C J Bacon, A P Kenna, H R Ingham, et al.
Archives of Ophthalmology (Chicago, Ill. : 1960)|October 1, 1991
Ocular findings associated with a rhodopsin gene codon 58 transversion mutation in autosomal dominant retinitis pigmentosaG A Fishman, E M Stone, L D Gilbert, et al.
Human Molecular Genetics|July 1, 1993
Exclusion of the involvement of all known retinitis pigmentosa loci in the disease present in a family of Irish origin provides evidence for a sixth autosomal dominant locus (RP8)R Kumar-Singh, G J Farrar, F Mansergh, et al.
Human Molecular Genetics|December 1, 1992
Autosomal dominant retinitis pigmentosa: a novel mutation in the rhodopsin gene in the original 3q linked familyG J Farrar, J B Findlay, R Kumar-Singh, et al.
Human Molecular Genetics|September 1, 1992
Autosomal dominant retinitis pigmentosa (adRP): exclusion of a gene from three mapped loci provides evidence for the existence of a fourth locusS A Jordan, T del Rio, N Soriano, et al.
The British Journal of Ophthalmology|March 1, 1997
Clinical and molecular genetic characterisation of a family segregating autosomal dominant retinitis pigmentosa and sensorineural deafnessP Kenna, F Mansergh, S Millington-Ward, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 4, 2018
Transcription factor Pebbled/RREB1 regulates injury-induced axon degenerationJonathan E Farley, Thomas C Burdett, Romina Barria, et al.
Current Opinion in Neurology|August 3, 2021
Advances in the genetic classification of amyotrophic lateral sclerosisJohnathan Cooper-Knock, Calum Harvey, Sai Zhang, et al.
Genomics|February 1, 1993
Autosomal dominant retinitis pigmentosa: a novel mutation at the peripherin/RDS locus in the original 6p-linked pedigreeG J Farrar, P Kenna, S A Jordan, et al.
Pageof 8