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M M Humphries

Showing results (11-20 of 35) with videos related to

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Genomics|October 1, 1989
Autosomal dominant retinitis pigmentosa: exclusion of a gene from extensive regions of chromosomes 6, 13, 20, and 21G J Farrar, P McWilliam, E M Sharp, et al.
Genomics|November 1, 1992
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.
Journal of Evolutionary Biology|April 8, 2015
Post-weaning parental care increases fitness but is not heritable in North American red squirrelsJ E Lane, A G McAdam, A Charmantier, et al.
American Journal of Human Genetics|March 1, 1992
Autosomal dominant retinitis pigmentosa (adRP; RP6): cosegregation of RP6 and the peripherin-RDS locus in a late-onset family of Irish originS A Jordan, G J Farrar, R Kumar-Singh, et al.
Human Mutation|January 15, 1999
A novel mutation within the rhodopsin gene (Thr-94-Ile) causing autosomal dominant congenital stationary night blindnessN al-Jandal, G J Farrar, A S Kiang, et al.
Ecology Letters|March 20, 2020
Optimisation of energetic and reproductive gains explains behavioural responses to environmental variation across seasons and yearsE K Studd, A K Menzies, E R Siracusa, et al.
Nature|December 12, 1991
A three-base-pair deletion in the peripherin-RDS gene in one form of retinitis pigmentosaG J Farrar, P Kenna, S A Jordan, et al.
Genomics|December 1, 1991
Autosomal dominant retinitis pigmentosa: localization of a disease gene (RP6) to the short arm of chromosome 6G J Farrar, S A Jordan, P Kenna, et al.
Journal of Evolutionary Biology|January 25, 2012
Low heritabilities, but genetic and maternal correlations between red squirrel behavioursRyan W Taylor, A K Boon, B Dantzer, et al.
Experimental Eye Research|September 7, 2000
Apoptotic photoreceptor death in the rhodopsin knockout mouse in the presence and absence of c-fosA H Hobson, M Donovan, M M Humphries, et al.
Pageof 4

Showing results (11-20 of 35) with videos related to

Sort By:
Pageof 4
Genomics|October 1, 1989
Autosomal dominant retinitis pigmentosa: exclusion of a gene from extensive regions of chromosomes 6, 13, 20, and 21G J Farrar, P McWilliam, E M Sharp, et al.
Genomics|November 1, 1992
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.
Journal of Evolutionary Biology|April 8, 2015
Post-weaning parental care increases fitness but is not heritable in North American red squirrelsJ E Lane, A G McAdam, A Charmantier, et al.
American Journal of Human Genetics|March 1, 1992
Autosomal dominant retinitis pigmentosa (adRP; RP6): cosegregation of RP6 and the peripherin-RDS locus in a late-onset family of Irish originS A Jordan, G J Farrar, R Kumar-Singh, et al.
Human Mutation|January 15, 1999
A novel mutation within the rhodopsin gene (Thr-94-Ile) causing autosomal dominant congenital stationary night blindnessN al-Jandal, G J Farrar, A S Kiang, et al.
Ecology Letters|March 20, 2020
Optimisation of energetic and reproductive gains explains behavioural responses to environmental variation across seasons and yearsE K Studd, A K Menzies, E R Siracusa, et al.
Nature|December 12, 1991
A three-base-pair deletion in the peripherin-RDS gene in one form of retinitis pigmentosaG J Farrar, P Kenna, S A Jordan, et al.
Genomics|December 1, 1991
Autosomal dominant retinitis pigmentosa: localization of a disease gene (RP6) to the short arm of chromosome 6G J Farrar, S A Jordan, P Kenna, et al.
Journal of Evolutionary Biology|January 25, 2012
Low heritabilities, but genetic and maternal correlations between red squirrel behavioursRyan W Taylor, A K Boon, B Dantzer, et al.
Experimental Eye Research|September 7, 2000
Apoptotic photoreceptor death in the rhodopsin knockout mouse in the presence and absence of c-fosA H Hobson, M Donovan, M M Humphries, et al.
Pageof 4