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P Humphries

Showing results (41-50 of 156) with videos related to

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Human Mutation|January 1, 1992
Polymorphic variation within "conserved" sequences at the 3' end of the human RDS gene which results in amino acid substitutionsS A Jordan, G J Farrar, P Kenna, et al.
Visual Neuroscience|June 15, 1999
The electroretinogram of the rhodopsin knockout mouseK Toda, R A Bush, P Humphries, et al.
The Biochemical Journal|January 1, 1988
Long-term dosing studies using mutagenic carcinogens indicate a highly significant correlation between elevations in the level of rat glutathione S-transferase P messenger RNA and liver tumours of hepatocellular originS E Russell, C Pearson, M Kelly, et al.
Nucleic Acids Research|October 25, 1991
Poly (T/A) polymorphism at the human retinal degeneration slow (RDS) locusR Kumar-Singh, S A Jordan, G J Farrar, et al.
Journal of Computer Assisted Tomography|February 1, 1981
Posterior fossa hemorrhages in the newbornG Scotti, O Flodmark, D C Harwood-Nash, et al.
Journal of Medical Genetics|February 25, 1998
Lack of evidence for genetic heterogeneity in Best vitelliform macular dystrophyF Mansergh, T Meitinger, G Rodolph, et al.
Genomics|January 1, 1993
Evidence for further genetic heterogeneity in autosomal dominant retinitis pigmentosaR Kumar-Singh, P F Kenna, G J Farrar, et al.
Molecular & General Genetics : MGG|January 1, 1983
Isolation of a polymorphic DNA segment unique to human chromosome 7 by molecular cloning of hybrid cell DNAP Humphries, D Barton, A M McKay, et al.
American Journal of Human Genetics|August 1, 1993
Evidence against a second autosomal dominant retinitis pigmentosa locus close to rhodopsin on chromosome 3qC Inglehearn, J Farrar, M Denton, et al.
Experimental Eye Research|April 29, 2006
Aberrant retinal tight junction and adherens junction protein expression in an animal model of autosomal dominant Retinitis pigmentosa: the Rho(-/-) mouseM Campbell, M Humphries, A Kennan, et al.
Pageof 16

Showing results (41-50 of 156) with videos related to

Sort By:
Pageof 16
Human Mutation|January 1, 1992
Polymorphic variation within "conserved" sequences at the 3' end of the human RDS gene which results in amino acid substitutionsS A Jordan, G J Farrar, P Kenna, et al.
Visual Neuroscience|June 15, 1999
The electroretinogram of the rhodopsin knockout mouseK Toda, R A Bush, P Humphries, et al.
The Biochemical Journal|January 1, 1988
Long-term dosing studies using mutagenic carcinogens indicate a highly significant correlation between elevations in the level of rat glutathione S-transferase P messenger RNA and liver tumours of hepatocellular originS E Russell, C Pearson, M Kelly, et al.
Nucleic Acids Research|October 25, 1991
Poly (T/A) polymorphism at the human retinal degeneration slow (RDS) locusR Kumar-Singh, S A Jordan, G J Farrar, et al.
Journal of Computer Assisted Tomography|February 1, 1981
Posterior fossa hemorrhages in the newbornG Scotti, O Flodmark, D C Harwood-Nash, et al.
Journal of Medical Genetics|February 25, 1998
Lack of evidence for genetic heterogeneity in Best vitelliform macular dystrophyF Mansergh, T Meitinger, G Rodolph, et al.
Genomics|January 1, 1993
Evidence for further genetic heterogeneity in autosomal dominant retinitis pigmentosaR Kumar-Singh, P F Kenna, G J Farrar, et al.
Molecular & General Genetics : MGG|January 1, 1983
Isolation of a polymorphic DNA segment unique to human chromosome 7 by molecular cloning of hybrid cell DNAP Humphries, D Barton, A M McKay, et al.
American Journal of Human Genetics|August 1, 1993
Evidence against a second autosomal dominant retinitis pigmentosa locus close to rhodopsin on chromosome 3qC Inglehearn, J Farrar, M Denton, et al.
Experimental Eye Research|April 29, 2006
Aberrant retinal tight junction and adherens junction protein expression in an animal model of autosomal dominant Retinitis pigmentosa: the Rho(-/-) mouseM Campbell, M Humphries, A Kennan, et al.
Pageof 16