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R A Lewis

Showing results (331-340 of 381) with videos related to

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American Journal of Human Genetics|April 16, 1998
Mutations in CYP1B1, the gene for cytochrome P4501B1, are the predominant cause of primary congenital glaucoma in Saudi ArabiaB A Bejjani, R A Lewis, K F Tomey, et al.
Human Molecular Genetics|October 9, 2001
A recurrent deletion in the ubiquitously expressed NEMO (IKK-gamma) gene accounts for the vast majority of incontinentia pigmenti mutationsS Aradhya, H Woffendin, T Jakins, et al.
Neurology|March 14, 2007
CMT1X phenotypes represent loss of GJB1 gene functionM E Shy, C Siskind, E R Swan, et al.
Ophthalmology|January 1, 1989
A comparison of the ocular hypotensive efficacy of once-daily and twice-daily levobunolol treatmentS I Rakofsky, S Melamed, J S Cohen, et al.
Optics Express|June 13, 2014
Raman scattering reveals strong LO-phonon-hole-plasmon coupling in nominally undoped GaAsBi: optical determination of carrier concentrationJ A Steele, R A Lewis, M Henini, et al.
Blood|May 16, 1998
Membrane phospholipid asymmetry in human thalassemiaF A Kuypers, J Yuan, R A Lewis, et al.
Diabetes|October 1, 1982
Retinopathy in juvenile-onset type I diabetes of short durationR N Frank, W H Hoffman, M J Podgor, et al.
Ophthalmology|January 1, 1980
Retinopathy in juvenile-onset diabetes of short durationR N Frank, W H Hoffman, M J Podgor, et al.
American Journal of Human Genetics|December 1, 1994
Analysis of HLA and disease susceptibility: chromosome 6 genes and sex influence long-QT phenotypeL R Weitkamp, A J Moss, R A Lewis, et al.
The New England Journal of Medicine|May 9, 1985
Effect of dietary enrichment with eicosapentaenoic and docosahexaenoic acids on in vitro neutrophil and monocyte leukotriene generation and neutrophil functionT H Lee, R L Hoover, J D Williams, et al.
Pageof 39

Showing results (331-340 of 381) with videos related to

Sort By:
Pageof 39
American Journal of Human Genetics|April 16, 1998
Mutations in CYP1B1, the gene for cytochrome P4501B1, are the predominant cause of primary congenital glaucoma in Saudi ArabiaB A Bejjani, R A Lewis, K F Tomey, et al.
Human Molecular Genetics|October 9, 2001
A recurrent deletion in the ubiquitously expressed NEMO (IKK-gamma) gene accounts for the vast majority of incontinentia pigmenti mutationsS Aradhya, H Woffendin, T Jakins, et al.
Neurology|March 14, 2007
CMT1X phenotypes represent loss of GJB1 gene functionM E Shy, C Siskind, E R Swan, et al.
Ophthalmology|January 1, 1989
A comparison of the ocular hypotensive efficacy of once-daily and twice-daily levobunolol treatmentS I Rakofsky, S Melamed, J S Cohen, et al.
Optics Express|June 13, 2014
Raman scattering reveals strong LO-phonon-hole-plasmon coupling in nominally undoped GaAsBi: optical determination of carrier concentrationJ A Steele, R A Lewis, M Henini, et al.
Blood|May 16, 1998
Membrane phospholipid asymmetry in human thalassemiaF A Kuypers, J Yuan, R A Lewis, et al.
Diabetes|October 1, 1982
Retinopathy in juvenile-onset type I diabetes of short durationR N Frank, W H Hoffman, M J Podgor, et al.
Ophthalmology|January 1, 1980
Retinopathy in juvenile-onset diabetes of short durationR N Frank, W H Hoffman, M J Podgor, et al.
American Journal of Human Genetics|December 1, 1994
Analysis of HLA and disease susceptibility: chromosome 6 genes and sex influence long-QT phenotypeL R Weitkamp, A J Moss, R A Lewis, et al.
The New England Journal of Medicine|May 9, 1985
Effect of dietary enrichment with eicosapentaenoic and docosahexaenoic acids on in vitro neutrophil and monocyte leukotriene generation and neutrophil functionT H Lee, R L Hoover, J D Williams, et al.
Pageof 39