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J R Gilbert

Showing results (71-80 of 120) with videos related to

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Organic Letters|May 18, 2000
New diffusion-edited NMR experiments to expedite the dereplication of known compounds from natural product mixturesR T Williamson, E L Chapin, A W Carr, et al.
American Journal of Medical Genetics|May 16, 2001
De novo partial duplication of chromosome 7p in a male with autistic disorderC M Wolpert, S L Donnelly, M L Cuccaro, et al.
Autism Research : Official Journal of the International Society for Autism Research|April 11, 2009
Examination of association to autism of common genetic variationin genes related to dopamineB M Anderson, N Schnetz-Boutaud, J Bartlett, et al.
Journal of Hypertension|June 1, 1986
Hypertension control in two Canadian communities: evidence for better treatment and overlabellingN J Birkett, C E Evans, R B Haynes, et al.
American Journal of Human Genetics|August 1, 1993
Evidence for heterogeneity in facioscapulohumeral muscular dystrophy (FSHD)J R Gilbert, J M Stajich, S Wall, et al.
Molecular Vision|January 5, 2001
Mutations in corneal carbohydrate sulfotransferase 6 gene (CHST6) cause macular corneal dystrophy in IcelandN P Liu, S Dew-Knight, M Rayner, et al.
Experimental Neurology|February 1, 1994
Hypothesis: microtubule instability and paired helical filament formation in the Alzheimer disease brain are related to apolipoprotein E genotypeW J Strittmatter, K H Weisgraber, M Goedert, et al.
American Journal of Human Genetics|August 1, 1992
Linkage studies in facioscapulohumeral muscular dystrophy (FSHD)J R Gilbert, J M Stajich, M C Speer, et al.
The International Journal of Tuberculosis and Lung Disease : the Official Journal of the International Union Against Tuberculosis and Lung Disease|September 3, 2009
Association of SLC11A1 with tuberculosis and interactions with NOS2A and TLR2 in African-Americans and CaucasiansD R Velez, W F Hulme, J L Myers, et al.
The Journal of Biological Chemistry|June 27, 1997
Interferon-gamma modulates a p53-independent apoptotic pathway and apoptosis-related gene expressionN K Ossina, A Cannas, V C Powers, et al.
Pageof 12

Showing results (71-80 of 120) with videos related to

Sort By:
Pageof 12
Organic Letters|May 18, 2000
New diffusion-edited NMR experiments to expedite the dereplication of known compounds from natural product mixturesR T Williamson, E L Chapin, A W Carr, et al.
American Journal of Medical Genetics|May 16, 2001
De novo partial duplication of chromosome 7p in a male with autistic disorderC M Wolpert, S L Donnelly, M L Cuccaro, et al.
Autism Research : Official Journal of the International Society for Autism Research|April 11, 2009
Examination of association to autism of common genetic variationin genes related to dopamineB M Anderson, N Schnetz-Boutaud, J Bartlett, et al.
Journal of Hypertension|June 1, 1986
Hypertension control in two Canadian communities: evidence for better treatment and overlabellingN J Birkett, C E Evans, R B Haynes, et al.
American Journal of Human Genetics|August 1, 1993
Evidence for heterogeneity in facioscapulohumeral muscular dystrophy (FSHD)J R Gilbert, J M Stajich, S Wall, et al.
Molecular Vision|January 5, 2001
Mutations in corneal carbohydrate sulfotransferase 6 gene (CHST6) cause macular corneal dystrophy in IcelandN P Liu, S Dew-Knight, M Rayner, et al.
Experimental Neurology|February 1, 1994
Hypothesis: microtubule instability and paired helical filament formation in the Alzheimer disease brain are related to apolipoprotein E genotypeW J Strittmatter, K H Weisgraber, M Goedert, et al.
American Journal of Human Genetics|August 1, 1992
Linkage studies in facioscapulohumeral muscular dystrophy (FSHD)J R Gilbert, J M Stajich, M C Speer, et al.
The International Journal of Tuberculosis and Lung Disease : the Official Journal of the International Union Against Tuberculosis and Lung Disease|September 3, 2009
Association of SLC11A1 with tuberculosis and interactions with NOS2A and TLR2 in African-Americans and CaucasiansD R Velez, W F Hulme, J L Myers, et al.
The Journal of Biological Chemistry|June 27, 1997
Interferon-gamma modulates a p53-independent apoptotic pathway and apoptosis-related gene expressionN K Ossina, A Cannas, V C Powers, et al.
Pageof 12