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G Cole

Showing results (611-620 of 805) with videos related to

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BMC Family Practice|April 21, 2005
Psychiatric outpatient consultation for seniors. Perspectives of family physicians, consultants, and patients/family: a descriptive studyMark J Yaffe, Francois Primeau, Jane McCusker, et al.
Molecular Biology of the Cell|June 10, 2005
Mutant kinesin-2 motor subunits increase chromosome lossMark S Miller, Jessica M Esparza, Andrew M Lippa, et al.
Journal of Lipid Research|May 1, 1999
Known mutations of apoB account for only a small minority of hypobetalipoproteinemiaJ Wu, J Kim, Q Li, et al.
Optics Express|October 1, 2008
Three-dimensional parallel holographic micropatterning using a spatial light modulatorNathan J Jenness, Kurt D Wulff, Matthew S Johannes, et al.
The American Journal of Clinical Nutrition|February 1, 1992
Insulin-like growth factor I and low-density-lipoprotein cholesterol in women during high- and low-fat feedingT E Prewitt, T G Unterman, R Glick, et al.
Human Mutation|November 16, 2005
Multiple epiphyseal dysplasia mutations in MATN3 cause misfolding of the A-domain and prevent secretion of mutant matrilin-3Sally L Cotterill, Gail C Jackson, Matthew P Leighton, et al.
Genomics|October 1, 1992
A random STS strategy for construction of YAC contigs spanning defined chromosomal regionsC G Cole, I Dunham, A J Coffey, et al.
Skin Research and Technology : Official Journal of International Society for Bioengineering and the Skin (ISBS) [And] International Society for Digital Imaging of Skin (ISDIS) [And] International Society for Skin Imaging (ISSI)|March 27, 2015
Real-time supervised detection of pink areas in dermoscopic images of melanoma: importance of color shades, texture and locationR Kaur, P P Albano, J G Cole, et al.
Journal of Advanced Nursing|June 5, 2009
Type 1 diabetes: children and adolescents' knowledge and questionsSusanne Olsen Roper, Amanda Call, Joan Leishman, et al.
American Journal of Medical Genetics|September 13, 2000
Rapid determination of COL2A1 mutations in individuals with Stickler syndrome: analysis of potential premature termination codonsD J Wilkin, R Liberfarb, J Davis, et al.
Pageof 81

Showing results (611-620 of 805) with videos related to

Sort By:
Pageof 81
BMC Family Practice|April 21, 2005
Psychiatric outpatient consultation for seniors. Perspectives of family physicians, consultants, and patients/family: a descriptive studyMark J Yaffe, Francois Primeau, Jane McCusker, et al.
Molecular Biology of the Cell|June 10, 2005
Mutant kinesin-2 motor subunits increase chromosome lossMark S Miller, Jessica M Esparza, Andrew M Lippa, et al.
Journal of Lipid Research|May 1, 1999
Known mutations of apoB account for only a small minority of hypobetalipoproteinemiaJ Wu, J Kim, Q Li, et al.
Optics Express|October 1, 2008
Three-dimensional parallel holographic micropatterning using a spatial light modulatorNathan J Jenness, Kurt D Wulff, Matthew S Johannes, et al.
The American Journal of Clinical Nutrition|February 1, 1992
Insulin-like growth factor I and low-density-lipoprotein cholesterol in women during high- and low-fat feedingT E Prewitt, T G Unterman, R Glick, et al.
Human Mutation|November 16, 2005
Multiple epiphyseal dysplasia mutations in MATN3 cause misfolding of the A-domain and prevent secretion of mutant matrilin-3Sally L Cotterill, Gail C Jackson, Matthew P Leighton, et al.
Genomics|October 1, 1992
A random STS strategy for construction of YAC contigs spanning defined chromosomal regionsC G Cole, I Dunham, A J Coffey, et al.
Skin Research and Technology : Official Journal of International Society for Bioengineering and the Skin (ISBS) [And] International Society for Digital Imaging of Skin (ISDIS) [And] International Society for Skin Imaging (ISSI)|March 27, 2015
Real-time supervised detection of pink areas in dermoscopic images of melanoma: importance of color shades, texture and locationR Kaur, P P Albano, J G Cole, et al.
Journal of Advanced Nursing|June 5, 2009
Type 1 diabetes: children and adolescents' knowledge and questionsSusanne Olsen Roper, Amanda Call, Joan Leishman, et al.
American Journal of Medical Genetics|September 13, 2000
Rapid determination of COL2A1 mutations in individuals with Stickler syndrome: analysis of potential premature termination codonsD J Wilkin, R Liberfarb, J Davis, et al.
Pageof 81