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K Vass

Showing results (81-90 of 99) with videos related to

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Arteriosclerosis, Thrombosis, and Vascular Biology|August 1, 1995
Independent mutations at codon 3500 of the apolipoprotein B gene are associated with hyperlipidemiaD Gaffney, J M Reid, I M Cameron, et al.
Nucleic Acids Research|August 11, 1980
Repetitive DNA sequences near three human beta-type globin genesL W Coggins, G J Grindlay, J K Vass, et al.
Neuron|March 1, 2016
Oscillations Go the Distance: Low-Frequency Human Hippocampal Oscillations Code Spatial Distance in the Absence of Sensory Cues during TeleportationLindsay K Vass, Milagros S Copara, Masud Seyal, et al.
Progress in Clinical and Biological Research|January 1, 1985
Distant sequences which regulate globin genesJ Paul, M Allan, S Gilmour, et al.
European Journal of Neurology|January 27, 2010
Decision-making for and impact of early immunomodulatory treatment: the Austrian Clinically Isolated Syndrome Study (ACISS)F Fazekas, U Baumhackl, T Berger, et al.
Oncogene|December 5, 2000
Regulation of a multigenic invasion programme by the transcription factor, AP-1: re-expression of a down-regulated gene, TSC-36, inhibits invasionI M Johnston, H J Spence, J N Winnie, et al.
Neurology|October 26, 2005
Inclusion body myopathy and Paget disease is linked to a novel mutation in the VCP geneD Haubenberger, R E Bittner, S Rauch-Shorny, et al.
Fertility and Sterility|October 3, 1998
No evidence of the inactivating mutation (C566T) in the follicle-stimulating hormone receptor gene in Brazilian women with premature ovarian failureM B da Fonte Kohek, M C Batista, A J Russell, et al.
Scottish Medical Journal|December 26, 2009
Two novel mutations causing familial benign hypocalciuric hypercalcaemia in three Scottish familiesJ Hinnie, J K Vass, E Rolfe, et al.
Journal of Molecular Endocrinology|October 1, 1995
The human 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) gene cluster on chromosome 1p13 contains a presumptive pseudogene; 3 beta-HSD and CYP17 do not segregate with dominantly inherited hirsutismM W McBride, A J Russell, K Vass, et al.
Pageof 10

Showing results (81-90 of 99) with videos related to

Sort By:
Pageof 10
Arteriosclerosis, Thrombosis, and Vascular Biology|August 1, 1995
Independent mutations at codon 3500 of the apolipoprotein B gene are associated with hyperlipidemiaD Gaffney, J M Reid, I M Cameron, et al.
Nucleic Acids Research|August 11, 1980
Repetitive DNA sequences near three human beta-type globin genesL W Coggins, G J Grindlay, J K Vass, et al.
Neuron|March 1, 2016
Oscillations Go the Distance: Low-Frequency Human Hippocampal Oscillations Code Spatial Distance in the Absence of Sensory Cues during TeleportationLindsay K Vass, Milagros S Copara, Masud Seyal, et al.
Progress in Clinical and Biological Research|January 1, 1985
Distant sequences which regulate globin genesJ Paul, M Allan, S Gilmour, et al.
European Journal of Neurology|January 27, 2010
Decision-making for and impact of early immunomodulatory treatment: the Austrian Clinically Isolated Syndrome Study (ACISS)F Fazekas, U Baumhackl, T Berger, et al.
Oncogene|December 5, 2000
Regulation of a multigenic invasion programme by the transcription factor, AP-1: re-expression of a down-regulated gene, TSC-36, inhibits invasionI M Johnston, H J Spence, J N Winnie, et al.
Neurology|October 26, 2005
Inclusion body myopathy and Paget disease is linked to a novel mutation in the VCP geneD Haubenberger, R E Bittner, S Rauch-Shorny, et al.
Fertility and Sterility|October 3, 1998
No evidence of the inactivating mutation (C566T) in the follicle-stimulating hormone receptor gene in Brazilian women with premature ovarian failureM B da Fonte Kohek, M C Batista, A J Russell, et al.
Scottish Medical Journal|December 26, 2009
Two novel mutations causing familial benign hypocalciuric hypercalcaemia in three Scottish familiesJ Hinnie, J K Vass, E Rolfe, et al.
Journal of Molecular Endocrinology|October 1, 1995
The human 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) gene cluster on chromosome 1p13 contains a presumptive pseudogene; 3 beta-HSD and CYP17 do not segregate with dominantly inherited hirsutismM W McBride, A J Russell, K Vass, et al.
Pageof 10