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Showing results (51-60 of 59) with videos related to

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Psychopharmacology|June 20, 2026
The relationship between duration of access to intravenous oxycodone self-administration, economic demand for oxycodone, and cognition in ratsSydney Dick, Amy Heaton, Aaron D Claypool, et al.
Journal of Medical Genetics|February 1, 1996
Clinical features in 27 patients with Angelman syndrome resulting from DNA deletionA Smith, C Wiles, E Haan, et al.
Nature Genetics|August 4, 1999
Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tardaA K Gedeon, A Colley, R Jamieson, et al.
Clinical Genetics|February 22, 2013
Novel mutations of the PRKAR1A gene in patients with acrodysostosisF Muhn, E Klopocki, L Graul-Neumann, et al.
Human Genetics|September 15, 2000
Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHMK L Friend, D Crimmins, T G Phan, et al.
Journal of Medical Genetics|February 21, 2008
Molecular characterisation of SMARCB1 and NF2 in familial and sporadic schwannomatosisK D Hadfield, W G Newman, N L Bowers, et al.
Yeast (Chichester, England)|July 20, 2000
Genome-wide protein interaction screens reveal functional networks involving Sm-like proteinsM Fromont-Racine, A E Mayes, A Brunet-Simon, et al.
Neuromuscular Disorders : NMD|February 5, 2003
Principal mutation hotspot for central core disease and related myopathies in the C-terminal transmembrane region of the RYR1 geneM R Davis, E Haan, H Jungbluth, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 16, 2013
Genotype and clinical care correlations in craniosynostosis: findings from a cohort of 630 Australian and New Zealand patientsT Roscioli, G Elakis, T C Cox, et al.
Pageof 6

Showing results (51-60 of 59) with videos related to

Sort By:
Pageof 6
You have reached the last page of results.This site can display upto 59 results.
Psychopharmacology|June 20, 2026
The relationship between duration of access to intravenous oxycodone self-administration, economic demand for oxycodone, and cognition in ratsSydney Dick, Amy Heaton, Aaron D Claypool, et al.
Journal of Medical Genetics|February 1, 1996
Clinical features in 27 patients with Angelman syndrome resulting from DNA deletionA Smith, C Wiles, E Haan, et al.
Nature Genetics|August 4, 1999
Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tardaA K Gedeon, A Colley, R Jamieson, et al.
Clinical Genetics|February 22, 2013
Novel mutations of the PRKAR1A gene in patients with acrodysostosisF Muhn, E Klopocki, L Graul-Neumann, et al.
Human Genetics|September 15, 2000
Detection of a novel missense mutation and second recurrent mutation in the CACNA1A gene in individuals with EA-2 and FHMK L Friend, D Crimmins, T G Phan, et al.
Journal of Medical Genetics|February 21, 2008
Molecular characterisation of SMARCB1 and NF2 in familial and sporadic schwannomatosisK D Hadfield, W G Newman, N L Bowers, et al.
Yeast (Chichester, England)|July 20, 2000
Genome-wide protein interaction screens reveal functional networks involving Sm-like proteinsM Fromont-Racine, A E Mayes, A Brunet-Simon, et al.
Neuromuscular Disorders : NMD|February 5, 2003
Principal mutation hotspot for central core disease and related myopathies in the C-terminal transmembrane region of the RYR1 geneM R Davis, E Haan, H Jungbluth, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|October 16, 2013
Genotype and clinical care correlations in craniosynostosis: findings from a cohort of 630 Australian and New Zealand patientsT Roscioli, G Elakis, T C Cox, et al.
Pageof 6