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J McKinlay

Showing results (61-70 of 112) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|September 12, 2018
mRNA vaccination with charge-altering releasable transporters elicits human T cell responses and cures established tumors in miceOle A W Haabeth, Timothy R Blake, Colin J McKinlay, et al.
Journal of Medical Genetics|January 20, 2004
Isolated Robin sequence associated with a balanced t(2;17) chromosomal translocationN Jamshidi, I Macciocca, P A Dargaville, et al.
Familial Cancer|October 24, 2003
Profuse familial adenomatous polyposis with an adenomatous polyposis coli exon 3 mutationS Nasioulas, I T Jones, D J St John, et al.
ACS Central Science|November 10, 2018
Delivery of Inorganic Polyphosphate into Cells Using Amphipathic Oligocarbonate TransportersGabriella M Fernandes-Cunha, Colin J McKinlay, Jessica R Vargas, et al.
Experimental Physiology|July 2, 2025
Individuals with persisting post-concussion symptoms with physiological subtype demonstrate altered cardiovascular and autonomic responses to face coolingPhillip J Wallace, Steve Lidstone, Josh G Nowlan, et al.
Deutsche Medizinische Wochenschrift (1946)|February 19, 2011
[Medical decision making in symptoms of type 2 diabetes mellitus in general practice]W de Cruppé, O von dem Knesebeck, E Gerstenberger, et al.
Brain : a Journal of Neurology|March 5, 2004
Dominantly inherited ataxia and dysphonia with dentate calcification: spinocerebellar ataxia type 20Melanie A Knight, R J McKinlay Gardner, Melanie Bahlo, et al.
BMC Medical Genetics|May 10, 2005
Molecular breakpoint cloning and gene expression studies of a novel translocation t(4;15)(q27;q11.2) associated with Prader-Willi syndromeBirgitt Schüle, Mohammed Albalwi, Emma Northrop, et al.
Human Molecular Genetics|June 13, 1998
Reduced collagen VI causes Bethlem myopathy: a heterozygous COL6A1 nonsense mutation results in mRNA decay and functional haploinsufficiencyS R Lamandé, J F Bateman, W Hutchison, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|March 31, 2020
Having caregiving responsibilities affects management of fragility fractures and bone healthJ E M Sale, L Frankel, J Paiva, et al.
Pageof 12

Showing results (61-70 of 112) with videos related to

Sort By:
Pageof 12
Proceedings of the National Academy of Sciences of the United States of America|September 12, 2018
mRNA vaccination with charge-altering releasable transporters elicits human T cell responses and cures established tumors in miceOle A W Haabeth, Timothy R Blake, Colin J McKinlay, et al.
Journal of Medical Genetics|January 20, 2004
Isolated Robin sequence associated with a balanced t(2;17) chromosomal translocationN Jamshidi, I Macciocca, P A Dargaville, et al.
Familial Cancer|October 24, 2003
Profuse familial adenomatous polyposis with an adenomatous polyposis coli exon 3 mutationS Nasioulas, I T Jones, D J St John, et al.
ACS Central Science|November 10, 2018
Delivery of Inorganic Polyphosphate into Cells Using Amphipathic Oligocarbonate TransportersGabriella M Fernandes-Cunha, Colin J McKinlay, Jessica R Vargas, et al.
Experimental Physiology|July 2, 2025
Individuals with persisting post-concussion symptoms with physiological subtype demonstrate altered cardiovascular and autonomic responses to face coolingPhillip J Wallace, Steve Lidstone, Josh G Nowlan, et al.
Deutsche Medizinische Wochenschrift (1946)|February 19, 2011
[Medical decision making in symptoms of type 2 diabetes mellitus in general practice]W de Cruppé, O von dem Knesebeck, E Gerstenberger, et al.
Brain : a Journal of Neurology|March 5, 2004
Dominantly inherited ataxia and dysphonia with dentate calcification: spinocerebellar ataxia type 20Melanie A Knight, R J McKinlay Gardner, Melanie Bahlo, et al.
BMC Medical Genetics|May 10, 2005
Molecular breakpoint cloning and gene expression studies of a novel translocation t(4;15)(q27;q11.2) associated with Prader-Willi syndromeBirgitt Schüle, Mohammed Albalwi, Emma Northrop, et al.
Human Molecular Genetics|June 13, 1998
Reduced collagen VI causes Bethlem myopathy: a heterozygous COL6A1 nonsense mutation results in mRNA decay and functional haploinsufficiencyS R Lamandé, J F Bateman, W Hutchison, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|March 31, 2020
Having caregiving responsibilities affects management of fragility fractures and bone healthJ E M Sale, L Frankel, J Paiva, et al.
Pageof 12