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S Harper

Showing results (521-530 of 1,225) with videos related to

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Gels (Basel, Switzerland)|June 27, 2023
Developing Biomimetic Hydrogels of the Arterial Wall as a Prothrombotic Substrate for In Vitro Human Thrombosis ModelsJacob Ranjbar, Wanjiku Njoroge, Jonathan M Gibbins, et al.
Journal of Thrombosis and Haemostasis : JTH|August 11, 2022
Clot-targeted magnetic hyperthermia permeabilizes blood clots to make them more susceptible to thrombolysisDavid Cabrera, Maneea Eizadi Sharifabad, Jacob A Ranjbar, et al.
Journal of Medical Genetics|December 1, 1986
Duchenne muscular dystrophy with adrenal insufficiency and glycerol kinase deficiency: high resolution cytogenetic analysis with molecular, biochemical, and clinical studiesA Clarke, S H Roberts, N S Thomas, et al.
Human Molecular Genetics|April 1, 1996
Partial characterisation of murine huntingtin and apparent variations in the subcellular localisation of huntingtin in human, mouse and rat brainJ D Wood, J C MacMillan, P S Harper, et al.
Applied Optics|February 23, 2010
Gallium arsenide laser-array-on-silicon packageJ D Crow, L D Comerford, J S Harper, et al.
Lancet (London, England)|June 6, 1987
Exclusion testing for Huntington's disease in pregnancy with a closely linked DNA markerO W Quarrell, A L Meredith, A Tyler, et al.
Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association|August 6, 2009
N-acetyl-glutamic acid: evaluation of acute and 28-day repeated dose oral toxicity and genotoxicityMarc S Harper, Z Amanda Shen, John F Barnett, et al.
The Journal of Pediatrics|March 18, 2014
Yield of skeletal survey by age in children referred to abuse specialistsDaniel M Lindberg, Rachel P Berger, Maegan S Reynolds, et al.
Journal of Medical Genetics|August 1, 1983
The use of linked DNA polymorphisms for genotype prediction in families with Duchenne muscular dystrophyP S Harper, T O'Brien, J M Murray, et al.
Clinical Genetics|November 1, 1982
Mannosidosis in two brothers: prolonged survival in the severe phenotypeM A Patton, I C Barnes, I D Young, et al.
Pageof 123

Showing results (521-530 of 1,225) with videos related to

Sort By:
Pageof 123
Gels (Basel, Switzerland)|June 27, 2023
Developing Biomimetic Hydrogels of the Arterial Wall as a Prothrombotic Substrate for In Vitro Human Thrombosis ModelsJacob Ranjbar, Wanjiku Njoroge, Jonathan M Gibbins, et al.
Journal of Thrombosis and Haemostasis : JTH|August 11, 2022
Clot-targeted magnetic hyperthermia permeabilizes blood clots to make them more susceptible to thrombolysisDavid Cabrera, Maneea Eizadi Sharifabad, Jacob A Ranjbar, et al.
Journal of Medical Genetics|December 1, 1986
Duchenne muscular dystrophy with adrenal insufficiency and glycerol kinase deficiency: high resolution cytogenetic analysis with molecular, biochemical, and clinical studiesA Clarke, S H Roberts, N S Thomas, et al.
Human Molecular Genetics|April 1, 1996
Partial characterisation of murine huntingtin and apparent variations in the subcellular localisation of huntingtin in human, mouse and rat brainJ D Wood, J C MacMillan, P S Harper, et al.
Applied Optics|February 23, 2010
Gallium arsenide laser-array-on-silicon packageJ D Crow, L D Comerford, J S Harper, et al.
Lancet (London, England)|June 6, 1987
Exclusion testing for Huntington's disease in pregnancy with a closely linked DNA markerO W Quarrell, A L Meredith, A Tyler, et al.
Food and Chemical Toxicology : an International Journal Published for the British Industrial Biological Research Association|August 6, 2009
N-acetyl-glutamic acid: evaluation of acute and 28-day repeated dose oral toxicity and genotoxicityMarc S Harper, Z Amanda Shen, John F Barnett, et al.
The Journal of Pediatrics|March 18, 2014
Yield of skeletal survey by age in children referred to abuse specialistsDaniel M Lindberg, Rachel P Berger, Maegan S Reynolds, et al.
Journal of Medical Genetics|August 1, 1983
The use of linked DNA polymorphisms for genotype prediction in families with Duchenne muscular dystrophyP S Harper, T O'Brien, J M Murray, et al.
Clinical Genetics|November 1, 1982
Mannosidosis in two brothers: prolonged survival in the severe phenotypeM A Patton, I C Barnes, I D Young, et al.
Pageof 123