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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 Models
Jacob 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 thrombolysis
David 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 studies
A 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 brain
J D Wood, J C MacMillan, P S Harper, et al.
Applied Optics
|
February 23, 2010
Gallium arsenide laser-array-on-silicon package
J 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 marker
O 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 genotoxicity
Marc 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 specialists
Daniel 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 dystrophy
P S Harper, T O'Brien, J M Murray, et al.
Clinical Genetics
|
November 1, 1982
Mannosidosis in two brothers: prolonged survival in the severe phenotype
M A Patton, I C Barnes, I D Young, et al.
Page
of 123
Search research articles
Search
Showing results (521-530 of 1,225) with videos related to
Sort By:
Page
of 123
Gels (Basel, Switzerland)
|
June 27, 2023
Developing Biomimetic Hydrogels of the Arterial Wall as a Prothrombotic Substrate for In Vitro Human Thrombosis Models
Jacob 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 thrombolysis
David 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 studies
A 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 brain
J D Wood, J C MacMillan, P S Harper, et al.
Applied Optics
|
February 23, 2010
Gallium arsenide laser-array-on-silicon package
J 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 marker
O 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 genotoxicity
Marc 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 specialists
Daniel 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 dystrophy
P S Harper, T O'Brien, J M Murray, et al.
Clinical Genetics
|
November 1, 1982
Mannosidosis in two brothers: prolonged survival in the severe phenotype
M A Patton, I C Barnes, I D Young, et al.
Page
of 123