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M E Daly

Showing results (21-30 of 35) with videos related to

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British Journal of Haematology|September 1, 1999
The GPIa C807T dimorphism associated with platelet collagen receptor density is not a risk factor for myocardial infarctionS A Croft, K K Hampton, J A Sorrell, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1986
Specificity analysis of human monoclonal antibodies reactive with cell surface and intracellular antigensR J Cote, D M Morrissey, A N Houghton, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|January 18, 2006
Short-term effects of severe dietary carbohydrate-restriction advice in Type 2 diabetes--a randomized controlled trialM E Daly, R Paisey, R Paisey, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1984
Cell surface antigens of human bladder cancer defined by mouse monoclonal antibodiesY Fradet, C Cordon-Cardo, T Thomson, et al.
The British Journal of Radiology|October 30, 2013
Clinical-dosimetric relationship between lacrimal gland dose and ocular toxicity after intensity-modulated radiotherapy for sinonasal tumoursS S Batth, R Sreeraman, E Dienes, et al.
British Journal of Haematology|May 1, 1994
Prevalence of antithrombin deficiency in the healthy populationR C Tait, I D Walker, D J Perry, et al.
Blood|July 11, 2000
A novel von Willebrand disease-causing mutation (Arg273Trp) in the von Willebrand factor propeptide that results in defective multimerization and secretionS Allen, A M Abuzenadah, J Hinks, et al.
Thrombosis and Haemostasis|January 10, 1998
Co-inheritance of the 20210A allele of the prothrombin gene increases the risk of thrombosis in subjects with familial thrombophiliaM Makris, F E Preston, N J Beauchamp, et al.
British Journal of Haematology|December 12, 2001
The -1185 A/G and -1051 G/A dimorphisms in the von Willebrand factor gene promoter and risk of myocardial infarctionR Di Bitondo, C L Cameron, M E Daly, et al.
Blood|March 9, 2000
Two novel type 2N von Willebrand disease-causing mutations that result in defective factor VIII binding, multimerization, and secretion of von Willebrand factorS Allen, A M Abuzenadah, J L Blagg, et al.
Pageof 4

Showing results (21-30 of 35) with videos related to

Sort By:
Pageof 4
British Journal of Haematology|September 1, 1999
The GPIa C807T dimorphism associated with platelet collagen receptor density is not a risk factor for myocardial infarctionS A Croft, K K Hampton, J A Sorrell, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 1, 1986
Specificity analysis of human monoclonal antibodies reactive with cell surface and intracellular antigensR J Cote, D M Morrissey, A N Houghton, et al.
Diabetic Medicine : a Journal of the British Diabetic Association|January 18, 2006
Short-term effects of severe dietary carbohydrate-restriction advice in Type 2 diabetes--a randomized controlled trialM E Daly, R Paisey, R Paisey, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 1, 1984
Cell surface antigens of human bladder cancer defined by mouse monoclonal antibodiesY Fradet, C Cordon-Cardo, T Thomson, et al.
The British Journal of Radiology|October 30, 2013
Clinical-dosimetric relationship between lacrimal gland dose and ocular toxicity after intensity-modulated radiotherapy for sinonasal tumoursS S Batth, R Sreeraman, E Dienes, et al.
British Journal of Haematology|May 1, 1994
Prevalence of antithrombin deficiency in the healthy populationR C Tait, I D Walker, D J Perry, et al.
Blood|July 11, 2000
A novel von Willebrand disease-causing mutation (Arg273Trp) in the von Willebrand factor propeptide that results in defective multimerization and secretionS Allen, A M Abuzenadah, J Hinks, et al.
Thrombosis and Haemostasis|January 10, 1998
Co-inheritance of the 20210A allele of the prothrombin gene increases the risk of thrombosis in subjects with familial thrombophiliaM Makris, F E Preston, N J Beauchamp, et al.
British Journal of Haematology|December 12, 2001
The -1185 A/G and -1051 G/A dimorphisms in the von Willebrand factor gene promoter and risk of myocardial infarctionR Di Bitondo, C L Cameron, M E Daly, et al.
Blood|March 9, 2000
Two novel type 2N von Willebrand disease-causing mutations that result in defective factor VIII binding, multimerization, and secretion of von Willebrand factorS Allen, A M Abuzenadah, J L Blagg, et al.
Pageof 4