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D Paterson

Showing results (361-370 of 540) with videos related to

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Physical Review Letters|August 16, 2006
Fresnel coherent diffractive imagingG J Williams, H M Quiney, B B Dhal, et al.
Blood|December 17, 2009
Persons with Quebec platelet disorder have a tandem duplication of PLAU, the urokinase plasminogen activator geneAndrew D Paterson, Johanna M Rommens, Bhupinder Bharaj, et al.
British Journal of Cancer|May 1, 1985
Treatment of malignant hypercalcaemia with clodronateR C Percival, A D Paterson, A J Yates, et al.
Journal of Synchrotron Radiation|June 17, 2008
Differential phase contrast with a segmented detector in a scanning X-ray microprobeB Hornberger, M D de Jonge, M Feser, et al.
Journal of the American Society of Nephrology : JASN|January 29, 2005
Progressive loss of renal function is an age-dependent heritable trait in type 1 autosomal dominant polycystic kidney diseaseAndrew D Paterson, Riccardo Magistroni, Ning He, et al.
British Journal of Cancer|July 1, 1990
Gene expression in oestrogen-dependent human breast cancer xenograft tumoursA M Thompson, C M Steel, M E Foster, et al.
BMC Endocrine Disorders|January 13, 2021
Skin autofluorescence predicts new cardiovascular disease and mortality in people with type 2 diabetesHenderikus E Boersma, Robert P van Waateringe, Melanie M van der Klauw, et al.
ESC Heart Failure|March 9, 2022
Heart failure with mildly reduced ejection fraction: retrospective study of ejection fraction trajectory riskRobert J H Miller, Majid Nabipoor, Erik Youngson, et al.
American Journal of Human Genetics|January 13, 2001
Bilineal disease and trans-heterozygotes in autosomal dominant polycystic kidney diseaseY Pei, A D Paterson, K R Wang, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 10, 2017
Molecular phenotype and bleeding risks of an inherited platelet disorder in a family with a RUNX1 frameshift mutationM S Badin, J K Iyer, M Chong, et al.
Pageof 54

Showing results (361-370 of 540) with videos related to

Sort By:
Pageof 54
Physical Review Letters|August 16, 2006
Fresnel coherent diffractive imagingG J Williams, H M Quiney, B B Dhal, et al.
Blood|December 17, 2009
Persons with Quebec platelet disorder have a tandem duplication of PLAU, the urokinase plasminogen activator geneAndrew D Paterson, Johanna M Rommens, Bhupinder Bharaj, et al.
British Journal of Cancer|May 1, 1985
Treatment of malignant hypercalcaemia with clodronateR C Percival, A D Paterson, A J Yates, et al.
Journal of Synchrotron Radiation|June 17, 2008
Differential phase contrast with a segmented detector in a scanning X-ray microprobeB Hornberger, M D de Jonge, M Feser, et al.
Journal of the American Society of Nephrology : JASN|January 29, 2005
Progressive loss of renal function is an age-dependent heritable trait in type 1 autosomal dominant polycystic kidney diseaseAndrew D Paterson, Riccardo Magistroni, Ning He, et al.
British Journal of Cancer|July 1, 1990
Gene expression in oestrogen-dependent human breast cancer xenograft tumoursA M Thompson, C M Steel, M E Foster, et al.
BMC Endocrine Disorders|January 13, 2021
Skin autofluorescence predicts new cardiovascular disease and mortality in people with type 2 diabetesHenderikus E Boersma, Robert P van Waateringe, Melanie M van der Klauw, et al.
ESC Heart Failure|March 9, 2022
Heart failure with mildly reduced ejection fraction: retrospective study of ejection fraction trajectory riskRobert J H Miller, Majid Nabipoor, Erik Youngson, et al.
American Journal of Human Genetics|January 13, 2001
Bilineal disease and trans-heterozygotes in autosomal dominant polycystic kidney diseaseY Pei, A D Paterson, K R Wang, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|February 10, 2017
Molecular phenotype and bleeding risks of an inherited platelet disorder in a family with a RUNX1 frameshift mutationM S Badin, J K Iyer, M Chong, et al.
Pageof 54