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van den Born

Showing results (591-600 of 717) with videos related to

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Journal of the American Heart Association|June 24, 2020
Prevalence of ECGs Exceeding Thresholds for ST-Segment-Elevation Myocardial Infarction in Apparently Healthy Individuals: The Role of EthnicityC Cato Ter Haar, Jan A Kors, Ron J G Peters, et al.
Atherosclerosis|January 7, 2022
Lipoprotein(a), venous thromboembolism and COVID-19: A pilot studyNick S Nurmohamed, Didier Collard, Laurens F Reeskamp, et al.
Scientific Reports|March 9, 2022
Pretransplant endotrophin predicts delayed graft function after kidney transplantationMartin Tepel, Firas F Alkaff, Daan Kremer, et al.
Molecular Immunology|December 17, 2011
Lectin complement pathway gene profile of the donor and recipient does not influence graft outcome after kidney transplantationJeffrey Damman, Julian L Kok, Harold Snieder, et al.
BMJ Open Diabetes Research & Care|July 16, 2020
Association between C reactive protein and microvascular and macrovascular dysfunction in sub-Saharan Africans with and without diabetes: the RODAM studyCharles Frederick Hayfron-Benjamin, Anke H Maitland-van der Zee, Bert-Jan van den Born, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 31, 2016
Reg4+ deep crypt secretory cells function as epithelial niche for Lgr5+ stem cells in colonNobuo Sasaki, Norman Sachs, Kay Wiebrands, et al.
Ophthalmology|January 19, 2010
Comprehensive analysis of the achromatopsia genes CNGA3 and CNGB3 in progressive cone dystrophyAlberta A H J Thiadens, Susanne Roosing, Rob W J Collin, et al.
Acta Ophthalmologica|November 12, 2014
Retinitis pigmentosa caused by mutations in the ciliary MAK gene is relatively mild and is not associated with apparent extra-ocular featuresRamon A C van Huet, Anna M Siemiatkowska, Riza K Özgül, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 24, 2022
Biallelic KIF24 Variants Are Responsible for a Spectrum of Skeletal Disorders Ranging From Lethal Skeletal Ciliopathy to Severe Acromesomelic DysplasiaMadeline Louise Reilly, Noor Ul Ain, Mari Muurinen, et al.
The Journal of General Virology|October 18, 2024
A broadly reactive ultralong bovine antibody that can determine the integrity of foot-and-mouth disease virus capsidsJohn D Clarke, Helen M E Duyvesteyn, Eva Perez-Martin, et al.
Pageof 72

Showing results (591-600 of 717) with videos related to

Sort By:
Pageof 72
Journal of the American Heart Association|June 24, 2020
Prevalence of ECGs Exceeding Thresholds for ST-Segment-Elevation Myocardial Infarction in Apparently Healthy Individuals: The Role of EthnicityC Cato Ter Haar, Jan A Kors, Ron J G Peters, et al.
Atherosclerosis|January 7, 2022
Lipoprotein(a), venous thromboembolism and COVID-19: A pilot studyNick S Nurmohamed, Didier Collard, Laurens F Reeskamp, et al.
Scientific Reports|March 9, 2022
Pretransplant endotrophin predicts delayed graft function after kidney transplantationMartin Tepel, Firas F Alkaff, Daan Kremer, et al.
Molecular Immunology|December 17, 2011
Lectin complement pathway gene profile of the donor and recipient does not influence graft outcome after kidney transplantationJeffrey Damman, Julian L Kok, Harold Snieder, et al.
BMJ Open Diabetes Research & Care|July 16, 2020
Association between C reactive protein and microvascular and macrovascular dysfunction in sub-Saharan Africans with and without diabetes: the RODAM studyCharles Frederick Hayfron-Benjamin, Anke H Maitland-van der Zee, Bert-Jan van den Born, et al.
Proceedings of the National Academy of Sciences of the United States of America|August 31, 2016
Reg4+ deep crypt secretory cells function as epithelial niche for Lgr5+ stem cells in colonNobuo Sasaki, Norman Sachs, Kay Wiebrands, et al.
Ophthalmology|January 19, 2010
Comprehensive analysis of the achromatopsia genes CNGA3 and CNGB3 in progressive cone dystrophyAlberta A H J Thiadens, Susanne Roosing, Rob W J Collin, et al.
Acta Ophthalmologica|November 12, 2014
Retinitis pigmentosa caused by mutations in the ciliary MAK gene is relatively mild and is not associated with apparent extra-ocular featuresRamon A C van Huet, Anna M Siemiatkowska, Riza K Özgül, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|June 24, 2022
Biallelic KIF24 Variants Are Responsible for a Spectrum of Skeletal Disorders Ranging From Lethal Skeletal Ciliopathy to Severe Acromesomelic DysplasiaMadeline Louise Reilly, Noor Ul Ain, Mari Muurinen, et al.
The Journal of General Virology|October 18, 2024
A broadly reactive ultralong bovine antibody that can determine the integrity of foot-and-mouth disease virus capsidsJohn D Clarke, Helen M E Duyvesteyn, Eva Perez-Martin, et al.
Pageof 72