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Showing results (151-160 of 172) with videos related to

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Circulation Research|May 21, 2016
CD74-Downregulation of Placental Macrophage-Trophoblastic Interactions in PreeclampsiaLukasz Przybyl, Nadine Haase, Michaela Golic, et al.
Expert Review of Hematology|March 15, 2023
Building the foundation for a community-generated national research blueprint for inherited bleeding disorders: research priorities to transform the care of people with hemophiliaDuc Q Tran, Craig C Benson, Judith A Boice, et al.
Genetic Epidemiology|February 1, 2014
A variational Bayes discrete mixture test for rare variant associationBenjamin A Logsdon, James Y Dai, Paul L Auer, et al.
American Journal of Human Genetics|October 30, 2012
Imputation of exome sequence variants into population- based samples and blood-cell-trait-associated loci in African Americans: NHLBI GO Exome Sequencing ProjectPaul L Auer, Jill M Johnsen, Andrew D Johnson, et al.
Human Molecular Genetics|October 12, 2018
Whole genome sequence association with E-selectin levels reveals loss-of-function variant in African AmericansLinda M Polfus, Laura M Raffield, Marsha M Wheeler, et al.
Journal of Thrombosis and Haemostasis : JTH|February 12, 2023
Heterogeneity in the half-life of factor VIII concentrate in patients with hemophilia A is due to variability in the clearance of endogenous von Willebrand factorEinas Elsheikh, Michelle Lavin, Lilian Antunes Heck, et al.
Human Molecular Genetics|May 13, 2022
Whole-exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factorsNathan Pankratz, Peng Wei, Jennifer A Brody, et al.
Placenta|December 14, 2011
IFPA Meeting 2011 workshop report III: Placental immunology; epigenetic and microRNA-dependent gene regulation; comparative placentation; trophoblast differentiation; stem cellsW E Ackerman, J N Bulmer, A M Carter, et al.
Journal of Thrombosis and Haemostasis : JTH|May 14, 2025
Genetic study of von Willebrand factor antigen levels ≤ 50 IU/dL identifies variants associated with increased risk of von Willebrand disease and bleedingRachel K Friedman, Adam S Heath, Jennifer E Huffman, et al.
American Journal of Human Genetics|September 3, 2016
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human HematopoiesisLinda M Polfus, Rajiv K Khajuria, Ursula M Schick, et al.
Pageof 18

Showing results (151-160 of 172) with videos related to

Sort By:
Pageof 18
Circulation Research|May 21, 2016
CD74-Downregulation of Placental Macrophage-Trophoblastic Interactions in PreeclampsiaLukasz Przybyl, Nadine Haase, Michaela Golic, et al.
Expert Review of Hematology|March 15, 2023
Building the foundation for a community-generated national research blueprint for inherited bleeding disorders: research priorities to transform the care of people with hemophiliaDuc Q Tran, Craig C Benson, Judith A Boice, et al.
Genetic Epidemiology|February 1, 2014
A variational Bayes discrete mixture test for rare variant associationBenjamin A Logsdon, James Y Dai, Paul L Auer, et al.
American Journal of Human Genetics|October 30, 2012
Imputation of exome sequence variants into population- based samples and blood-cell-trait-associated loci in African Americans: NHLBI GO Exome Sequencing ProjectPaul L Auer, Jill M Johnsen, Andrew D Johnson, et al.
Human Molecular Genetics|October 12, 2018
Whole genome sequence association with E-selectin levels reveals loss-of-function variant in African AmericansLinda M Polfus, Laura M Raffield, Marsha M Wheeler, et al.
Journal of Thrombosis and Haemostasis : JTH|February 12, 2023
Heterogeneity in the half-life of factor VIII concentrate in patients with hemophilia A is due to variability in the clearance of endogenous von Willebrand factorEinas Elsheikh, Michelle Lavin, Lilian Antunes Heck, et al.
Human Molecular Genetics|May 13, 2022
Whole-exome sequencing of 14 389 individuals from the ESP and CHARGE consortia identifies novel rare variation associated with hemostatic factorsNathan Pankratz, Peng Wei, Jennifer A Brody, et al.
Placenta|December 14, 2011
IFPA Meeting 2011 workshop report III: Placental immunology; epigenetic and microRNA-dependent gene regulation; comparative placentation; trophoblast differentiation; stem cellsW E Ackerman, J N Bulmer, A M Carter, et al.
Journal of Thrombosis and Haemostasis : JTH|May 14, 2025
Genetic study of von Willebrand factor antigen levels ≤ 50 IU/dL identifies variants associated with increased risk of von Willebrand disease and bleedingRachel K Friedman, Adam S Heath, Jennifer E Huffman, et al.
American Journal of Human Genetics|September 3, 2016
Whole-Exome Sequencing Identifies Loci Associated with Blood Cell Traits and Reveals a Role for Alternative GFI1B Splice Variants in Human HematopoiesisLinda M Polfus, Rajiv K Khajuria, Ursula M Schick, et al.
Pageof 18