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Martin de Boer

Showing results (61-70 of 74) with videos related to

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Journal of Medical Genetics|January 15, 2018
A false-carrier state for the c.579G>A mutation in the NCF1 gene in Ashkenazi JewsMartin De Boer, Ronit Gavrieli, Karin van Leeuwen, et al.
Human Mutation|December 3, 2009
Alu-repeat-induced deletions within the NCF2 gene causing p67-phox-deficient chronic granulomatous disease (CGD)Marcus Gentsch, Aneta Kaczmarczyk, Karin van Leeuwen, et al.
British Journal of Haematology|June 7, 2019
Identification of genetic biomarkers for alloimmunization in sickle cell diseaseSanne M Meinderts, Jorn J Gerritsma, Joep W R Sins, et al.
Blood Cells, Molecules & Diseases|January 25, 2023
Hematologically important mutations: Leukocyte adhesion deficiency (second update)Dirk Roos, Karin van Leeuwen, Manisha Madkaikar, et al.
Blood Cells, Molecules & Diseases|December 3, 2011
Hematologically important mutations: leukocyte adhesion deficiency (first update)Edith van de Vijver, Anne Maddalena, Özden Sanal, et al.
Blood|June 21, 2024
Genotype-phenotype correlations in chronic granulomatous disease: insights from a large national cohortBaruch Wolach, Ronit Gavrieli, Ofir Wolach, et al.
The Journal of Allergy and Clinical Immunology|December 15, 2016
Combined immunodeficiency with severe inflammation and allergy caused by ARPC1B deficiencyTaco W Kuijpers, Anton T J Tool, Ivo van der Bijl, et al.
Blood Cells, Molecules & Diseases|August 24, 2010
Hematologically important mutations: X-linked chronic granulomatous disease (third update)Dirk Roos, Douglas B Kuhns, Anne Maddalena, et al.
Frontiers in Immunology|April 6, 2019
Extensive Ethnic Variation and Linkage Disequilibrium at the <i>FCGR2/3</i> Locus: Different Genetic Associations Revealed in Kawasaki DiseaseSietse Q Nagelkerke, Carline E Tacke, Willemijn B Breunis, et al.
Blood|March 5, 2020
MKL1 deficiency results in a severe neutrophil motility defect due to impaired actin polymerizationEvelien G G Sprenkeler, Stefanie S V Henriet, Anton T J Tool, et al.
Pageof 8

Showing results (61-70 of 74) with videos related to

Sort By:
Pageof 8
Journal of Medical Genetics|January 15, 2018
A false-carrier state for the c.579G>A mutation in the NCF1 gene in Ashkenazi JewsMartin De Boer, Ronit Gavrieli, Karin van Leeuwen, et al.
Human Mutation|December 3, 2009
Alu-repeat-induced deletions within the NCF2 gene causing p67-phox-deficient chronic granulomatous disease (CGD)Marcus Gentsch, Aneta Kaczmarczyk, Karin van Leeuwen, et al.
British Journal of Haematology|June 7, 2019
Identification of genetic biomarkers for alloimmunization in sickle cell diseaseSanne M Meinderts, Jorn J Gerritsma, Joep W R Sins, et al.
Blood Cells, Molecules & Diseases|January 25, 2023
Hematologically important mutations: Leukocyte adhesion deficiency (second update)Dirk Roos, Karin van Leeuwen, Manisha Madkaikar, et al.
Blood Cells, Molecules & Diseases|December 3, 2011
Hematologically important mutations: leukocyte adhesion deficiency (first update)Edith van de Vijver, Anne Maddalena, Özden Sanal, et al.
Blood|June 21, 2024
Genotype-phenotype correlations in chronic granulomatous disease: insights from a large national cohortBaruch Wolach, Ronit Gavrieli, Ofir Wolach, et al.
The Journal of Allergy and Clinical Immunology|December 15, 2016
Combined immunodeficiency with severe inflammation and allergy caused by ARPC1B deficiencyTaco W Kuijpers, Anton T J Tool, Ivo van der Bijl, et al.
Blood Cells, Molecules & Diseases|August 24, 2010
Hematologically important mutations: X-linked chronic granulomatous disease (third update)Dirk Roos, Douglas B Kuhns, Anne Maddalena, et al.
Frontiers in Immunology|April 6, 2019
Extensive Ethnic Variation and Linkage Disequilibrium at the <i>FCGR2/3</i> Locus: Different Genetic Associations Revealed in Kawasaki DiseaseSietse Q Nagelkerke, Carline E Tacke, Willemijn B Breunis, et al.
Blood|March 5, 2020
MKL1 deficiency results in a severe neutrophil motility defect due to impaired actin polymerizationEvelien G G Sprenkeler, Stefanie S V Henriet, Anton T J Tool, et al.
Pageof 8