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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 Jews
Martin De Boer, Ronit Gavrieli, Karin van Leeuwen, et al.
Haematologica
|
January 24, 2016
Impaired killing of Candida albicans by granulocytes mobilized for transfusion purposes: a role for granule components
Roel P Gazendam, Annemarie van de Geer, John L van Hamme, 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.
Plos One
|
April 22, 2009
Chronic granulomatous disease: the European experience
J Merlijn van den Berg, Elsbeth van Koppen, Anders Ahlin, 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 cohort
Baruch Wolach, Ronit Gavrieli, Ofir Wolach, et al.
Apoptosis : an International Journal on Programmed Cell Death
|
April 19, 2007
Homocysteine affects cardiomyocyte viability: concentration-dependent effects on reversible flip-flop, apoptosis and necrosis
Jessica A Sipkens, Paul A J Krijnen, Christof Meischl, et al.
Cell Biochemistry and Biophysics
|
November 1, 2011
Homocysteine-induced apoptosis in endothelial cells coincides with nuclear NOX2 and peri-nuclear NOX4 activity
Jessica A Sipkens, Nynke Hahn, Carlien S van den Brand, et al.
The Journal of Allergy and Clinical Immunology
|
December 15, 2016
Combined immunodeficiency with severe inflammation and allergy caused by ARPC1B deficiency
Taco W Kuijpers, Anton T J Tool, Ivo van der Bijl, et al.
Page
of 15
Search research articles
Search
Showing results (131-140 of 146) with videos related to
Sort By:
Page
of 15
Journal of Medical Genetics
|
January 15, 2018
A false-carrier state for the c.579G>A mutation in the NCF1 gene in Ashkenazi Jews
Martin De Boer, Ronit Gavrieli, Karin van Leeuwen, et al.
Haematologica
|
January 24, 2016
Impaired killing of Candida albicans by granulocytes mobilized for transfusion purposes: a role for granule components
Roel P Gazendam, Annemarie van de Geer, John L van Hamme, 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.
Plos One
|
April 22, 2009
Chronic granulomatous disease: the European experience
J Merlijn van den Berg, Elsbeth van Koppen, Anders Ahlin, 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 cohort
Baruch Wolach, Ronit Gavrieli, Ofir Wolach, et al.
Apoptosis : an International Journal on Programmed Cell Death
|
April 19, 2007
Homocysteine affects cardiomyocyte viability: concentration-dependent effects on reversible flip-flop, apoptosis and necrosis
Jessica A Sipkens, Paul A J Krijnen, Christof Meischl, et al.
Cell Biochemistry and Biophysics
|
November 1, 2011
Homocysteine-induced apoptosis in endothelial cells coincides with nuclear NOX2 and peri-nuclear NOX4 activity
Jessica A Sipkens, Nynke Hahn, Carlien S van den Brand, et al.
The Journal of Allergy and Clinical Immunology
|
December 15, 2016
Combined immunodeficiency with severe inflammation and allergy caused by ARPC1B deficiency
Taco W Kuijpers, Anton T J Tool, Ivo van der Bijl, et al.
Page
of 15