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Martin de Boer

Showing results (51-60 of 74) with videos related to

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Journal of Clinical & Cellular Immunology|May 5, 2015
Two CGD Families with a Hypomorphic Mutation in the Activation Domain of p67<sup>phox</sup>Dirk Roos, Jaap D van Buul, Anton Tj Tool, et al.
The Journal of Allergy and Clinical Immunology|August 6, 2013
Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patientsMustafa Yavuz Köker, Yıldız Camcıoğlu, Karin van Leeuwen, et al.
Plos One|July 11, 2013
Extensive variation in gene copy number at the killer immunoglobulin-like receptor locus in humansSanne Vendelbosch, Martin de Boer, Remko A T W Gouw, et al.
Blood Cells, Molecules & Diseases|February 20, 2010
Hematologically important mutations: the autosomal recessive forms of chronic granulomatous disease (second update)Dirk Roos, Douglas B Kuhns, Anne Maddalena, et al.
Human Mutation|June 7, 2017
Hermansky-Pudlak syndrome type 2: Aberrant pre-mRNA splicing and mislocalization of granule proteins in neutrophilsMartin de Boer, Karin van Leeuwen, Judy Geissler, et al.
European Journal of Human Genetics : EJHG|January 24, 2013
Functional and genetic characterization of two extremely rare cases of Williams-Beuren syndrome associated with chronic granulomatous diseaseMarie J Stasia, Michèle Mollin, Cécile Martel, et al.
The Journal of Molecular Diagnostics : JMD|March 16, 2010
Rapid genetic analysis of x-linked chronic granulomatous disease by high-resolution meltingHarry R Hill, Nancy H Augustine, Robert J Pryor, et al.
European Journal of Immunology|September 28, 2017
Genetic variation of human neutrophil Fcγ receptors and SIRPα in antibody-dependent cellular cytotoxicity towards cancer cellsLouise W Treffers, Xi Wen Zhao, Joris van der Heijden, et al.
Blood|December 10, 2008
LAD-1/variant syndrome is caused by mutations in FERMT3Taco W Kuijpers, Edith van de Vijver, Marian A J Weterman, et al.
American Journal of Hematology|October 5, 2016
Chronic granulomatous disease: Clinical, functional, molecular, and genetic studies. The Israeli experience with 84 patientsBaruch Wolach, Ronit Gavrieli, Martin de Boer, et al.
Pageof 8

Showing results (51-60 of 74) with videos related to

Sort By:
Pageof 8
Journal of Clinical & Cellular Immunology|May 5, 2015
Two CGD Families with a Hypomorphic Mutation in the Activation Domain of p67<sup>phox</sup>Dirk Roos, Jaap D van Buul, Anton Tj Tool, et al.
The Journal of Allergy and Clinical Immunology|August 6, 2013
Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patientsMustafa Yavuz Köker, Yıldız Camcıoğlu, Karin van Leeuwen, et al.
Plos One|July 11, 2013
Extensive variation in gene copy number at the killer immunoglobulin-like receptor locus in humansSanne Vendelbosch, Martin de Boer, Remko A T W Gouw, et al.
Blood Cells, Molecules & Diseases|February 20, 2010
Hematologically important mutations: the autosomal recessive forms of chronic granulomatous disease (second update)Dirk Roos, Douglas B Kuhns, Anne Maddalena, et al.
Human Mutation|June 7, 2017
Hermansky-Pudlak syndrome type 2: Aberrant pre-mRNA splicing and mislocalization of granule proteins in neutrophilsMartin de Boer, Karin van Leeuwen, Judy Geissler, et al.
European Journal of Human Genetics : EJHG|January 24, 2013
Functional and genetic characterization of two extremely rare cases of Williams-Beuren syndrome associated with chronic granulomatous diseaseMarie J Stasia, Michèle Mollin, Cécile Martel, et al.
The Journal of Molecular Diagnostics : JMD|March 16, 2010
Rapid genetic analysis of x-linked chronic granulomatous disease by high-resolution meltingHarry R Hill, Nancy H Augustine, Robert J Pryor, et al.
European Journal of Immunology|September 28, 2017
Genetic variation of human neutrophil Fcγ receptors and SIRPα in antibody-dependent cellular cytotoxicity towards cancer cellsLouise W Treffers, Xi Wen Zhao, Joris van der Heijden, et al.
Blood|December 10, 2008
LAD-1/variant syndrome is caused by mutations in FERMT3Taco W Kuijpers, Edith van de Vijver, Marian A J Weterman, et al.
American Journal of Hematology|October 5, 2016
Chronic granulomatous disease: Clinical, functional, molecular, and genetic studies. The Israeli experience with 84 patientsBaruch Wolach, Ronit Gavrieli, Martin de Boer, et al.
Pageof 8