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Martin de Boer

Showing results (41-50 of 74) with videos related to

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International Archives of Allergy and Immunology|June 9, 2020
Genetic Characteristics, Infectious, and Noninfectious Manifestations of 32 Patients with Chronic Granulomatous DiseaseDeniz Aygun, Mustafa Yavuz Koker, Serdar Nepesov, et al.
Blood Cells, Molecules & Diseases|October 14, 2015
A founder effect for p47(phox)Trp193Ter chronic granulomatous disease in Kavkazi JewsMartin de Boer, Shay Tzur, Karin van Leeuwen, et al.
International Journal of Molecular and Cellular Medicine|September 14, 2019
Diagnostic Challenges in the Early Onset of Inflammatory Bowel Disease: A Case ReportNaghi Dara, Sharam Nemati, Sharam Teimourian, et al.
Blood|December 23, 2006
Molecular basis of glutathione reductase deficiency in human blood cellsNanne M Kamerbeek, Rob van Zwieten, Martin de Boer, et al.
Journal of Pediatric Hematology/Oncology|May 12, 2018
Genetic Analysis of 13 Iranian Families With Leukocyte Adhesion Deficiency Type 1Shahram Teimourian, Martin De Boer, Dirk Roos, et al.
Research and Practice in Thrombosis and Haemostasis|October 19, 2019
Alternative trafficking of Weibel-Palade body proteins in CRISPR/Cas9-engineered von Willebrand factor-deficient blood outgrowth endothelial cellsMaaike Schillemans, Marije Kat, Jurjen Westeneng, et al.
Blood|July 20, 2002
Deletion of leucine 61 in glucose-6-phosphate dehydrogenase leads to chronic nonspherocytic anemia, granulocyte dysfunction, and increased susceptibility to infectionsRobin van Bruggen, José M Bautista, Theoni Petropoulou, et al.
Frontiers in Immunology|November 3, 2017
Factor H-Related (FHR)-1 and FHR-2 Form Homo- and Heterodimers, while FHR-5 Circulates Only As Homodimer in Human PlasmaAnna E van Beek, Richard B Pouw, Mieke C Brouwer, et al.
European Journal of Medical Genetics|September 3, 2017
Very early onset inflammatory bowel disease: Investigation of the IL-10 signaling pathway in Iranian childrenShahram Nemati, Shahram Teimourian, Mina Tabrizi, et al.
Journal of Clinical Immunology|March 3, 2012
Rare duplication or deletion of exons 6, 7 and 8 in CYBB leading to X-linked chronic granulomatous disease in two patients from different familiesMarie José Stasia, Karin van Leeuwen, Martin de Boer, et al.
Pageof 8

Showing results (41-50 of 74) with videos related to

Sort By:
Pageof 8
International Archives of Allergy and Immunology|June 9, 2020
Genetic Characteristics, Infectious, and Noninfectious Manifestations of 32 Patients with Chronic Granulomatous DiseaseDeniz Aygun, Mustafa Yavuz Koker, Serdar Nepesov, et al.
Blood Cells, Molecules & Diseases|October 14, 2015
A founder effect for p47(phox)Trp193Ter chronic granulomatous disease in Kavkazi JewsMartin de Boer, Shay Tzur, Karin van Leeuwen, et al.
International Journal of Molecular and Cellular Medicine|September 14, 2019
Diagnostic Challenges in the Early Onset of Inflammatory Bowel Disease: A Case ReportNaghi Dara, Sharam Nemati, Sharam Teimourian, et al.
Blood|December 23, 2006
Molecular basis of glutathione reductase deficiency in human blood cellsNanne M Kamerbeek, Rob van Zwieten, Martin de Boer, et al.
Journal of Pediatric Hematology/Oncology|May 12, 2018
Genetic Analysis of 13 Iranian Families With Leukocyte Adhesion Deficiency Type 1Shahram Teimourian, Martin De Boer, Dirk Roos, et al.
Research and Practice in Thrombosis and Haemostasis|October 19, 2019
Alternative trafficking of Weibel-Palade body proteins in CRISPR/Cas9-engineered von Willebrand factor-deficient blood outgrowth endothelial cellsMaaike Schillemans, Marije Kat, Jurjen Westeneng, et al.
Blood|July 20, 2002
Deletion of leucine 61 in glucose-6-phosphate dehydrogenase leads to chronic nonspherocytic anemia, granulocyte dysfunction, and increased susceptibility to infectionsRobin van Bruggen, José M Bautista, Theoni Petropoulou, et al.
Frontiers in Immunology|November 3, 2017
Factor H-Related (FHR)-1 and FHR-2 Form Homo- and Heterodimers, while FHR-5 Circulates Only As Homodimer in Human PlasmaAnna E van Beek, Richard B Pouw, Mieke C Brouwer, et al.
European Journal of Medical Genetics|September 3, 2017
Very early onset inflammatory bowel disease: Investigation of the IL-10 signaling pathway in Iranian childrenShahram Nemati, Shahram Teimourian, Mina Tabrizi, et al.
Journal of Clinical Immunology|March 3, 2012
Rare duplication or deletion of exons 6, 7 and 8 in CYBB leading to X-linked chronic granulomatous disease in two patients from different familiesMarie José Stasia, Karin van Leeuwen, Martin de Boer, et al.
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