Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Dirk Roos

Showing results (31-40 of 146) with videos related to

Pageof 15
Sort By:
Blood Cells, Molecules & Diseases|September 15, 2005
A donor splice site mutation in intron 1 of CYBA, leading to chronic granulomatous diseaseMartin de Boer, Dominik Hartl, Uwe Wintergerst, et al.
Journal of Immunology (Baltimore, Md. : 1950)|December 10, 2002
Repression of rac2 mRNA expression by Anaplasma phagocytophila is essential to the inhibition of superoxide production and bacterial proliferationJason A Carlyon, Wai-Tsing Chan, Jorge Galán, et al.
Iranian Journal of Allergy, Asthma, and Immunology|March 13, 2009
Prenatal diagnosis of chronic granulomatous disease in a male fetusM Yavuz Köker, Ayşe Metin, Tuba T Ozgür, et al.
Journal of the American Chemical Society|October 2, 2003
Resonance Raman imaging of the NADPH oxidase subunit cytochrome b558 in single neutrophilic granulocytesHenk-Jan van Manen, Natallia Uzunbajakava, Robin van Bruggen, et al.
Prenatal Diagnosis|March 29, 2002
Prenatal diagnosis in two families with autosomal, p47(phox)-deficient chronic granulomatous disease due to a novel point mutation in NCF1Martin de Boer, Vinita Singh, Jan Dekker, et al.
Annals of Hematology|January 1, 2013
Alu repeat-induced deletions in chronic granulomatous disease: a cause not only for p67-phox, but also for p47-phox deficiencyStefan Winkler, Karin van Leeuwen, Martin Deboer, et al.
Free Radical Biology & Medicine|November 22, 2005
Activation of AP-1 through reactive oxygen species by angiotensin II in rat cardiomyocytesShuling Wu, Jianping Gao, Carsten Ohlemeyer, et al.
Biochimica Et Biophysica Acta|May 22, 2013
Different unequal cross-over events between NCF1 and its pseudogenes in autosomal p47(phox)-deficient chronic granulomatous diseaseAstghik Hayrapetyan, Paula C D Dencher, Karin van Leeuwen, et al.
Pediatric Research|February 20, 2004
Diurnal fluctuation of leukocyte G6PD activity. A possible explanation for the normal neutrophil bactericidal activity and the low incidence of pyogenic infections in patients with severe G6PD deficiency in IsraelBaruch Wolach, Meir Ashkenazi, Rami Grossmann, et al.
Journal of Cosmetic Dermatology|March 11, 2020
Recurrent skin abscesses in a female X-linked chronic granulomatous disease carrierBurak Altintas, Deniz Cagdas, Karin van Leeuwen, et al.
Pageof 15

Showing results (31-40 of 146) with videos related to

Sort By:
Pageof 15
Blood Cells, Molecules & Diseases|September 15, 2005
A donor splice site mutation in intron 1 of CYBA, leading to chronic granulomatous diseaseMartin de Boer, Dominik Hartl, Uwe Wintergerst, et al.
Journal of Immunology (Baltimore, Md. : 1950)|December 10, 2002
Repression of rac2 mRNA expression by Anaplasma phagocytophila is essential to the inhibition of superoxide production and bacterial proliferationJason A Carlyon, Wai-Tsing Chan, Jorge Galán, et al.
Iranian Journal of Allergy, Asthma, and Immunology|March 13, 2009
Prenatal diagnosis of chronic granulomatous disease in a male fetusM Yavuz Köker, Ayşe Metin, Tuba T Ozgür, et al.
Journal of the American Chemical Society|October 2, 2003
Resonance Raman imaging of the NADPH oxidase subunit cytochrome b558 in single neutrophilic granulocytesHenk-Jan van Manen, Natallia Uzunbajakava, Robin van Bruggen, et al.
Prenatal Diagnosis|March 29, 2002
Prenatal diagnosis in two families with autosomal, p47(phox)-deficient chronic granulomatous disease due to a novel point mutation in NCF1Martin de Boer, Vinita Singh, Jan Dekker, et al.
Annals of Hematology|January 1, 2013
Alu repeat-induced deletions in chronic granulomatous disease: a cause not only for p67-phox, but also for p47-phox deficiencyStefan Winkler, Karin van Leeuwen, Martin Deboer, et al.
Free Radical Biology & Medicine|November 22, 2005
Activation of AP-1 through reactive oxygen species by angiotensin II in rat cardiomyocytesShuling Wu, Jianping Gao, Carsten Ohlemeyer, et al.
Biochimica Et Biophysica Acta|May 22, 2013
Different unequal cross-over events between NCF1 and its pseudogenes in autosomal p47(phox)-deficient chronic granulomatous diseaseAstghik Hayrapetyan, Paula C D Dencher, Karin van Leeuwen, et al.
Pediatric Research|February 20, 2004
Diurnal fluctuation of leukocyte G6PD activity. A possible explanation for the normal neutrophil bactericidal activity and the low incidence of pyogenic infections in patients with severe G6PD deficiency in IsraelBaruch Wolach, Meir Ashkenazi, Rami Grossmann, et al.
Journal of Cosmetic Dermatology|March 11, 2020
Recurrent skin abscesses in a female X-linked chronic granulomatous disease carrierBurak Altintas, Deniz Cagdas, Karin van Leeuwen, et al.
Pageof 15