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Baruch Wolach

Showing results (31-40 of 53) with videos related to

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European Journal of Clinical Investigation|November 10, 2018
Leucocyte adhesion deficiency-A multicentre national experienceBaruch Wolach, Ronit Gavrieli, Ofir Wolach, et al.
American Journal of Hematology|June 30, 2004
Hydrops fetalis associated with homozygosity for hemoglobin Taybe (alpha 38/39 THR deletion) in newborn tripletsShmuel Arnon, Hannah Tamary, Orly Dgany, et al.
Plos One|November 25, 2010
The effect of gentamicin-induced readthrough on a novel premature termination codon of CD18 leukocyte adhesion deficiency patientsAmos J Simon, Atar Lev, Baruch Wolach, et al.
Journal of Pediatric Hematology/Oncology|July 30, 2014
Leukocyte adhesion deficiency type III: clinical features and treatment with stem cell transplantationPolina Y Stepensky, Baruch Wolach, Ronit Gavrieli, et al.
Experimental Hematology|March 24, 2007
Growth factors G-CSF and GM-CSF differentially preserve chemotaxis of neutrophils aging in vitroBaruch Wolach, Luc J W van der Laan, Nikolai A Maianski, et al.
Journal of Clinical Immunology|February 8, 2018
Analysis of Chronic Granulomatous Disease in the Kavkazi Population in Israel Reveals Phenotypic Heterogeneity in Patients with the Same NCF1 mutation (c.579G>A)Baruch Wolach, Ronit Gavrieli, Martin de Boer, et al.
Clinical Immunology (Orlando, Fla.)|August 19, 2008
Chronic granulomatous disease in Israel: clinical, functional and molecular studies of 38 patientsBaruch Wolach, Ronit Gavrieli, Martin de Boer, et al.
The Journal of Biological Chemistry|September 4, 2008
Cytosolic phospholipase A2alpha is targeted to the p47phox-PX domain of the assembled NADPH oxidase via a novel binding site in its C2 domainZeev Shmelzer, Maria Karter, Miriam Eisenstein, et al.
Human Mutation|September 15, 2006
Chronic granulomatous disease caused by mutations other than the common GT deletion in NCF1, the gene encoding the p47phox component of the phagocyte NADPH oxidaseDirk Roos, Martin de Boer, M Yavuz Köker, 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.
Pageof 6

Showing results (31-40 of 53) with videos related to

Sort By:
Pageof 6
European Journal of Clinical Investigation|November 10, 2018
Leucocyte adhesion deficiency-A multicentre national experienceBaruch Wolach, Ronit Gavrieli, Ofir Wolach, et al.
American Journal of Hematology|June 30, 2004
Hydrops fetalis associated with homozygosity for hemoglobin Taybe (alpha 38/39 THR deletion) in newborn tripletsShmuel Arnon, Hannah Tamary, Orly Dgany, et al.
Plos One|November 25, 2010
The effect of gentamicin-induced readthrough on a novel premature termination codon of CD18 leukocyte adhesion deficiency patientsAmos J Simon, Atar Lev, Baruch Wolach, et al.
Journal of Pediatric Hematology/Oncology|July 30, 2014
Leukocyte adhesion deficiency type III: clinical features and treatment with stem cell transplantationPolina Y Stepensky, Baruch Wolach, Ronit Gavrieli, et al.
Experimental Hematology|March 24, 2007
Growth factors G-CSF and GM-CSF differentially preserve chemotaxis of neutrophils aging in vitroBaruch Wolach, Luc J W van der Laan, Nikolai A Maianski, et al.
Journal of Clinical Immunology|February 8, 2018
Analysis of Chronic Granulomatous Disease in the Kavkazi Population in Israel Reveals Phenotypic Heterogeneity in Patients with the Same NCF1 mutation (c.579G>A)Baruch Wolach, Ronit Gavrieli, Martin de Boer, et al.
Clinical Immunology (Orlando, Fla.)|August 19, 2008
Chronic granulomatous disease in Israel: clinical, functional and molecular studies of 38 patientsBaruch Wolach, Ronit Gavrieli, Martin de Boer, et al.
The Journal of Biological Chemistry|September 4, 2008
Cytosolic phospholipase A2alpha is targeted to the p47phox-PX domain of the assembled NADPH oxidase via a novel binding site in its C2 domainZeev Shmelzer, Maria Karter, Miriam Eisenstein, et al.
Human Mutation|September 15, 2006
Chronic granulomatous disease caused by mutations other than the common GT deletion in NCF1, the gene encoding the p47phox component of the phagocyte NADPH oxidaseDirk Roos, Martin de Boer, M Yavuz Köker, 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.
Pageof 6