Page 1 | Search Results | Blood | American Society of Hematology

1-5 of 5

Sort by

Sort Order Select

Journal Articles

NOX5 and p22phox are 2 novel regulators of human monocytic differentiation into dendritic cells

Viviana Marzaioli, Margarita Hurtado-Nedelec, Coralie Pintard, Asma Tlili, Jean-Claude Marie, Renato C. Monteiro, Marie-Anne Gougerot-Pocidalo, Pham My-Chan Dang, Jamel El-Benna

Blood (2017) 130 (15): 1734–1745.

https://doi.org/10.1182/blood-2016-10-746347

Published: 2017

Includes: Supplemental data

Journal Articles

Inflammasome activation in NADPH oxidase defective mononuclear phagocytes from patients with chronic granulomatous disease

Felix Meissner, Reinhard A. Seger, Despina Moshous, Alain Fischer, Janine Reichenbach, Arturo Zychlinsky

Blood (2010) 116 (9): 1570–1573.

https://doi.org/10.1182/blood-2010-01-264218

Published: 2010

Includes: Supplemental data

Journal Articles

Essential role of nuclear factor-κB for NADPH oxidase activity in normal and anhidrotic ectodermal dysplasia leukocytes

Marcos Luengo-Blanco, Carolina Prando, Jacinta Bustamante, Walmir Cutrim Aragão-Filho, Paulo Vitor Soeiro Pereira, Jussara Rehder, Carolyn Padden, Jean-Laurent Casanova, Peter E. Newburger, Antonio Condino-Neto

Blood (2008) 112 (4): 1453–1460.

https://doi.org/10.1182/blood-2007-07-099267

Published: 2008

Includes: Supplemental data

Journal Articles

Molecular analysis of 9 new families with chronic granulomatous disease caused by mutations in CYBA , the gene encoding p22 phox

Julie Rae, Deborah Noack, Paul G. Heyworth, Beverly A. Ellis, John T. Curnutte, Andrew R. Cross

Blood (2000) 96 (3): 1106–1112.

https://doi.org/10.1182/blood.V96.3.1106

Published: 2000

Journal Articles

Recombination events between the p47-phox gene and its highly homologous pseudogenes are the main cause of autosomal recessive chronic granulomatous disease

Joachim Roesler, John T. Curnutte, Julie Rae, David Barrett, Pablo Patino, Stephen J. Chanock, Agnes Goerlach

Blood (2000) 95 (6): 2150–2156.

https://doi.org/10.1182/blood.V95.6.2150

Published: 2000

NARROW

NOX5 and p22phox are 2 novel regulators of human monocytic differentiation into dendritic cells

Inflammasome activation in NADPH oxidase defective mononuclear phagocytes from patients with chronic granulomatous disease

Essential role of nuclear factor-κB for NADPH oxidase activity in normal and anhidrotic ectodermal dysplasia leukocytes

Molecular analysis of 9 new families with chronic granulomatous disease caused by mutations in CYBA , the gene encoding p22 phox

Recombination events between the p47-phox gene and its highly homologous pseudogenes are the main cause of autosomal recessive chronic granulomatous disease

Email alerts

ASH Publications

American Society of Hematology

NOX5 and p22phox are 2 novel regulators of human monocytic differentiation into dendritic cells

Inflammasome activation in NADPH oxidase defective mononuclear phagocytes from patients with chronic granulomatous disease

Essential role of nuclear factor-κB for NADPH oxidase activity in normal and anhidrotic ectodermal dysplasia leukocytes

Molecular analysis of 9 new families with chronic granulomatous disease caused by mutations in CYBA , the gene encoding p22 phox

Recombination events between the p47-phox gene and its highly homologous pseudogenes are the main cause of autosomal recessive chronic granulomatous disease

Email alerts

ASH Publications

American Society of Hematology

This Feature Is Available To Subscribers Only