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Journal Articles

Autosomal recessive chronic granulomatous disease caused by defects in NCF-1 , the gene encoding the phagocyte p47- phox : mutations not arising in the NCF-1 pseudogenes

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

Blood (2001) 97 (1): 305–311.

https://doi.org/10.1182/blood.V97.1.305

Published: 2001

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

Journal Articles

Molecular Characterization of Autosomal Recessive Chronic Granulomatous Disease Caused by a Defect of the Nicotinamide Adenine Dinucleotide Phosphate (Reduced Form) Oxidase Component p67- phox

Pablo J. Patiño, Julie Rae, Deborah Noack, Rich Erickson, Jiabing Ding, Diana Garcı́a de Olarte, John T. Curnutte

Blood (1999) 94 (7): 2505–2514.

https://doi.org/10.1182/blood.V94.7.2505.419k10_2505_2514

Published: 1999

Journal Articles

Increased Phagocyte FcγRI Expression and Improved Fcγ-Receptor–Mediated Phagocytosis After In Vivo Recombinant Human Interferon-γ Treatment of Normal Human Subjects

Deborah E. Schiff, Julie Rae, Thomas R. Martin, Bruce H. Davis, John T. Curnutte

Blood (1997) 90 (8): 3187–3194.

https://doi.org/10.1182/blood.V90.8.3187

Published: 1997

NARROW

Autosomal recessive chronic granulomatous disease caused by defects in NCF-1 , the gene encoding the phagocyte p47- phox : mutations not arising in the NCF-1 pseudogenes

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

Molecular Characterization of Autosomal Recessive Chronic Granulomatous Disease Caused by a Defect of the Nicotinamide Adenine Dinucleotide Phosphate (Reduced Form) Oxidase Component p67- phox

Increased Phagocyte FcγRI Expression and Improved Fcγ-Receptor–Mediated Phagocytosis After In Vivo Recombinant Human Interferon-γ Treatment of Normal Human Subjects

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ASH Publications

American Society of Hematology

Autosomal recessive chronic granulomatous disease caused by defects in NCF-1 , the gene encoding the phagocyte p47- phox : mutations not arising in the NCF-1 pseudogenes

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

Molecular Characterization of Autosomal Recessive Chronic Granulomatous Disease Caused by a Defect of the Nicotinamide Adenine Dinucleotide Phosphate (Reduced Form) Oxidase Component p67- phox

Increased Phagocyte FcγRI Expression and Improved Fcγ-Receptor–Mediated Phagocytosis After In Vivo Recombinant Human Interferon-γ Treatment of Normal Human Subjects

Email alerts

ASH Publications

American Society of Hematology

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