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Results: 1-10 |
Results: 10
Hematologically important mutations: X-linked chronic granulomatous disease (Second update)
Authors: Heyworth, PG Curnutte, JT Rae, J Noack, D Roos, D van Koppen, E Cross, AR
Citation: Pg. Heyworth et al., Hematologically important mutations: X-linked chronic granulomatous disease (Second update), BL CELL M D, 27(1), 2001, pp. 16-26
An unusual intronic mutation in the CYBB gene giving rise to chronic granulomatous disease
Authors: Noack, D Heyworth, PG Newburger, PE Cross, AR
Citation: D. Noack et al., An unusual intronic mutation in the CYBB gene giving rise to chronic granulomatous disease, BBA-MOL BAS, 1537(2), 2001, pp. 125-131
A second case of somatic triple mosaicism in the CYBB gene causing chronicgranulomatous disease
Authors: Noack, D Heyworth, PG Kyono, W Cross, AR
Citation: D. Noack et al., A second case of somatic triple mosaicism in the CYBB gene causing chronicgranulomatous disease, HUM GENET, 109(2), 2001, pp. 234-238
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
Authors: Noack, D Rae, J Cross, AR Ellis, BA Newburger, PE Curnutte, JT Heyworth, PG
Citation: D. Noack et al., 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, BLOOD, 97(1), 2001, pp. 305-311
Hematologically important mutations: The autosomal recessive forms of chronic granulomatous disease (First update)
Authors: Cross, AR Noack, D Rae, J Curnutte, JT Heyworth, PG
Citation: Ar. Cross et al., Hematologically important mutations: The autosomal recessive forms of chronic granulomatous disease (First update), BL CELL M D, 26(5), 2000, pp. 561
Molecular analysis of 9 new families with chronic granulomatous disease caused by mutations in CYBA, the gene encoding p22(phox)
Authors: Rae, J Noack, D Heyworth, PG Ellis, BA Curnutte, JT Cross, AR
Citation: J. Rae et al., Molecular analysis of 9 new families with chronic granulomatous disease caused by mutations in CYBA, the gene encoding p22(phox), BLOOD, 96(3), 2000, pp. 1106-1112
A novel mutation in the CYBB gene resulting in an unexpected pattern of exon skipping and chronic granulomatous disease
Authors: Noack, D Heyworth, PG Curnutte, JT Rae, J Cross, AR
Citation: D. Noack et al., A novel mutation in the CYBB gene resulting in an unexpected pattern of exon skipping and chronic granulomatous disease, BBA-MOL BAS, 1454(3), 1999, pp. 270-274
Autosomal recessive chronic granulomatous disease caused by novel mutations in NCF-2, the gene encoding the p67-phox component of phagocyte NADPH oxidase
Authors: Noack, D Rae, J Cross, AR Munoz, J Salmen, S Mendoza, JA Rossi, N Curnutte, JT Heyworth, PG
Citation: D. Noack et al., Autosomal recessive chronic granulomatous disease caused by novel mutations in NCF-2, the gene encoding the p67-phox component of phagocyte NADPH oxidase, HUM GENET, 105(5), 1999, pp. 460-467
Activation of human neutrophil NADPH oxidase by phosphatidic acid or diacylglycerol in a cell-free system - Activity of diacylglycerol is dependent on its conversion to phosphatidic acid
Authors: Erickson, RW Langel-Peveri, P Traynor-Kaplan, AE Heyworth, PG Curnutte, JT
Citation: Rw. Erickson et al., Activation of human neutrophil NADPH oxidase by phosphatidic acid or diacylglycerol in a cell-free system - Activity of diacylglycerol is dependent on its conversion to phosphatidic acid, J BIOL CHEM, 274(32), 1999, pp. 22243-22250
Structure and regulation of NADPH oxidase of phagocytic leukocytes - Insights from chronic granulomatous disease
Authors: Heyworth, PG Curnutte, JT Badwey, JA
Citation: Pg. Heyworth et al., Structure and regulation of NADPH oxidase of phagocytic leukocytes - Insights from chronic granulomatous disease, CUR INF RES, 1999, pp. 165-191
Risultati: 1-10 |