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Results: 1-15 |
Results: 15
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
Organizing participation in interaction: Doing participation framework
Authors: Rae, J
Citation: J. Rae, Organizing participation in interaction: Doing participation framework, RES LANG S, 34(2), 2001, pp. 253-278
Induction of gp91-phox, a component of the phagocyte NADPH oxidase, in microglial cells during central nervous system inflammation
Authors: Green, SP Cairns, B Rae, J Errett-Baroncini, C Hongo, JAS Erickson, RW Curnutte, JT
Citation: Sp. Green et al., Induction of gp91-phox, a component of the phagocyte NADPH oxidase, in microglial cells during central nervous system inflammation, J CEREBR B, 21(4), 2001, pp. 374-384
Transplantation of a fetus with paternal Thy-1(+)CD34(+) cells for chronicgranulomatous disease
Authors: Muench, MO Rae, J Barcena, A Leemhuis, T Farrell, J Humeau, L Maxwell-Wiggins, JR Capper, J Mychaliska, GB Albanese, CT Martin, T Tsukamoto, A Curnutte, JT Harrison, MR
Citation: Mo. Muench et al., Transplantation of a fetus with paternal Thy-1(+)CD34(+) cells for chronicgranulomatous disease, BONE MAR TR, 27(4), 2001, pp. 355-364
High resolution mapping of the binding site on human IgG1 for Fc gamma RI,Fc gamma RII, Fc gamma RIII, and FcRn and design of IgG1 variants with improved binding to the Fc gamma R
Authors: Shields, RL Namenuk, AK Hong, K Meng, YG Rae, J Briggs, J Xie, D Lai, J Stadlen, A Li, B Fox, JA Presta, LG
Citation: Rl. Shields et al., High resolution mapping of the binding site on human IgG1 for Fc gamma RI,Fc gamma RII, Fc gamma RIII, and FcRn and design of IgG1 variants with improved binding to the Fc gamma R, J BIOL CHEM, 276(9), 2001, pp. 6591-6604
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
Recombination events between the p47-phox gene and its highly homologous pseudogenes are the main cause of autosomal recessive chronic granulomatous disease
Authors: Roesler, J Curnutte, JT Rae, J Barrett, D Patino, P Chanock, SJ Goerlach, A
Citation: J. Roesler et al., Recombination events between the p47-phox gene and its highly homologous pseudogenes are the main cause of autosomal recessive chronic granulomatous disease, BLOOD, 95(6), 2000, pp. 2150-2156
Roundtable II: Cost concerns for rheumatoid arthritis treatment
Authors: Kavanaugh, AF Wolfe, F Auslander, M Bresloff, T Clark, DL Hillman, D Lewis, DL Martinez, L Milgram, L Newcomer, D Nguyen, T Rae, J
Citation: Af. Kavanaugh et al., Roundtable II: Cost concerns for rheumatoid arthritis treatment, AM J M CARE, 5(14), 1999, pp. S880-S888
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
Molecular characterization of autosomal recessive chronic granulomatous disease caused by a defect of the nicotinamide adenine dinucleotide phosphate(reduced form) oxidase component p67-phox
Authors: Patino, PJ Rae, J Noack, D Erickson, R Ding, JB de Olarte, DG Curnutte, JT
Citation: Pj. Patino et al., Molecular characterization of autosomal recessive chronic granulomatous disease caused by a defect of the nicotinamide adenine dinucleotide phosphate(reduced form) oxidase component p67-phox, BLOOD, 94(7), 1999, pp. 2505-2514
Moral identity in action: Young offenders' reports of encounters with the police
Authors: Kerby, J Rae, J
Citation: J. Kerby et J. Rae, Moral identity in action: Young offenders' reports of encounters with the police, BR J SOC P, 37, 1998, pp. 439-456
Host defense molecule polymorphisms influence the risk for immune-mediatedcomplications in chronic granulomatous disease
Authors: Foster, CB Lehrnbecher, T Mol, F Steinberg, SM Venzon, DJ Walsh, TJ Noack, D Rae, J Winkelstein, JA Curnutte, JT Chanock, SJ
Citation: Cb. Foster et al., Host defense molecule polymorphisms influence the risk for immune-mediatedcomplications in chronic granulomatous disease, J CLIN INV, 102(12), 1998, pp. 2146-2155
Risultati: 1-15 |