-
1
-
-
8544270180
-
Direct interaction of the novel Nox proteins with p22phox is required for the formation of a functionally active NADPH oxidase
-
Ambasta R.K., Kumar P., Griendling K.K., Schmidt H.H., Busse R., Brandes R.P. Direct interaction of the novel Nox proteins with p22phox is required for the formation of a functionally active NADPH oxidase. J. Biol. Chem. 2004, 279:45935-45941.
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 45935-45941
-
-
Ambasta, R.K.1
Kumar, P.2
Griendling, K.K.3
Schmidt, H.H.4
Busse, R.5
Brandes, R.P.6
-
2
-
-
42249101584
-
C242T polymorphism of NADPH oxidase p22phox and recurrence of cardiovascular events in coronary artery disease
-
Arca M., Conti B., Montali A., Pignatelli P., Campagna F., Barilla F., Tanzilli G., Verna R., Vestri A., Gaudio C., Violi F. C242T polymorphism of NADPH oxidase p22phox and recurrence of cardiovascular events in coronary artery disease. Arterioscler. Thromb. Vasc. Biol. 2008, 28:752-757.
-
(2008)
Arterioscler. Thromb. Vasc. Biol.
, vol.28
, pp. 752-757
-
-
Arca, M.1
Conti, B.2
Montali, A.3
Pignatelli, P.4
Campagna, F.5
Barilla, F.6
Tanzilli, G.7
Verna, R.8
Vestri, A.9
Gaudio, C.10
Violi, F.11
-
3
-
-
61849102269
-
First report of clinical, functional, and molecular investigation of chronic granulomatous disease in nine Jordanian families
-
Bakri F.G., Martel C., Khuri-Bulos N., Mahafzah A., El-Khateeb M.S., Al-Wahadneh A.M., Hayajneh W.A., Hamamy H.A., Maquet E., Molin M., Stasia M.J. First report of clinical, functional, and molecular investigation of chronic granulomatous disease in nine Jordanian families. J. Clin. Immunol. 2009, 29:215-230.
-
(2009)
J. Clin. Immunol.
, vol.29
, pp. 215-230
-
-
Bakri, F.G.1
Martel, C.2
Khuri-Bulos, N.3
Mahafzah, A.4
El-Khateeb, M.S.5
Al-Wahadneh, A.M.6
Hayajneh, W.A.7
Hamamy, H.A.8
Maquet, E.9
Molin, M.10
Stasia, M.J.11
-
4
-
-
8544273753
-
NOX3, a superoxide-generating NADPH oxidase of the inner ear
-
Banfi B., Malgrange B., Knisz J., Steger K., Dubois-Dauphin M., Krause K.H. NOX3, a superoxide-generating NADPH oxidase of the inner ear. J. Biol. Chem. 2004, 279:46065-46072.
-
(2004)
J. Biol. Chem.
, vol.279
, pp. 46065-46072
-
-
Banfi, B.1
Malgrange, B.2
Knisz, J.3
Steger, K.4
Dubois-Dauphin, M.5
Krause, K.H.6
-
5
-
-
0032485387
-
Biochemical and immunochemical properties of B lymphocyte cytochrome b558
-
Batot G., Paclet M.H., Doussiere J., Vergnaud S., Martel C., Vignais P.V., Morel F. Biochemical and immunochemical properties of B lymphocyte cytochrome b558. Biochim. Biophys. Acta 1998, 1406:188-202.
-
(1998)
Biochim. Biophys. Acta
, vol.1406
, pp. 188-202
-
-
Batot, G.1
Paclet, M.H.2
Doussiere, J.3
Vergnaud, S.4
Martel, C.5
Vignais, P.V.6
Morel, F.7
-
6
-
-
84919360635
-
Identification of NOX2 regions for normal biosynthesis of cytochrome b558 in phagocytes highlighting essential residues for p22phox binding
-
Beaumel S., Grunwald D., Fieschi F., Stasia M.J. Identification of NOX2 regions for normal biosynthesis of cytochrome b558 in phagocytes highlighting essential residues for p22phox binding. Biochem. J. 2014, 464:425-437.
-
(2014)
Biochem. J.
, vol.464
, pp. 425-437
-
-
Beaumel, S.1
Grunwald, D.2
Fieschi, F.3
Stasia, M.J.4
-
7
-
-
33846794822
-
The NOX family of ROS-generating NADPH oxidases: physiology and pathophysiology
-
Bedard K., Krause K.H. The NOX family of ROS-generating NADPH oxidases: physiology and pathophysiology. Physiol. Rev. 2007, 87:245-313.
-
(2007)
Physiol. Rev.
, vol.87
, pp. 245-313
-
-
Bedard, K.1
Krause, K.H.2
-
8
-
-
67649771733
-
Three common polymorphisms in the CYBA gene form a haplotype associated with decreased ROS generation
-
Bedard K., Attar H., Bonnefont J., Jaquet V., Borel C., Plastre O., Stasia M.J., Antonarakis S.E., Krause K.H. Three common polymorphisms in the CYBA gene form a haplotype associated with decreased ROS generation. Hum. Mutat. 2009, 30:1123-1133.
-
(2009)
Hum. Mutat.
, vol.30
, pp. 1123-1133
-
-
Bedard, K.1
Attar, H.2
Bonnefont, J.3
Jaquet, V.4
Borel, C.5
Plastre, O.6
Stasia, M.J.7
Antonarakis, S.E.8
Krause, K.H.9
-
9
-
-
0035903206
-
Heme-ligating histidines in flavocytochrome b(558): identification of specific histidines in gp91(phox)
-
Biberstine-Kinkade K.J., DeLeo F.R., Epstein R.I., LeRoy B.A., Nauseef W.M., Dinauer M.C. Heme-ligating histidines in flavocytochrome b(558): identification of specific histidines in gp91(phox). J. Biol. Chem. 2001, 276:31105-31112.
-
(2001)
J. Biol. Chem.
, vol.276
, pp. 31105-31112
-
-
Biberstine-Kinkade, K.J.1
DeLeo, F.R.2
Epstein, R.I.3
LeRoy, B.A.4
Nauseef, W.M.5
Dinauer, M.C.6
-
10
-
-
84901451026
-
First report on the Moroccan registry of primary immunodeficiencies: 15 years of experience (1998-2012)
-
Bousfiha A.A., Jeddane L., El Hafidi N., Benajiba N., Rada N., El Bakkouri J., Kili A., Benmiloud S., Benhsaien I., Faiz I., Maataoui O., Aadam Z., Aglaguel A., Baba L.A., Jouhadi Z., Abilkassem R., Bouskraoui M., Hida M., Najib J., Alj H.S., Ailal F., Moroccan Society for Primary, I. First report on the Moroccan registry of primary immunodeficiencies: 15 years of experience (1998-2012). J. Clin. Immunol. 2014, 34:459-468.
-
(2014)
J. Clin. Immunol.
, vol.34
, pp. 459-468
-
-
Bousfiha, A.A.1
Jeddane, L.2
El Hafidi, N.3
Benajiba, N.4
Rada, N.5
El Bakkouri, J.6
Kili, A.7
Benmiloud, S.8
Benhsaien, I.9
Faiz, I.10
Maataoui, O.11
Aadam, Z.12
Aglaguel, A.13
Baba, L.A.14
Jouhadi, Z.15
Abilkassem, R.16
Bouskraoui, M.17
Hida, M.18
Najib, J.19
Alj, H.S.20
Ailal, F.21
more..
-
11
-
-
84937773825
-
Optimized Generation of Functional Neutrophils and Macrophages from Patient-Specific Induced Pluripotent Stem Cells: Ex Vivo Models of X(0)-Linked, AR22(0)- and AR47(0)- Chronic Granulomatous Diseases
-
Brault J., Goutagny E., Telugu N., Shao K., Baquie M., Satre V., Coutton C., Grunwald D., Brion J.P., Barlogis V., Stephan J.L., Plantaz D., Hescheler J., Krause K.H., Saric T., Stasia M.J. Optimized Generation of Functional Neutrophils and Macrophages from Patient-Specific Induced Pluripotent Stem Cells: Ex Vivo Models of X(0)-Linked, AR22(0)- and AR47(0)- Chronic Granulomatous Diseases. Biores. Open Access 2014, 3:311-326.
-
(2014)
Biores. Open Access
, vol.3
, pp. 311-326
-
-
Brault, J.1
Goutagny, E.2
Telugu, N.3
Shao, K.4
Baquie, M.5
Satre, V.6
Coutton, C.7
Grunwald, D.8
Brion, J.P.9
Barlogis, V.10
Stephan, J.L.11
Plantaz, D.12
Hescheler, J.13
Krause, K.H.14
Saric, T.15
Stasia, M.J.16
-
12
-
-
0025223839
-
The alpha subunit of cytochrome b-245 mapped to chromosome 16
-
Bu-Ghanim H.N., Casimir C.M., Povey S., Segal A.W. The alpha subunit of cytochrome b-245 mapped to chromosome 16. Genomics 1990, 8:568-570.
-
(1990)
Genomics
, vol.8
, pp. 568-570
-
-
Bu-Ghanim, H.N.1
Casimir, C.M.2
Povey, S.3
Segal, A.W.4
-
13
-
-
0032544589
-
Antibody imprint of a membrane protein surface. Phagocyte flavocytochrome b
-
Burritt J.B., Busse S.C., Gizachew D., Siemsen D.W., Quinn M.T., Bond C.W., Dratz E.A., Jesaitis A.J. Antibody imprint of a membrane protein surface. Phagocyte flavocytochrome b. J Biol Chem 1998, 273:24847-24852.
-
(1998)
J Biol Chem
, vol.273
, pp. 24847-24852
-
-
Burritt, J.B.1
Busse, S.C.2
Gizachew, D.3
Siemsen, D.W.4
Quinn, M.T.5
Bond, C.W.6
Dratz, E.A.7
Jesaitis, A.J.8
-
14
-
-
0035897653
-
Homologs of gp91phox: cloning and tissue expression of Nox3, Nox4, and Nox5
-
Cheng G., Cao Z., Xu X., van Meir E.G., Lambeth J.D. Homologs of gp91phox: cloning and tissue expression of Nox3, Nox4, and Nox5. Gene 2001, 269:131-140.
-
(2001)
Gene
, vol.269
, pp. 131-140
-
-
Cheng, G.1
Cao, Z.2
Xu, X.3
van Meir, E.G.4
Lambeth, J.D.5
-
15
-
-
0037040940
-
Mapping of functional domains in the p22(phox) subunit of flavocytochrome b(559) participating in the assembly of the NADPH oxidase complex by "peptide walking"
-
Dahan I., Issaeva I., Gorzalczany Y., Sigal N., Hirshberg M., Pick E. Mapping of functional domains in the p22(phox) subunit of flavocytochrome b(559) participating in the assembly of the NADPH oxidase complex by "peptide walking". J. Biol. Chem. 2002, 277:8421-8432.
-
(2002)
J. Biol. Chem.
, vol.277
, pp. 8421-8432
-
-
Dahan, I.1
Issaeva, I.2
Gorzalczany, Y.3
Sigal, N.4
Hirshberg, M.5
Pick, E.6
-
16
-
-
80053968646
-
The NADPH oxidase cytosolic component p67phox is constitutively phosphorylated in human neutrophils: Regulation by a protein tyrosine kinase, MEK1/2 and phosphatases 1/2A
-
Dang P.M., Raad H., Derkawi R.A., Boussetta T., Paclet M.H., Belambri S.A., Makni-Maalej K., Kroviarski Y., Morel F., Gougerot-Pocidalo M.A., El-Benna J. The NADPH oxidase cytosolic component p67phox is constitutively phosphorylated in human neutrophils: Regulation by a protein tyrosine kinase, MEK1/2 and phosphatases 1/2A. Biochem. Pharmacol. 2011, 82:1145-1152.
-
(2011)
Biochem. Pharmacol.
, vol.82
, pp. 1145-1152
-
-
Dang, P.M.1
Raad, H.2
Derkawi, R.A.3
Boussetta, T.4
Paclet, M.H.5
Belambri, S.A.6
Makni-Maalej, K.7
Kroviarski, Y.8
Morel, F.9
Gougerot-Pocidalo, M.A.10
El-Benna, J.11
-
17
-
-
0026616852
-
Cytochrome b558-negative, autosomal recessive chronic granulomatous disease: two new mutations in the cytochrome b558 light chain of the NADPH oxidase (p22-phox)
-
de Boer M., de Klein A., Hossle J.P., Seger R., Corbeel L., Weening R.S., Roos D. Cytochrome b558-negative, autosomal recessive chronic granulomatous disease: two new mutations in the cytochrome b558 light chain of the NADPH oxidase (p22-phox). Am. J. Hum. Genet. 1992, 51:1127-1135.
-
(1992)
Am. J. Hum. Genet.
, vol.51
, pp. 1127-1135
-
-
de Boer, M.1
de Klein, A.2
Hossle, J.P.3
Seger, R.4
Corbeel, L.5
Weening, R.S.6
Roos, D.7
-
18
-
-
0034607821
-
Processing and maturation of flavocytochrome b558 include incorporation of heme as a prerequisite for heterodimer assembly
-
DeLeo F.R., Burritt J.B., Yu L., Jesaitis A.J., Dinauer M.C., Nauseef W.M. Processing and maturation of flavocytochrome b558 include incorporation of heme as a prerequisite for heterodimer assembly. J. Biol. Chem. 2000, 275:13986-13993.
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 13986-13993
-
-
DeLeo, F.R.1
Burritt, J.B.2
Yu, L.3
Jesaitis, A.J.4
Dinauer, M.C.5
Nauseef, W.M.6
-
19
-
-
0023251352
-
The glycoprotein encoded by the X-linked chronic granulomatous disease locus is a component of the neutrophil cytochrome b complex
-
Dinauer M.C., Orkin S.H., Brown R., Jesaitis A.J., Parkos C.A. The glycoprotein encoded by the X-linked chronic granulomatous disease locus is a component of the neutrophil cytochrome b complex. Nature 1987, 327:717-720.
-
(1987)
Nature
, vol.327
, pp. 717-720
-
-
Dinauer, M.C.1
Orkin, S.H.2
Brown, R.3
Jesaitis, A.J.4
Parkos, C.A.5
-
20
-
-
0025114585
-
Human neutrophil cytochrome b light chain (p22-phox). Gene structure, chromosomal location, and mutations in cytochrome-negative autosomal recessive chronic granulomatous disease
-
Dinauer M.C., Pierce E.A., Bruns G.A., Curnutte J.T., Orkin S.H. Human neutrophil cytochrome b light chain (p22-phox). Gene structure, chromosomal location, and mutations in cytochrome-negative autosomal recessive chronic granulomatous disease. J. Clin. Invest. 1990, 86:1729-1737.
-
(1990)
J. Clin. Invest.
, vol.86
, pp. 1729-1737
-
-
Dinauer, M.C.1
Pierce, E.A.2
Bruns, G.A.3
Curnutte, J.T.4
Orkin, S.H.5
-
21
-
-
28844467210
-
Haplotype analysis of NAD(P)H oxidase p22phox polymorphisms in end-stage renal disease
-
Doi K., Noiri E., Nakao A., Fujita T., Kobayashi S., Tokunaga K. Haplotype analysis of NAD(P)H oxidase p22phox polymorphisms in end-stage renal disease. J. Hum. Genet. 2005, 50:641-647.
-
(2005)
J. Hum. Genet.
, vol.50
, pp. 641-647
-
-
Doi, K.1
Noiri, E.2
Nakao, A.3
Fujita, T.4
Kobayashi, S.5
Tokunaga, K.6
-
22
-
-
33749047901
-
Genetic and mutational heterogeneity of autosomal recessive chronic granulomatous disease in Tunisia
-
El Kares R., Barbouche M.R., Elloumi-Zghal H., Bejaoui M., Chemli J., Mellouli F., Tebib N., Abdelmoula M.S., Boukthir S., Fitouri Z., M'Rad S., Bouslama K., Touiri H., Abdelhak S., Dellagi M.K. Genetic and mutational heterogeneity of autosomal recessive chronic granulomatous disease in Tunisia. J. Hum. Genet. 2006, 51:887-895.
-
(2006)
J. Hum. Genet.
, vol.51
, pp. 887-895
-
-
El Kares, R.1
Barbouche, M.R.2
Elloumi-Zghal, H.3
Bejaoui, M.4
Chemli, J.5
Mellouli, F.6
Tebib, N.7
Abdelmoula, M.S.8
Boukthir, S.9
Fitouri, Z.10
M'Rad, S.11
Bouslama, K.12
Touiri, H.13
Abdelhak, S.14
Dellagi, M.K.15
-
23
-
-
65949102522
-
P47phox, the phagocyte NADPH oxidase/NOX2 organizer: structure, phosphorylation and implication in diseases
-
El-Benna J., Dang P.M., Gougerot-Pocidalo M.A., Marie J.C., Braut-Boucher F. p47phox, the phagocyte NADPH oxidase/NOX2 organizer: structure, phosphorylation and implication in diseases. Exp. Mol. Med. 2009, 41:217-225.
-
(2009)
Exp. Mol. Med.
, vol.41
, pp. 217-225
-
-
El-Benna, J.1
Dang, P.M.2
Gougerot-Pocidalo, M.A.3
Marie, J.C.4
Braut-Boucher, F.5
-
24
-
-
77951666823
-
Association of p22phox gene C242T polymorphism with coronary artery disease: a meta-analysis
-
Fang S., Wang L., Jia C. Association of p22phox gene C242T polymorphism with coronary artery disease: a meta-analysis. Thromb. Res. 2010, 125:e197-e201.
-
(2010)
Thromb. Res.
, vol.125
, pp. e197-e201
-
-
Fang, S.1
Wang, L.2
Jia, C.3
-
25
-
-
84971607692
-
RAGE and CYBA polymorphisms are associated with microalbuminuria and end-stage renal disease onset in a cohort of type 1 diabetes mellitus patients over a 20-year follow-up
-
Franko B., Benhamou P.Y., Genty C., Jouve T., Nasse L., Rzeoecki V., Semeraro P., Stasia M.J., Zaoui P. RAGE and CYBA polymorphisms are associated with microalbuminuria and end-stage renal disease onset in a cohort of type 1 diabetes mellitus patients over a 20-year follow-up. Acta Diabetol. 2015.
-
(2015)
Acta Diabetol.
-
-
Franko, B.1
Benhamou, P.Y.2
Genty, C.3
Jouve, T.4
Nasse, L.5
Rzeoecki, V.6
Semeraro, P.7
Stasia, M.J.8
Zaoui, P.9
-
26
-
-
0028982606
-
Cytochrome b-558 alpha-subunit cloning and expression in rat aortic smooth muscle cells
-
Fukui T., Lassegue B., Kai H., Alexander R.W., Griendling K.K. Cytochrome b-558 alpha-subunit cloning and expression in rat aortic smooth muscle cells. Biochim. Biophys. Acta 1995, 1231:215-219.
-
(1995)
Biochim. Biophys. Acta
, vol.1231
, pp. 215-219
-
-
Fukui, T.1
Lassegue, B.2
Kai, H.3
Alexander, R.W.4
Griendling, K.K.5
-
27
-
-
0032588543
-
The p22 phox A640G gene polymorphism but not the C242T gene variation is associated with coronary heart disease in younger individuals
-
Gardemann A., Mages P., Katz N., Tillmanns H., Haberbosch W. The p22 phox A640G gene polymorphism but not the C242T gene variation is associated with coronary heart disease in younger individuals. Atherosclerosis 1999, 145:315-323.
-
(1999)
Atherosclerosis
, vol.145
, pp. 315-323
-
-
Gardemann, A.1
Mages, P.2
Katz, N.3
Tillmanns, H.4
Haberbosch, W.5
-
28
-
-
15944372262
-
Activation and assembly of the NADPH oxidase: a structural perspective
-
Groemping Y., Rittinger K. Activation and assembly of the NADPH oxidase: a structural perspective. Biochem. J. 2005, 386:401-416.
-
(2005)
Biochem. J.
, vol.386
, pp. 401-416
-
-
Groemping, Y.1
Rittinger, K.2
-
29
-
-
0037722978
-
Molecular basis of phosphorylation-induced activation of the NADPH oxidase
-
Groemping Y., Lapouge K., Smerdon S.J., Rittinger K. Molecular basis of phosphorylation-induced activation of the NADPH oxidase. Cell 2003, 113:343-355.
-
(2003)
Cell
, vol.113
, pp. 343-355
-
-
Groemping, Y.1
Lapouge, K.2
Smerdon, S.J.3
Rittinger, K.4
-
30
-
-
84878615779
-
Association between the C242T polymorphism of p22phox gene and ischemic stroke: a meta-analysis
-
Gu L., Su L., Liang B., Tang N., Long J., Tan J., Chen Q., Xie J., Wu G., Yan Y., Huang G., Zu X. Association between the C242T polymorphism of p22phox gene and ischemic stroke: a meta-analysis. J. Neurol. Sci. 2013, 330:100-110.
-
(2013)
J. Neurol. Sci.
, vol.330
, pp. 100-110
-
-
Gu, L.1
Su, L.2
Liang, B.3
Tang, N.4
Long, J.5
Tan, J.6
Chen, Q.7
Xie, J.8
Wu, G.9
Yan, Y.10
Huang, G.11
Zu, X.12
-
31
-
-
0021763208
-
Purification of cytochrome b-245 from human neutrophils
-
Harper A.M., Dunne M.J., Segal A.W. Purification of cytochrome b-245 from human neutrophils. Biochem. J. 1984, 219:519-527.
-
(1984)
Biochem. J.
, vol.219
, pp. 519-527
-
-
Harper, A.M.1
Dunne, M.J.2
Segal, A.W.3
-
32
-
-
84929157603
-
Meta-analysis of C242T polymorphism in CYBA genes: risk of acute coronary syndrome is lower in Asians but not in Caucasians
-
Hu P., Huang M.Y., Hu X.Y., Xie X.J., Xiang M.X., Liu X.B., Wang J.A. Meta-analysis of C242T polymorphism in CYBA genes: risk of acute coronary syndrome is lower in Asians but not in Caucasians. J. Zhejiang Univ. Sci. B 2015, 16:370-379.
-
(2015)
J. Zhejiang Univ. Sci. B
, vol.16
, pp. 370-379
-
-
Hu, P.1
Huang, M.Y.2
Hu, X.Y.3
Xie, X.J.4
Xiang, M.X.5
Liu, X.B.6
Wang, J.A.7
-
33
-
-
0026610275
-
Topology of cytochrome b558 in neutrophil membrane analyzed by anti-peptide antibodies and proteolysis
-
Imajoh-Ohmi S., Tokita K., Ochiai H., Nakamura M., Kanegasaki S. Topology of cytochrome b558 in neutrophil membrane analyzed by anti-peptide antibodies and proteolysis. J. Biol. Chem. 1992, 267:180-184.
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 180-184
-
-
Imajoh-Ohmi, S.1
Tokita, K.2
Ochiai, H.3
Nakamura, M.4
Kanegasaki, S.5
-
34
-
-
0031940241
-
Polymorphism of the NADH/NADPH oxidase p22 phox gene in patients with coronary artery disease
-
Inoue N., Kawashima S., Kanazawa K., Yamada S., Akita H., Yokoyama M. Polymorphism of the NADH/NADPH oxidase p22 phox gene in patients with coronary artery disease. Circulation 1998, 97:135-137.
-
(1998)
Circulation
, vol.97
, pp. 135-137
-
-
Inoue, N.1
Kawashima, S.2
Kanazawa, K.3
Yamada, S.4
Akita, H.5
Yokoyama, M.6
-
35
-
-
84867418899
-
Genetical analysis of all Danish patients diagnosed with chronic granulomatous disease
-
Jakobsen M.A., Katzenstein T.L., Valerius N.H., Roos D., Fisker N., Mogensen T.H., Jensen P.O., Barington T. Genetical analysis of all Danish patients diagnosed with chronic granulomatous disease. Scand. J. Immunol. 2012, 76:505-511.
-
(2012)
Scand. J. Immunol.
, vol.76
, pp. 505-511
-
-
Jakobsen, M.A.1
Katzenstein, T.L.2
Valerius, N.H.3
Roos, D.4
Fisker, N.5
Mogensen, T.H.6
Jensen, P.O.7
Barington, T.8
-
36
-
-
84921473820
-
Accumulation of oxidative stress-related gene polymorphisms and the risk of coronary heart disease events in patients with type 2 diabetes-an 8-year prospective study
-
Katakami N., Kaneto H., Matsuoka T.A., Takahara M., Osonoi T., Saitou M., Kawai K., Ishibashi F., Kashiwagi A., Kawamori R., Shimomura I., Yamasaki Y. Accumulation of oxidative stress-related gene polymorphisms and the risk of coronary heart disease events in patients with type 2 diabetes-an 8-year prospective study. Atherosclerosis 2014, 235:408-414.
-
(2014)
Atherosclerosis
, vol.235
, pp. 408-414
-
-
Katakami, N.1
Kaneto, H.2
Matsuoka, T.A.3
Takahara, M.4
Osonoi, T.5
Saitou, M.6
Kawai, K.7
Ishibashi, F.8
Kashiwagi, A.9
Kawamori, R.10
Shimomura, I.11
Yamasaki, Y.12
-
37
-
-
84887019423
-
Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patients
-
(e5)
-
Koker M.Y., Camcioglu Y., van Leeuwen K., Kilic S.S., Barlan I., Yilmaz M., Metin A., de Boer M., Avcilar H., Patiroglu T., Yildiran A., Yegin O., Tezcan I., Sanal O., Roos D. Clinical, functional, and genetic characterization of chronic granulomatous disease in 89 Turkish patients. J. Allergy Clin. Immunol. 2013, 132:1156-1163. (e5).
-
(2013)
J. Allergy Clin. Immunol.
, vol.132
, pp. 1156-1163
-
-
Koker, M.Y.1
Camcioglu, Y.2
van Leeuwen, K.3
Kilic, S.S.4
Barlan, I.5
Yilmaz, M.6
Metin, A.7
de Boer, M.8
Avcilar, H.9
Patiroglu, T.10
Yildiran, A.11
Yegin, O.12
Tezcan, I.13
Sanal, O.14
Roos, D.15
-
38
-
-
62349107356
-
Six different CYBA mutations including three novel mutations in ten families from Turkey, resulting in autosomal recessive chronic granulomatous disease
-
Koker M.Y., van Leeuwen K., de Boer M., Celmeli F., Metin A., Ozgur T.T., Tezcan I., Sanal O., Roos D. Six different CYBA mutations including three novel mutations in ten families from Turkey, resulting in autosomal recessive chronic granulomatous disease. Eur. J. Clin. Investig. 2009, 39:311-319.
-
(2009)
Eur. J. Clin. Investig.
, vol.39
, pp. 311-319
-
-
Koker, M.Y.1
van Leeuwen, K.2
de Boer, M.3
Celmeli, F.4
Metin, A.5
Ozgur, T.T.6
Tezcan, I.7
Sanal, O.8
Roos, D.9
-
40
-
-
78650918337
-
Residual NADPH oxidase and survival in chronic granulomatous disease
-
Kuhns D.B., Alvord W.G., Heller T., Feld J.J., Pike K.M., Marciano B.E., Uzel G., DeRavin S.S., Priel D.A., Soule B.P., Zarember K.A., Malech H.L., Holland S.M., Gallin J.I. Residual NADPH oxidase and survival in chronic granulomatous disease. N. Engl. J. Med. 2010, 363:2600-2610.
-
(2010)
N. Engl. J. Med.
, vol.363
, pp. 2600-2610
-
-
Kuhns, D.B.1
Alvord, W.G.2
Heller, T.3
Feld, J.J.4
Pike, K.M.5
Marciano, B.E.6
Uzel, G.7
DeRavin, S.S.8
Priel, D.A.9
Soule, B.P.10
Zarember, K.A.11
Malech, H.L.12
Holland, S.M.13
Gallin, J.I.14
-
41
-
-
84897019491
-
Nox enzymes and new thinking on reactive oxygen: a double-edged sword revisited
-
Lambeth J.D., Neish A.S. Nox enzymes and new thinking on reactive oxygen: a double-edged sword revisited. Annu. Rev. Pathol. 2014, 9:119-145.
-
(2014)
Annu. Rev. Pathol.
, vol.9
, pp. 119-145
-
-
Lambeth, J.D.1
Neish, A.S.2
-
42
-
-
0027973549
-
Assembly of the phagocyte NADPH oxidase: binding of Src homology 3 domains to proline-rich targets
-
Leto T.L., Adams A.G., de Mendez I. Assembly of the phagocyte NADPH oxidase: binding of Src homology 3 domains to proline-rich targets. Proc. Natl. Acad. Sci. U. S. A. 1994, 91:10650-10654.
-
(1994)
Proc. Natl. Acad. Sci. U. S. A.
, vol.91
, pp. 10650-10654
-
-
Leto, T.L.1
Adams, A.G.2
de Mendez, I.3
-
43
-
-
0028170628
-
156Pro->Gln substitution in the light chain of cytochrome b558 of the human NADPH oxidase (p22-phox) leads to defective translocation of the cytosolic proteins p47-phox and p67-phox
-
Leusen J.H., Bolscher B.G., Hilarius P.M., Weening R.S., Kaulfersch W., Seger R.A., Roos D., Verhoeven A.J. 156Pro->Gln substitution in the light chain of cytochrome b558 of the human NADPH oxidase (p22-phox) leads to defective translocation of the cytosolic proteins p47-phox and p67-phox. J. Exp. Med. 1994, 180:2329-2334.
-
(1994)
J. Exp. Med.
, vol.180
, pp. 2329-2334
-
-
Leusen, J.H.1
Bolscher, B.G.2
Hilarius, P.M.3
Weening, R.S.4
Kaulfersch, W.5
Seger, R.A.6
Roos, D.7
Verhoeven, A.J.8
-
44
-
-
77449086400
-
Phosphorylation of p22phox on threonine 147 enhances NADPH oxidase activity by promoting p47phox binding
-
Lewis E.M., Sergeant S., Ledford B., Stull N., Dinauer M.C., McPhail L.C. Phosphorylation of p22phox on threonine 147 enhances NADPH oxidase activity by promoting p47phox binding. J. Biol. Chem. 2010, 285:2959-2967.
-
(2010)
J. Biol. Chem.
, vol.285
, pp. 2959-2967
-
-
Lewis, E.M.1
Sergeant, S.2
Ledford, B.3
Stull, N.4
Dinauer, M.C.5
McPhail, L.C.6
-
45
-
-
84873654722
-
Association between NADPH oxidase p22(phox) C242T polymorphism and ischemic cerebrovascular disease: a meta-analysis
-
Li B.H., Zhang L.L., Zhang B.B., Yin Y.W., Dai L.M., Pi Y., Guo L., Gao C.Y., Fang C.Q., Wang J.Z., Li J.C. Association between NADPH oxidase p22(phox) C242T polymorphism and ischemic cerebrovascular disease: a meta-analysis. PLoS One 2013, 8:e56478.
-
(2013)
PLoS One
, vol.8
, pp. e56478
-
-
Li, B.H.1
Zhang, L.L.2
Zhang, B.B.3
Yin, Y.W.4
Dai, L.M.5
Pi, Y.6
Guo, L.7
Gao, C.Y.8
Fang, C.Q.9
Wang, J.Z.10
Li, J.C.11
-
46
-
-
84921290589
-
NADPH oxidase p22phox C242T polymorphism and ischemic cerebrovascular disease: an updated meta-analysis
-
Li P., Qiu T., Qin C. NADPH oxidase p22phox C242T polymorphism and ischemic cerebrovascular disease: an updated meta-analysis. Med. Sci. Monit. 2015, 21:231-238.
-
(2015)
Med. Sci. Monit.
, vol.21
, pp. 231-238
-
-
Li, P.1
Qiu, T.2
Qin, C.3
-
47
-
-
84897113517
-
The A640G polymorphism in the NAD(P)H oxidase p22phox gene (CYBA) is associated with risk reduction of coronary heart disease: a meta-analysis
-
Liang B., Wei Q., Shen T., Su L., Yan Y., Wu G., Lu J., Gu L. The A640G polymorphism in the NAD(P)H oxidase p22phox gene (CYBA) is associated with risk reduction of coronary heart disease: a meta-analysis. Clin. Biochem. 2014, 47:409-416.
-
(2014)
Clin. Biochem.
, vol.47
, pp. 409-416
-
-
Liang, B.1
Wei, Q.2
Shen, T.3
Su, L.4
Yan, Y.5
Wu, G.6
Lu, J.7
Gu, L.8
-
48
-
-
0027361152
-
Restitution of superoxide generation in autosomal cytochrome-negative chronic granulomatous disease (A22(0) CGD)-derived B lymphocyte cell lines by transfection with p22phax cDNA
-
Maly F.E., Schuerer-Maly C.C., Quilliam L., Cochrane C.G., Newburger P.E., Curnutte J.T., Gifford M., Dinauer M.C. Restitution of superoxide generation in autosomal cytochrome-negative chronic granulomatous disease (A22(0) CGD)-derived B lymphocyte cell lines by transfection with p22phax cDNA. J. Exp. Med. 1993, 178:2047-2053.
-
(1993)
J. Exp. Med.
, vol.178
, pp. 2047-2053
-
-
Maly, F.E.1
Schuerer-Maly, C.C.2
Quilliam, L.3
Cochrane, C.G.4
Newburger, P.E.5
Curnutte, J.T.6
Gifford, M.7
Dinauer, M.C.8
-
49
-
-
26244444476
-
Functional analysis of Nox4 reveals unique characteristics compared to other NADPH oxidases
-
Martyn K.D., Frederick L.M., von Loehneysen K., Dinauer M.C., Knaus U.G. Functional analysis of Nox4 reveals unique characteristics compared to other NADPH oxidases. Cell. Signal. 2006, 18:69-82.
-
(2006)
Cell. Signal.
, vol.18
, pp. 69-82
-
-
Martyn, K.D.1
Frederick, L.M.2
von Loehneysen, K.3
Dinauer, M.C.4
Knaus, U.G.5
-
50
-
-
84861434584
-
Consensus in silico computational modelling of the p22phox subunit of the NADPH oxidase
-
Meijles D.N., Howlin B.J., Li J.M. Consensus in silico computational modelling of the p22phox subunit of the NADPH oxidase. Comput. Biol. Chem. 2012, 39:6-13.
-
(2012)
Comput. Biol. Chem.
, vol.39
, pp. 6-13
-
-
Meijles, D.N.1
Howlin, B.J.2
Li, J.M.3
-
51
-
-
77955896068
-
CYBA gene variants as biomarkers for coronary artery disease
-
Moreno M.U., Zalba G. CYBA gene variants as biomarkers for coronary artery disease. Drug News Perspect. 2010, 23:316-324.
-
(2010)
Drug News Perspect.
, vol.23
, pp. 316-324
-
-
Moreno, M.U.1
Zalba, G.2
-
52
-
-
34447309993
-
A novel CYBA variant, the -675A/T polymorphism, is associated with essential hypertension
-
Moreno M.U., San Jose G., Fortuno A., Beloqui O., Redon J., Chaves F.J., Corella D., Diez J., Zalba G. A novel CYBA variant, the -675A/T polymorphism, is associated with essential hypertension. J. Hypertens. 2007, 25:1620-1626.
-
(2007)
J. Hypertens.
, vol.25
, pp. 1620-1626
-
-
Moreno, M.U.1
San Jose, G.2
Fortuno, A.3
Beloqui, O.4
Redon, J.5
Chaves, F.J.6
Corella, D.7
Diez, J.8
Zalba, G.9
-
53
-
-
0038363762
-
Preliminary characterisation of the promoter of the human p22(phox) gene: identification of a new polymorphism associated with hypertension
-
Moreno M.U., San Jose G., Orbe J., Paramo J.A., Beloqui O., Diez J., Zalba G. Preliminary characterisation of the promoter of the human p22(phox) gene: identification of a new polymorphism associated with hypertension. FEBS Lett. 2003, 542:27-31.
-
(2003)
FEBS Lett.
, vol.542
, pp. 27-31
-
-
Moreno, M.U.1
San Jose, G.2
Orbe, J.3
Paramo, J.A.4
Beloqui, O.5
Diez, J.6
Zalba, G.7
-
54
-
-
70149091507
-
Pivotal Advance: Eosinophilia in the MES rat strain is caused by a loss-of-function mutation in the gene for cytochrome b(-245), alpha polypeptide (Cyba)
-
Mori M., Li G., Hashimoto M., Nishio A., Tomozawa H., Suzuki N., Usami S., Higuchi K., Matsumoto K. Pivotal Advance: Eosinophilia in the MES rat strain is caused by a loss-of-function mutation in the gene for cytochrome b(-245), alpha polypeptide (Cyba). J. Leukoc. Biol. 2009, 86:473-478.
-
(2009)
J. Leukoc. Biol.
, vol.86
, pp. 473-478
-
-
Mori, M.1
Li, G.2
Hashimoto, M.3
Nishio, A.4
Tomozawa, H.5
Suzuki, N.6
Usami, S.7
Higuchi, K.8
Matsumoto, K.9
-
55
-
-
34147130314
-
Critical roles for p22phox in the structural maturation and subcellular targeting of Nox3
-
Nakano Y., Banfi B., Jesaitis A.J., Dinauer M.C., Allen L.A., Nauseef W.M. Critical roles for p22phox in the structural maturation and subcellular targeting of Nox3. Biochem. J. 2007, 403:97-108.
-
(2007)
Biochem. J.
, vol.403
, pp. 97-108
-
-
Nakano, Y.1
Banfi, B.2
Jesaitis, A.J.3
Dinauer, M.C.4
Allen, L.A.5
Nauseef, W.M.6
-
56
-
-
40549116310
-
Mutation of the Cyba gene encoding p22phox causes vestibular and immune defects in mice
-
Nakano Y., Longo-Guess C.M., Bergstrom D.E., Nauseef W.M., Jones S.M., Banfi B. Mutation of the Cyba gene encoding p22phox causes vestibular and immune defects in mice. J. Clin. Invest. 2008, 118:1176-1185.
-
(2008)
J. Clin. Invest.
, vol.118
, pp. 1176-1185
-
-
Nakano, Y.1
Longo-Guess, C.M.2
Bergstrom, D.E.3
Nauseef, W.M.4
Jones, S.M.5
Banfi, B.6
-
57
-
-
84876931396
-
Beyond oxidative stress: an immunologist's guide to reactive oxygen species
-
Nathan C., Cunningham-Bussel A. Beyond oxidative stress: an immunologist's guide to reactive oxygen species. Nat. Rev. Immunol. 2013, 13:349-361.
-
(2013)
Nat. Rev. Immunol.
, vol.13
, pp. 349-361
-
-
Nathan, C.1
Cunningham-Bussel, A.2
-
58
-
-
77956154620
-
Association of the CYBA, PPARGC1A, PPARG3, and PPARD gene variants with coronary artery disease and metabolic risk factors of coronary atherosclerosis in a Russian population
-
Nikitin A.G., Chistiakov D.A., Minushkina L.O., Zateyshchikov D.A., Nosikov V.V. Association of the CYBA, PPARGC1A, PPARG3, and PPARD gene variants with coronary artery disease and metabolic risk factors of coronary atherosclerosis in a Russian population. Heart Vessel. 2010, 25:229-236.
-
(2010)
Heart Vessel.
, vol.25
, pp. 229-236
-
-
Nikitin, A.G.1
Chistiakov, D.A.2
Minushkina, L.O.3
Zateyshchikov, D.A.4
Nosikov, V.V.5
-
59
-
-
33645641343
-
NMR solution structure of the tandem Src homology 3 domains of p47phox complexed with a p22phox-derived proline-rich peptide
-
Ogura K., Nobuhisa I., Yuzawa S., Takeya R., Torikai S., Saikawa K., Sumimoto H., Inagaki F. NMR solution structure of the tandem Src homology 3 domains of p47phox complexed with a p22phox-derived proline-rich peptide. J. Biol. Chem. 2006, 281:3660-3668.
-
(2006)
J. Biol. Chem.
, vol.281
, pp. 3660-3668
-
-
Ogura, K.1
Nobuhisa, I.2
Yuzawa, S.3
Takeya, R.4
Torikai, S.5
Saikawa, K.6
Sumimoto, H.7
Inagaki, F.8
-
60
-
-
12144287044
-
Vestibular defects in head-tilt mice result from mutations in Nox3, encoding an NADPH oxidase
-
Paffenholz R., Bergstrom R.A., Pasutto F., Wabnitz P., Munroe R.J., Jagla W., Heinzmann U., Marquardt A., Bareiss A., Laufs J., Russ A., Stumm G., Schimenti J.C., Bergstrom D.E. Vestibular defects in head-tilt mice result from mutations in Nox3, encoding an NADPH oxidase. Genes Dev. 2004, 18:486-491.
-
(2004)
Genes Dev.
, vol.18
, pp. 486-491
-
-
Paffenholz, R.1
Bergstrom, R.A.2
Pasutto, F.3
Wabnitz, P.4
Munroe, R.J.5
Jagla, W.6
Heinzmann, U.7
Marquardt, A.8
Bareiss, A.9
Laufs, J.10
Russ, A.11
Stumm, G.12
Schimenti, J.C.13
Bergstrom, D.E.14
-
61
-
-
0023483148
-
Purified cytochrome b from human granulocyte plasma membrane is comprised of two polypeptides with relative molecular weights of 91,000 and 22,000
-
Parkos C.A., Allen R.A., Cochrane C.G., Jesaitis A.J. Purified cytochrome b from human granulocyte plasma membrane is comprised of two polypeptides with relative molecular weights of 91,000 and 22,000. J. Clin. Investig. 1987, 80:732-742.
-
(1987)
J. Clin. Investig.
, vol.80
, pp. 732-742
-
-
Parkos, C.A.1
Allen, R.A.2
Cochrane, C.G.3
Jesaitis, A.J.4
-
62
-
-
0024513954
-
Absence of both the 91kD and 22kD subunits of human neutrophil cytochrome b in two genetic forms of chronic granulomatous disease
-
Parkos C.A., Dinauer M.C., Jesaitis A.J., Orkin S.H., Curnutte J.T. Absence of both the 91kD and 22kD subunits of human neutrophil cytochrome b in two genetic forms of chronic granulomatous disease. Blood 1989, 73:1416-1420.
-
(1989)
Blood
, vol.73
, pp. 1416-1420
-
-
Parkos, C.A.1
Dinauer, M.C.2
Jesaitis, A.J.3
Orkin, S.H.4
Curnutte, J.T.5
-
63
-
-
1842350863
-
Primary structure and unique expression of the 22-kilodalton light chain of human neutrophil cytochrome b
-
Parkos C.A., Dinauer M.C., Walker L.E., Allen R.A., Jesaitis A.J., Orkin S.H. Primary structure and unique expression of the 22-kilodalton light chain of human neutrophil cytochrome b. Proc. Natl. Acad. Sci. U. S. A. 1988, 85:3319-3323.
-
(1988)
Proc. Natl. Acad. Sci. U. S. A.
, vol.85
, pp. 3319-3323
-
-
Parkos, C.A.1
Dinauer, M.C.2
Walker, L.E.3
Allen, R.A.4
Jesaitis, A.J.5
Orkin, S.H.6
-
64
-
-
84930621494
-
Allelic variations in the CYBA gene of NADPH oxidase and risk of kidney complications in patients with type 1 diabetes
-
Patente T.A., Mohammedi K., Bellili-Munoz N., Driss F., Sanchez M., Fumeron F., Roussel R., Hadjadj S., Correa-Giannella M.L., Marre M., Velho G. Allelic variations in the CYBA gene of NADPH oxidase and risk of kidney complications in patients with type 1 diabetes. Free Radic. Biol. Med. 2015, 86:16-24.
-
(2015)
Free Radic. Biol. Med.
, vol.86
, pp. 16-24
-
-
Patente, T.A.1
Mohammedi, K.2
Bellili-Munoz, N.3
Driss, F.4
Sanchez, M.5
Fumeron, F.6
Roussel, R.7
Hadjadj, S.8
Correa-Giannella, M.L.9
Marre, M.10
Velho, G.11
-
65
-
-
0036528750
-
Increased free radical production in hypertension due to increased expression of the NADPH oxidase subunit p22(phox) in lymphoblast cell lines
-
Pettit A.I., Wong R.K., Lee V., Jennings S., Quinn P.A., Ng L.L. Increased free radical production in hypertension due to increased expression of the NADPH oxidase subunit p22(phox) in lymphoblast cell lines. J. Hypertens. 2002, 20:677-683.
-
(2002)
J. Hypertens.
, vol.20
, pp. 677-683
-
-
Pettit, A.I.1
Wong, R.K.2
Lee, V.3
Jennings, S.4
Quinn, P.A.5
Ng, L.L.6
-
66
-
-
0028063050
-
P22-phox-deficient chronic granulomatous disease: reconstitution by retrovirus-mediated expression and identification of a biosynthetic intermediate of gp91-phox
-
Porter C.D., Parkar M.H., Verhoeven A.J., Levinsky R.J., Collins M.K., Kinnon C. p22-phox-deficient chronic granulomatous disease: reconstitution by retrovirus-mediated expression and identification of a biosynthetic intermediate of gp91-phox. Blood 1994, 84:2767-2775.
-
(1994)
Blood
, vol.84
, pp. 2767-2775
-
-
Porter, C.D.1
Parkar, M.H.2
Verhoeven, A.J.3
Levinsky, R.J.4
Collins, M.K.5
Kinnon, C.6
-
67
-
-
84891955093
-
The A930G polymorphism ofP22phox (CYBA) gene but not C242T variation is associated with hypertension: a meta-analysis
-
Qin Y.W., Peng J., Liang B.Y., Su L., Chen Q., Xie J.J., Gu L. The A930G polymorphism ofP22phox (CYBA) gene but not C242T variation is associated with hypertension: a meta-analysis. PLoS One 2013, 8.
-
(2013)
PLoS One
, vol.8
-
-
Qin, Y.W.1
Peng, J.2
Liang, B.Y.3
Su, L.4
Chen, Q.5
Xie, J.J.6
Gu, L.7
-
68
-
-
0026754805
-
Human neutrophil cytochrome b contains multiple hemes. Evidence for heme associated with both subunits
-
Quinn M.T., Mullen M.L., Jesaitis A.J. Human neutrophil cytochrome b contains multiple hemes. Evidence for heme associated with both subunits. J. Biol. Chem. 1992, 267:7303-7309.
-
(1992)
J. Biol. Chem.
, vol.267
, pp. 7303-7309
-
-
Quinn, M.T.1
Mullen, M.L.2
Jesaitis, A.J.3
-
69
-
-
65349153053
-
Regulation of the phagocyte NADPH oxidase activity: phosphorylation of gp91phox/NOX2 by protein kinase C enhances its diaphorase activity and binding to Rac2, p67phox, and p47phox
-
Raad H., Paclet M.H., Boussetta T., Kroviarski Y., Morel F., Quinn M.T., Gougerot-Pocidalo M.A., Dang P.M., El-Benna J. Regulation of the phagocyte NADPH oxidase activity: phosphorylation of gp91phox/NOX2 by protein kinase C enhances its diaphorase activity and binding to Rac2, p67phox, and p47phox. FASEB J. 2009, 23:1011-1022.
-
(2009)
FASEB J.
, vol.23
, pp. 1011-1022
-
-
Raad, H.1
Paclet, M.H.2
Boussetta, T.3
Kroviarski, Y.4
Morel, F.5
Quinn, M.T.6
Gougerot-Pocidalo, M.A.7
Dang, P.M.8
El-Benna, J.9
-
70
-
-
0034254771
-
Molecular analysis of 9 new families with chronic granulomatous disease caused by mutations in CYBA, the gene encoding p22(phox)
-
Rae J., Noack D., Heyworth P.G., Ellis B.A., Curnutte J.T., Cross A.R. Molecular analysis of 9 new families with chronic granulomatous disease caused by mutations in CYBA, the gene encoding p22(phox). Blood 2000, 96:1106-1112.
-
(2000)
Blood
, vol.96
, pp. 1106-1112
-
-
Rae, J.1
Noack, D.2
Heyworth, P.G.3
Ellis, B.A.4
Curnutte, J.T.5
Cross, A.R.6
-
71
-
-
77950299675
-
Hematologically important mutations: the autosomal recessive forms of chronic granulomatous disease (second update)
-
Roos D., Kuhns D.B., Maddalena A., Bustamante J., Kannengiesser C., de Boer M., van Leeuwen K., Koker M.Y., Wolach B., Roesler J., Malech H.L., Holland S.M., Gallin J.I., Stasia M.J. Hematologically important mutations: the autosomal recessive forms of chronic granulomatous disease (second update). Blood Cells Mol. Dis. 2010, 44:291-299.
-
(2010)
Blood Cells Mol. Dis.
, vol.44
, pp. 291-299
-
-
Roos, D.1
Kuhns, D.B.2
Maddalena, A.3
Bustamante, J.4
Kannengiesser, C.5
de Boer, M.6
van Leeuwen, K.7
Koker, M.Y.8
Wolach, B.9
Roesler, J.10
Malech, H.L.11
Holland, S.M.12
Gallin, J.I.13
Stasia, M.J.14
-
72
-
-
77956879800
-
Hematologically important mutations: X-linked chronic granulomatous disease (third update)
-
Roos D., Kuhns D.B., Maddalena A., Roesler J., Lopez J.A., Ariga T., Avcin T., de Boer M., Bustamante J., Condino-Neto A., Di Matteo G., He J., Hill H.R., Holland S.M., Kannengiesser C., Koker M.Y., Kondratenko I., van Leeuwen K., Malech H.L., Marodi L., Nunoi H., Stasia M.J., Ventura A.M., Witwer C.T., Wolach B., Gallin J.I. Hematologically important mutations: X-linked chronic granulomatous disease (third update). Blood Cells Mol. Dis. 2010, 45:246-265.
-
(2010)
Blood Cells Mol. Dis.
, vol.45
, pp. 246-265
-
-
Roos, D.1
Kuhns, D.B.2
Maddalena, A.3
Roesler, J.4
Lopez, J.A.5
Ariga, T.6
Avcin, T.7
de Boer, M.8
Bustamante, J.9
Condino-Neto, A.10
Di Matteo, G.11
He, J.12
Hill, H.R.13
Holland, S.M.14
Kannengiesser, C.15
Koker, M.Y.16
Kondratenko, I.17
van Leeuwen, K.18
Malech, H.L.19
Marodi, L.20
Nunoi, H.21
Stasia, M.J.22
Ventura, A.M.23
Witwer, C.T.24
Wolach, B.25
Gallin, J.I.26
more..
-
73
-
-
38949165231
-
NADPH oxidase CYBA polymorphisms, oxidative stress and cardiovascular diseases
-
San Jose G., Fortuno A., Beloqui O., Diez J., Zalba G. NADPH oxidase CYBA polymorphisms, oxidative stress and cardiovascular diseases. Clin. Sci. (Lond.) 2008, 114:173-182.
-
(2008)
Clin. Sci. (Lond.)
, vol.114
, pp. 173-182
-
-
San Jose, G.1
Fortuno, A.2
Beloqui, O.3
Diez, J.4
Zalba, G.5
-
74
-
-
0019870665
-
The nature and function of the microbicidal oxidase system of neutrophils
-
Segal A.W., Harper A., Garcia R., Jones O.T., Cross A.R. The nature and function of the microbicidal oxidase system of neutrophils. Bull. Eur. Physiopathol. Respir. 1981, 17(Suppl.):187-191.
-
(1981)
Bull. Eur. Physiopathol. Respir.
, vol.17
, pp. 187-191
-
-
Segal, A.W.1
Harper, A.2
Garcia, R.3
Jones, O.T.4
Cross, A.R.5
-
75
-
-
44949106317
-
Structure, regulation and evolution of Nox-family NADPH oxidases that produce reactive oxygen species
-
Sumimoto H. Structure, regulation and evolution of Nox-family NADPH oxidases that produce reactive oxygen species. FEBS J. 2008, 275:3249-3277.
-
(2008)
FEBS J.
, vol.275
, pp. 3249-3277
-
-
Sumimoto, H.1
-
76
-
-
0029806925
-
Assembly and activation of the phagocyte NADPH oxidase. Specific interaction of the N-terminal Src homology 3 domain of p47phox with p22phox is required for activation of the NADPH oxidase
-
Sumimoto H., Hata K., Mizuki K., Ito T., Kage Y., Sakaki Y., Fukumaki Y., Nakamura M., Takeshige K. Assembly and activation of the phagocyte NADPH oxidase. Specific interaction of the N-terminal Src homology 3 domain of p47phox with p22phox is required for activation of the NADPH oxidase. J. Biol. Chem. 1996, 271:22152-22158.
-
(1996)
J. Biol. Chem.
, vol.271
, pp. 22152-22158
-
-
Sumimoto, H.1
Hata, K.2
Mizuki, K.3
Ito, T.4
Kage, Y.5
Sakaki, Y.6
Fukumaki, Y.7
Nakamura, M.8
Takeshige, K.9
-
77
-
-
33845990565
-
Analysis of human phagocyte flavocytochrome b(558) by mass spectrometry
-
Taylor R.M., Baniulis D., Burritt J.B., Gripentrog J.M., Lord C.I., Riesselman M.H., Maaty W.S., Bothner B.P., Angel T.E., Dratz E.A., Linton G.F., Malech H.L., Jesaitis A.J. Analysis of human phagocyte flavocytochrome b(558) by mass spectrometry. J. Biol. Chem. 2006, 281:37045-37056.
-
(2006)
J. Biol. Chem.
, vol.281
, pp. 37045-37056
-
-
Taylor, R.M.1
Baniulis, D.2
Burritt, J.B.3
Gripentrog, J.M.4
Lord, C.I.5
Riesselman, M.H.6
Maaty, W.S.7
Bothner, B.P.8
Angel, T.E.9
Dratz, E.A.10
Linton, G.F.11
Malech, H.L.12
Jesaitis, A.J.13
-
78
-
-
10344262907
-
Site-specific inhibitors of NADPH oxidase activity and structural probes of flavocytochrome b: characterization of six monoclonal antibodies to the p22phox subunit
-
Taylor R.M., Burritt J.B., Baniulis D., Foubert T.R., Lord C.I., Dinauer M.C., Parkos C.A., Jesaitis A.J. Site-specific inhibitors of NADPH oxidase activity and structural probes of flavocytochrome b: characterization of six monoclonal antibodies to the p22phox subunit. J. Immunol. 2004, 173:7349-7357.
-
(2004)
J. Immunol.
, vol.173
, pp. 7349-7357
-
-
Taylor, R.M.1
Burritt, J.B.2
Baniulis, D.3
Foubert, T.R.4
Lord, C.I.5
Dinauer, M.C.6
Parkos, C.A.7
Jesaitis, A.J.8
-
79
-
-
79960845452
-
Invariant local conformation in p22phox p.Y72H polymorphisms suggested by mass spectral analysis of crosslinked human neutrophil flavocytochrome b
-
Taylor R.M., Dratz E.A., Jesaitis A.J. Invariant local conformation in p22phox p.Y72H polymorphisms suggested by mass spectral analysis of crosslinked human neutrophil flavocytochrome b. Biochimie 2011, 93:1502-1509.
-
(2011)
Biochimie
, vol.93
, pp. 1502-1509
-
-
Taylor, R.M.1
Dratz, E.A.2
Jesaitis, A.J.3
-
80
-
-
0023191301
-
The X-linked chronic granulomatous disease gene codes for the beta-chain of cytochrome b-245
-
Teahan C., Rowe P., Parker P., Totty N., Segal A.W. The X-linked chronic granulomatous disease gene codes for the beta-chain of cytochrome b-245. Nature 1987, 327:720-721.
-
(1987)
Nature
, vol.327
, pp. 720-721
-
-
Teahan, C.1
Rowe, P.2
Parker, P.3
Totty, N.4
Segal, A.W.5
-
81
-
-
44249093014
-
Characterization of six novel mutations in CYBA: the gene causing autosomal recessive chronic granulomatous disease
-
Teimourian S., Zomorodian E., Badalzadeh M., Pouya A., Kannengiesser C., Mansouri D., Cheraghi T., Parvaneh N. Characterization of six novel mutations in CYBA: the gene causing autosomal recessive chronic granulomatous disease. Br. J. Haematol. 2008, 141:848-851.
-
(2008)
Br. J. Haematol.
, vol.141
, pp. 848-851
-
-
Teimourian, S.1
Zomorodian, E.2
Badalzadeh, M.3
Pouya, A.4
Kannengiesser, C.5
Mansouri, D.6
Cheraghi, T.7
Parvaneh, N.8
-
82
-
-
65349179624
-
Chronic granulomatous disease: the European experience
-
van den Berg J.M., van Koppen E., Ahlin A., Belohradsky B.H., Bernatowska E., Corbeel L., Espanol T., Fischer A., Kurenko-Deptuch M., Mouy R., Petropoulou T., Roesler J., Seger R., Stasia M.J., Valerius N.H., Weening R.S., Wolach B., Roos D., Kuijpers T.W. Chronic granulomatous disease: the European experience. PLoS One 2009, 4:e5234.
-
(2009)
PLoS One
, vol.4
, pp. e5234
-
-
van den Berg, J.M.1
van Koppen, E.2
Ahlin, A.3
Belohradsky, B.H.4
Bernatowska, E.5
Corbeel, L.6
Espanol, T.7
Fischer, A.8
Kurenko-Deptuch, M.9
Mouy, R.10
Petropoulou, T.11
Roesler, J.12
Seger, R.13
Stasia, M.J.14
Valerius, N.H.15
Weening, R.S.16
Wolach, B.17
Roos, D.18
Kuijpers, T.W.19
-
83
-
-
58049200120
-
Mutational analysis reveals distinct features of the Nox4-p22 phox complex
-
von Lohneysen K., Noack D., Jesaitis A.J., Dinauer M.C., Knaus U.G. Mutational analysis reveals distinct features of the Nox4-p22 phox complex. J. Biol. Chem. 2008, 283:35273-35282.
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 35273-35282
-
-
von Lohneysen, K.1
Noack, D.2
Jesaitis, A.J.3
Dinauer, M.C.4
Knaus, U.G.5
-
84
-
-
75749118290
-
Structural insights into Nox4 and Nox2: motifs involved in function and cellular localization
-
von Lohneysen K., Noack D., Wood M.R., Friedman J.S., Knaus U.G. Structural insights into Nox4 and Nox2: motifs involved in function and cellular localization. Mol. Cell. Biol. 2010, 30:961-975.
-
(2010)
Mol. Cell. Biol.
, vol.30
, pp. 961-975
-
-
von Lohneysen, K.1
Noack, D.2
Wood, M.R.3
Friedman, J.S.4
Knaus, U.G.5
-
85
-
-
51249086031
-
Chronic granulomatous disease in Israel: clinical, functional and molecular studies of 38 patients
-
Wolach B., Gavrieli R., de Boer M., Gottesman G., Ben-Ari J., Rottem M., Schlesinger Y., Grisaru-Soen G., Etzioni A., Roos D. Chronic granulomatous disease in Israel: clinical, functional and molecular studies of 38 patients. Clin. Immunol. 2008, 129:103-114.
-
(2008)
Clin. Immunol.
, vol.129
, pp. 103-114
-
-
Wolach, B.1
Gavrieli, R.2
de Boer, M.3
Gottesman, G.4
Ben-Ari, J.5
Rottem, M.6
Schlesinger, Y.7
Grisaru-Soen, G.8
Etzioni, A.9
Roos, D.10
-
86
-
-
84883518358
-
Relationship of the p22phox (CYBA) gene polymorphism C242T with risk of coronary artery disease: a meta-analysis
-
Wu Z., Lou Y., Jin W., Liu Y., Lu L., Chen Q., Xie Y., Lu G. Relationship of the p22phox (CYBA) gene polymorphism C242T with risk of coronary artery disease: a meta-analysis. PLoS One 2013, 8:e70885.
-
(2013)
PLoS One
, vol.8
, pp. e70885
-
-
Wu, Z.1
Lou, Y.2
Jin, W.3
Liu, Y.4
Lu, L.5
Chen, Q.6
Xie, Y.7
Lu, G.8
-
87
-
-
84919951136
-
Clinical and molecular features of 38 children with chronic granulomatous disease in mainland china
-
Xu H., Tian W., Li S.J., Zhang L.Y., Liu W., Zhao Y., Zhang Z.Y., Tang X.M., Wang M., Wu D.Q., Shi J.S., Ding Y., Zhao X.D., Yang X.Q., Jiang L.P. Clinical and molecular features of 38 children with chronic granulomatous disease in mainland china. J. Clin. Immunol. 2014, 34:633-641.
-
(2014)
J. Clin. Immunol.
, vol.34
, pp. 633-641
-
-
Xu, H.1
Tian, W.2
Li, S.J.3
Zhang, L.Y.4
Liu, W.5
Zhao, Y.6
Zhang, Z.Y.7
Tang, X.M.8
Wang, M.9
Wu, D.Q.10
Shi, J.S.11
Ding, Y.12
Zhao, X.D.13
Yang, X.Q.14
Jiang, L.P.15
-
88
-
-
84894280949
-
Polymorphisms of C242T and A640G in CYBA gene and the risk of coronary artery disease: a meta-analysis
-
Xu Q., Yuan F., Shen X., Wen H., Li W., Cheng B., Wu J. Polymorphisms of C242T and A640G in CYBA gene and the risk of coronary artery disease: a meta-analysis. PLoS One 2014, 9:e84251.
-
(2014)
PLoS One
, vol.9
, pp. e84251
-
-
Xu, Q.1
Yuan, F.2
Shen, X.3
Wen, H.4
Li, W.5
Cheng, B.6
Wu, J.7
-
89
-
-
0033547877
-
Biosynthesis of flavocytochrome b558. gp91(phox) is synthesized as a 65-kDa precursor (p65) in the endoplasmic reticulum
-
Yu L., DeLeo F.R., Biberstine-Kinkade K.J., Renee J., Nauseef W.M., Dinauer M.C. Biosynthesis of flavocytochrome b558. gp91(phox) is synthesized as a 65-kDa precursor (p65) in the endoplasmic reticulum. J. Biol. Chem. 1999, 274:4364-4369.
-
(1999)
J. Biol. Chem.
, vol.274
, pp. 4364-4369
-
-
Yu, L.1
DeLeo, F.R.2
Biberstine-Kinkade, K.J.3
Renee, J.4
Nauseef, W.M.5
Dinauer, M.C.6
-
90
-
-
0032493445
-
Gp91(phox) is the heme binding subunit of the superoxide-generating NADPH oxidase
-
Yu L., Quinn M.T., Cross A.R., Dinauer M.C. Gp91(phox) is the heme binding subunit of the superoxide-generating NADPH oxidase. Proc. Natl. Acad. Sci. U. S. A. 1998, 95:7993-7998.
-
(1998)
Proc. Natl. Acad. Sci. U. S. A.
, vol.95
, pp. 7993-7998
-
-
Yu, L.1
Quinn, M.T.2
Cross, A.R.3
Dinauer, M.C.4
-
91
-
-
0030827909
-
Biosynthesis of the phagocyte NADPH oxidase cytochrome b558. Role of heme incorporation and heterodimer formation in maturation and stability of gp91phox and p22phox subunits
-
Yu L., Zhen L., Dinauer M.C. Biosynthesis of the phagocyte NADPH oxidase cytochrome b558. Role of heme incorporation and heterodimer formation in maturation and stability of gp91phox and p22phox subunits. J. Biol. Chem. 1997, 272:27288-27294.
-
(1997)
J. Biol. Chem.
, vol.272
, pp. 27288-27294
-
-
Yu, L.1
Zhen, L.2
Dinauer, M.C.3
-
92
-
-
33750083602
-
Deletion mutagenesis of p22phox subunit of flavocytochrome b558: identification of regions critical for gp91phox maturation and NADPH oxidase activity
-
Zhu Y., Marchal C.C., Casbon A.J., Stull N., von Lohneysen K., Knaus U.G., Jesaitis A.J., McCormick S., Nauseef W.M., Dinauer M.C. Deletion mutagenesis of p22phox subunit of flavocytochrome b558: identification of regions critical for gp91phox maturation and NADPH oxidase activity. J. Biol. Chem. 2006, 281:30336-30346.
-
(2006)
J. Biol. Chem.
, vol.281
, pp. 30336-30346
-
-
Zhu, Y.1
Marchal, C.C.2
Casbon, A.J.3
Stull, N.4
von Lohneysen, K.5
Knaus, U.G.6
Jesaitis, A.J.7
McCormick, S.8
Nauseef, W.M.9
Dinauer, M.C.10
-
93
-
-
79957587075
-
Oxidase-deficient neutrophils from X-linked chronic granulomatous disease iPS cells: functional correction by zinc finger nuclease-mediated safe harbor targeting
-
Zou J., Sweeney C.L., Chou B.K., Choi U., Pan J., Wang H., Dowey S.N., Cheng L., Malech H.L. Oxidase-deficient neutrophils from X-linked chronic granulomatous disease iPS cells: functional correction by zinc finger nuclease-mediated safe harbor targeting. Blood 2011, 117:5561-5572.
-
(2011)
Blood
, vol.117
, pp. 5561-5572
-
-
Zou, J.1
Sweeney, C.L.2
Chou, B.K.3
Choi, U.4
Pan, J.5
Wang, H.6
Dowey, S.N.7
Cheng, L.8
Malech, H.L.9
|