-
1
-
-
0033105874
-
NADPH oxidase: An update
-
B.M. Babior NADPH oxidase: an update Blood 93 1999 1464 1476
-
(1999)
Blood
, vol.93
, pp. 1464-1476
-
-
Babior, B.M.1
-
2
-
-
0033391007
-
Activation of the neutrophil respiratory burst oxidase
-
R.A. Clark Activation of the neutrophil respiratory burst oxidase J Infect Dis 179 1999 309 317
-
(1999)
J Infect Dis
, vol.179
, pp. 309-317
-
-
Clark, R.A.1
-
3
-
-
0023483148
-
Purified cytochrome b from human plasma membrane is comprised of two polypeptides with relative molecular weights of 91,000 and 22,000
-
C.A. Parkos, R.A. Allen, C.G. Cochrane, and A.J. Jesaitis Purified cytochrome b from human plasma membrane is comprised of two polypeptides with relative molecular weights of 91,000 and 22,000 J Clin Invest 80 1987 732 742
-
(1987)
J Clin Invest
, vol.80
, pp. 732-742
-
-
Parkos, C.A.1
Allen, R.A.2
Cochrane, C.G.3
Jesaitis, A.J.4
-
4
-
-
0025114585
-
Human neutrophil cytochrome b light chain (p22-phox): Gene structure, chromosomal location, and mutations in cytochrome-negative autosomal recessive chronic granulomatous disease
-
M.C. Dinauer, E.A. Pierce, G.A. Bruns, J.T. Curnutte, and S.H. Orkin 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 86 1990 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
-
5
-
-
0029099413
-
Purification of human neutrophil NADPH oxidase cytochrome b-558 and association with Rap 1A
-
M.T. Quinn, C.A. Parkos, and A.J. Jesaitis Purification of human neutrophil NADPH oxidase cytochrome b-558 and association with Rap 1A Methods Enzymol 255 1995 476 487
-
(1995)
Methods Enzymol
, vol.255
, pp. 476-487
-
-
Quinn, M.T.1
Parkos, C.A.2
Jesaitis, A.J.3
-
6
-
-
0342266916
-
Cloning of the cDNA and functional expression of the 47-kilodalton cytosolic component of human neutrophil respiratory burst oxidase
-
B.D. Volpp, W.M. Nauseef, J.E. Donelson, D.R. Moser, and R.A. Clark Cloning of the cDNA and functional expression of the 47-kilodalton cytosolic component of human neutrophil respiratory burst oxidase Proc Natl Acad Sci U S A 86 1989 7195 7199 [Erratum in Proc Natl Acad Sci U S A. 1989;86:9563]
-
(1989)
Proc Natl Acad Sci U S a
, vol.86
, pp. 7195-7199
-
-
Volpp, B.D.1
Nauseef, W.M.2
Donelson, J.E.3
Moser, D.R.4
Clark, R.A.5
-
7
-
-
0025292583
-
Cloning of a 67-kD neutrophil oxidase factor with similarity to a noncatalytic region of p60c-src
-
T.L. Leto, K.J. Lomax, and B.D. Volpp Cloning of a 67-kD neutrophil oxidase factor with similarity to a noncatalytic region of p60c-src Science 248 1990 727 730
-
(1990)
Science
, vol.248
, pp. 727-730
-
-
Leto, T.L.1
Lomax, K.J.2
Volpp, B.D.3
-
8
-
-
0027787417
-
P40phox, a third cytosolic component of the activation complex of the NADPH oxidase to contain src homology 3 domains
-
F.B. Wientjes, J.J. Hsuan, N.F. Totty, and A.W. Segal P40phox, a third cytosolic component of the activation complex of the NADPH oxidase to contain src homology 3 domains Biochem J 296 1993 557 561
-
(1993)
Biochem J
, vol.296
, pp. 557-561
-
-
Wientjes, F.B.1
Hsuan, J.J.2
Totty, N.F.3
Segal, A.W.4
-
9
-
-
0028305414
-
A novel cytosolic component, p40phox, of respiratory burst oxidase associates with p67phox and is absent in patients with chronic granulomatous disease who lack p67phox
-
S. Tsunawaki, H. Mizunari, M. Nagata, O. Tatsuzawa, and T. Kuratsuji A novel cytosolic component, p40phox, of respiratory burst oxidase associates with p67phox and is absent in patients with chronic granulomatous disease who lack p67phox Biochem Biophys Res Commun 199 1994 1378 1387
-
(1994)
Biochem Biophys Res Commun
, vol.199
, pp. 1378-1387
-
-
Tsunawaki, S.1
Mizunari, H.2
Nagata, M.3
Tatsuzawa, O.4
Kuratsuji, T.5
-
10
-
-
0026787468
-
The cytosolic components of the respiratory burst oxidase exist as a M(r) approximately 240,000 complex that acquires a membrane-binding site during activation of the oxidase in a cell-free system
-
J.W. Park, M. Ma, J.M. Ruedi, R.M. Smith, and B.M. Babior The cytosolic components of the respiratory burst oxidase exist as a M(r) approximately 240,000 complex that acquires a membrane-binding site during activation of the oxidase in a cell-free system J Biol Chem 267 1992 17,327 17,332
-
(1992)
J Biol Chem
, vol.267
, pp. 17
-
-
Park, J.W.1
Ma, M.2
Ruedi, J.M.3
Smith, R.M.4
Babior, B.M.5
-
11
-
-
0025259712
-
Two cytosolic components of the human neutrophil respiratory burst oxidase translocate to the plasma membrane during cell activation
-
R.A. Clark, B.D. Volpp, K.G. Leidal, and W.M. Nauseef Two cytosolic components of the human neutrophil respiratory burst oxidase translocate to the plasma membrane during cell activation J Clin Invest 85 1990 714 721
-
(1990)
J Clin Invest
, vol.85
, pp. 714-721
-
-
Clark, R.A.1
Volpp, B.D.2
Leidal, K.G.3
Nauseef, W.M.4
-
13
-
-
13344293679
-
Mutations in the X-linked and autosomal recessive forms of chronic granulomatous disease
-
D. Roos, M. de Boer, and F. Kuribayashi Mutations in the X-linked and autosomal recessive forms of chronic granulomatous disease Blood 87 1996 1663 1681
-
(1996)
Blood
, vol.87
, pp. 1663-1681
-
-
Roos, D.1
De Boer, M.2
Kuribayashi, F.3
-
14
-
-
0031896343
-
The molecular basis of chronic granulomatous disease
-
C. Meischl, and D. Roos The molecular basis of chronic granulomatous disease Springer Semin Immunopathol 19 1998 417 434
-
(1998)
Springer Semin Immunopathol
, vol.19
, pp. 417-434
-
-
Meischl, C.1
Roos, D.2
-
16
-
-
0003053791
-
Chronic granulomatous disease
-
H.D. Ochs C.I. Smith J.M. Puck Oxford University Press New York
-
D. Roos, and J.T. Curnutte Chronic granulomatous disease H.D. Ochs C.I. Smith J.M. Puck Primary immunodeficiency diseases 1999 Oxford University Press New York 353 374
-
(1999)
Primary Immunodeficiency Diseases
, pp. 353-374
-
-
Roos, D.1
Curnutte, J.T.2
-
17
-
-
0035054158
-
Hematologically important mutations: X-linked chronic granulomatous disease - Second update
-
P.G. Heyworth, J.T. Curnutte, and J. Rae Hematologically important mutations: X-linked chronic granulomatous disease - second update Blood Cells Mol Dis 27 2001 16 26
-
(2001)
Blood Cells Mol Dis
, vol.27
, pp. 16-26
-
-
Heyworth, P.G.1
Curnutte, J.T.2
Rae, J.3
-
18
-
-
0031777032
-
X-linked chronic granulomatous disease: Mutations in the CYBB gene encoding the gp91-phox component of respiratory-burst oxidase
-
J. Rae, P.E. Newburger, and M.C. Dinauer X-linked chronic granulomatous disease: mutations in the CYBB gene encoding the gp91-phox component of respiratory-burst oxidase Am J Hum Genet 62 1998 1320 1331
-
(1998)
Am J Hum Genet
, vol.62
, pp. 1320-1331
-
-
Rae, J.1
Newburger, P.E.2
Dinauer, M.C.3
-
19
-
-
12944257362
-
Four novel mutations in the gene encoding gp91-phox of human NADPH oxidase: Consequences for oxidase assembly
-
J.H. Leusen, C. Meischl, and M.H. Eppink Four novel mutations in the gene encoding gp91-phox of human NADPH oxidase: consequences for oxidase assembly Blood 95 2000 666 673
-
(2000)
Blood
, vol.95
, pp. 666-673
-
-
Leusen, J.H.1
Meischl, C.2
Eppink, M.H.3
-
20
-
-
0022522125
-
Heterogeneity in chronic granulomatous disease detected with an improved nitroblue tetrazolium slide test
-
L.J. Meerhof, and D. Roos Heterogeneity in chronic granulomatous disease detected with an improved nitroblue tetrazolium slide test J Leukoc Biol 39 1996 699 711
-
(1996)
J Leukoc Biol
, vol.39
, pp. 699-711
-
-
Meerhof, L.J.1
Roos, D.2
-
21
-
-
0018922106
-
Activity and activation of the granulocyte superoxide-generating system
-
P.E. Newburger, M.E. Chovaniec, and H.J. Cohen Activity and activation of the granulocyte superoxide-generating system Blood 55 1980 85 92
-
(1980)
Blood
, vol.55
, pp. 85-92
-
-
Newburger, P.E.1
Chovaniec, M.E.2
Cohen, H.J.3
-
22
-
-
0025294129
-
A fast and easy method to determine the production of reactive oxygen intermediates by human and murine phagocytes using dihydrorhodamine 123
-
A. Emmendörffer, M. Hecht, M.L. Lohmann-Mathes, and J. Roesler A fast and easy method to determine the production of reactive oxygen intermediates by human and murine phagocytes using dihydrorhodamine 123 J Immunol Methods 131 1990 269 275
-
(1990)
J Immunol Methods
, vol.131
, pp. 269-275
-
-
Emmendörffer, A.1
Hecht, M.2
Lohmann-Mathes, M.L.3
Roesler, J.4
-
23
-
-
0021928992
-
Purification and partial characterization of the b-type cytochrome from human polymorphonuclear leucocytes
-
R. Lutter, M.L. van Schaik, R. van Zwieten, R. Wever, D. Roos, and M.N. Hamers Purification and partial characterization of the b-type cytochrome from human polymorphonuclear leucocytes J Biol Chem 260 1985 2237 2244
-
(1985)
J Biol Chem
, vol.260
, pp. 2237-2244
-
-
Lutter, R.1
Van Schaik, M.L.2
Van Zwieten, R.3
Wever, R.4
Roos, D.5
Hamers, M.N.6
-
24
-
-
0023198590
-
558 of human neutrophils: Immunocytochemical detection of the antigen in peripheral phagocytes of normal subjects, patients with chronic granulomatous disease and their carrier mothers
-
558 of human neutrophils: immunocytochemical detection of the antigen in peripheral phagocytes of normal subjects, patients with chronic granulomatous disease and their carrier mothers Blood 69 1987 1404 1408
-
(1987)
Blood
, vol.69
, pp. 1404-1408
-
-
Nakamura, M.1
Kobayashi, S.2
Sendo, S.3
Koga, T.4
Kanegasaki, S.5
-
26
-
-
0024595101
-
Detection of polymorphisms of human DNA by gel electrophoresis as single strand conformations polymorphisms
-
M. Orita, H. Iwahana, H. Kanazawa, K. Hayashi, and T. Sekiya Detection of polymorphisms of human DNA by gel electrophoresis as single strand conformations polymorphisms Proc Natl Acad Sci U S A 88 1989 2766 2770
-
(1989)
Proc Natl Acad Sci U S a
, vol.88
, pp. 2766-2770
-
-
Orita, M.1
Iwahana, H.2
Kanazawa, H.3
Hayashi, K.4
Sekiya, T.5
-
27
-
-
0032772838
-
Two buffer PAGE system-based SSCP/HD analysis: A general protocol for rapid and sensitive mutation screening in cystic fibrosis and any other human genetic disease
-
S. Liechti-Gallati, V. Schneider, D. Neeser, and R. Kraemer Two buffer PAGE system-based SSCP/HD analysis: a general protocol for rapid and sensitive mutation screening in cystic fibrosis and any other human genetic disease Eur J Hum Genet 7 1999 590 598
-
(1999)
Eur J Hum Genet
, vol.7
, pp. 590-598
-
-
Liechti-Gallati, S.1
Schneider, V.2
Neeser, D.3
Kraemer, R.4
-
28
-
-
0026726139
-
Splice site mutations are a common cause of X-linked chronic granulomatous disease
-
M. De Boer, B.G. Bolscher, and M.C. Dinauer Splice site mutations are a common cause of X-linked chronic granulomatous disease Blood 80 1992 1553 1558
-
(1992)
Blood
, vol.80
, pp. 1553-1558
-
-
De Boer, M.1
Bolscher, B.G.2
Dinauer, M.C.3
-
29
-
-
0027278605
-
Chronic granulomatous disease: The solving of a clinical riddle at the molecular level
-
J.T. Curnutte Chronic granulomatous disease: the solving of a clinical riddle at the molecular level Clin Immunol Immunopathol 67 1993 2 15
-
(1993)
Clin Immunol Immunopathol
, vol.67
, pp. 2-15
-
-
Curnutte, J.T.1
-
30
-
-
0030296689
-
X-CGDbase: A database of X-CGD-causing mutations
-
D. Roos, J.T. Curnutte, and J.P. Hossle X-CGDbase: a database of X-CGD-causing mutations Immunol Today 17 1996 517 521
-
(1996)
Immunol Today
, vol.17
, pp. 517-521
-
-
Roos, D.1
Curnutte, J.T.2
Hossle, J.P.3
-
31
-
-
0035432944
-
Characterization of 11 novel mutations in the X-linked chronic granulomatous disease (CYBB Gene)
-
B. Gerard, J. El Benna, F. Alcain, M.-A. Gougerot-Pocidalo, B. Grandchamp, and S. Chollet-Martin Characterization of 11 novel mutations in the X-linked chronic granulomatous disease (CYBB Gene) Hum Mutat 18 2001 163
-
(2001)
Hum Mutat
, vol.18
, pp. 163
-
-
Gerard, B.1
El Benna, J.2
Alcain, F.3
Gougerot-Pocidalo, M.-A.4
Grandchamp, B.5
Chollet-Martin, S.6
-
32
-
-
0036347927
-
Loss of the muscle-specific chloride channel in type 1 myotonic dystrophy due to misregulated alternative splicing
-
B.N. Charlet-, R. Savkur, G. Singh, A. Philips, E. Grice, and T.A. Cooper Loss of the muscle-specific chloride channel in type 1 myotonic dystrophy due to misregulated alternative splicing Mol Cell 10 2002 45 53
-
(2002)
Mol Cell
, vol.10
, pp. 45-53
-
-
Charlet-, B.N.1
Savkur, R.2
Singh, G.3
Philips, A.4
Grice, E.5
Cooper, T.A.6
-
33
-
-
0035146628
-
The CELF family of RNA binding proteins is implicated in cell-specific and developmentally regulated alternative splicing
-
A.N. Ladd, B.N. Charlet-, and T.A. Cooper The CELF family of RNA binding proteins is implicated in cell-specific and developmentally regulated alternative splicing Mol Cell Biol 21 2001 1285 1296
-
(2001)
Mol Cell Biol
, vol.21
, pp. 1285-1296
-
-
Ladd, A.N.1
Charlet-, B.N.2
Cooper, T.A.3
-
34
-
-
0030068638
-
Chronic granulomatous disease in adults
-
J.G. Liese, V. Jendrossek, and A. Jansson Chronic granulomatous disease in adults Lancet 347 1996 220 223
-
(1996)
Lancet
, vol.347
, pp. 220-223
-
-
Liese, J.G.1
Jendrossek, V.2
Jansson, A.3
-
35
-
-
0035116245
-
Increased susceptibility of a carrier of X-linked chronic granulomatous disease (CGD) to Aspergillus fumigatus infection associated with age-related skewing of lyonization
-
A. Rosen-Wolff, W. Soldan, K. Heyne, J. Bickhardt, M. Gahr, and J. Roesler Increased susceptibility of a carrier of X-linked chronic granulomatous disease (CGD) to Aspergillus fumigatus infection associated with age-related skewing of lyonization Ann Hematol 80 2001 113 115
-
(2001)
Ann Hematol
, vol.80
, pp. 113-115
-
-
Rosen-Wolff, A.1
Soldan, W.2
Heyne, K.3
Bickhardt, J.4
Gahr, M.5
Roesler, J.6
-
36
-
-
0029901946
-
Nonrandom X-inactivation patterns in normal females: Lyonization ratios vary with age
-
L. Busque, R. Mio, and J. Mattioli Nonrandom X-inactivation patterns in normal females: lyonization ratios vary with age Blood 88 1996 59 65
-
(1996)
Blood
, vol.88
, pp. 59-65
-
-
Busque, L.1
Mio, R.2
Mattioli, J.3
-
37
-
-
0036228428
-
Unusual late onset of X-linked chronic granulomatous disease in an adult woman after unsuspicious childhood
-
A. Lun, J. Roesler, and H. Renz Unusual late onset of X-linked chronic granulomatous disease in an adult woman after unsuspicious childhood Clin Chem 48 2002 780 781
-
(2002)
Clin Chem
, vol.48
, pp. 780-781
-
-
Lun, A.1
Roesler, J.2
Renz, H.3
-
38
-
-
11144232335
-
Unusual late presentation of X-linked chronic granulomatous disease in an adult female with a somatic mosaic for a novel mutation in CYBB
-
B. Wolach, Y. Scharf, R. Gavrieli, M. de Boer, and D. Roos Unusual late presentation of X-linked chronic granulomatous disease in an adult female with a somatic mosaic for a novel mutation in CYBB Blood 105 2005 61 66
-
(2005)
Blood
, vol.105
, pp. 61-66
-
-
Wolach, B.1
Scharf, Y.2
Gavrieli, R.3
De Boer, M.4
Roos, D.5
-
39
-
-
0029058898
-
Ocular pathologic findings of chronic granulomatous disease of childhood
-
S. Valluri, F.C. Chi, and M.E. Smith Ocular pathologic findings of chronic granulomatous disease of childhood Am J Ophthalmol 120 1995 120 123
-
(1995)
Am J Ophthalmol
, vol.120
, pp. 120-123
-
-
Valluri, S.1
Chi, F.C.2
Smith, M.E.3
-
40
-
-
0026613011
-
Cytochrome b558: The flavin-binding component of the phagocyte NADPH oxidase
-
D. Rotrosen, C.L. Yeung, T.L. Leto, H.L. Malech, and C.H. Kwong Cytochrome b558: the flavin-binding component of the phagocyte NADPH oxidase Science 256 1992 1459 1462
-
(1992)
Science
, vol.256
, pp. 1459-1462
-
-
Rotrosen, D.1
Yeung, C.L.2
Leto, T.L.3
Malech, H.L.4
Kwong, C.H.5
-
41
-
-
0027007734
-
Cytochrome b558, a component of the phagocyte NADPH oxidase, is a flavoprotein
-
H. Sumimoto, N. Sakamoto, M. Nozaki, Y. Sakaki, K. Takeshige, and S. Minakami Cytochrome b558, a component of the phagocyte NADPH oxidase, is a flavoprotein Biochem Biophys Res Commun 186 1992 1368 1375
-
(1992)
Biochem Biophys Res Commun
, vol.186
, pp. 1368-1375
-
-
Sumimoto, H.1
Sakamoto, N.2
Nozaki, M.3
Sakaki, Y.4
Takeshige, K.5
Minakami, S.6
-
42
-
-
0026642394
-
Cytochrome b-245 is a flavocytochrome containing FAD and the NADPH-binding site of the microbicidal oxidase of phagocytes
-
A.W. Segal, I. West, and F. Wientjes Cytochrome b-245 is a flavocytochrome containing FAD and the NADPH-binding site of the microbicidal oxidase of phagocytes Biochem J 284 1992 781 788
-
(1992)
Biochem J
, vol.284
, pp. 781-788
-
-
Segal, A.W.1
West, I.2
Wientjes, F.3
-
43
-
-
0032561317
-
Mutation of histidine 338 of gp91-phox depletes FAD and affects expression of cytochrome b558 of the human NADPH oxidase
-
L.S. Yoshida, F. Saruta, K. Yoshikawa, O. Tatsuzawa, and S. Tsunawaki Mutation of histidine 338 of gp91-phox depletes FAD and affects expression of cytochrome b558 of the human NADPH oxidase J Biol Chem 273 1998 879 886
-
(1998)
J Biol Chem
, vol.273
, pp. 879-886
-
-
Yoshida, L.S.1
Saruta, F.2
Yoshikawa, K.3
Tatsuzawa, O.4
Tsunawaki, S.5
-
44
-
-
0036613395
-
Gene therapy of hematopoietic stem cells: Strategies for improvement
-
J.P. Hossle, R.A. Seger, and D. Steinhoff Gene therapy of hematopoietic stem cells: strategies for improvement News Physiol Sci 17 2002 87 92
-
(2002)
News Physiol Sci
, vol.17
, pp. 87-92
-
-
Hossle, J.P.1
Seger, R.A.2
Steinhoff, D.3
|