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Volumn 101, Issue 8, 2003, Pages 3337-

Association between p47phox pseudogenes and inflammatory bowel disease [1]

Author keywords

[No Author keywords available]

Indexed keywords

DINUCLEOTIDE; PHORBOL 13 ACETATE 12 MYRISTATE; PROTEIN P47; ZYMOSAN; CANTHARIDIN; IRRITANT AGENT; NEUTROPHIL CYTOSOLIC FACTOR 1; PHOSPHOPROTEIN; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE OXIDASE;

EID: 0037605983     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood-2002-10-3060     Document Type: Letter
Times cited : (10)

References (10)
  • 1
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    • Identification of a novel NCF-1 (p47-phox) pseudogene not containing the signature GT deletion: Significance for A47 degrees chronic granulomatous disease carrier detection
    • Heyworth PG, Noack D, Cross AR. Identification of a novel NCF-1 (p47-phox) pseudogene not containing the signature GT deletion: significance for A47 degrees chronic granulomatous disease carrier detection. Blood. 2002;100:1845-1851.
    • (2002) Blood , vol.100 , pp. 1845-1851
    • Heyworth, P.G.1    Noack, D.2    Cross, A.R.3
  • 2
    • 0033036631 scopus 로고    scopus 로고
    • Comparative mapping of the region of human chromosome 7 deleted in Williams syndrome
    • DeSilva U, Massa H, Trask BJ, Green ED. Comparative mapping of the region of human chromosome 7 deleted in Williams syndrome. Genome Res. 1999;9:428-436.
    • (1999) Genome Res , vol.9 , pp. 428-436
    • DeSilva, U.1    Massa, H.2    Trask, B.J.3    Green, E.D.4
  • 3
    • 0040945789 scopus 로고    scopus 로고
    • A p47-phox pseudogene carries the most common mutation causing p47-phox-deficient chronic granulomatous disease
    • Gorlach A, Lee PL, Roesler J, et al. A p47-phox pseudogene carries the most common mutation causing p47-phox-deficient chronic granulomatous disease. J Clin Invest. 1997;100:1907-1918.
    • (1997) J Clin Invest , vol.100 , pp. 1907-1918
    • Gorlach, A.1    Lee, P.L.2    Roesler, J.3
  • 4
    • 0034653483 scopus 로고    scopus 로고
    • Recombination events between the p47-phox gene and its highly homologous pseudogenes are the main cause of autosomal recessive chronic granulomatous disease
    • Roesler J, Curnutte JT, Rae J, 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. 2000;95:2150-2156.
    • (2000) Blood , vol.95 , pp. 2150-2156
    • Roesler, J.1    Curnutte, J.T.2    Rae, J.3
  • 5
    • 0034764060 scopus 로고    scopus 로고
    • Gene-scan method for the recognition of carriers and patients with p47(phox)-deficient autosomal recessive chronic granulomatous disease
    • Dekker J, de Boer M, Roos D. Gene-scan method for the recognition of carriers and patients with p47(phox)-deficient autosomal recessive chronic granulomatous disease. Exp Hematol. 2001;29:1319-1325.
    • (2001) Exp Hematol , vol.29 , pp. 1319-1325
    • Dekker, J.1    De Boer, M.2    Roos, D.3
  • 6
    • 0017162599 scopus 로고
    • Neutrophil dysfunction in Crohn's disease
    • Segal AW, Loewi G. Neutrophil dysfunction in Crohn's disease. Lancet. 1976;2:219-221.
    • (1976) Lancet , vol.2 , pp. 219-221
    • Segal, A.W.1    Loewi, G.2
  • 7
    • 0035978533 scopus 로고    scopus 로고
    • A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease
    • Ogura Y, Bonen D, Inohara N, et al. A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease. Nature. 2001;411:603-606.
    • (2001) Nature , vol.411 , pp. 603-606
    • Ogura, Y.1    Bonen, D.2    Inohara, N.3
  • 8
    • 16044373177 scopus 로고    scopus 로고
    • Two stage genome-wide search in inflammatory bowel disease provides evidence for susceptibility loci on chromosomes 3, 7 and 12
    • Satsangi J, Parkes M, Louis E, et al. Two stage genome-wide search in inflammatory bowel disease provides evidence for susceptibility loci on chromosomes 3, 7 and 12. Nat Genet. 1996;14:199-202.
    • (1996) Nat Genet , vol.14 , pp. 199-202
    • Satsangi, J.1    Parkes, M.2    Louis, E.3
  • 9
    • 0023839784 scopus 로고
    • Detection of carriers of the autosomal form of chronic granulomatous disease
    • Verhoeven AJ, van-Schaik ML, Roos D, Weening RS. Detection of carriers of the autosomal form of chronic granulomatous disease. Blood. 1988;71:505-507.
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    • Verhoeven, A.J.1    Van-Schaik, M.L.2    Roos, D.3    Weening, R.S.4
  • 10
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    • Cantharidin blisters: A technique for investigating leukocyte trafficking and cytokine production at sites of inflammation in humans
    • Day RM, Harbord M, Forbes A, Segal AW. Cantharidin blisters: a technique for investigating leukocyte trafficking and cytokine production at sites of inflammation in humans. J Immunol Methods. 2001;257:213-220.
    • (2001) J Immunol Methods , vol.257 , pp. 213-220
    • Day, R.M.1    Harbord, M.2    Forbes, A.3    Segal, A.W.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.