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    Results: 1 to 20 of 116

    1.

    NCF1 gene and pseudogene pattern: association with parasitic infection and autoimmunity.

    Greve B, Hoffmann P, Vonthein R, Kun J, Lell B, Mycko MP, Selmaj KW, Berger K, Weissert R, Kremsner PG.

    Malar J. 2008 Dec 11;7:251.PMID: 19077231 [PubMed - indexed for MEDLINE]Related articlesFree article

    2.

    NCF1 (p47phox) and ncf1 pseudogenes are not associated with inflammatory bowel disease.

    Suraweera N, Zampeli E, Rogers P, Atkin W, Forbes A, Harbord M, Silver A.

    Inflamm Bowel Dis. 2004 Nov;10(6):758-62.PMID: 15626894 [PubMed - indexed for MEDLINE]Related articles

    3.

    DNA phasing by TA dinucleotide microsatellite length determines in vitro and in vivo expression of the gp91phox subunit of NADPH oxidase and mediates protection against severe malaria.

    Uhlemann AC, Szlezák NA, Vonthein R, Tomiuk J, Emmer SA, Lell B, Kremsner PG, Kun JF.

    J Infect Dis. 2004 Jun 15;189(12):2227-34. Epub 2004 May 25.PMID: 15181570 [PubMed - indexed for MEDLINE]Related articles

    4.

    Chronic granulomatous disease caused by mutations other than the common GT deletion in NCF1, the gene encoding the p47phox component of the phagocyte NADPH oxidase.

    Roos D, de Boer M, Köker MY, Dekker J, Singh-Gupta V, Ahlin A, Palmblad J, Sanal O, Kurenko-Deptuch M, Jolles S, Wolach B.

    Hum Mutat. 2006 Dec;27(12):1218-29.PMID: 16972229 [PubMed - indexed for MEDLINE]Related articles

    5.

    High oxygen radical production is associated with fast parasite clearance in children with Plasmodium falciparum malaria.

    Greve B, Lehman LG, Lell B, Luckner D, Schmidt-Ott R, Kremsner PG.

    J Infect Dis. 1999 Jun;179(6):1584-6.PMID: 10228089 [PubMed - indexed for MEDLINE]Related articles

    6.

    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.

    Exp Hematol. 2001 Nov;29(11):1319-25.PMID: 11698128 [PubMed - indexed for MEDLINE]Related articles

    7.

    Inconsistent susceptibility to autoimmunity in inbred LEW rats is due to genetic crossbreeding involving segregation of the arthritis-regulating gene Ncf1.

    Olofsson P, Johansson A, Wedekind D, Klöting I, Klinga-Levan K, Lu S, Holmdahl R.

    Genomics. 2004 May;83(5):765-71.PMID: 15081107 [PubMed - indexed for MEDLINE]Related articles

    9.

    Enhanced autoimmunity, arthritis, and encephalomyelitis in mice with a reduced oxidative burst due to a mutation in the Ncf1 gene.

    Hultqvist M, Olofsson P, Holmberg J, Bäckström BT, Tordsson J, Holmdahl R.

    Proc Natl Acad Sci U S A. 2004 Aug 24;101(34):12646-51. Epub 2004 Aug 13.PMID: 15310853 [PubMed - indexed for MEDLINE]Related articlesFree article

    10.

    A copy number variation in human NCF1 and its pseudogenes.

    Brunson T, Wang Q, Chambers I, Song Q.

    BMC Genet. 2010 Feb 23;11(1):13. [Epub ahead of print]PMID: 20178640 [PubMed - as supplied by publisher]Related articlesFree article

    11.

    Haplotype specific-sequencing reveals MBL2 association with asymptomatic Plasmodium falciparum infection.

    Boldt AB, Messias-Reason IJ, Lell B, Issifou S, Pedroso ML, Kremsner PG, Kun JF.

    Malar J. 2009 May 11;8:97.PMID: 19432958 [PubMed - indexed for MEDLINE]Related articlesFree article

    12.

    CR1 levels and gene polymorphisms exhibit differential association with falciparum malaria in regions of varying disease endemicity.

    Sinha S, Jha GN, Anand P, Qidwai T, Pati SS, Mohanty S, Mishra SK, Tyagi PK, Sharma SK, Venkatesh V, Habib S.

    Hum Immunol. 2009 Apr;70(4):244-50. Epub 2009 Feb 10.PMID: 19480840 [PubMed - indexed for MEDLINE]Related articles

    13.

    Ncf1-associated reduced oxidative burst promotes IL-33R+ T cell-mediated adjuvant-free arthritis in mice.

    Hagenow K, Gelderman KA, Hultqvist M, Merky P, Bäcklund J, Frey O, Kamradt T, Holmdahl R.

    J Immunol. 2009 Jul 15;183(2):874-81. Epub 2009 Jun 24.PMID: 19553535 [PubMed - indexed for MEDLINE]Related articles

    14.

    Malarial anaemia in African children associated with high oxygen-radical production.

    Greve B, Kremsner PG, Lell B, Luckner D, Schmid D.

    Lancet. 2000 Jan 1;355(9197):40-1. Erratum in: Lancet 2000 Feb 26;355(9205):758. PMID: 10615892 [PubMed - indexed for MEDLINE]Related articles

    15.

    Hygiene hypothesis: innate immunity, malaria and multiple sclerosis.

    Sotgiu S, Angius A, Embry A, Rosati G, Musumeci S.

    Med Hypotheses. 2008;70(4):819-25. Epub 2007 Sep 21.PMID: 17889443 [PubMed - indexed for MEDLINE]Related articles

    16.

    Common genotypic polymorphisms in glutathione S-transferases in mild and severe falciparum malaria in Tanzanian children.

    Kavishe RA, Bousema T, Shekalaghe SA, Sauerwein RW, Mosha FW, van der Ven AJ, Russel FG, Koenderink JB.

    Am J Trop Med Hyg. 2009 Aug;81(2):363-5.PMID: 19635899 [PubMed - indexed for MEDLINE]Related articles

    17.

    A novel mutation in NCF1 in an adult CGD patient with a liver abscess as first presentation.

    van de Vosse E, van Wengen A, van Geelen JA, de Boer M, Roos D, van Dissel JT.

    J Hum Genet. 2009 Jun;54(6):313-6. Epub 2009 Mar 27.PMID: 19329991 [PubMed - indexed for MEDLINE]Related articles

    18.

    IL2RA genetic heterogeneity in multiple sclerosis and type 1 diabetes susceptibility and soluble interleukin-2 receptor production.

    Maier LM, Lowe CE, Cooper J, Downes K, Anderson DE, Severson C, Clark PM, Healy B, Walker N, Aubin C, Oksenberg JR, Hauser SL, Compston A, Sawcer S; International Multiple Sclerosis Genetics Consortium, De Jager PL, Wicker LS, Todd JA, Hafler DA.

    PLoS Genet. 2009 Jan;5(1):e1000322. Epub 2009 Jan 2.PMID: 19119414 [PubMed - indexed for MEDLINE]Related articlesFree article

    19.

    Oxygen radical production in leukocytes and disease severity in multiple sclerosis.

    Mossberg N, Movitz C, Hellstrand K, Bergström T, Nilsson S, Andersen O.

    J Neuroimmunol. 2009 Aug 18;213(1-2):131-4. Epub 2009 Jul 8.PMID: 19589606 [PubMed - indexed for MEDLINE]Related articles

    20.

    Modification of Multiple Sclerosis Phenotypes by African Ancestry at HLA.

    Cree BA, Reich DE, Khan O, De Jager PL, Nakashima I, Takahashi T, Bar-Or A, Tong C, Hauser SL, Oksenberg JR.

    Arch Neurol. 2009 Feb;66(2):226-33.PMID: 19204159 [PubMed - indexed for MEDLINE]Related articlesFree article

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