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Journal Abstract Search

117 related items for PubMed ID: 7913005

  • 21.
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  • 23. Ethnic differences in allelic associations of the interleukin-1 gene cluster in South African patients with inflammatory bowel disease (IBD) and in control individuals.
    Mwantembe O, Gaillard MC, Barkhuizen M, Pillay V, Berry SD, Dewar JB, Song E.
    Immunogenetics; 2001; 52(3-4):249-54. PubMed ID: 11220627
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  • 26. Predominance of one T-cell antigen receptor BV haplotype in African populations.
    Craddock TP, Zumla AM, Ollier WE, Chintu CZ, Muyinda GP, Lancaster FC, Boylston AW.
    Immunogenetics; 2000 Mar; 51(3):231-7. PubMed ID: 10752633
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  • 27. Z-type alpha 1-antitrypsin is less competent than M1-type alpha 1-antitrypsin as an inhibitor of neutrophil elastase.
    Ogushi F, Fells GA, Hubbard RC, Straus SD, Crystal RG.
    J Clin Invest; 1987 Nov; 80(5):1366-74. PubMed ID: 3500183
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  • 29. SSCP analysis of the tyrosine kinase domain of the insulin receptor gene: polymorphisms detected in South African black and white subjects.
    Panz VR, Ruff P, Joffe BI, Kedda MA, Seftel HC.
    Hum Genet; 1996 Apr; 97(4):438-40. PubMed ID: 8834239
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  • 30. Unique TCR beta-subunit variable gene haplotypes in Africans.
    Donaldson IJ, Shefta J, Lawson CA, Bushnell JR, Morgan AW, Isaacs JD, Carpenter D, Shaw MA, Rooth I, Quinnell RJ, Zumla AM, Ollier WR, Chintu CZ, Muyinda GP, Hill AS, Boylston AW.
    Immunogenetics; 2002 Feb; 53(10-11):884-93. PubMed ID: 11862388
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  • 31. Five novel missense mutations of the Lewis gene (FUT3) in African (Xhosa) and Caucasian populations in South Africa.
    Pang H, Liu Y, Koda Y, Soejima M, Jia J, Schlaphoff T, Du Toit ED, Kimura H.
    Hum Genet; 1998 Jun; 102(6):675-80. PubMed ID: 9703429
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  • 32. Haplotypes of the alpha-1 antitrypsin gene in healthy controls and Z deficiency patients.
    Chappell S, Guetta-Baranés T, Batowski K, Yiannakis E, Morgan K, O'Connor C, MacNee W, Kalsheker N.
    Hum Mutat; 2004 Dec; 24(6):535-6. PubMed ID: 15532029
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  • 33. Characterization of the gene and protein of the alpha 1-antitrypsin "deficiency" allele Mprocida.
    Takahashi H, Nukiwa T, Satoh K, Ogushi F, Brantly M, Fells G, Stier L, Courtney M, Crystal RG.
    J Biol Chem; 1988 Oct 25; 263(30):15528-34. PubMed ID: 3262617
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  • 34. Alpha 1-antitrypsin Wbethesda: molecular basis of an unusual alpha 1-antitrypsin deficiency variant.
    Holmes MD, Brantly ML, Fells GA, Crystal RG.
    Biochem Biophys Res Commun; 1990 Aug 16; 170(3):1013-20. PubMed ID: 2390072
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  • 35. D1S80 locus variability in three Brazilian ethnic groups.
    Heidrich EM, Hutz MH, Salzano FM, Coimbra CE, Santos RV.
    Hum Biol; 1995 Apr 16; 67(2):311-9. PubMed ID: 7729831
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  • 36. IL-4 receptor genetic polymorphisms and asthma in Asian populations.
    Zhang W, Zhang X, Qiu D, Sandford A, Tan WC.
    Respir Med; 2007 Jan 16; 101(1):186-90. PubMed ID: 16757160
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  • 37. Immunogenetics of atopic asthma: association of DRB1*1101 DQA1*0501 DQB1*0301 haplotype with Dermatophagoides spp.-sensitive asthma in a sample of the Venezuelan population.
    Lara-Marquez ML, Yunis JJ, Layrisse Z, Ortega F, Carvallo-Gil E, Montagnani S, Makhatadze NJ, Pocino M, Granja C, Yunis E.
    Clin Exp Allergy; 1999 Jan 16; 29(1):60-71. PubMed ID: 10051703
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  • 38. Genetic characterization and origin of Tunisian Berbers.
    Chaâbani H, Cox DW.
    Hum Hered; 1988 Jan 16; 38(5):308-16. PubMed ID: 3266184
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  • 39. Ethnic differences in the association between lipid metabolism genes and lipid levels in black and white South African women.
    Ellman N, Keswell D, Collins M, Tootla M, Goedecke JH.
    Atherosclerosis; 2015 Jun 16; 240(2):311-7. PubMed ID: 25864161
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  • 40. Molecular-based haplotype analysis of the beta 2-adrenergic receptor gene (ADRB2) in Japanese asthmatic and non-asthmatic subjects.
    Munakata M, Harada Y, Ishida T, Saito J, Nagabukuro A, Matsushita H, Koga N, Ohsaki M, Imagawa K, Shiratsuchi T.
    Allergol Int; 2006 Jun 16; 55(2):191-8. PubMed ID: 17075257
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