Alpha 1-antichymotrypsin von Kalsheker, N A

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On the potential significance of the enzymatic activity of mite allergens to immunogenicity. Clues to structure and function revealed by molecular characterization von ROBINSON, C., KALSHEKER, N. A., SRINIVASAN, N., KING, C. M., GARROD, D. R., THOMPSON, P. J., STEWART, G. A.

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Enzymatically Active Papain Preferentially Induces an Allergic Response in Mice von Chambers, Louise, Brown, Alan, Pritchard, David I., Sreedharan, Suneal, Brocklehurst, Keith, Kalsheker, Noor A.

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Point mutation in a 3′ flanking sequence of the alpha-1-antitrypsin gene associated with chronic respiratory disease occurs in a regulatory sequence von Morgan, Kevin, Scobie, Graeme, Kalsheker, Noor A.

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Greater frequency of K-ras Val-12 mutation in colorectal cancer as detected with sensitive methods von Carpenter, KM, Durrant, LG, Morgan, K, Bennett, D, Hardcastle, JD, Kalsheker, NA

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On the potential significance of the enzymatic activity of mite allergens to immunogenicity. Clues to structure and function revealed by molecular characterization von ROBINSON, C, KALSHEKER, N. A, SRINIVASAN, N, KING, C. M, GARROD, D. R, THOMPSON, . P. J, STEWART, G. A

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The house dust mite allergen Der p1 catalytically inactivates alpha sub(1)-antitrypsin by specific reactive centre loop cleavage: A mechanism that promotes airway inflammation and... von Kalsheker, NA, Deam, S, Chambers, L, Sreedharan, S, Brocklehurst, K, Lomas, DA

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Acute intermittent porphyria caused by a C----T mutation that produces a stop codon in the porphobilinogen deaminase gene von Scobie, G A, Llewellyn, D H, Urquhart, A J, Smyth, S J, Kalsheker, N A, Harrison, P R, Elder, G H

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DNA polymorphism of human porphobilinogen deaminase gene in acute intermittent porphyria von LLEWELLYN, D. H, KALSHEKER, N. A, HARRISSON, P. R, PICAT, C, ROMEO, P. H, ELDER, G. H, MARSH, O. W. M, GRANDCHAMP, B, NORDMANN, Y, GOOSSENS, M

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Characterization of the alpha-1-antitrypsin M3 gene, a normal variant von GRAHAM, A, HAYES, K, WEIDINGER, S, NEWTON, C. R, MARKHAM, A. F, KALSHEKER, N. A

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Heterozygosity and localisation of normal allelic fragments for an alpha sub(1)-antitrypsin homologous sequence von Kalsheker, NA, Watkins, G L

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Alpha 1 antitrypsin deficiency due to Pi null: clinical presentation and evidence for molecular heterogeneity von Bamforth, F J, Kalsheker, N A

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Development of a rapid DNA screening procedure for the Factor V Leiden mutation von Scobie, G A, Ho, S T, Dolan, G., Kalsheker, N A

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Heterozygosity and localisation of normal allelic fragments for an alpha 1-antitrypsin homologous sequence von Kalsheker, N A, Watkins, G L

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Linkage disequilibrium between DNA polymorphisms within the porphobilinogen deaminase gene von Scobie, G A, Urquhart, A J, Elder, G H, Kalsheker, N A, Llewellyn, D H, Smyth, J, Harrison, P R

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A MspI polymorphism for the human porphobilinogen deaminase gene von Llewellyn, D H, Kalsheker, N A, Elder, G H, Harrison, P R, Chretien, S, Goossens, M

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Deoxyribonucleic acid (DNA) polymorphism of the alpha 1-antitrypsin gene in chronic lung disease von Kalsheker, N A, Hodgson, I J, Watkins, G L, White, J P, Morrison, H M, Stockley, R A

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Molecular characterisation of two alpha-1-antitrypsin deficiency variants: Proteinase inhibitor (Pi) Null sub(Newport) (Gly super(115) arrow right Ser) and (Pi) Z Wrexham (Ser supe... von Graham, A, Kalsheker, NA, Bamforth, F J, Newton, C R, Markham, A F

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Phenotyping alpha-1-antitrypsin ( α1AT) variants by isoelectric focusing in agarose and immunoblotting von Kalsheker, Noor A., Warner, Justin T., Watkins, Glyn L.

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Comparative modelling of major house dust mite allergen Der p I : structure validation using an extended environmental amino acid propensity table von TOPHAM, C. M, SRINIVASAN, N, THORPE, C. J, OVERINGTON, J. P, KALSHEKER, N. A

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