Wilson P - Search Results

1

Modelling the impact of wastewater flows and management practices on antimicrobial resistance in dairy farms.

Todman H, Helliwell R, King L, Blanchard A, Gray-Hammerton CJ, Hooton SP, Baker M, Margerison J, Wilson P, Dodd CER, Morris C, Raman S, Hudson C, Kreft JU, Hobman JL, Kypraios T, Stekel DJ. Todman H, et al. Among authors: wilson p. NPJ Antimicrob Resist. 2024;2(1):13. doi: 10.1038/s44259-024-00029-4. Epub 2024 May 14. NPJ Antimicrob Resist. 2024. PMID: 38757121 Free PMC article.

2

Sequence of the human iduronate 2-sulfatase (IDS) gene.

Wilson PJ, Meaney CA, Hopwood JJ, Morris CP. Wilson PJ, et al. Genomics. 1993 Sep;17(3):773-5. doi: 10.1006/geno.1993.1406. Genomics. 1993. PMID: 8244397

3

Molecular analysis of patients with Hunter syndrome: implication of a region prone to structural alterations within the IDS gene.

Steén-Bondeson ML, Dahl N, Tönnesen T, Kleijer WJ, Seidlitz G, Gustavson KH, Wilson PJ, Morris CP, Hopwood JJ, Pettersson U. Steén-Bondeson ML, et al. Among authors: wilson pj. Hum Mol Genet. 1992 Jun;1(3):195-8. doi: 10.1093/hmg/1.3.195. Hum Mol Genet. 1992. PMID: 1303177

4

Molecular basis of mucopolysaccharidosis type II: mutations in the iduronate-2-sulphatase gene.

Hopwood JJ, Bunge S, Morris CP, Wilson PJ, Steglich C, Beck M, Schwinger E, Gal A. Hopwood JJ, et al. Among authors: wilson pj. Hum Mutat. 1993;2(6):435-42. doi: 10.1002/humu.1380020603. Hum Mutat. 1993. PMID: 8111411 Review.

5

Hunter syndrome: isolation of an iduronate-2-sulfatase cDNA clone and analysis of patient DNA.

Wilson PJ, Morris CP, Anson DS, Occhiodoro T, Bielicki J, Clements PR, Hopwood JJ. Wilson PJ, et al. Proc Natl Acad Sci U S A. 1990 Nov;87(21):8531-5. doi: 10.1073/pnas.87.21.8531. Proc Natl Acad Sci U S A. 1990. PMID: 2122463 Free PMC article.

6

Genetic mapping of new RFLPs at Xq27-q28.

Suthers GK, Oberlé I, Nancarrow J, Mulley JC, Hyland VJ, Wilson PJ, McCure J, Morris CP, Hopwood JJ, Mandel JL, et al. Suthers GK, et al. Among authors: wilson pj. Genomics. 1991 Jan;9(1):37-43. doi: 10.1016/0888-7543(91)90218-4. Genomics. 1991. PMID: 1672291

7

Frequent deletions at Xq28 indicate genetic heterogeneity in Hunter syndrome.

Wilson PJ, Suthers GK, Callen DF, Baker E, Nelson PV, Cooper A, Wraith JE, Sutherland GR, Morris CP, Hopwood JJ. Wilson PJ, et al. Hum Genet. 1991 Mar;86(5):505-8. doi: 10.1007/BF00194643. Hum Genet. 1991. PMID: 1901826

8

Genetic mapping on the mouse X chromosome of human cDNA clones for the fragile X and Hunter syndromes.

Faust CJ, Verkerk AJ, Wilson PJ, Morris CP, Hopwood JJ, Oostra BA, Herman GE. Faust CJ, et al. Among authors: wilson pj. Genomics. 1992 Apr;12(4):814-7. doi: 10.1016/0888-7543(92)90314-i. Genomics. 1992. PMID: 1572654

9

The clinical phenotype of two patients with a complete deletion of the iduronate-2-sulphatase gene (mucopolysaccharidosis II--Hunter syndrome).

Wraith JE, Cooper A, Thornley M, Wilson PJ, Nelson PV, Morris CP, Hopwood JJ. Wraith JE, et al. Among authors: wilson pj. Hum Genet. 1991 Jun;87(2):205-6. doi: 10.1007/BF00204183. Hum Genet. 1991. PMID: 1906048

10

Characterization of a deletion at Xq27-q28 associated with unbalanced inactivation of the nonmutant X chromosome.

Clarke JT, Wilson PJ, Morris CP, Hopwood JJ, Richards RI, Sutherland GR, Ray PN. Clarke JT, et al. Among authors: wilson pj. Am J Hum Genet. 1992 Aug;51(2):316-22. Am J Hum Genet. 1992. PMID: 1642233 Free PMC article.

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