Hopwood JJ - Search Results

1

Family 39 alpha-l-iduronidases and beta-D-xylosidases react through similar glycosyl-enzyme intermediates: identification of the human iduronidase nucleophile.

Nieman CE, Wong AW, He S, Clarke L, Hopwood JJ, Withers SG. Nieman CE, et al. Among authors: hopwood jj. Biochemistry. 2003 Jul 8;42(26):8054-65. doi: 10.1021/bi034293v. Biochemistry. 2003. PMID: 12834357

2

Mutation analysis of 19 North American mucopolysaccharidosis type I patients: identification of two additional frequent mutations.

Clarke LA, Nelson PV, Warrington CL, Morris CP, Hopwood JJ, Scott HS. Clarke LA, et al. Among authors: hopwood jj. Hum Mutat. 1994;3(3):275-82. doi: 10.1002/humu.1380030316. Hum Mutat. 1994. PMID: 8019563

3

Molecular genetics of mucopolysaccharidosis type I: diagnostic, clinical, and biological implications.

Scott HS, Bunge S, Gal A, Clarke LA, Morris CP, Hopwood JJ. Scott HS, et al. Among authors: hopwood jj. Hum Mutat. 1995;6(4):288-302. doi: 10.1002/humu.1380060403. Hum Mutat. 1995. PMID: 8680403 Review.

4

Human alpha-L-iduronidase. 2. Catalytic properties.

Clements PR, Muller V, Hopwood JJ. Clements PR, et al. Among authors: hopwood jj. Eur J Biochem. 1985 Oct 1;152(1):29-34. doi: 10.1111/j.1432-1033.1985.tb09159.x. Eur J Biochem. 1985. PMID: 4043083 Free article.

5

Human alpha-L-iduronidase. 1. Purification, monoclonal antibody production, native and subunit molecular mass.

Clements PR, Brooks DA, Saccone GT, Hopwood JJ. Clements PR, et al. Among authors: hopwood jj. Eur J Biochem. 1985 Oct 1;152(1):21-8. doi: 10.1111/j.1432-1033.1985.tb09158.x. Eur J Biochem. 1985. PMID: 4043081 Free article.

6

Glycosidase active site mutations in human alpha-L-iduronidase.

Brooks DA, Fabrega S, Hein LK, Parkinson EJ, Durand P, Yogalingam G, Matte U, Giugliani R, Dasvarma A, Eslahpazire J, Henrissat B, Mornon JP, Hopwood JJ, Lehn P. Brooks DA, et al. Among authors: hopwood jj. Glycobiology. 2001 Sep;11(9):741-50. doi: 10.1093/glycob/11.9.741. Glycobiology. 2001. PMID: 11555618

7

Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome): a Y210C mutation causes either altered protein handling or altered protein function of N-acetylgalactosamine 4-sulfatase at multiple points in the vacuolar network.

Bradford TM, Litjens T, Parkinson EJ, Hopwood JJ, Brooks DA. Bradford TM, et al. Among authors: hopwood jj. Biochemistry. 2002 Apr 16;41(15):4962-71. doi: 10.1021/bi0121149. Biochemistry. 2002. PMID: 11939792

8

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: hopwood jj. Hum Genet. 1991 Jun;87(2):205-6. doi: 10.1007/BF00204183. Hum Genet. 1991. PMID: 1906048

9

Mucopolysaccharidosis type I: identification of 8 novel mutations and determination of the frequency of the two common alpha-L-iduronidase mutations (W402X and Q70X) among European patients.

Bunge S, Kleijer WJ, Steglich C, Beck M, Zuther C, Morris CP, Schwinger E, Hopwood JJ, Scott HS, Gal A. Bunge S, et al. Among authors: hopwood jj. Hum Mol Genet. 1994 Jun;3(6):861-6. doi: 10.1093/hmg/3.6.861. Hum Mol Genet. 1994. PMID: 7951228

10

Identification of mutations in the alpha-L-iduronidase gene (IDUA) that cause Hurler and Scheie syndromes.

Scott HS, Litjens T, Nelson PV, Thompson PR, Brooks DA, Hopwood JJ, Morris CP. Scott HS, et al. Among authors: hopwood jj. Am J Hum Genet. 1993 Nov;53(5):973-86. Am J Hum Genet. 1993. PMID: 8213840 Free PMC article.

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