Hopwood JJ - Search Results

1

Aminoglycoside-Induced Premature Stop Codon Read-Through of Mucopolysaccharidosis Type I Patient Q70X and W402X Mutations in Cultured Cells.

Kamei M, Kasperski K, Fuller M, Parkinson-Lawrence EJ, Karageorgos L, Belakhov V, Baasov T, Hopwood JJ, Brooks DA. Kamei M, et al. Among authors: hopwood jj. JIMD Rep. 2014;13:139-47. doi: 10.1007/8904_2013_270. Epub 2013 Nov 6. JIMD Rep. 2014. PMID: 24193436 Free PMC article.

2

Stop-codon read-through for patients affected by a lysosomal storage disorder.

Brooks DA, Muller VJ, Hopwood JJ. Brooks DA, et al. Among authors: hopwood jj. Trends Mol Med. 2006 Aug;12(8):367-73. doi: 10.1016/j.molmed.2006.06.001. Epub 2006 Jun 23. Trends Mol Med. 2006. PMID: 16798086 Review.

3

Prediction of neuropathology in mucopolysaccharidosis I patients.

Fuller M, Brooks DA, Evangelista M, Hein LK, Hopwood JJ, Meikle PJ. Fuller M, et al. Among authors: hopwood jj. Mol Genet Metab. 2005 Jan;84(1):18-24. doi: 10.1016/j.ymgme.2004.09.004. Mol Genet Metab. 2005. PMID: 15639191

4

N-acetylgalactosamine-6-sulfatase protein detection in MPS IVA patient and unaffected control samples.

Parkinson-Lawrence EJ, Muller VJ, Hopwood JJ, Brooks DA. Parkinson-Lawrence EJ, et al. Among authors: hopwood jj. Clin Chim Acta. 2007 Feb;377(1-2):88-91. doi: 10.1016/j.cca.2006.08.030. Epub 2006 Sep 1. Clin Chim Acta. 2007. PMID: 17027703

5

Drug induced exocytosis of glycogen in Pompe disease.

Turner CT, Fuller M, Hopwood JJ, Meikle PJ, Brooks DA. Turner CT, et al. Among authors: hopwood jj. Biochem Biophys Res Commun. 2016 Oct 28;479(4):721-727. doi: 10.1016/j.bbrc.2016.09.145. Epub 2016 Sep 28. Biochem Biophys Res Commun. 2016. PMID: 27693584

6

The alpha-L-iduronidase mutations R89Q and R89W result in an attenuated mucopolysaccharidosis type I clinical presentation.

Hein LK, Hopwood JJ, Clements PR, Brooks DA. Hein LK, et al. Among authors: hopwood jj. Biochim Biophys Acta. 2003 Oct 15;1639(2):95-103. doi: 10.1016/s0925-4439(03)00129-7. Biochim Biophys Acta. 2003. PMID: 14559116 Free article.

7

Enzyme replacement therapy in mucopolysaccharidosis I: altered distribution and targeting of alpha-L-iduronidase in immunized rats.

Turner CT, Hopwood JJ, Brooks DA. Turner CT, et al. Among authors: hopwood jj. Mol Genet Metab. 2000 Apr;69(4):277-85. doi: 10.1006/mgme.2000.2979. Mol Genet Metab. 2000. PMID: 10870845

8

Exocytosis is impaired in mucopolysaccharidosis IIIA mouse chromaffin cells.

Keating DJ, Winter MA, Hemsley KM, Mackenzie KD, Teo EH, Hopwood JJ, Brooks DA, Parkinson-Lawrence EJ. Keating DJ, et al. Among authors: hopwood jj. Neuroscience. 2012 Dec 27;227:110-8. doi: 10.1016/j.neuroscience.2012.09.034. Epub 2012 Sep 25. Neuroscience. 2012. PMID: 23022219

9

alpha-L-iduronidase premature stop codons and potential read-through in mucopolysaccharidosis type I patients.

Hein LK, Bawden M, Muller VJ, Sillence D, Hopwood JJ, Brooks DA. Hein LK, et al. Among authors: hopwood jj. J Mol Biol. 2004 Apr 30;338(3):453-62. doi: 10.1016/j.jmb.2004.03.012. J Mol Biol. 2004. PMID: 15081804

10

Glycosaminoglycan degradation fragments in mucopolysaccharidosis I.

Fuller M, Meikle PJ, Hopwood JJ. Fuller M, et al. Among authors: hopwood jj. Glycobiology. 2004 May;14(5):443-50. doi: 10.1093/glycob/cwh049. Epub 2004 Jan 12. Glycobiology. 2004. PMID: 14718373

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