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1. Monoclonal antibodies against the muscle specific N-terminus of dystrophin: Characterizaton of dystrophin in a muscular dystrophy patient with a frameshift deletion of exons 3-7 Le Thiet Thanh, Nguyen thi Man, D. R. Love, T. R. Helliwell, K. E. Davies and G. E. Morris American J. Human Genetics 53 (1993) 131-139

2. Specificity and VH sequence of two monoclonal antibodies against the N-terminus of dystrophin G. E. Morris, C. Nguyen and Nguyen thi Man Biochemical Journal 309 (1995) 355-359

3. Is myoblast transplantation effective? T. Partridge, Q. Lu, G. E. Morris and E. Hoffmann Nature Med. 4 (1998) 1208-1209

4. In vivo targeted repair of a point mutation in the canine dystrophin gene by a chimeric RNA/DNA oligonucleotide. R.J. Bartlett, S. Stockinger, M.M. Denis, W.T. Bartlett, L. Inverardi, T.T. Le, Nguyen thi Man, G.E. Morris, D.J. Bogan, J. Metcalf-Brogan and J.N. Kornegay Nature Biotechnol. 18 (2000) 615-622

5. Flexible hinges in dystrophin N. Ahmed, Nguyen thi Man and G. E. Morris Biochem. Soc. Trans. 26 (1998) S310

6. Monoclonal antibodies against defined regions of the muscular dystrophy protein, dystrophin Nguyen thi Man, A. J. Cartwright, G. E. Morris, D. Love, J. F. Bloomfield and K. E. Davies FEBS Letters 262 (1990) 237-240

7. Use of epitope libraries to identify exon-specific monoclonal antibodies for characterization of altered dystrophins in muscular dystrophy Nguyen thi Man and G. E. Morris American J. Human Genetics 52 (1993) 1057-1066

8. Monoclonal antibodies for dystrophin analysis: epitope mapping and improved binding to SDS-treated muscle sections Nguyen thi Man, H.B. Ginjaar, G.J.B. van Ommen and G.E. Morris Biochem. J. 288 (1992) 663-668.

9. Monoclonal antibody evidence for structural similarities between the central rod regions of actinin and dystrophin Nguyen thi Man, J.M. Ellis, I.B. Ginjaar, M.M.B. van Paassen, G.-J. B. van Ommen, A.F.M. Moorman, A.J. Cartwright and G.E. Morris FEBS Lett. 272 (1990) 109-112

10. The molecular basis for cross-reactiom of an anti-dystrophin antibody with alpha-actinin M. James, Nguyen thi Man, Y.H. Edwards and G.E. Morris Biochim. biophys. acta 1360 (1997) 169-176

11. Alpha-actinin in nemaline bodies in congenital nemaline myopathy: Immunological confirmation by light and electron microscopy C. Wallgren-Pettersson, B. Jasani, G.R. Newman, S. Jones, S. Singharao, G.E. Morris, A. Clarke, I. Virtanen, C. Holmberg and J. Rapola Neuromusc. Disord. 5 (1995) 93-104

12. A truncated dystrophin lacking the C-terminal domains is localized at the muscle membrane T.R. Helliwell, J.M. Ellis, R.C. Mountford, R.E. Appleton and G.E. Morris American. J. Human. Genetics 50 (1992) 508-514

13. Characterization of genetic deletions in Becker Muscular Dystrophy using monoclonal antibodies against a deletion-prone region of dystrophin Le Thiet Thanh, Nguyen thi Man, S. Hori, C.A. Sewry, V. Dubowitz and G.E. Morris American J. of Medical Genetics 58 (1995) 177-186

14. Characterization of revertant muscle fibres in Duchenne Muscular Dystrophy using exon-specific monoclonal antibodies against dystrophin Le Thiet Thanh, Nguyen thi Man, T.R. Helliwell and G.E. Morris American J. of Human Genetics 56 (1995) 725-731

15. Localization of the DMDL-gene-encoded dystrophin-related protein using a panel of 19 monoclonal antibodies. Presence at neuromuscular junctions, in the sarcolemma of dystrophic skeletal muscle, in vascular and other smooth muscles and in proliferating brain cell lines Nguyen thi Man, J.M. Ellis, D.R. Love, K.E. Davies, K.C. Gatter, G.Dickson and G.E. Morris J. Cell Biol. 115 (1991) 1695-1700

16. An epitope structure for the C-terminal domain of dystrophin and utrophin G.E. Morris, S. G. Sedgwick, J. M. Ellis, A. Pereboev, J. S. Chamberlain and Nguyen thi Man Biochemistry 37 (1998) 11117-11127

17. Monoclonal antibody studies of an alternatively-spliced region of dystrophin C. Simmons (1997) M. Phil. thesis (University of Salford)

18. The N-terminal half of dystrophin is protected from proteolysis in situ S. Hori, S. Ohtani, Nguyen thi Man and G.E. Morris Biochem. Biophys. Res. Commun., 209 (1995) 1062-1067

19. Apo-dystrophins (Dp140 and Dp71) and dystrophin splicing isoforms in developing brain G.E. Morris, C. Simmons and Nguyen thi Man Biochem. Biophys. Res. Commun. 215 (1995) 361-367

20. Full-length and short forms of utrophin, the dystrophin-related protein Nguyen thi Man, T.R. Helliwell, C. Simmons, S.J. Winder, J. Kendrick-Jones, K.E. Davies and G.E. Morris FEBS Letters 358 (1995) 262-266

21. Disruption of the utrophin-actin interaction by monoclonal antibodies and prediction of an actin-binding surface of utrophin Morris G. E., Nguyen thi Man, Nguyen thi Ngoc Huyen, A. Pereboev, J. Kendrick-Jones and Winder S. J. Biochem. J. 337 (1999) 119-123

22. Expression of the 43kD dystrophin-associated glycoprotein in human neuromuscular disease T.R. Helliwell, Nguyen thi Man and G.E. Morris Neuromusc. Disord. 4 (1994) 101-113

23. Dystrophin-related protein, utrophin, in normal and dystrophic human foetal skeletal muscle A. Clerk, G.E. Morris, V. Dubowitz, K.E. Davies, P.N. Strong and C.A. Sewry Histochem. J. 25 (1993) 554-561

24. A novel dystrophin isoform is required for normal retinal electrophysiology V.N. d'Souza, Nguyen thi Man, G.E. Morris, W. Karges, D.M. Pillers and P.N. Ray Human Molec. Genet. 4 (1995) 837-842

25. Myoblast transfer in the treatment of Duchenne's Muscular Dystrophy J.R. Mendell, J.T. Kissel, A.A. Amato, W. King, L. Signore, T.W. Prior, Z. Sahenk, S. Benson, P.E. McAndrew, R. Rice, H. Nagaraja, R. Stephens, L. Lantry, G.E. Morris and A.H.M. Burghes New England J. Med. 333 (1995) 832-838

26. A utrophin-glycoprotein complex in membranes of adherent cultured cells M. James, Nguyen thi Man, C.J. Wise, G.E. Jones and G.E. Morris Cell Motil. Cytoskeleton. 33 (1996) 163-174

27. Laminin-induced clustering of dystroglycan on embryonic muscle cells M.W. Cohen, C. Jacobson, P.D. Yurchenko, G.E. Morris and S. Carbonetto J. Cell Biol. 136 (1997) 1047-1058

28. Dystrophin is replaced by utrophin in frog heart; implications for muscular dystrophy G.E. Morris Neuromuscular Disorders 7 (1997) 493-498

29. An investigation into the effects of dystrophin on the lateral mobility of muscle membrane components A.L. Dutton Ph.D. thesis, University of Durham, submitted

30. Localization of rabbit huntingtin using a new panel of monoclonal antibodies. F.L. Wilkinson, Nguyen thi Man, S.B. Manilal, P. Thomas, J.W. Neal, P.S. Harper, A.L. Jones and G.E. Morris. Molec. Brain. Res. 69 (1999) 10-20.

31. The Emery-Dreifuss muscular dystrophy protein, emerin, is a nuclear membrane protein. S. Manilal, Nguyen thi Man, C.A. Sewry and G.E. Morris Hum. Mol. Genet. 5 (1996) 801-808.

32.Distibution of emerin and lamins in the heart and implications for Emery-Dreifuss muscular dystrophy. S. Manilal, C.A. Sewry, A. Pereboev, Nguyen thi Man, P. Gobbi, S. Hawkes, D.R. Love and G.E. Morris. Hum. Mol. Genet. 8 (1999) 353-359.

33. Heart to heart: from nuclear proteins to Emery-Dreifuss muscular dystrophy. G.E.Morris and S. Manilal. Hum. Mol. Genet. 8 (1999) 1847-1851.

34. The relationship between SMN, the spinal muscular atrophy protein, and nuclear coiled bodies in differentiated tissues and cultured cells. P.J. Young, T.T. Le, Nguyen thi Man, A.H.M. Burghes and G. E. Morris. Exp. Cell Res. 256 (2000) 365-374. [PubMed abstract]

35. Localization of myotonic dystrophy protein kinase in human and rabbit tissues using a new panel of monoclonal antibodies. Y. C. N. Pham, Nguyen thi Man, Le Thanh Lam and G.E. Morris. Hum. Mol. Genet., 7 (1998) 1957-1965.

36. Characterization of a monoclonal antibody panel shows that the myotonic dystrophy protein kinase, DMPK, is expressed almost exclusively in muscle and heart. L. T. Lam, Y. C. N. Pham, Nguyen thi Man and G. E. Morris. Hum. Mol. Genet. 9 (2000) 2167-2173.

37. Distinct nuclear assembly pathways for lamins A and C lead to their increase during quiescence in Swiss 3T3 cells. Pugh GE, Coates PJ, Lane EB, Raymond Y, Quinlan RA. J. Cell Sci. 110 (1997) 2483.

38. Mutations in the nuclear lamin proteins resulting in their aberrant assembly in the cytoplasm. Loewinger L, McKeon F EMBO J. 7 (1988) 2301.

39. A carboxyl-terminal interaction of lamin B1 is dependent on the CAAX endoprotease Rce1 and carboxymethylation. Maske CP, Hollinshead MS, Higbee NC, Bergo MO, Young SG, Vaux DJ J. Cell Biol. 162 (2003) 1223.

40. Characterisation of the Transcription Factor, Six5, using a new Panel of Monoclonal Antibodies. Y.C.N. Pham, Nguyen thi Man, I. Holt, C.A. Sewry, G. Pall, K.J. Johnson and G.E. Morris J. Cell Biochem. 95 (2005) 990.

41. A lamin A/C beta-strand containing the site of lipodystrophy mutations is a major surface epitope for a new panel of monoclonal antibodies.BR> Manilal S, Randles KN, Aunac C, Nguyen thi Man and Morris GE. Biochimica Biophysica Acta 1671 (2004) 87-92.

42. Absence of gemin5 from SMN complexes in nuclear Cajal bodies. Hao le T, Fuller HR, Lam le T, Le TT, Burghes AH, Morris GE. .BMC Cell Biol. 2007 8:28.

43. A role for complexes of survival of motor neurons (SMN) protein with gemins and profilin in neurite-like cytoplasmic extensions of cultured nerve cells. Sharma A, Lambrechts A, Hao le T, Le TT, Sewry CA, Ampe C, Burghes AH, Morris GE. . Exp Cell Res.309(2005)185-197.

44. Endosomal location of dopamine receptors in neuronal cell cytoplasm. Wolstencroft EC, Simic G, Man NT, Holt I, Lam le T, Buckland PR, Morris GE. .J Mol Histol. 38 (2007) 333-340.

45. Defective mRNA in myotonic dystrophy accumulates at the periphery of nuclear splicing speckles. Holt I, Mittal S, Furling D,Butler-Browne GS, Brook JD and Morris GE. .Genes to Cells 12:(2007)1035-1048 .

46. Treatment of human muscle creatine kinase with glutaraldehyde preferentially increases the immunogenicity of the native conformation and permits production of high-affinity monoclonal antibodies which recognize two distinct surface epitopes. Nguyen thi Man, A.J. Cartwright, K. Andrews and G.E. Morris. .J. Immunol.Methods 125 (1989) 251-259.

47. Monoclonal antibody studies of creatine kinase. Antibody-binding sites in the N-terminal region of creatine kinase and effects of antibody on enzyme refolding G.E,. Morris, L.C. Frost, P.A. Newport & N. Hudson .Biochem. J. 248 (1987) 53-59.

48. Monoclonal antibody studies suggest a catalytic site at the interface between domains in creatine kinase G.E. Morris and A.J. Cartwright, .Biochim. Biophys. Acta 1039 (1990) 318-322

49. A monoclonal antibody against the skeletal muscle enzyme creatine kinase G. E. Morris & L.P.Head FEBS Lett. 145 (1982) 163-168

50. Monoclonal antibody studies of creatine kinase. The ART epitope:evidence for an intermediate in protein folding G.E. Morris Biochem. J. 257 (1989) 461-469.

51. Spatial distribution of tissue-specific antigens in developing human heart and skeletal muscle:1)An immunohistochemical analysis of creatine kinase isoenzyme expression patterns A. Wessels, J.L.M. Vermeulen, S. Viragh, F. Kalman, G.E.Morris, Nguyen thi Man, W.H. Lamers & A.F.M. Moorman Anat. Rec. 228 (1990) 163-176

52. Muscleblind-like proteins: similarities and differences in normal and myotonic dystrophy muscle.Holt I, Jacquemin V, Fardaei M. Sewry CA, Butler-Browne GS, Furling D, Brook JD and Morris GE. Amer. J. Pathol., 174,(2009) 216-227.

53. Nesprins, but not Sun proteins, switch isoforms at the nuclear envelope during muscle development. K. Natalie Randles, Le Thanh Lam, Caroline A.Sewry, Megan Puckelwartz, Denis Furling, Manfred Wehnert, Elizabeth M. McNally and Glenn E. Morris. Dev Dyn. 239 (2010) 998-1009.

54. Exon-specific dystrophin antibodies for studies of Duchenne muscular dystrophy. Le Thanh Lam,Giang H. Nguyen,Nguyen Thi Man, Caroline A. Sewry,Glenn E. Morris. Translation Neuroscience.Vol1(2010) 233-237.

55. The mouse mismatch repair protein, MSH3, is a nucleoplasmic protein that aggregates into denser nuclear bodies under conditions of stress . Holt I, Lam LT, Tome S, Wansink, DG, te Riele, H, Gourdon G and Morris GE J Cell Biochem. 112:(2011)1612-1621.

56. Detection of the dystroglycanopathy protein, fukutin, using a new panel of site-specific monoclonal antibodies. Lynch TA, Lam le T, Man Nt, Kobayashi K, Toda T, Morris GE. Biochem Biophys Res Commun. 424 (2012) 354-357.

57. A new monoclonal antibody DAG-6F4 against human alpha-dystroglycan reveals reduced core protein in some, but not all, dystroglycanopathy patients. Humphrey EL, Lacey E, Le TL, Feng L, Sciandra F, Morris CR, Hewitt JE, Holt I, Brancaccio A, Barresi R, Sewry CA, Brown SC, Morris GE. Neuromuscul. Disord. (2014) Epub. Sep 16

58. Nesprins: tissue-specific expression of epsilon and other short isoforms. Duong NT, Morris GE, Lam le T, Zhang Q, Sewry CA, Shanahan CM, Holt I. (2014) PLoS One. 9(4):e94380.

59. Specific localization of nesprin-1-alpha2, the short isoform of nesprin-1 with a KASH domain, in developing, fetal and regenerating muscle, using a new monoclonal antibody. Holt I, Duong NT, Zhang Q, Lam le T, Sewry CA, Mamchaoui K, Shanahan CM, Morris GE. BMC Cell Biol. 2016 Jun 27;17(1):26.