A novel dystrophin isoform is required for normal retinal electrophysiology von D'Souza, Vinita N., Man, Nguyen thi, Morris, Glenn E., Karges, Wolfram, Pillers, De-Ann M., Ray, Peter N.

Volltext

The Emery-Dreifuss Muscular Dystrophy Protein, Emerin, is a Nuclear Membrane Protein von Manilal, S., Man, Nguyen thi, Sewry, C. A., Morris, G. E.

Volltext

Effect of pathogenic mis-sense mutations in lamin A on its interaction with emerin in vivo von Holt, Ian, Ostlund, Cecilia, Stewart, Colin L, Man, Nguyen thi, Worman, Howard J, Morris, Glenn E

Volltext

Does the survival motor neuron protein (SMN) interact with Bcl-2? von COOVERT, DANIEL D, LE, THANH T, MORRIS, GLENN E, MAN, NGUYEN THI, KRALEWSKI, MARTINA, SENDTNER, MICHAEL, BURGHES, ARTHUR H M

Volltext

The exon 2b region of the spinal muscular atrophy protein, SMN, is involved in self-association and SIP1 binding von YOUNG, Philip J, NGUYEN THI MAN, LORSON, Christian L, LE, Thanh T, ANDROPHY, Elliot J, BURGHES, Arthur H. M, MORRIS, Glenn E

Volltext

Distribution of Emerin and Lamins in the Heart and Implications for Emery-Dreifuss Muscular Dystrophy von Manilal, S., Sewry, C. A., Pereboev, A., thi Man, Nguyen, Gobbi, P., Hawkes, S., Love, D. R., Morris, G. E.

Volltext

Characterization of a monoclonal antibody panel shows that the myotonic dystrophy protein kinase, DMPK, is expressed almost exclusively in muscle and heart von LAM, L. T, PHAM, Y. C. N, NGUYEN THI MAN, MORRIS, G. E

Volltext

Localization of Myotonic Dystrophy Protein Kinase in Human and Rabbit Tissues using a new Panel of Monoclonal Antibodies von Pham, Y. C. N., thi Man, Nguyen, Thanh Lam, Le, Morris, G. E.

Volltext

Apo-Dystrophins (DP140 and DP71) and Dystrophin-Splicing Isoforms in Developing Brain von Morris, G.E., Simmons, C., Man, N.T.

Volltext

Optimization of culture conditions for callus proliferation of Curculigo orchioides Gaertn von Nguyen, Tran Thi Thao, Nhung, Doan Thi Phuong, Man, Nguyen Thi Nguyen, Y, Tran Thi Nhu, An, Nguyen Hoang, Phuong, Truong Thi Bich

Volltext

The dystrophin-related protein, utrophin, is expressed on the sarcolemma of regenerating human skeletal muscle fibres in dystrophies and inflammatory myopathies von Helliwell, T.R., Nguyen thi, Man, Morris, G.E., Davies, K.E.

Volltext

A two-site ELISA can quantify upregulation of SMN protein by drugs for spinal muscular atrophy von NGUYEN THI MAN, HUMPHREY, E, LAM, L. T, FULLER, H. R, LYNCH, T. A, SEWRY, C. A, GOODWIN, P. R, MACKENZIE, A. E, MORRIS, G. E

Volltext

The molecular basis for cross-reaction of an anti-dystrophin antibody with alpha-actinin von James, Marian, Man, Nguyen thi, Edwards, Yvonne H., Morris, Glenn E.

Volltext

Absence of utrophin in intercalated discs of human cardiac muscle von Sewry, C A, Man, N T, Lynch, T, Morris, G E

Volltext

The Relationship between SMN, the Spinal Muscular Atrophy Protein, and Nuclear Coiled Bodies in Differentiated Tissues and Cultured Cells von Young, Philip J., Le, Thanh T., thi Man, Nguyen, Burghes, Arthur H.M., Morris, Glenn E.

Volltext

In vivo targeted repair of a point mutation in the canine dystrophin gene by a chimeric RNA/DNA oligonucleotide von Bartlett, Richard J., Stockinger, Sabine, Denis, Melvin M., Bartlett, William T., Inverardi, Luca, Le, T.T., Man, Nguyen thi, Morris, Glenn E., Bogan, Daniel J., Metcalf-Bogan, Janet, Kornegay, Joe N.

Volltext

Epitope mapping of recombinant antigens by transposon mutagenesis von MORRIS, G. E, NGUYEN THI MAN, SEDGWICK, S. G

Volltext

Specificity of dystrophin analysis improved with monoclonal antibodies von Ellis, J.M., Thi Man, Nguyen, Morris, G.E., Ginjaar, I.B., Moorman, A.F.M., Van Ommen, G.-J.B.

Volltext

Nuclear Gems and Cajal (Coiled) Bodies in Fetal Tissues: Nucleolar Distribution of the Spinal Muscular Atrophy Protein, SMN von Young, P.J., Le, T.T., Dunckley, M., thi Man, Nguyen, Burghes, A.H.M., Morris, G.E.

Volltext

Construction of dystrophin fusion proteins to raise targeted antibodies to different epitopes von Ginjaar, H.B., van Paassen, H.B.M., den Dunnen, J.T., thi Man, Nguyen, Morris, G.E., Moorman, A.F.M., van Ommen, G.J.B.

Volltext