Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Lucy E. Walmsley"'
Autor:
Qingshan Teng, Mary Garrity-Moses, Thais Federici, Diana Tanase, James K. Liu, Nicholas D. Mazarakis, Mimoun Azzouz, Lucy E. Walmsley, Erin Carlton, Nicholas M. Boulis
Publikováno v:
Neurobiology of Disease, Vol 20, Iss 3, Pp 694-700 (2005)
The present study examines gene delivery to cultured motor neurons (MNs) with the Rabies G protein (RabG)-pseudotyped lentiviral equine infectious anemia virus (RabG.EIAV) vector. RabG.EIAV-mediated β-galactosidase (RabG.EIAV-LacZ) gene expression i
Externí odkaz:
https://doaj.org/article/fadd0179677e4a0992f20be438f51d4e
Autor:
Nicholas D. Mazarakis, Mary E. Garrity-Moses, Lucy E. Walmsley, Mimoun Azzouz, Erin Carlton, James K. Liu, Diana Tanase, Qingshan Teng, Nicholas M. Boulis, Thais Federici
Publikováno v:
Neurobiology of Disease, Vol 20, Iss 3, Pp 694-700 (2005)
The present study examines gene delivery to cultured motor neurons (MNs) with the Rabies G protein (RabG)-pseudotyped lentiviral equine infectious anemia virus (RabG.EIAV) vector. RabG.EIAV-mediated β-galactosidase (RabG.EIAV-LacZ) gene expression i
Autor:
Mimoun Azzouz, Umrao R. Monani, G. Scott Ralph, Fraser J. Wilkes, Debbie C.P. Lee, Susan M. Kingsman, Lucy E. Walmsley, Arthur H.M. Burghes, Kyriacos A. Mitrophanous, Nicholas D. Mazarakis, Thanh Le
Publikováno v:
Journal of Clinical Investigation. 114:1726-1731
Spinal muscular atrophy (SMA) is a frequent recessive autosomal disorder. It is caused by mutations or deletion of the telomeric copy of the survival motor neuron (SMN) gene, leading to depletion in SMN protein levels. The treatment rationale for SMA
Lentiviral-mediated delivery of Bcl-2 or GDNF protects against excitotoxicity in the rat hippocampus
Autor:
Stephen Parham, Susan M. Kingsman, Nicholas D. Mazarakis, G. Scott Ralph, Liang-Fong Wong, Alison S. Bienemann, James B. Uney, Lucy E. Walmsley
Publikováno v:
Molecular therapy : the journal of the American Society of Gene Therapy. 11(1)
Nutrient deprivation during ischemia leads to severe insult to neurons causing widespread excitotoxic damage in specific brain regions such as the hippocampus. One possible strategy for preventing neurodegeneration is to express therapeutic proteins
Autor:
L Lawrence, Kyriacos A. Mitrophanous, Lucy E. Walmsley, Brian W. Bigger, Simon N. Waddington, Maxine V. Holder, Charles Coutelle, Michael Themis, Faisal A. Al-Allaf, Suzanne M. K. Buckley, K. Mosley, Susan M. Kingsman, Lisa G. Gregory, F M Ellard
Publikováno v:
Gene therapy. 11(14)
Gene therapy for Duchenne muscular dystrophy has so far not been successful because of the difficulty in achieving efficient and permanent gene transfer to the large number of affected muscles and the development of immune reactions against vector an
Autor:
Susan M. Kingsman, Mimoun Azzouz, Peter Carmeliet, Kyriacos A. Mitrophanous, G. Scott Ralph, Nicholas D. Mazarakis, Lucy E. Walmsley, Erik Storkebaum
Publikováno v:
Nature. 429(6990)
Amyotrophic lateral sclerosis (ALS) causes adult-onset, progressive motor neuron degeneration in the brain and spinal cord, resulting in paralysis and death three to five years after onset in most patients. ALS is still incurable, in part because its
Autor:
Nicholas D. Mazarakis, Susan M. Kingsman, Lucy E. Walmsley, Kyriacos A. Mitrophanous, Liang-Fong Wong, Mimoun Azzouz, Zoe Askham, Fraser J. Wilkes
Publikováno v:
Molecular therapy : the journal of the American Society of Gene Therapy. 9(1)
We have developed a non-primate-based lentiviral vector based on the equine infectious anemia virus (EIAV) for efficient gene transfer to the central and peripheral nervous systems. Previously we have demonstrated that pseudotyping lentiviral vectors
Autor:
Suzanne M. K. Buckley, Charles Coutelle, Pippa A Radcliffe, Terrence Cook, L Lawrence, Michael Themis, Kyriacos A. Mitrophanous, Nick Mazarakis, Faisal A. Allaf, Lisa G. Gregory, Brian W. Bigger, Susan M. Kingsman, Fiona E. Ellard, Mimoun Azzouz, Simon N. Waddington, Maxine V. Holder, Lucy E. Walmsley
Publikováno v:
Molecular Therapy. 9:S91
Top of pageAbstract Gene therapy for Duchenne muscular dystrophy has so far not been successful because of the difficulty in achieving efficient and permanent gene transfer to the large number of affected muscles and the development of immune reactio
Autor:
James K. Liu, Qingshan Teng, Mimoun Azzouz, Lucy E. Walmsley, Nicholas D. Mazarakis, Diana Tanase, Ajit A. Krishnaney, Nicholas M. Boulis, Mary E. Garrity-Moses
Publikováno v:
Molecular Therapy. 9:S201
Objective: Recent work has suggested that injection of lentiviral vectors might constitute means of therapeutic gene delivery to diseased motor neurons in ALS. However, as implied by the name, Amyotrophic Lateral Sclerosis, this disorder results in s
Autor:
Liang-Fong Wong, Mimoun Azzouz, Nicholas D. Mazarakis, Fraser J. Wilkes, Lucy E. Walmsley, Zoe Askham, Kyriacos A. Mitrophanous, Susan M. Kingsman
Publikováno v:
Molecular Therapy. 9:765
The publisher regrets that a proof correction requested by the author was misinterpreted. On page 109, left-hand column, lines 15 and 16 should read: "In differentiated PC12 cells, p75NTR has been shown to internalize into vesicles bound to its ligan