Works matching AU Jackson, Mandy

Results: 20

Current issues and challenges in research on virtual reality therapy for children with neurodisability.

Published in:

Journal of Alternative Medicine Research, 2018, v. 10, n. 1, p. 7

By:

Farr, William J.;
Male, Ian;
Green, Dido;
Morris, Christopher;
Gage, Heather;
Bailey, Sarah;
Speller, Sandra;
Colville, Valerie;
Jackson, Mandy;
Bremner, Stephen;
Memon, Anjum

Publication type:

Article

Feasibility of a randomised controlled trial to evaluate home-based virtual reality therapy in children with cerebral palsy.

Published in:

Disability & Rehabilitation, 2021, v. 43, n. 1, p. 85, doi. 10.1080/09638288.2019.1618400

By:

Farr, William J.;
Green, Dido;
Bremner, Stephen;
Male, Ian;
Gage, Heather;
Bailey, Sarah;
Speller, Sandra;
Colville, Valerie;
Jackson, Mandy;
Memon, Anjum;
Morris, Christopher

Publication type:

Article

Objective Assessment of Adherence to Inhalers by Patients with Chronic Obstructive Pulmonary Disease.

Published in:

2017

By:

Sulaiman, Imran;
Cushen, Breda;
Greene, Garrett;
Seheult, Jansen;
Seow, Dexter;
Rawat, Fiona;
MacHale, Elaine;
Mokoka, Matshediso;
Moran, Catherine Nora;
Bhreathnach, Aoife Sartini;
MacHale, Philippa;
Tappuni, Shahed;
Deering, Brenda;
Jackson, Mandy;
McCarthy, Hannah;
Mellon, Lisa;
Doyle, Frank;
Boland, Fiona;
Reilly, Richard B.;
Costello, Richard W.

Publication type:

journal article

Combining Comparative Proteomics and Molecular Genetics Uncovers Regulators of Synaptic and Axonal Stability and Degeneration In Vivo.

Published in:

PLoS Genetics, 2012, v. 8, n. 8, p. 1, doi. 10.1371/journal.pgen.1002936

By:

Wishart, Thomas M.;
Rooney, Timothy M.;
Lamont, Douglas J.;
Wright, Ann K.;
Morton, A. Jennifer;
Jackson, Mandy;
Freeman, Marc R.;
Gillingwater, Thomas H.

Publication type:

Article

A Novel Mutation in the Arylsulfatase A Gene Associated with Adult-Onset Metachromatic Leukodystrophy without Clinical Evidence of Neuropathy.

Published in:

European Neurology, 2008, v. 60, n. 6, p. 310, doi. 10.1159/000159928

By:

Suzuki, Chieko;
Watanabe, Mitsunori;
Tomiyama, Masahiko;
Sugimoto, Kazuhiro;
Nanba, Eiji;
Jackson, Mandy;
Kimura, Tamaki;
Seino, Yusuke;
Wakasaya, Yasuhito;
Kawarabayashi, Takeshi;
Miki, Yasuo;
Yamamoto-Watanabe, Yukiko;
Shoji, Mikio

Publication type:

Article

β-III Spectrin Is Critical for Development of Purkinje Cell Dendritic Tree and Spine Morphogenesis.

Published in:

Journal of Neuroscience, 2011, v. 31, n. 46, p. 16581, doi. 10.1523/JNEUROSCI.3332-11.2011

By:

Yuanzheng Gao;
Perkins, Emma M.;
Clarkson, Yvonne L.;
Tobia, Steven;
Lyndon, Alastair R.;
Jackson, Mandy;
Rothstein, Jeffrey D.

Publication type:

Article

Loss of β-III Spectrin Leads to Purkinje Cell Dysfunction Recapitulating the Behavior and Neuropathology of Spinocerebellar Ataxia Type 5 in Humans.

Published in:

Journal of Neuroscience, 2010, v. 30, n. 14, p. 4857, doi. 10.1523/JNEUROSCI.6065-09.2010

By:

Perkins, Emma M.;
Clarkson, Yvonne L.;
Sabatier, Nancy;
Longhurst, David M.;
Millward, Christopher P.;
Jack, Jennifer;
Toraiwa, Junko;
Watanabe, Mitsunori;
Rothstein, Jeffrey D.;
Lyndon, Alastair R.;
Wyllie, David J. A.;
Dutia, Mayank B.;
Jackson, Mandy

Publication type:

Article

Copper/zinc superoxide dismutase 1 and sporadic amyotrophic lateral sclerosis: Analysis of 155 cases and identification of novel insertion mutation.

Published in:

Annals of Neurology, 1997, v. 42, n. 5, p. 803, doi. 10.1002/ana.410420518

By:

Jackson, Mandy;
Al-Chalabi, Ammar;
Enayat, Zinat E.;
Chioza, Barry;
Leigh, Peter N.;
Morrison, Karen E.

Publication type:

Article

Analysis of chromosome 5q13 genes in amyotrophic lateral sclerosis: Homozygous naip deletion in a sporadic case.

Published in:

Annals of Neurology, 1996, v. 39, n. 6, p. 796, doi. 10.1002/ana.410390616

By:

Jackson, Mandy;
Morrison, Karen E.;
Al-Chalabi, Ammar;
Baldier, Martijn;
Leigh, Peter N.

Publication type:

Article

The role of the host culture as a resource for developing intercultural understanding in a Dutch international secondary school.

Published in:

Journal of Research in International Education, 2005, v. 4, n. 2, p. 193, doi. 10.1177/1475240905054390

By:

Jackson, Mandy

Publication type:

Article

Cerebellar ataxias: β-III spectrin's interactions suggest common pathogenic pathways.

Published in:

Journal of Physiology, 2016, v. 594, n. 16, p. 4661, doi. 10.1113/JP271195

By:

Perkins, Emma;
Suminaite, Daumante;
Jackson, Mandy

Publication type:

Article

Control of synaptic vesicle endocytosis by an extracellular signalling molecule.

Published in:

Nature Communications, 2013, v. 4, n. 9, p. 2394, doi. 10.1038/ncomms3394

By:

Smillie, Karen J.;
Pawson, Jonathan;
Perkins, Emma M.;
Jackson, Mandy;
Cousin, Michael A.

Publication type:

Article

Therapeutic potential and ownership of commercially available consoles in children with cerebral palsy.

Published in:

British Journal of Occupational Therapy, 2017, v. 80, n. 2, p. 108, doi. 10.1177/0308022616678635

By:

Farr, William;
Green, Dido;
Male, Ian;
Morris, Christopher;
Bailey, Sarah;
Gage, Heather;
Speller, Sandra;
Colville, Val;
Jackson, Mandy;
Bremner, Stephen;
Memon, Anjum

Publication type:

Article

De novo point mutations in patients diagnosed with ataxic cerebral palsy.

Published in:

2015

By:

Schnekenberg, Ricardo Parolin;
Perkins, Emma M.;
Miller, Jack W.;
Davies, Wayne I. L.;
D'Adamo, Maria Cristina;
Pessia, Mauro;
Fawcett, Katherine A.;
Sims, David;
Gillard, Elodie;
Hudspith, Karl;
Skehel, Paul;
Williams, Jonathan;
O'Regan, Mary;
Jayawant, Sandeep;
Jefferson, Rosalind;
Hughes, Sarah;
Lustenberger, Andrea;
Ragoussis, Jiannis;
Jackson, Mandy;
Tucker, Stephen J.

Publication type:

journal article

Modulation of the neuronal glutamate transporter EAAT4 by two interacting proteins.

Published in:

Nature, 2001, v. 410, n. 6824, p. 89, doi. 10.1038/35065091

By:

Jackson, Mandy;
Wei Song;
Mu-Ya Liu;
Lin Jin;
Dykes-Hoberg, Margaret;
Chien-Iiang G. Lin;
Bowers, William J.;
Federoff, Howard J.;
Sternweis, Paul C.;
Rothstein, Jeffrey D.

Publication type:

Article

Modulation of the neuronal glutamate transporter EAAC1 by the interacting protein GTRAP3-18.

Published in:

Nature, 2001, v. 410, n. 6824, p. 84, doi. 10.1038/35065084

By:

Chien-Iiang Glenn Lin;
Orlov, Irina;
Ruggiero, Alicia M.;
Dykes-Hoberg, Margaret;
Lee, Andy;
Jackson, Mandy;
Rothstein, Jeffrey D.

Publication type:

Article

Spinal cord neurone loss and foot placement changes in a rat knock-in model of amyotrophic lateral sclerosis Type 8.

Published in:

Brain Communications, 2024, v. 6, n. 3, p. 1, doi. 10.1093/braincomms/fcae184

By:

Murage, Brenda;
Tan, Han;
Mashimo, Tomoji;
Jackson, Mandy;
Skehel, Paul A

Publication type:

Article

Posterior cerebellar Purkinje cells in an SCA5/SPARCA1 mouse model are especially vulnerable to the synergistic effect of loss of β-III spectrin and GLAST.

Published in:

Human Molecular Genetics, 2016, v. 25, n. 20, p. 4448, doi. 10.1093/hmg/ddw274

By:

Perkins, Emma M.;
Suminaite, Daumante;
Clarkson, Yvonne L.;
Sin Kwan Lee;
Lyndon, Alastair R.;
Rothstein, Jeffrey D.;
Wyllie, David J. A.;
Kohichi Tanaka;
Jackson, Mandy

Publication type:

Article

β-III spectrin underpins ankyrin R function in Purkinje cell dendritic trees: protein complex critical for sodium channel activity is impaired by SCA5-associated mutations.

Published in:

Human Molecular Genetics, 2014, v. 23, n. 14, p. 3875, doi. 10.1093/hmg/ddu103

By:

Clarkson, Yvonne L.;
Perkins, Emma M.;
Cairncross, Callum J.;
Lyndon, Alastair R.;
Skehel, Paul A.;
Jackson, Mandy

Publication type:

Article

β-III spectrin mutation L253P associated with spinocerebellar ataxia type 5 interferes with binding to Arp1 and protein trafficking from the Golgi.

Published in:

Human Molecular Genetics, 2010, v. 19, n. 18, p. 3634, doi. 10.1093/hmg/ddq279

By:

Clarkson, Yvonne L.;
Gillespie, Trudi;
Perkins, Emma M.;
Lyndon, Alastair R.;
Jackson, Mandy

Publication type:

Article