Browse by UCL people
Group by: Type | Date
Number of items: 9.
Article
Baruteau, J;
Perocheau, DP;
Hanley, J;
Lorvellec, M;
Rocha-Ferreira, E;
Karda, R;
Ng, J;
... Waddington, SN; + view all
(2018)
Argininosuccinic aciduria fosters neuronal nitrosative stress reversed by Asl gene transfer.
Nature Communications
, 9
(1)
, Article 3505. 10.1038/s41467-018-05972-1.
|
Holthaus, S-MK;
Herranz-Martin, S;
Massaro, G;
Aristorena, M;
Hoke, J;
Hughes, MP;
Maswood, R;
... Ali, RR; + view all
(2019)
Neonatal brain-directed gene therapy rescues a mouse model of neurodegenerative CLN6 Batten disease.
Human Molecular Genetics
, 28
(23)
pp. 3867-3879.
10.1093/hmg/ddz210.
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Hughes, MP;
Smith, DA;
Morris, L;
Fletcher, C;
Colaco, A;
Huebecker, M;
Tordo, J;
... Rahim, AA; + view all
(2018)
AAV9 intracerebroventricular gene therapy improves lifespan, locomotor function and pathology in a mouse model of Niemann-Pick type C1 disease.
Human Molecular Genetics
, 27
(17)
pp. 3079-3098.
10.1093/hmg/ddy212.
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Karda, R;
Buckley, SM;
Mattar, CN;
Ng, J;
Massaro, G;
Hughes, MP;
Kurian, MA;
... Rahim, AA; + view all
(2014)
Perinatal systemic gene delivery using adeno-associated viral vectors.
Front Mol Neurosci
, 7
, Article 89. 10.3389/fnmol.2014.00089.
|
Karda, R;
Rahim, AA;
Wong, AMS;
Suff, N;
Diaz, JA;
Perocheau, DP;
Tijani, M;
... Waddington, SN; + view all
(2020)
Generation of light-producing somatic-transgenic mice using adeno-associated virus vectors.
Scientific Reports
, 10
(1)
, Article 2121. 10.1038/s41598-020-59075-3.
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Massaro, G;
Hughes, MP;
Whaler, SM;
Wallom, K-L;
Priestman, DA;
Platt, FM;
Waddington, SN;
(2020)
Systemic AAV9 gene therapy using the synapsin I promoter rescues a mouse model of neuronopathic Gaucher disease but with limited cross-correction potential to astrocytes.
Human Molecular Genetics
10.1093/hmg/ddz317.
(In press).
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Rocha-Ferreira, E;
Rudge, B;
Hughes, MP;
Rahim, AA;
Hristova, M;
Robertson, NJ;
(2016)
Immediate Remote Ischemic Postconditioning Reduces Brain Nitrotyrosine Formation in a Piglet Asphyxia Model.
Oxidative Medicine and Cellular Longevity
, 2016
, Article 5763743. 10.1155/2016/5763743.
|
Snowball, A;
Chabrol, E;
Wykes, RC;
Shekh-Ahmad, T;
Cornford, JH;
Lieb, A;
Hughes, MP;
... Schorge, S; + view all
(2019)
Epilepsy Gene Therapy Using an Engineered Potassium Channel.
Journal of Neuroscience
, 39
(16)
pp. 3159-3169.
10.1523/JNEUROSCI.1143-18.2019.
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Thesis
Hughes, Michael;
(2017)
The development of gene therapy for Niemann-Pick Type C disease.
Doctoral thesis (Ph.D), UCL (University College London).
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