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Number of items at this level: 11.

B

Bain, J., Ruiz-Perez, L., Kennerley, A.J. et al. (4 more authors) (2015) In situ formation of magnetopolymersomes via electroporation for MRI. Scientific Reports, 5. 14311 . ISSN 2045-2322

D

Das, D. orcid.org/0000-0001-8501-8696, Faridounnia, M., Kovacic, L. et al. (3 more authors) (2017) Single-strand DNA Binding by the Helix-Hairpin-Helix Domain of XPF Contributes to Substrate Specificity of ERCC1-XPF. Journal of Biological Chemistry, 292 (7). pp. 2842-2853. ISSN 0021-9258

Das, D., Haas, R., Veltien, A. et al. (2 more authors) (2015) Complex 1 deficiency in the brain of mice causes white matter lesions, defective energy metabolism and morphology, and increased perfusion. In: Magnetic Resonance Materials in Physics, Biology and Medicine. ESMRMB 2015, 01.10.15 - 03.10.15, Edinburgh, UK. Springer Berlin Heidelberg , pp. 110-111.

de Haas, R., Das, D. orcid.org/0000-0001-8501-8696, Garanto, A. et al. (10 more authors) (2017) Therapeutic effects of the mitochondrial ROS-redox modulator KH176 in a mammalian model of Leigh Disease. Scientific Reports, 7 (1). 11733. ISSN 2045-2322

G

Grant, R.A., Sharp, P.S., Kennerley, A.J. et al. (4 more authors) (2014) Abnormalities in whisking behaviour are associated with lesions in brain stem nuclei in a mouse model of amyotrophic lateral sclerosis. Behavioural Brain Research , 259. pp. 274-283. ISSN 0166-4328

K

Kazan, S.M., Mohammadi, S., Callaghan, M.F. et al. (6 more authors) (2016) Vascular autorescaling of fMRI (VasA fMRI) improves sensitivity of population studies: A pilot study. NeuroImage, 124 (A). pp. 794-805. ISSN 1053-8119

Kennerley, A.J., Mayhew, J.E., Redgrave, P. et al. (1 more author) (2010) Vascular Origins of BOLD and CBV fMRI Signals: Statistical Mapping and Histological Sections Compared. Open Neuroimaging Journal, 4. pp. 1-8. ISSN 1874-4400

M

Mead, P.J. (2011) Optimised and rapid pre-clinical screening in the SOD1<sup>G93A</sup> transgenic mouse model of amyotrophic lateral sclerosis (ALS). PLoS ONE, 6. e23244. ISSN 1932-6203

S

Stockebrand, M., Sasani, A., Das, D. orcid.org/0000-0001-8501-8696 et al. (8 more authors) (2018) A mouse model of creatine transporter deficiency reveals impaired motor function and muscle energy metabolism. Frontiers in Physiology, 9.

T

Tripsianes, K., Folkers, G.E., Zheng, C. et al. (4 more authors) (2007) Analysis of the XPA and ssDNA-binding surfaces on the central domain of human ERCC1 reveals evidence for subfunctionalization. Nucleic Acids Res, 35 (17). pp. 5789-5798. ISSN 0305-1048

V

van der Pluijm, I., Burger, J., van Heijningen, P.M. et al. (21 more authors) (2018) Decreased mitochondrial respiration in aneurysmal aortas of Fibulin-4 mutant mice is linked to PGC1A regulation. Cardiovascular Research. cvy150. ISSN 0008-6363

This list was generated on Fri Aug 17 03:54:21 2018 BST.