Search results - ORA - Oxford University Research Archive

1 - 8 of 8

1

Journal article

Depletion of mitochondrial DNA in fibroglast cultures from patients with POLG1 mutations is a consequence of catalytic mutations

Ashley, N, O'Rourke, A, Smith, C, et al.
2008-08-01

2

Journal article

Defects in maintenance of mitochondrial DNA are associated with intramitochondrial nucleotide imbalances

Ashley, N, Adams, S, Slama, A, et al.
2007-06-01

3

Journal article

Crystal structure of the GluR2 amino-terminal domain provides insights into the architecture and assembly of ionotropic glutamate receptors

Clayton, A, Siebold, C, Gilbert, R, et al.
2009-10-01

4

Journal article

Genetic constraints and the adaptive evolution of rabies virus in nature

Holmes, E, Woelk, C, Kassis, R, et al.
2002-01-01

5

Journal article

Assessing the impact of FOXP1 mutations on developmental verbal dyspraxia

Vernes, S, MacDermot, K, Monaco, A, et al.
2009-10-01

6

Journal article

Disease model distortion in association studies

Vukcevic, D, Hechter, E, Spencer, C, et al.
2011-05-01

7

Journal article

Mutations of the same conserved glutamate residue in NBD2 of the sulfonylurea receptor 1 subunit of the KATP channel can result in either hyperinsulinism or neonatal diabetes.

Männikkö, R, Flanagan, SE, Sim, X, et al.
2011-06-01

8

Journal article

The genetic relationship between handedness and neurodevelopmental disorders

Brandler, W, Paracchini, S
2014-02-01

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