ORA - Oxford University Research Archive

1 - 10 of 10

1

Journal article

The brain-derived neurotrophic factor Val66Met polymorphism is associated with sense of coherence in a non-clinical community sample of 7335 adults.

Surtees, PG, Wainwright, NW, Willis-Owen, SA, et al.
2007-10-05

2

Journal article

Genomic organization and mutation screening of the human ortholog of Pkdr1 associated with polycystic kidney disease in the rat.

Kaisaki, PJ, Bergmann, C, Brown, JH, et al.
2008

3

Journal article

A humanized version of Foxp2 affects cortico-basal ganglia circuits in mice.

Enard, W, Gehre, S, Hammerschmidt, K, et al.
2009-05-05

4

Journal article

Cancer. Puzzling patterns of predisposition.

Pollard, PJ, Ratcliffe, PJ
2009-04-05

5

Journal article

Common variants in HNF-1 alpha and risk of type 2 diabetes.

Holmkvist, J, Cervin, C, Lyssenko, V, et al.
2006-12-05

6

Journal article

Denaturing high-performance liquid chromatography of the myotubularin-related 2 gene (MTMR2) in unrelated patients with Charcot-Marie-Tooth disease suggests a low frequency of mutation in inherited neuropathy.

Bolino, A, Lonie, LJ, Zimmer, M, et al.
2001-03-05

7

Journal article

Lack of association of the COMT (Val158/108 Met) gene and schizophrenia: a meta-analysis of case-control studies.

Munafo, MR, Bowes, L, Clark, TG, et al.
2005-08-05

8

Journal article

The P446L variant in GCKR associated with fasting plasma glucose and triglyceride levels exerts its effect through increased glucokinase activity in liver.

Beer, NL, Tribble, ND, McCulloch, LJ, et al.
2009-11-05

9

Journal article

Molecular evolution of FOXP2, a gene involved in speech and language.

Enard, W, Przeworski, M, Fisher, SE, et al.
2002-08-05

10

Journal article

Mutations in the beta-tubulin gene TUBB2B result in asymmetrical polymicrogyria.

Jaglin, XH, Poirier, K, Saillour, Y, et al.
2009-06-05

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