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Comparison of mouse models reveals a molecular distinction between psychotic illness in PWS and schizophrenia.
Published in:
Translational Psychiatry, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41398-021-01561-x
By:
- Zahova, Simona K.;
- Humby, Trevor;
- Davies, Jennifer R.;
- Morgan, Joanne E.;
- Isles, Anthony R.
Publication type:
Article
A behavioral task for investigating action discovery, selection and switching: comparison between types of reinforcer.
Published in:
Frontiers in Behavioral Neuroscience, 2014, v. 8, p. 1, doi. 10.3389/fnbeh.2014.00398
By:
- Fisher, Simon D.;
- Gray, Jason P.;
- Black, Melony J.;
- Davies, Jennifer R.;
- Bednark, Jeffery G.;
- Redgrave, Peter;
- Franz, Elizabeth A.;
- Abraham, Wickliffe C.;
- Reynolds, John N. J.
Publication type:
Article
A missense mutation in the murine Opa3 gene models human Costeff syndrome.
Published in:
Brain: A Journal of Neurology, 2008, v. 131, n. 2, p. 368, doi. 10.1093/brain/awm333
By:
- Vanessa J. Davies;
- Kate A. Powell;
- Kathryn E. White;
- Wanfen Yip;
- Vanessa Hogan;
- Andrew J. Hollins;
- Jennifer R. Davies;
- Malgorzata Piechota;
- David G. Brownstein;
- Stuart J. Moat;
- Philip P. Nichols;
- Michael A. Wride;
- Michael E. Boulton;
- Marcela Votruba
Publication type:
Article
Prader–Willi syndrome imprinting centre deletion mice have impaired baseline and 5-HT2CR-mediated response inhibition.
Published in:
Human Molecular Genetics, 2019, v. 28, n. 18, p. 3013, doi. 10.1093/hmg/ddz100
By:
- Davies, Jennifer R;
- Wilkinson, Lawrence S;
- Isles, Anthony R;
- Humby, Trevor
Publication type:
Article
Disrupted mitochondrial function in the Opa3L122P mouse model for Costeff Syndrome impairs skeletal integrity.
Published in:
Human Molecular Genetics, 2016, v. 25, n. 12, p. 2404, doi. 10.1093/hmg/ddw107
By:
- Navein, Alice E.;
- Cooke, Esther J.;
- Davies, Jennifer R.;
- Smith, Terence G.;
- Wells, Lois H. M.;
- Ohazama, Atsushi;
- Healy, Christopher;
- Sharpe, Paul T.;
- Evans, Sam L.;
- Evans, Bronwen A. J.;
- Votruba, Marcela;
- Wells, Timothy
Publication type:
Article
Opa3, a novel regulator of mitochondrial function, controls thermogenesis and abdominal fat mass in a mouse model for Costeff syndrome.
Published in:
Human Molecular Genetics, 2012, v. 21, n. 22, p. 4836, doi. 10.1093/hmg/dds315
By:
- Wells, Timothy;
- Davies, Jennifer R.;
- Guschina, Irina A.;
- Ball, Daniel J.;
- Davies, Jeffrey S.;
- Davies, Vanessa J.;
- Evans, Bronwen A. J.;
- Votruba, Marcela
Publication type:
Article
Increased alternate splicing of Htr2c in a mouse model for Prader-Willi syndrome leads disruption of 5HT2C receptor mediated appetite.
Published in:
Molecular Brain, 2016, v. 9, p. 1, doi. 10.1186/s13041-016-0277-4
By:
- Garfield, Alastair S.;
- Davies, Jennifer R.;
- Burke, Luke K.;
- Furby, Hannah V.;
- Wilkinson, Lawrence S.;
- Heisler, Lora K.;
- Isles, Anthony R.
Publication type:
Article
Genetic, physical, and phenotypic characterization of the Del(13)Svea36H mouse.
Published in:
Mammalian Genome, 2001, v. 12, n. 9, p. 687, doi. 10.1007/s00335-001-2066-2
By:
- Arkell, Ruth M.;
- Cadman, Matthew;
- Marsland, Tracy;
- Southwell, Anne;
- Thaung, Caroline;
- Davies, Jennifer R.;
- Clay, Toni;
- Beechey, Colin V.;
- Evans, Edward P.;
- Strivens, Mark A.;
- Brown, Steve D.M.;
- Denny, Paul
Publication type:
Article
Calorie seeking, but not hedonic response, contributes to hyperphagia in a mouse model for Prader-Willi syndrome.
Published in:
European Journal of Neuroscience, 2015, v. 42, n. 4, p. 2105, doi. 10.1111/ejn.12972
By:
- Davies, Jennifer R.;
- Humby, Trevor;
- Dwyer, Dominic M.;
- Garfield, Alastair S.;
- Furby, Hannah;
- Wilkinson, Lawrence S.;
- Wells, Timothy;
- Isles, Anthony R.
Publication type:
Article
Opa1 deficiency in a mouse model of autosomal dominant optic atrophy impairs mitochondrial morphology, optic nerve structure and visual function.
Published in:
Human Molecular Genetics, 2007, v. 16, n. 11, p. 1307, doi. 10.1093/hmg/ddm079
By:
- Davies, Vanessa J.;
- Hollins, Andrew J.;
- Piechota, Malgorzata J.;
- Yip, Wanfen;
- Davies, Jennifer R.;
- White, Kathryn E.;
- Nicols, Phillip P.;
- Boulton, Michael E.;
- Votruba, Marcela
Publication type:
Article
Correction: Davies et al. Impact of Refinements to Handling and Restraint Methods in Mice. Animals 2022, 12 , 2173.
Published in:
2023
By:
- Davies, Jennifer R.;
- Purawijaya, Dandri A.;
- Bartlett, Julia M.;
- Robinson, Emma S. J.
Publication type:
Correction Notice
Impact of Refinements to Handling and Restraint Methods in Mice.
Published in:
Animals (2076-2615), 2022, v. 12, n. 17, p. 2173, doi. 10.3390/ani12172173
By:
- Davies, Jennifer R.;
- Purawijaya, Dandri A.;
- Bartlett, Julia M.;
- Robinson, Emma S. J.
Publication type:
Article

Found: 12

Comparison of mouse models reveals a molecular distinction between psychotic illness in PWS and schizophrenia.

A behavioral task for investigating action discovery, selection and switching: comparison between types of reinforcer.

A missense mutation in the murine Opa3 gene models human Costeff syndrome.

Prader–Willi syndrome imprinting centre deletion mice have impaired baseline and 5-HT<sub>2C</sub>R-mediated response inhibition.

Disrupted mitochondrial function in the Opa3<sup>L122P</sup> mouse model for Costeff Syndrome impairs skeletal integrity.

Opa3, a novel regulator of mitochondrial function, controls thermogenesis and abdominal fat mass in a mouse model for Costeff syndrome.

Increased alternate splicing of Htr2c in a mouse model for Prader-Willi syndrome leads disruption of 5HT<sub>2C</sub> receptor mediated appetite.

Genetic, physical, and phenotypic characterization of the Del(13)Svea36H mouse.

Calorie seeking, but not hedonic response, contributes to hyperphagia in a mouse model for Prader-Willi syndrome.

Opa1 deficiency in a mouse model of autosomal dominant optic atrophy impairs mitochondrial morphology, optic nerve structure and visual function.

Correction: Davies et al. Impact of Refinements to Handling and Restraint Methods in Mice. Animals 2022, 12 , 2173.

Impact of Refinements to Handling and Restraint Methods in Mice.