-Peter Day Researcher Activity Profile

Research Author Detailed Information 

Peter Day Publication Rate By Year

Peter Day has published 1 paper(s) in 2002, 4 paper(s) in 2007, 3 paper(s) in 2008, for a total of 8 research publications in total.

Peter P Day Author Information

LAST NAME: day

FIRST NAME: peter

INITIALS: P

AFFILIATION:

Papers

Peter Day's Publication Record

1. Synthesis of bis(ethylenedithio)tetrathiafulvalene (BEDT-TTF) derivatives functionalised with two, four or eight hydroxyl groups. Year Published: 2007
School of Biomedical and Natural Sciences, Nottingham Trent University, Nottingham, UK.
2. Mixed valence: origins and developments. Year Published: 2007
Davy Faraday Research Laboratory, The Royal Institution of Great Britain, 21 Albemarle Street, London W1S 4BS, UK.
3. Effect of included guest molecules on the normal state conductivity and superconductivity of beta''-(ET)(4)[(H(3)O)Ga(C(2)O(4))(3)].G (G = pyridine, nitrobenzene). Year Published: 2002
Davy Faraday Research Laboratory, The Royal Institution of Great Britain, 21 Albemarle Street, London W1S 4BS, UK.
4. Signaling from beta(1)- and beta(2)-adrenergic receptors is defined by differential interactions with PDE4. Year Published: 2008
Division of Reproductive Biology, Department of Obstetrics and Gynecology, Stanford University School of Medicine, Stanford, CA, USA.
5. Signaling from beta1- and beta2-adrenergic receptors is defined by differential interactions with PDE4. Year Published: 2008
Division of Reproductive Biology, Department of Obstetrics and Gynecology, Stanford University School of Medicine, Stanford, CA 94305-5317, USA.
6. Mixed valence: origins and developments. Year Published: 2007
Davy Faraday Research Laboratory, The Royal Institution of Great Britain, 21 Albemarle Street, London W1S 4BS, UK.
7. Mixed valence: origins and developments. Year Published: 2007
Davy Faraday Research Laboratory, The Royal Institution of Great Britain, 21 Albemarle Street, London W1S 4BS, UK.
8. Signaling from beta1- and beta2-adrenergic receptors is defined by differential interactions with PDE4. Year Published: 2008
Division of Reproductive Biology, Department of Obstetrics and Gynecology, Stanford University School of Medicine, Stanford, CA 94305-5317, USA.