| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
Allosteric modulation of adenosine receptors
|
Göblyös, Anikó
|
|
2008
|
5 |
1 |
p. 51-61
|
artikel
|
| 2 |
Application of the functionalized congener approach to dendrimer-based signaling agents acting through A2A adenosine receptors
|
Kim, Yoonkyung
|
|
2008
|
5 |
1 |
p. 39-50
|
artikel
|
| 3 |
Development of selective agonists and antagonists of P2Y receptors
|
Jacobson, Kenneth A.
|
|
2008
|
5 |
1 |
p. 75-89
|
artikel
|
| 4 |
Kinase inhibitors for the treatment of inflammatory and autoimmune disorders
|
Bhagwat, Shripad S.
|
|
2008
|
5 |
1 |
p. 107-115
|
artikel
|
| 5 |
Preface: special issue on medicinal chemistry of purines
|
Jacobson, Kenneth A.
|
|
2008
|
5 |
1 |
p. 1
|
artikel
|
| 6 |
Progress in the discovery of selective, high affinity A2B adenosine receptor antagonists as clinical candidates
|
Kalla, Rao V.
|
|
2008
|
5 |
1 |
p. 21-29
|
artikel
|
| 7 |
Protein and lipid kinase inhibitors as targeted anticancer agents of the Ras/Raf/MEK and PI3K/PKB pathways
|
García-Echeverría, Carlos
|
|
2008
|
5 |
1 |
p. 117-125
|
artikel
|
| 8 |
Recent improvements in the development of A2B adenosine receptor agonists
|
Baraldi, Pier Giovanni
|
|
2009
|
5 |
1 |
p. 3-19
|
artikel
|
| 9 |
Selective P2X7 receptor antagonists for chronic inflammation and pain
|
Carroll, William A.
|
|
2008
|
5 |
1 |
p. 63-73
|
artikel
|
| 10 |
Structure-activity relationships of anthraquinone derivatives derived from bromaminic acid as inhibitors of ectonucleoside triphosphate diphosphohydrolases (E-NTPDases)
|
Baqi, Younis
|
|
2008
|
5 |
1 |
p. 91-106
|
artikel
|
| 11 |
Synthesis and pharmacological characterization of [125I]MRS1898, a high-affinity, selective radioligand for the rat A3 adenosine receptor
|
Gao, Zhan-Guo
|
|
2008
|
5 |
1 |
p. 31-37
|
artikel
|
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