nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
1 |
Anticancer bisquaternary heterocyclic compounds: a ras-ional design
|
Campos, Joaquı́n |
|
2003 |
58 |
3 |
p. 221-229 9 p. |
artikel |
2 |
Anti-HIV agents: design and discovery of new potent RT inhibitors
|
Barreca, Maria Letizia |
|
2003 |
58 |
3 |
p. 259-263 5 p. |
artikel |
3 |
Ceramide analogues in apoptosis: a new strategy for anticancer drug development
|
Macchia, Marco |
|
2003 |
58 |
3 |
p. 205-211 7 p. |
artikel |
4 |
Cytisine derivatives as ligands for neuronal nicotine receptors and with various pharmacological activities
|
Boido, Caterina Canu |
|
2003 |
58 |
3 |
p. 265-277 13 p. |
artikel |
5 |
H3 receptor ligands: new imidazole H3-antagonists endowed with NO-donor properties
|
Bertinaria, Massimo |
|
2003 |
58 |
3 |
p. 279-283 5 p. |
artikel |
6 |
In memoriam of the work of Pietro Pratesi in the field of the Italian medicinal chemistry
|
Villa, Luigi |
|
2003 |
58 |
3 |
p. 169-172 4 p. |
artikel |
7 |
In silico screening with benzofurane- and benzopyrane-type MDR-modulators
|
Rebitzer, Sascha |
|
2003 |
58 |
3 |
p. 185-191 7 p. |
artikel |
8 |
Ligands for expression cloning and isolation of GABAB receptors
|
Froestl, Wolfgang |
|
2003 |
58 |
3 |
p. 173-183 11 p. |
artikel |
9 |
Purine and deazapurine nucleosides: synthetic approaches, molecular modelling and biological activity
|
Cristalli, Gloria |
|
2003 |
58 |
3 |
p. 193-204 12 p. |
artikel |
10 |
Structural modifications of antisense oligonucleotides
|
Urban, Ernst |
|
2003 |
58 |
3 |
p. 243-258 16 p. |
artikel |
11 |
Synthesis and biological evaluation of enantiomerically pure pyrrolyl-oxazolidinones as a new class of potent and selective monoamine oxidase type A inhibitors
|
Mai, A. |
|
2003 |
58 |
3 |
p. 231-241 11 p. |
artikel |
12 |
The discovery of a new potential anticancer drug: a case history
|
Cozzi, Paolo |
|
2003 |
58 |
3 |
p. 213-220 8 p. |
artikel |