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                             23 gevonden resultaten
nr titel auteur tijdschrift jaar jaarg. afl. pagina('s) type
1 A comparison between genetically humanized and chimeric liver humanized mouse models for studies in drug metabolism and toxicity Scheer, Nico
2016
21 2 p. 250-263
14 p.
artikel
2 An analysis of FDA-approved drugs: natural products and their derivatives Patridge, Eric
2016
21 2 p. 204-207
4 p.
artikel
3 Bridging the translational gap: collaborative drug development and dispelling the stigma of commercialization Yu, Helen W.H.
2016
21 2 p. 299-305
7 p.
artikel
4 Conformational stability and self-association equilibrium in biologics Clarkson, Benjamin R.
2016
21 2 p. 342-347
6 p.
artikel
5 Contents page 2 2016
21 2 p. ii-
1 p.
artikel
6 Contents page 1 2016
21 2 p. i-
1 p.
artikel
7 Cyclodextrins in pharmaceutical formulations II: solubilization, binding constant, and complexation efficiency Jambhekar, Sunil S.
2016
21 2 p. 363-368
6 p.
artikel
8 Cyclodextrins in pharmaceutical formulations I: structure and physicochemical properties, formation of complexes, and types of complex Jambhekar, Sunil S.
2016
21 2 p. 356-362
7 p.
artikel
9 Drug regulators and ethics: which GCP issues are also ethical issues? Bernabe, Rosemarie D.L.C.
2016
21 2 p. 217-224
8 p.
artikel
10 Emerging therapeutic targets for the treatment of hepatic fibrosis Fagone, Paolo
2016
21 2 p. 369-375
7 p.
artikel
11 Extensions of indication throughout the drug product lifecycle: a quantitative analysis Langedijk, Joris
2016
21 2 p. 348-355
8 p.
artikel
12 Immunotoxin therapy for hematologic malignancies: where are we heading? Madhumathi, Jayaprakasam
2016
21 2 p. 325-332
8 p.
artikel
13 In silico methods to address polypharmacology: current status, applications and future perspectives Lavecchia, Antonio
2016
21 2 p. 288-298
11 p.
artikel
14 Key strategic factors for stakeholders in the current global biosimilar market Casey, Daniel
2016
21 2 p. 208-211
4 p.
artikel
15 Kynurenine-3-monooxygenase: a review of structure, mechanism, and inhibitors Smith, Jason R.
2016
21 2 p. 315-324
10 p.
artikel
16 Mapping lifecycle management activities for blockbuster drugs in Japan based on drug approvals and patent term extensions Yamanaka, Takayuki
2016
21 2 p. 306-314
9 p.
artikel
17 Modelling of compound combination effects and applications to efficacy and toxicity: state-of-the-art, challenges and perspectives Bulusu, Krishna C.
2016
21 2 p. 225-238
14 p.
artikel
18 Natural polyphenols: potential in the prevention of sexually transmitted viral infections Date, Abhijit A.
2016
21 2 p. 333-341
9 p.
artikel
19 Proteomics and drug discovery in cancer Dias, Matheus H.
2016
21 2 p. 264-277
14 p.
artikel
20 Repurposing historical control clinical trial data to provide safety context Bhuyan, Prakash
2016
21 2 p. 212-216
5 p.
artikel
21 The prescription's prescription: enhanced pharmaceutical planning through use of a product health assessment Ashkenazy, Rebecca
2016
21 2 p. 201-203
3 p.
artikel
22 The role of the 14-3-3 protein family in health, disease, and drug development Aghazadeh, Yasaman
2016
21 2 p. 278-287
10 p.
artikel
23 Why and how have drug discovery strategies in pharma changed? What are the new mindsets? Mignani, Serge
2016
21 2 p. 239-249
11 p.
artikel
                             23 gevonden resultaten
 
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