Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Aslam M. Ansari"'
Autor:
Aslam M. Ansari, Sydney O. Ugwu
Publikováno v:
Synthetic Communications. 38:2330-2340
A general and efficient synthetic route to α-amino acids by alkylation of the sodium salt of Schiff base ester 1 has been described previously. The α-substituted ethyl glycinates 4a–g are prepared in excellent yield by a two-step sequence involvi
Autor:
Frank Y. Xie, Puthupparampil V. Scaria, Aslam M. Ansari, Barry T. Rouse, Bumseok Kim, Raymond M. Schiffelers, Partha S. Biswas, Jun Xu, Patrick Y. Lu, Qingquan Tang, Martin C. Woodle
Publikováno v:
The American Journal of Pathology. 165:2177-2185
Ocular neovascularization often results in vision impairment. Frequently vascular endothelial cell growth factors (VEGFs) are mainly responsible for the pathological neovascularization as in the case in neovascularization induced by CpG oligodeoxynuc
Autor:
Aslam M. Ansari, Sydney O. Ugwu
Publikováno v:
ChemInform. 39
A general and efficient synthetic route to α-amino acids by alkylation of the sodium salt of Schiff base ester 1 has been described previously. The α-substituted ethyl glycinates 4a–g are prepared in excellent yield by a two-step sequence involvi
Autor:
Aslam M. Ansari, Grietje Molema, Marcel H.A.M. Fens, Qin Zhou, Puthupparampil V. Scaria, Martin C. Woodle, A. J. Mixson, Raymond M. Schiffelers, Gert Storm, Quingquan Tang, Jun Xu, Patrick Y. Lu
Publikováno v:
Journal of Controlled Release, 109(1-3), 5-14. Elsevier Bedrijfsinformatie b.v.
The recently developed siRNA oligonucleotides are an attractive alternative to antisense as a therapeutic modality because of their robust, gene selective silencing of drug target protein expression. To achieve therapeutic success, however, several h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::28f4a3274348382b75a33ceedb2c6932
https://research.rug.nl/en/publications/bc832285-6a43-4130-98c0-de8a4f460118
https://research.rug.nl/en/publications/bc832285-6a43-4130-98c0-de8a4f460118
Autor:
J. Cymerman Craig, Aslam M. Ansari
Publikováno v:
Synthesis. 1995:147-149
Autor:
Aslam M. Ansari, J. Cymerman Craiga
Publikováno v:
Chirality. 5:188-190
Evidence is accumulating that 7-chloro-4-[4-diethylamino-1-methylbutyl] amino quinoline (chloroquine) displays considerable stereoselectivity in its metabolism, pharmacokinetics, macromolecular interactions, and biological activity. The availability
Autor:
Qin Zhou, Raymond M. Schiffelers, Martin C. Woodle, Aslam M. Ansari, Gert Storm, Puthupparampil V. Scaria
Publikováno v:
Molecular Therapy. 9:S316-S317
Gene therapy, in principle, can be applicable to the management and cure of a variety of diseases, but efficient and targeted delivery of the therapeutic gene to the disease site has been a formidable challenge. Local delivery of genes has some limit
Metabolites of chloroquine: some observations on desethylchloroquine and N-acetyldesethylchloroquine
Autor:
Aslam M. Ansari, J. Cymerman Craig
Publikováno v:
Journal of pharmaceutical sciences. 83(7)
The major metabolite of chloroquine, (+)‐desethylchlo‐roquine, produced by stereoselective N‐dealkylation of the drug, was obtained in 81.5% enantiomeric purity by resolution of racemic desethylchloroquine using an atropisomeric resolving agent
Autor:
Raymond M. Schiffelers, Puthupparampil V. Scaria, Martin C. Woodle, Qin Zhou, Aslam M. Ansari
Publikováno v:
Molecular Therapy. 11:S124
Recent advances in the nucleic acid delivery technology have renewed interest in gene therapy. These advances can benefit not only gene therapy but also nucleic acid therapeutic approaches based on RNA interference, antisense etc. To realize the full
Autor:
Qingquan Tang, Qin Zhou, Grietje Molema, Gert Storm, Jun Xu, Aslam M. Ansari, Patrick Y. Lu, Raymond M. Schiffelers, Puthupparampil V. Scaria, Martin C. Woodle
Publikováno v:
Scopus-Elsevier
Nucleic Acids Research, 32(19):149. Oxford University Press
Nucleic Acids Research, 32(19):149. Oxford University Press
Potent sequence selective gene inhibition by siRNA 'targeted' therapeutics promises the ultimate level of specificity, but siRNA therapeutics is hindered by poor intracellular uptake, limited blood stability and non-specific immune stimulation. To ad