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Akademický článek
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Autor:
M. Lebl, Wayne L. Cody, Ana Maria de Lauro Castrucci, M. E. Hadley, Brian C. Wilkes, Victor J. Hruby
Publikováno v:
International Journal of Peptide and Protein Research. 24:472-479
The highly potent cyclic analogue of alpha-MSH, Ac-[Cys4,Cys10]-alpha-MSH4-13-NH2, was structurally modified in position 4. Four analogues were prepared and their biological activities in the in vitro frog and lizard skin bioassays were determined. I
Publikováno v:
IEEE Sensors Journal. 7:506-514
This paper presents a neuromorphic approach for sensor-based machine olfaction that combines a portable chemical detection system based on microbead array technology with a biologically inspired model of signal processing in the olfactory bulb. The s
Publikováno v:
Molecular Diversity. 1:177-182
A small-molecule synthetic combinatorial library was designed and synthesized that features potential pharmacophores attached to a variety of small cyclic scaffolds. The synthesis of the library involved randomization of three types of building block
Autor:
M. Lebl, Viktor Krchňák, V. Pokorný, P. Mudra, M. Pavlı́k, K. Ženı́šek, Z. Barták, J. Kalousek, Sydney E. Salmon, Z. Vobůrka, J. Bolf, M. Rinnová, Kit S. Lam
Publikováno v:
Methods. 6:432-437
An automatic peptide library synthesizer capable of randomizing 20 building blocks in 20 reaction vessels is described. The design is based on uniform bead distribution by gravity sedimentation after thorough mixing by inert gas bubbling and stirring
Autor:
M. Lebl, Kit S. Lam
Publikováno v:
Methods. 6:372-380
The Selectide process is a random synthetic chemical library method based on the one-bead one-peptide (structure) concept. A "split-synthesis" method is used to generate huge random libraries (10 6 -10 8 ). At the end of the synthesis, each bead expr
Publikováno v:
Methods. 6:381-387
A method for the synthesis and screening of polymeric libraries for biologic activities in solution is described. Libraries are constructed on a completely random basis with one structure on one particle of solid support (bead). The screened structur
Publikováno v:
Drug Development Research. 33:146-156
A synthetic chemical library comprised of alkylated and acylated amino acids was synthesized and screened to determine structures that bind to a model target, streptavidin. The library was prepared using "split synthesis" and screened in a solid phas
Publikováno v:
Drug Development Research. 33:157-160
Using a "one-bead one-peptide" rombinatorial peptide library method, we have been able to identify peptide ligands that interact specifically with various macromolecular targets such as monoclonal antibodies, streptavidin, avidin, MHC-Class I molecul