Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Om Prakash Edupuganti"'
Autor:
Om Prakash Edupuganti, Orla Moriarty, Jianghui Meng, John Nealon, Jiafu Wang, Laura Casals-Diaz, Oliver James Dolly, Tomas H. Zurawski
Publikováno v:
Neuropharmacology. 118:223-232
A pressing need exists for long-acting, non-addictive medicines to treat chronic pain, a major societal burden. Botulinum neurotoxin type A (BoNT/A) complex – a potent, specific and prolonged inhibitor of neuro-exocytosis – gives some relief in s
Publikováno v:
Food Control. 34:668-674
Recombinant scFvs to zearalenone were isolated by phage display, expressed in Escherichia coli and the analytical sensitivity of selected scFvs determined by competitive inhibition enzyme-linked immunoassay (CI-ELISA) and surface plasmon resonance (S
Publikováno v:
World Mycotoxin Journal. 6:273-280
Aflatoxins are highly carcinogenic in nature and occur in a variety of food and feed samples. To ensure food is free from aflatoxins and safe for human consumption, methods to detect these toxins are necessary. Both aflatoxin B1 and aflatoxin B2 (AFB
Publikováno v:
Bioconjugate Chemistry. 18:1831-1840
IRS-1 overexpression has been associated with breast cancer development, hormone independence and antiestrogen resistance. IRS-1 is a major downstream signaling protein for insulin and IGF1 receptors, conveying signals to PI-3K/Akt and ERK1/2 pathway
Autor:
Stéphanie Boullanger, Om Prakash Edupuganti, Richard O'Kennedy, Eric Defrancq, Soujanya Ratna Edupuganti
Publikováno v:
Journal of Chromatography B-Analytical Technologies in the Biomedical and Life Sciences
Journal of Chromatography B-Analytical Technologies in the Biomedical and Life Sciences, Elsevier, 2013, pp.98-101
Europe PubMed Central
Journal of Chromatography B-Analytical Technologies in the Biomedical and Life Sciences, Elsevier, 2013, pp.98-101
Europe PubMed Central
An affinity purification method that isolates T-2 toxin-specific IgY utilizing a T-2-toxin-immobilized column was developed. The T-2 toxin was covalently coupled via a carbonyldiimidazole-activated hydroxyl functional group to amine-activated sepharo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c063dd5e7ce92dde328c36445220a64c
https://hal.archives-ouvertes.fr/hal-00825418
https://hal.archives-ouvertes.fr/hal-00825418
Publikováno v:
The Journal of Organic Chemistry. 68:8708-8710
A convenient strategy for the synthesis of the analogue of cyclic oligodeoxyribonucleotides is presented. The cyclization of the oligonucleotide was accomplished through intramolecular oxime bond formation between a 5'-oxyamine moiety and a 3'-aldehy
Publikováno v:
Talanta. 115
A highly robust immunoassay applicable for the detection of aflatoxin B1 (AFB1) using a Fab antibody fragment was developed. A key factor was the use of covalently immobilized AFB1 which allowed an almost three fold increase in sensitivity, reduced a
Publikováno v:
Organic Letters
Organic Letters, American Chemical Society, 2007, 9, pp.219-222
Organic Letters, American Chemical Society, 2007, 9, pp.219-222
A novel solid support 1 was synthesized to incorporate glyoxylic aldehyde functionality at the oligonucleotide 3'-terminus. 6-mer and 11-mer oligonucleotide sequences containing 3'-glyoxylic aldehyde functionality were prepared by using this support.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::910622c9df73c9a17579ec5c8fea660f
https://hal.archives-ouvertes.fr/hal-00174223
https://hal.archives-ouvertes.fr/hal-00174223
Autor:
Noreen J. Hickok, Samuel B. King, Valentin Antoci, Binoy Jose, Javad Parvizi, Eric Wickstrom, Om Prakash Edupuganti, Irving M. Shapiro, Allen R. Zeiger, Christopher S. Adams
Publikováno v:
Bioorganicmedicinal chemistry letters. 17(10)
Self-protecting Ti6Al4V alloy pins were prepared by covalent bonding of bis(ethylene glycol) linkers, then vancomycin to the oxidized, aminopropylated Ti6Al4V alloy surface. Fluorescence modification-enabled estimation of yields of free amines on the
Publikováno v:
ChemInform. 37
Synthetic oligonucleotides are attracting considerable interest as potential therapeutic agents for the selective inhibition of gene expression. The attainment of effective cellular delivery however remains a problem. The conjugation of oligonucleoti