Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Joseph Wooters"'
Autor:
Ji Ming Wang, Joost J. Oppenheim, De Yang, Oleg Chertov, Albert P. Schmidt, G. Mark Anderson, Qian Chen, Joseph Wooters
Publikováno v:
The Journal of Experimental Medicine
We have previously shown that antimicrobial peptides like defensins have the capacity to mobilize leukocytes in host defense. LL-37 is the cleaved antimicrobial 37-residue, COOH-terminal peptide of hCAP18 (human cationic antimicrobial protein with a
Autor:
Maria Tereza Nunes, Michael K. May, Frank Loganzo, Sylvia Musto, and Arie Zask, Malathi Hari, Albert A. Minnick, Celine Shi, Lee M. Greenberger, Yongchang Qiu, Joseph Wooters, Girija Krishnamurthy, Carl Beyer, Joshua Kaplan, Semiramis Ayral-Kaloustian
Publikováno v:
Biochemistry. 44(18)
A synthetic analogue of the tripeptide hemiasterlin, designated HTI-286, depolymerizes microtubules, is a poor substrate for P-glycoprotein, and inhibits the growth of paclitaxel-resistant tumors in xenograft models. Two radiolabeled photoaffinity an
Autor:
Scott K. Durum, Oleg Chertov, Annette R. Khaled, Qiong Jiang, Naima Benbernou, Joseph Wooters
Publikováno v:
Cellular signalling. 16(2)
IL-7 induction of protein tyrosine phosphorylation was examined in an IL-7-dependent thymocyte cell line, D1, which was generated from a p53-/- mouse. Anti-phosphotyrosine antibody was used both to immunoprecipitate and Western blot, and showed that
Autor:
Steven H. Herrmann, Eugene L. Brown, Grant Cull, Holly Swiniarski, Joseph Wooters, Margot O'Toole, Lena Leger
Publikováno v:
Annals of the New York Academy of Sciences. 795
Publikováno v:
Peptides ISBN: 9789401050050
Peptides
Peptides
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f998e2a20a2a2ae8677ed6d222325b1d
https://doi.org/10.1007/978-94-011-2264-1_200
https://doi.org/10.1007/978-94-011-2264-1_200
Autor:
Eugene L. Brown, Joseph Wooters, Mary Collins, Rachel E. Meyers, Jonathan N. Kremsky, Joseph P. Dougherty
A general method for the immobilization of DNA through its 5'-end has been developed. A synthetic oligonucleotide, modified at its 5'-end with an aldehyde or carboxylic acid, was attached to latex microspheres containing hydrazide residues. Using T4
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0707fab862b14094700a3f7169b50534
https://europepmc.org/articles/PMC340705/
https://europepmc.org/articles/PMC340705/