Detalhe da pesquisa
1.
Myeloid-derived suppressor cells and tolerogenic dendritic cells are distinctively induced by PI3K and Wnt signaling pathways.
J Biol Chem
; 299(11): 105276, 2023 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-37739035
2.
Dual Site-Specific Chemoenzymatic Antibody Fragment Conjugation Using CRISPR-Based Hybridoma Engineering.
Bioconjug Chem
; 32(2): 301-310, 2021 02 17.
Artigo
em Inglês
| MEDLINE | ID: mdl-33476135
3.
Structure-Acid Lability Relationship of N-Alkylated α,α-Dialkylglycine Obtained via a Ugi Multicomponent Reaction.
Molecules
; 26(1)2021 Jan 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-33401754
4.
Bioconjugation through Mesitylene Thiol Alkylation.
Bioconjug Chem
; 29(4): 1199-1208, 2018 04 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-29433317
5.
Formylation of electron-rich aromatic rings mediated by dichloromethyl methyl ether and TiCl4: scope and limitations.
Molecules
; 20(4): 5409-22, 2015 Mar 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-25822080
6.
Understanding acid lability of cysteine protecting groups.
Molecules
; 18(5): 5155-62, 2013 May 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-23648593
7.
Cysteine-Based Perfluorinated Derivatives: A Theoretical and Experimental Study.
Chempluschem
; 88(5): e202300028, 2023 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-37134299
8.
Efficient targeting of NY-ESO-1 tumor antigen to human cDC1s by lymphotactin results in cross-presentation and antigen-specific T cell expansion.
J Immunother Cancer
; 10(4)2022 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-35428705
9.
From Ugi Multicomponent Reaction to Linkers for Bioconjugation.
ACS Omega
; 5(13): 7424-7431, 2020 Apr 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-32280884
10.
Tetrahydropyranyl: A Non-aromatic, Mild-Acid-Labile Group for Hydroxyl Protection in Solid-Phase Peptide Synthesis.
ChemistryOpen
; 6(2): 206-210, 2017 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-28413752
11.
Understanding Tetrahydropyranyl as a Protecting Group in Peptide Chemistry.
ChemistryOpen
; 6(2): 168-177, 2017 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-28413747
12.
Tetrahydropyranyl, a nonaromatic acid-labile Cys protecting group for Fmoc peptide chemistry.
Org Lett
; 17(7): 1680-3, 2015 Apr 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-25764355
13.
Acid-labile Cys-protecting groups for the Fmoc/tBu strategy: filling the gap.
Org Lett
; 14(21): 5472-5, 2012 Nov 02.
Artigo
em Inglês
| MEDLINE | ID: mdl-23075170