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1 dges but not by HILIC to enable quantitative glycoproteomics.
2 loped so far provide important insights into glycoproteomics.
3 implications for the application of FAIMS in glycoproteomics.
10 of sites of protein glycosylation; targeted glycoproteomics; and functional glycoproteomics, with a
15 lute quantification of glycans are needed in glycoproteomics, during development and production of bi
17 et al. (2017) provides a novel algorithm for glycoproteomics in which complex glycopeptides can be id
18 ectrometry methods (CE-MS) for glycomics and glycoproteomics is limited by the lack of convenient int
19 we describe the important role that chemical glycoproteomics methods are playing in such efforts.
21 c glycoprotein reporter system and performed glycoproteomics on endogenous parasite glycoproteins usi
22 present IsoTaG, a mass-independent chemical glycoproteomics platform for characterization of intact,
23 ort that the addition of IMS to conventional glycoproteomics platforms adds additional information re
25 ven the structural analysis of glycoproteins-glycoproteomics-remains in its infancy due to the scarci
27 sensitive sheathless CE-ESI-MS approaches in glycoproteomics research, by significantly improving sen
28 MMP-9 null mice (n=8 per group) analyzed by glycoproteomics showed that of 541 N-glycosylated protei
29 ill one of the greatest challenges in modern glycoproteomics, since multiple regio- and stereoisomers
30 ectin enrichment) and improves large-scale N-glycoproteomics studies due to greatly reduced sample co
32 nt in C. jejuni, we utilized high throughput glycoproteomics to characterize C. jejuni JHH1 and ident
33 mbined with sensitive and quantitative O-Man glycoproteomics to identify a homologous family of four
34 lycopeptides to select peptides for targeted glycoproteomics using directed MS and (ii) mass-independ
35 his technology and expand its usefulness for glycoproteomics, we have developed and improved methods
39 on; targeted glycoproteomics; and functional glycoproteomics, with a focus on probing interactions be
40 ta acquisition modes currently available for glycoproteomics within a rapid Top Speed DDA duty cycle.
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