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1 igase carboxyl terminus of HSC70-interacting protein (CHIP).
2 carboxyl terminal of Hsp70/Hsp90 interacting protein (CHIP).
3 tein, carboxyl terminus of Hsc70-interacting protein (CHIP).
4 nd are thus an ideal substrate for selective protein chips.
5 y of the problems previously associated with protein chips.
6 d analysed using 17 different substrates and protein chips.
7 ate with the C terminus of Hsp70 interacting protein (CHIP), a multidomain ubiquitin ligase, to media
8 nstrate that C terminus of HSC70-interacting protein (CHIP), a regulator of protein quality control,
10 The carboxyl terminus of Hsp70-interacting protein (CHIP), a ubiquitin ligase/cochaperone, particip
12 studies, the C terminus of Hsc70-interacting protein (CHIP), an E3 ubiquitin ligase that ubiquitinate
14 tein and the sampled analyte directly on the protein chip and subsequent in situ analysis by MALDI ma
15 two years has established the usefulness of protein chips and made important advances in preparing p
16 -down of the plasma membrane quality control proteins CHIP and Hsc70 partially restored DeltaF508CFTR
18 perones, the C terminus of Hsp70-interacting protein (CHIP) and the Hsp70/Hsp90 organizer protein, we
19 ligase carboxy terminus of Hsp70-interacting protein (CHIP) and the molecular chaperone Hsp90 are imp
22 scale monitoring of the immune response with protein chips are revealing new participants in the path
25 Enzyme-linked immunosorbent assays and/or protein-chip arrays indicated a timeline change of SP to
28 igase carboxyl terminus of Hsc70-interacting protein (CHIP) as a central microautophagy regulator tha
31 terminus of heat shock protein70-interacting protein (CHIP) as we show that Abeta accumulation decrea
34 t the carboxyl terminus of HSP70-interacting protein (CHIP) binds, ubiquitinates, and promotes the ub
35 ser desorption/ionization (MALDI)-compatible protein chips by ambient ion landing of proteins and suc
38 er of chromatin immunoprecipitated DNA-bound proteins (ChIP-chip) or of DNA adenine methyltransferase
39 n 70 (Hsp70):c-terminus of Hsp70-interacting protein (CHIP) complex facilitates the ubiquitination an
40 sfection with the C-terminal hsp-interacting protein (CHIP) construct, a TPR-containing ubiquitin lig
43 ablation of C-terminus of Hsc70-interacting protein (CHIP) E3 ubiquitin-ligase impairs hepatic cytoc
47 and successive utilization of the resulting protein chips for the development of bioanalytical assay
49 uitin ligase C-terminus of Hsc70 interacting protein (CHIP) has been shown in vitro and in vivo to as
51 with multivariate statistical analysis, RCA protein chips have the potential to identify multiplexed
52 8 and UbcH5a-C terminus of Hsc70-interacting protein (CHIP)-Hsc70-Hsp40) complexes, as well as protei
53 biquitin ligase C-terminal Hsp70-interacting protein (CHIP), if freed from chaperones during acute st
54 novel role of host cell E3 ubiquitin ligase protein CHIP in regulating HIV-1 replication through ubi
55 s between Ap, Bar and the LIM-domain binding protein Chip in tarsus four, and between Al, Lim1 and Ch
57 igase carboxyl terminus of Hsc70-interacting protein (CHIP) in the regulation of MLK3 protein levels.
58 tein, carboxyl terminus of Hsp70-interacting protein (CHIP), in a complex with Hsp90 plays an importa
59 erminus of heat shock protein 70-interacting protein (CHIP), increased SRF activity, as well as beta-
60 t the carboxyl terminus of Hsc70-interacting protein (CHIP) interacts with wild-type Slug (wtSlug).
64 e carboxyl terminus of the Hsc70-interacting protein (CHIP) is an Hsp70 co-chaperone as well as an E3
66 The carboxyl terminus of Hsc70-interacting protein (CHIP) is pivotal for managing misfolded and agg
67 al Hsp70 (heat shock protein 70)-interacting protein (CHIP) links the two major arms of protein quali
71 ases, carboxyl terminus of HSC70-interacting protein (CHIP) or DIP1/Mib1, enhanced DAPK degradation,
74 mic range and easy adaptability of plasmonic protein chips presents new opportunities in proteomic re
75 biquitin ligase C-terminal Hsp70-interacting protein (CHIP) recognizes and marks for degradation not
76 e we present the first study that integrates protein ChIP-seq and Hi-C data to systematically identif
77 nal significance of FoxO1 against other FoxO proteins, ChIP-seq was performed with chromatin from liv
78 u peptide MALDI sequencing; the lectin-based protein chips showed the ability to enrich glycopeptides
79 e samples were preadsorbed on four different protein chip surfaces, and the protein composition was a
80 and when used in conjunction with Ciphergen protein chip technology (also referred to as SELDI-Surfa
81 (ToF; MALDI-ToF) mass spectrometry utilizing protein chip technology and artificial neural networks (
82 res of protein kinases and demonstrates that protein chip technology is useful for high-throughput sc
85 , this method offers an improved approach to protein chip technology that should prove useful for dia
87 s spectrometry in conjunction with Ciphergen protein chip technology we have used relative importance
88 To this end, we have evaluated the use of Protein Chip technology, coupled with bioinformatics ana
91 shock cognate protein 70 (Hsc70)-interacting protein (CHIP) that leads to its ubiquitination/proteaso
92 square design for the sample allocation on a Protein chip, the use of the pairwise Pearson correlatio
94 e report two similar strategies to fabricate protein chips through capture onto a solid surface of th
95 ily member Apterous requires the LIM-binding protein Chip to execute patterned outgrowth of the Droso
96 verge on the C terminus of Hsc70-interacting protein (CHIP) to regulate tau levels, highlighting the
97 The carboxyl terminus of hsc70-interacting protein (CHIP) ubiquitin ligase was previously associate
98 e report the development and construction of protein chips using derivatized glass and nitrocellulose
102 (E3) carboxyl terminus of Hsp70-interacting protein (CHIP) were markedly increased in HG-treated car
103 d ion landing apparatus that can manufacture protein chips with a predefined array of sample position
104 ures with subsequent MALDI analysis, and the protein chips with immobilized antibodies were used for