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1 enes, one of which encodes a neuron-specific ubiquitin C-terminal hydrolase.
2 , glial fibrillary acidic protein (GFAP) and ubiquitin C-terminal hydrolase.
3 gy to the known de-ubiquitinating enzymes or ubiquitin C-terminal hydrolases.
4 served Cys and His domains characteristic of ubiquitin C-terminal hydrolases.
5 zymes, and UCH-L3, a member of the family of ubiquitin C-terminal hydrolases.
6 690 amino acid protein with high homology to ubiquitin C-terminal hydrolases.
11 form a protein complex with the unidentified ubiquitin C-terminal hydrolase and recruit UbC1 to this
12 lement-binding protein 1 (CREB1), CREB2, and ubiquitin C-terminal hydrolase (Ap-uch) have been implic
15 smodium falciparum homologue, members of the ubiquitin C-terminal hydrolase family, use a unique acti
18 quence of UCH-L1 is similar to that of other ubiquitin C-terminal hydrolases, including the ubiquitou
19 the unfolded state of the 52-knotted protein ubiquitin C-terminal hydrolase isoenzyme L1 (UCH-L1) and
20 f glial fibrillary acidic protein (GFAP) and ubiquitin C-terminal hydrolase L1 (UCH-L1) as day-of-inj
21 Glial fibrillary acidic protein (GFAP) and ubiquitin C-terminal hydrolase L1 (UCH-L1) have been wid
24 ifunctional molecule of the ubiquitin system ubiquitin C-terminal hydrolase L1 (UCH-L1) is induced in
27 key mechanism mediating the deficit involves ubiquitin C-terminal hydrolase L1 (UCH-L1), a deubiquiti
28 h harbor a deletion within the gene encoding ubiquitin C-terminal hydrolase L1 (Uch-L1), display sens
29 We now show that a component of the pathway, ubiquitin C-terminal hydrolase L1 (Uch-L1), is required
31 cantly increase the levels of Abeta, Tau and Ubiquitin C-Terminal Hydrolase L1 (UCHL1) in mouse cereb
33 al fibrillary acidic protein (GFAP), tau and ubiquitin c-terminal hydrolase L1 (UCHL1) were assessed
35 amyloid-beta 1-42, neuropeptide Y (NPY), and ubiquitin C-terminal hydrolase L1 (UCHL1), whose CSF lev
36 ic enolase, glial fibrillary acidic protein, ubiquitin C-terminal hydrolase L1 [UCH-L1], neurofilamen
37 3% decrease; annexin VII, 8.8-fold increase; ubiquitin C-terminal hydrolase L1, 2.5-fold increase; AI
38 the ubiquitin-proteasome system, parkin and ubiquitin C-terminal hydrolase L1, are also associated w
39 associated with neurodegenerative diseases (ubiquitin C-terminal hydrolase L1, rat ortholog of human
40 lues, 0.34; 95% CI, 0.18-0.50; P < .001) and ubiquitin C-terminal hydrolase-L1 (mean difference in ln
41 f Glial Fibrillary Acidic Protein (GFAP) and Ubiquitin C-Terminal Hydrolase-L1 (UCH-L1) in a cohort o
45 lenged by the linkage of the neuronal enzyme ubiquitin C-terminal hydrolase-L1 (UCH-L1) to Parkinson'
47 asma glial fibrillary acidic protein (GFAP), ubiquitin C-terminal hydrolase-L1 (UCH-L1), neurofilamen
48 asma glial fibrillary acidic protein (GFAP), ubiquitin c-terminal hydrolase-L1 (UCH-L1), neurofilamen
52 ed included glial fibrillary acidic protein, ubiquitin C-terminal hydrolase-L1, neurofilament light c
55 in (KIAA0603), a novel protein AK000009, the ubiquitin C-terminal hydrolase L3 (UCHL3) and an F-box/P
62 e approach to tag active DUBs, we identified ubiquitin C-terminal hydrolase (UCH) isoform L3 as the p
64 esent study measured serum concentrations of ubiquitin C-terminal hydrolase (UCH-L1) and glial fibril
65 Glial Fibrillary Acidic Protein (GFAP) and Ubiquitin C-terminal hydrolase (UCH-L1) have been FDA-ap
66 f glial fibrillary acidic protein (GFAP) and ubiquitin C-terminal hydrolase (UCH-L1) levels became th
68 e crystal structure of the recombinant human Ubiquitin C-terminal Hydrolase (UCH-L3) by X-ray crystal
72 report a novel interaction between Smads and ubiquitin C-terminal hydrolase UCH37, a deubiquitinating
73 members (USP4, USP15, USP11, and USP2), the ubiquitin C-terminal hydrolase UCHL3, and the Machado-Jo
74 d of K48 linkages, the proteasome-associated ubiquitin C-terminal hydrolase UCHL5/UCH37 serves as a p