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1 min reduced transcriptional up-regulation of acid ceramidase.
2 D2646, to inhibit the hydrolytic activity of acid ceramidase.
3 ped to produce and purify recombinant, human acid ceramidase.
7 (e) whether physiological hypoxia increased acid ceramidase (AC) expression; and (f) the effect of t
9 s regulating ulcerative colitis, the role of acid ceramidase (AC) in intestinal inflammation is yet t
15 Autoproteolytic cleavage of the inactive acid ceramidase (AC) precursor into the active heterodim
17 demonstrate that ceramide-deacylating enzyme acid ceramidase (AC) was preferentially upregulated in i
18 C12 myotubes that constitutively overexpress acid ceramidase (AC), an enzyme that catalyzes the lysos
19 ons revealed that desipramine down-regulated acid ceramidase (AC), but not sphingosine kinase, at the
21 show that the ceramide-metabolizing enzyme, acid ceramidase (AC), is expressed in human cumulus cell
22 in the gene (Asah1) encoding one ceramidase, acid ceramidase (AC), lead to the lysosomal storage diso
23 h cDNA and genomic sequences encoding murine acid ceramidase (AC; E.C. 3.5.1.23) have been isolated a
28 e detected, providing an accurate measure of acid ceramidase activity as low as 0.1 pmol/mg protein/h
29 phages revealed rapid internalization of the acid ceramidase activity from the hamster cell media but
30 s study reports a new assay method to detect acid ceramidase activity in vitro using Bodipy or lissam
33 ctate, perinuclear distribution, although no acid ceramidase activity was detected in the transfected
34 id, and highly sensitive method to determine acid ceramidase activity, and that it could be useful wh
35 Using mouse kidney extracts as the source of acid ceramidase activity, this new method was compared w
37 a provide important new information on human acid ceramidase and further document its central role in
38 s no effect on transcriptional activation of acid ceramidase and that CerS2 slightly but significantl
40 se analysis of sequences homologous to human acid ceramidase (ASAH) revealed a 1233-bp cDNA (previous
44 we report detailed characterization of this acid ceramidase-associated "reverse activity" and provid
46 rare autosomal recessive disorder caused by acid ceramidase deficiency that usually presents as earl
49 -(alpha) and 40 (beta)-kDa subunits as human acid ceramidase from natural sources, had an acidic pH o
51 S6 can mediate transcriptional activation of acid ceramidase in a JNK-dependent manner that is indepe
54 ure (renamed human ASAHL since it is a human acid ceramidase-like sequence), chromosomal location, pr
57 morpholino-1-propanol (PDMP), which inhibits acid ceramidase or glucosylceramide synthase and then in
59 s method utilizes purified human recombinant acid ceramidase to completely hydrolyze ceramide to sphi
62 tigated sphingolipid pathways and found that acid ceramidase was constitutively overexpressed in leuk
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