コーパス検索結果 (1語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 lfotranserases exist in mammals (up to seven isoenzymes).
2 that modulates the activity of MAT2A-encoded isoenzyme.
3 that modulates the activity of MAT2A-encoded isoenzyme.
4 inhibitors specific for the cyclooxygenase 2 isoenzyme.
5 de substrates were tested against each human isoenzyme.
6 N-1-methylheptylformamide inhibitor in this isoenzyme.
7 d not reduce the expression of any other PKC isoenzyme.
8 vity appear to be more dependent on the PLD2 isoenzyme.
9 ich had become fully dependent on the second isoenzyme.
10 ructure-activity relationships for each ALDH isoenzyme.
11 que and overlapping functions of the ALDH1/2 isoenzymes.
12 daidzin for selectivity against five ALDH1/2 isoenzymes.
13 specific pyruvate dehydrogenase kinase (PDK) isoenzymes.
14 failed to detect heterodimerization of these isoenzymes.
15 ween the beta(1)beta(1) and gamma(2)gamma(2) isoenzymes.
16 te preferences shown by these highly related isoenzymes.
17 ve inhibition of human alcohol dehydrogenase isoenzymes.
18 the tissue-specific expression of these two isoenzymes.
19 e amino acids have the same function in both isoenzymes.
20 substrate specificities and are, therefore, isoenzymes.
21 gesting a differential induction of distinct isoenzymes.
22 uggesting functional cooperation between the isoenzymes.
23 eta-hydroxysteroid dehydrogenase (17betaHSD) isoenzymes.
24 r human ALDH1A1 compared to eight other ALDH isoenzymes.
25 l as the alpha- and the gamma-subunit of NSE isoenzymes.
26 ynthesis, were transfected with human Has1-3 isoenzymes.
27 gulate all three nrd operons that encode RNR isoenzymes.
28 Plants commonly contain two AMADH isoenzymes.
29 12-fold selectivity for NEU2 over all other isoenzymes.
33 eased expression of steroid-5alpha-reductase isoenzyme-1 (SRD5A1) over SRD5A2, which is otherwise the
34 tumor markers, such as lactate dehydrogenase isoenzyme-1, may provide a greater risk stratification.
35 rt hairpin (sh) sequences for inhibiting PHD isoenzyme 2 and FIH were inserted into novel, nonviral,
37 ut not azithromycin, inhibit cytochrome P450 isoenzyme 3A4 (CYP3A4), and inhibition increases blood c
39 serum levels of creatine kinase muscle-brain isoenzyme, a myocardial-specific injury marker, and an i
44 rature at 30 degrees C in both years whereas isoenzyme A2 had maximum activity at 40 degrees C in 200
46 three lines of evidence that the thioredoxin isoenzymes actually have redundant activities as antioxi
48 ntial inhibition of hepatic cytochrome P-450 isoenzymes, affect CY metabolism and conditioning-relate
51 al analogues of the DMSO reductase family of isoenzymes allows mechanistic examination of the minimal
52 stained activation of protein kinase C (PKC) isoenzymes alpha and betaII leads to their translocation
53 sensitivity to MSA with Ca(2+)-dependent PKC isoenzymes (alpha, beta, and gamma) being the most susce
54 the selective translocation of classical PKC isoenzymes, alpha and betaII, to a juxtanuclear compartm
55 iological conditions, we have cloned rat ALT isoenzyme ALT1 and ALT2 complementary DNAs (cDNAs), exam
58 A content, species-specific surface markers, isoenzyme analysis, and karyotyping indicate that they a
59 n that contained each of the three described isoenzymes and 69 extended-spectrum beta-lactamase-produ
60 cells or HEK293 cells did not express any AP isoenzymes and did not display any NAADP 2'-phosphatase
63 xhibit brain-regional alterations in 5alphaR isoenzymes and neuroactive steroid levels; then, we asse
64 tudy provides evidence that in human TB, NOS isoenzymes and NO are present in specialized areas of th
65 a suppresses the activity of specific CYP450 isoenzymes and that this correlates with discrete toxici
66 causes of differences between catalytic GST isoenzymes and the effects of mutations and genetic poly
67 of help to determine the roles of different isoenzymes and the mining of genes involved in light res
70 rapid and accurate method to detect all KPC isoenzymes and was useful in documenting the presence an
72 rly the promitogenic and prosurvival epsilon isoenzyme, and this inactivation causes growth inhibitio
76 s that the intracellular distribution of PKD isoenzymes are distinct, and suggests that their signali
78 ased phosphorylated PKC, we suggest that PKC isoenzymes are involved in the neuroprotective action of
81 pear in gene families, and the corresponding isoenzymes are located to the thylakoid lumen of chlorop
85 f and variation between all the isoforms and isoenzymes, as well as covarying results with the conven
89 homodimerization of PLC-beta3 and PLC-beta1 isoenzymes but failed to detect heterodimerization of th
90 states are essentially the same for the two isoenzymes, but the S states are quite different, indica
91 s yeast's entire complement of 26 glycolytic isoenzymes by any alternative, functional glycolytic pat
92 ond dynamics of horseradish peroxidase (HRP) isoenzyme C in the free form and when ligated to a varie
94 ne sulfation is mediated by one of two Golgi isoenzymes, called tyrosylprotein sulfotransferases (TPS
95 of the hemA gene, which codes for one of two isoenzymes catalyzing 5-aminolevulinic acid synthesis.
97 s concept is applied here to creatine kinase isoenzyme (CK-MB), a cardiac biomarker in ischemic condi
98 o high affinity and selectivity toward MAO-A isoenzyme, compared to clorgyline and moclobemide, with
100 hanges in expression of specific PDK and PDP isoenzymes contribute to hyperphosphorylation and theref
101 ble mutants revealed that each AHAS and IPMS isoenzyme contributes to homeostasis rather than being f
103 d the inhibition of the cyclooxygenase (COX) isoenzymes, COX-1 and COX-2, affect memory function and
104 Leu at position 141 in the gamma(2)gamma(2) isoenzyme create an environment with stereoselectivity f
105 tly coordinated CRR1-dependent regulation of isoenzymes Cth1 and Crd1 reinforces the notion that copp
107 tat (COBI; an inactivator of cytochrome P450 isoenzyme CYP3A without anti-HIV activity) and a new int
109 te (S1P), produced by two sphingosine kinase isoenzymes, denoted SphK1 and SphK2, is the ligand for a
116 hologic Q waves or creatine phosphokinase-MB isoenzyme elevation >8 x upper limits of normal) was red
118 of stress cardiomyopathy, including cardiac isoenzyme elevation, QTc interval prolongation, and rapi
119 atohepatitis in which the gene for the MAT1A isoenzyme encoding AdoMet synthetase has been disrupted,
125 abolism, involving differential synthesis of isoenzymes for many oxidation and reduction reactions.
128 ione anion to CDNB in the wild-type M1-1 GST isoenzyme from rat and in three single point mutant (Tyr
131 KI isoforms, indicate that individual PIP5KI isoenzymes fulfill specific roles in embryonic developme
132 opsis (Arabidopsis thaliana) cytosolic GAPDH isoenzymes GAPC1 and GAPC2 to cadmium-induced stress in
133 ts close homolog, the maize beta-glucosidase isoenzyme Glu1, which shares 72% sequence identity, hydr
134 quential enzymatic reaction performed by two isoenzyme groups, cyclooxygenases (COX-1 and COX-2) and
137 additional knowledge also suggests that each isoenzyme has evolved different collagen sequence-prefer
138 nctions of individual protein kinase C (PKC) isoenzymes has emerged as an important goal in the study
140 itochondrial branched chain aminotransferase isoenzyme (hBCATm) must be stored in a reducing environm
142 data imply a very high degree of Na,K-ATPase isoenzyme heterogeneity in zebrafish, with the potential
143 i, noted for encoding the fourth hydrogenase isoenzyme (HYD4), is not expressed at a significant leve
144 derivatives were tested against human (h) CA isoenzymes I and II (cytosolic, ubiquitous isoforms) and
151 tes mellitus, but the role of individual COX isoenzymes in diabetic nephropathy remains unknown.
152 ported example is the loss of one of the two isoenzymes in glioblastoma cancer cells such that the us
158 sing data from a study of the inheritance of isoenzymes in selfed progeny of octoploid strawberry cul
162 e selectivity toward one of the five ALDH1/2 isoenzymes, including compound 36, a selective inhibitor
164 of glycogen metabolism and consists of three isoenzymes, including glycogen phosphorylase isoenzyme B
165 l classes of drugs are known to affect IMPDH isoenzymes, including nucleotide and NAD analogs, sugges
168 n of enzyme subunits and weak association of isoenzymes independently catalyzing the same reaction.
172 ompound 8 showed remarkable HDAC 1, 2, and 6 isoenzymes inhibitory activities with IC(50) values of 1
173 glutathione S-transferases (GSTs), phase II isoenzymes involved in cellular detoxification, on risk
174 by sphingosine kinase (SK), of which the SK1 isoenzyme is activated by tumor necrosis alpha (TNF-alph
176 hough metabolism mediated by cytochrome P450 isoenzymes is known to play a major part in the biotrans
181 activity of PKM2, the major pyruvate kinase isoenzyme known to regulate cellular glutathione levels.
182 amplicon was designed so that the genes for isoenzymes KPC-1, -2, and -3 could be easily distinguish
183 otted protein ubiquitin C-terminal hydrolase isoenzyme L1 (UCH-L1) and have therefore been able to qu
184 ound that CCR5 2-18 is sulfated by both TPST isoenzymes leading to a final product with four sulfotyr
186 elevated troponin and creatine phosphokinase isoenzyme levels with mortality and organ failure in sub
187 of the high active site homology of the hNEU isoenzymes, little progress in the design and synthesis
188 mics analysis, we identified pyruvate kinase isoenzyme M2 (PKM2), a critical regulator of glycolysis
192 th the variable activities of human aldolase isoenzymes modulated LacD.1's affinity for substrate.
194 sbuvir is not metabolized by cytochrome P450 isoenzymes, nor does it induce or inhibit the metabolism
197 decreased the levels of creatine kinase, MB isoenzyme of creatine kinase, blood urea nitrogen, creat
199 ilated in the chloroplast by a chloroplastic isoenzyme of glutamine synthetase (GS2), the predominant
202 The crystal structure of HPTP-B, a human isoenzyme of the low molecular weight phosphotyrosyl pho
205 ber of a family of genes that includes three isoenzymes of prolyl 3-hydroxylase (P3H), P3H1, P3H2, an
206 uggest that humans express two mitochondrial isoenzymes of tafazzin that have similar transacylase ac
207 lus, identifying three groups of homologues: Isoenzymes of the first group are found in all species a
208 indicate that parasites express multiple APD isoenzymes of various functions that can now be specific
212 fascinating question whether individual ADT isoenzymes (or combinations thereof) differentially modu
213 dized by two transhydrogenation cycles, i.e. isoenzyme pairs of dehydrogenases with different cofacto
214 nity of PKC, it specifically inactivates PKC isoenzymes, particularly the promitogenic and prosurviva
215 tochemical assessment of phosphodiesterase-5 isoenzyme (PDE-5) and PDE-2 expression, which are the ta
217 activation of PKC, particularly prosurvival isoenzyme PKCepsilon, resulting in preconditioning again
218 ontaining proteins, such as protein kinase C isoenzymes (PKCs), have been identified as molecular tar
219 eta-hydroxysteroid dehydrogenase (3beta-HSD) isoenzymes play a key role in cellular steroid hormone s
220 cular weight complexes of PORB with its twin isoenzyme, PORA, as encountered with (Cys303-->Ala)-PORB
224 NSR1 suggest that two sulfide dehydrogenase isoenzymes provide a compensatory NADPH-dependent S(0) r
226 fer reactions for analogue complexes and for isoenzymes provided the catalytic sites are isostructura
227 ion structure of the second human LMW PTPase isoenzyme provides the opportunity to examine the struct
228 lot and quantitative PCR survey of the BMP-1 isoenzymes revealed expression of mTLD in primary kerati
229 rioration, preangiography creatine kinase-MB isoenzyme rise >2 x normal, and time interval between pr
230 and the myosin head (S1) was separated into isoenzymes S1A1 and S1A2 by ion-exchange chromatography.
231 The two major forms of phospholipase A(2) isoenzymes, secretory phospholipase A(2) and cytosolic p
233 recently published by developing a class of isoenzyme-selective inhibitors using similar indole-2,3-
235 4), showed 6 nM potency against tankyrase 1, isoenzyme selectivity, and Wnt signaling inhibition.
237 s increased in MCK-PPARbeta/delta muscle, an isoenzyme shift that diverts pyruvate into the mitochond
239 he present studies we demonstrate that these isoenzymes show high GPx activity toward phospholipid hy
240 emical reactions, many hundreds of metabolic isoenzymes show significant and tumor-specific expressio
241 uman pyruvate dehydrogenase complex, has two isoenzymes, somatic cell-specific PDH1 and testis-specif
242 c steatosis and provide evidence that an ALT isoenzyme-specific assay may have more diagnostic value
243 Our data indicate PI3K-C2gamma supports an isoenzyme-specific forking of insulin-mediated signal tr
246 e basis for rational approach to design ALDH isoenzyme-specific inhibitors as research tools and perh
250 h can be distinguished by its sensitivity to isoenzyme-specific, substrate-competitive inhibitors.
251 103, differ from vorinostat in structure and isoenzyme specificity, and have shown activity against l
252 ipid mediator produced by sphingosine kinase isoenzymes (SphK1 and SphK2), regulates diverse cellular
253 h is produced by 2 sphingosine kinase (SphK) isoenzymes, SphK1 and SphK2, has been implicated in IgE-
256 metabolic redundancy given, for example, by isoenzymes, subcellular compartmentalization or the pres
257 useful for measurement of highly homologous isoenzymes such as ADHs where multiple signature peptide
259 two known articular chondrocyte-expressed TG isoenzymes (TG2) demonstrated that TG2 was essential for
261 e of localization for PKCalpha and PKCbetaII isoenzymes that arises with sustained stimulation of PKC
262 Sphingosine kinase 2 (SphK2), one of the isoenzymes that generates S1P, was associated with histo
263 to sphingosine kinase 1 (SphK1), one of the isoenzymes that generates the pro-survival lipid mediato
265 is characterized by expression of glycolytic isoenzymes that play key roles in parasite metabolism.
266 Sphingosine kinase 1 (SphK1), one of the two isoenzymes that produce sphingosine-1-phosphate, is up-r
267 bstrates by hyaluronan synthase 1-3 (HAS1-3) isoenzymes that transfer N-acetylglucosamine (GlcNAc) an
268 ugh there may be contributions by both major isoenzymes, the effects on viral infectivity appear to b
269 uences indicates that plants have two ALDH10 isoenzymes: those known to be GB accumulators have a hig
270 man thymidine kinase-1 and the mitochondrial isoenzyme thymidine kinase-2, the highest phosphorylatio
272 h its proposed function in targeting the PKA isoenzyme to organelles rich in PBR, i.e. mitochondria,
273 hese data indicate a general tendency of HAS isoenzymes to form both homomeric and heteromeric comple
275 Elevated serum levels of creatine kinase (MB isoenzyme), troponin I, and troponin T, usually in the p
276 cells, potential interactions among the HAS isoenzymes using fluorescence resonance energy transfer
282 ysiological affect of these mutations in AAT isoenzymes was determined by measuring growth and amino
283 ional (PKCbetaII) and novel (PKCepsilon) PKC isoenzymes were also observed which were synchronous wit
286 gainst the GalNAc-T1, -T2, -T3, -T4, and -T6 isoenzymes, were used for immunofluorescence microscopic
288 In plants, PPOs often occur as families of isoenzymes which are differentially expressed, but littl
289 ermined by serine palmitoyltransferase (SPT) isoenzymes, which are trimeric proteins composed of two
290 edly reduced hyaluronan synthesis by all HAS isoenzymes while raising its concentration from 5 to 25
291 ny one of the six different carboxylesterase isoenzymes will regulate the metabolism of retinyl palmi
292 be GB accumulators have a high-BAL-affinity isoenzyme with Ala or cysteine in this critical position
293 or rottlerin (3 microM) or knockdown of this isoenzyme with specific siRNA oligonucleotides blocked p
294 s with CaM is supported by pull-down of both isoenzymes with CaM-Sepharose beads from 1321N1 cell lys
295 CHS3 and CHS8, which encode chitin synthase isoenzymes with different biochemical properties and phy
297 d isolated and cloned the genes encoding the isoenzymes with plastidic localization: NbAsp5 and NbPAT
298 Surprisingly, the Sdh3p subunit can form SDH isoenzymes with Sdh4p or with Shh4p as well as be a subu
299 Therefore, we analyzed the different AOX isoenzymes with the aim to identify differences in their
300 s and nonsynonymous/synonymous rates for Pr1 isoenzymes within a lineage and between lineages showed
WebLSDに未収録の専門用語(用法)は "新規対訳" から投稿できます。