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1 ular xanthine and hypoxanthine by the purine catabolic enzyme.
2  mutants lacking Glo1, a Mrr1-independent MG catabolic enzyme.
3 tional repressor to a membrane-bound proline catabolic enzyme.
4 uster whose products have homology to purine catabolic enzymes.
5 changing the activity of local synthetic and catabolic enzymes.
6 ion of numerous genes which specify nitrogen catabolic enzymes.
7 tion and activities of both its anabolic and catabolic enzymes.
8 ripts encoding the relevant biosynthetic and catabolic enzymes.
9 gnalling, leading to subsequent induction of catabolic enzymes.
10 s is substrate for a variety of anabolic and catabolic enzymes.
11 ions also depend upon the levels of the PGE2 catabolic enzyme 15-hydroxyprostaglandin dehydrogenase (
12 nown about the role of the key prostaglandin catabolic enzyme 15-hydroxyprostaglandin dehydrogenase (
13 to cancer progression, is inactivated by the catabolic enzyme, 15-hydroxyprostaglandin dehydrogenase
14       Mutation of alh-6, a conserved proline catabolic enzyme, accelerates fat mobilization, enhances
15 t, be related to inhibition of prostaglandin catabolic enzyme activities.
16                     Recently, we showed that catabolic enzyme activity could be assessed by substrate
17 ctions both as a membrane-associated proline catabolic enzyme and as a transcriptional repressor of t
18  are intricately controlled by biosynthetic, catabolic enzymes and antizymes.
19 ic growth of Escherichia coli, expression of catabolic enzymes and envelope and periplasmic proteins
20 osis enabled induction of several additional catabolic enzymes and sugar transporters at the high pH,
21 ethylglycine, sarcosine, glycine, and serine catabolic enzymes and the BetX and CbcXWV quaternary ami
22 se provides curated information on microbial catabolic enzymes and their organization into metabolic
23 ehydrogenase (15-PGDH, the key prostaglandin catabolic enzyme) and the cell cycle inhibitor p21.
24             Indoleamine 2,3-dioxygenase 1, a catabolic enzyme, and inhibitory ligands were employed a
25 nflammatory cytokines, chemotactic proteins, catabolic enzymes, and the recruitment and activation of
26 s and is expressed in tissues in which these catabolic enzymes are expressed.
27    The structural genes that encode nitrogen catabolic enzymes are subject to nitrogen metabolite rep
28 rter, and nanA and nanE, predicted to encode catabolic enzymes, are essential for growth on Neu5Ac.
29 he administration of a pegylated form of the catabolic enzyme arginase I (peg-Arg I) has shown some p
30                        The Neurospora crassa catabolic enzyme, arginase (L-arginine amidinohydrolase,
31 g submergence in the SUB1A rice through a GA catabolic enzyme as part of an early response and may re
32 uman chondrocytes promoted the expression of catabolic enzymes associated with OA.
33 d and genes encoding many of the chlorophyll catabolic enzymes been identified.
34  Here we demonstrate that SOD1 is not just a catabolic enzyme, but can also directly regulate NADPH o
35  With the elucidation of myriad anabolic and catabolic enzyme-catalyzed cellular pathways crisscrossi
36 kdown, STAY-GREEN1 (SGR1) interacts with Chl catabolic enzymes (CCEs) and light-harvesting complex II
37 d Ile content, suggesting that these two Thr catabolic enzymes compete for a common substrate pool.
38 esses a potentially unique suite of secreted catabolic enzymes, consistent with E. muscae's species-s
39 iated with the known overexpression of lipid catabolic enzymes, could be detected through metabolomic
40 ncentrations, while proteomics revealed that catabolic enzymes (CphCI and CphCII) were differentially
41 idermis, as were the activities of two lipid catabolic enzymes critical to stratum corneum function,
42 pecifically examined the effect of its major catabolic enzyme, CYP24A1, in prostate cancer.
43  120% increase in the expression of the ATRA catabolic enzyme Cyp26a1 in Dhrs3(-/-) embryos vs. contr
44 dh ortholog, rdh1, and a major retinoic acid catabolic enzyme, cyp26a1, suggesting coordinate modulat
45 ation (by knocking out the gene encoding the catabolic enzyme CYP7B1) decreased estrogen-dependent ex
46                 Deficiency of the pyrimidine catabolic enzyme, dihydropyrimidine dehydrogenase (DPD),
47 f ADMA are controlled by two isoforms of its catabolic enzyme dimethylarginine dimethylaminohydrolase
48 re decreased in unloaded mice, with elevated catabolic enzymes (e.g., matrix metalloproteinases), and
49                      The Pdu MCP consists of catabolic enzymes encased within a protein shell, and it
50  is consumed by this microorganism using the catabolic enzymes encoded by genes hpdH, hbdH and mmsA.
51 nant proteins we characterized four inositol catabolic enzymes encoded in the TM0412-TM0416 chromosom
52 e of a RA sink in the form of the CYP26B1 RA catabolic enzyme expressed in deeper regions of the brai
53 r-2.1(0) and older wild-type males, enhanced catabolic enzymes expression, coupled with the reduced e
54 vels of anandamide and lower activity of its catabolic enzyme fatty acid amide hydrolase (FAAH) are a
55 de (AEA) signaling through inhibition of its catabolic enzyme fatty acid amide hydrolase (FAAH) in th
56 ed by the failure of an inhibitor of the AEA catabolic enzyme fatty acid amide hydrolase (FAAH) to af
57 r proteins that mediate AEA transport to its catabolic enzyme fatty acid amide hydrolase (FAAH).
58 ndocannabinoid anandamide is degraded by the catabolic enzyme fatty acid amide hydrolase (FAAH).
59 type 1 (CRF1) potentiation of the anandamide catabolic enzyme fatty acid amide hydrolase.
60  x 10(-53)), a gene that encodes the primary catabolic enzyme for 1,25-dihydroxyvitamin D and 25-dihy
61   Adenosine deaminase (ADA) is the principal catabolic enzyme for adenosine in vivo, and its deficien
62  of ethanolamine ammonia lyase (EA-lyase), a catabolic enzyme for ethanolamine.
63 ns in fatty acid amide hydrolase (FAAH), the catabolic enzyme for the endocannabinoid anandamide, may
64 rolase (FAAH) (C385A; rs324420), the primary catabolic enzyme for the endocannabinoid anandamide.
65 ce deficient in both CD73 and AMPD3, the key catabolic enzymes for extracellular and intra-erythrocyt
66 on acetate, Methanosarcina barkeri expresses catabolic enzymes for other methanogenic substrates such
67  information exists on the quinate/shikimate catabolic enzymes found in these organisms.
68                                These evolved catabolic enzymes have application for improving biodegr
69 st likely due to reduced activity of the HDL-catabolic enzyme hepatic lipase (Lipc) and increased exp
70 exible protein scaffold shared with the heme catabolic enzyme, HO, and a set of metal-binding residue
71 rgely layered structure consisting of mostly catabolic enzymes; (iii) an anabolic module with a simil
72 nto how circulating BCAAs and their aberrant catabolic enzymes impact both cancer cells and the surro
73 e (IDE, insulysin) is the best characterized catabolic enzyme implicated in proteolysis of insulin.
74 cond, phenylethylamine oxidase is an unusual catabolic enzyme in that it is localized in the periplas
75 resis demonstrated downregulation of several catabolic enzymes in 8-month-old offspring of NR ewes.
76 s are reflected in expression levels of BCAA catabolic enzymes in both mice and humans.
77 arkness regulates the gene expression of fat catabolic enzymes in mice.
78 ilage integrity, inhibited the production of catabolic enzymes in osteoarthritic joints, and suppress
79  In addition, we discovered a function of rN catabolic enzymes in the degradation of deoxyribonucleos
80 ased on the loss of essential amino acids by catabolic enzymes in the microenvironment is a critical
81  deacetylation steps, whereas the downstream catabolic enzymes in the pathway were largely conserved.
82                   To examine the role of the catabolic enzymes in the response of breast cancer cells
83                          The operon encoding catabolic enzymes in the utilization of L-ascorbate (ula
84            Overexpression of SSAT (polyamine catabolic enzyme) in female mice results in impaired ova
85                                           GA catabolic enzymes include GA 2-oxidases that are classif
86 ression of genes encoding putative cell wall catabolic enzymes (including those involved with pectin)
87 a is provided with a focus on the tryptophan catabolic enzyme indoleamine 2,3-dioxygenase (IDO) and i
88 -molecule inhibitors of the tryptophan (Trp) catabolic enzyme indoleamine 2,3-dioxygenase (IDO) repre
89 s are the first to show that endocannabinoid catabolic enzyme inhibitors reduce abrupt withdrawal in
90 anabolic enzymes and increased expression of catabolic enzymes involved in the metabolism of amino ac
91  the transcription of genes encoding several catabolic enzymes is increased.
92 covery of impaired branched chain amino acid catabolic enzyme isovaleryl-CoA dehydrogenase (encoded b
93  gene that encodes a rate-limiting polyamine catabolic enzyme, leads to lower intracellular polyamine
94 embers of the cytochrome P450 superfamily of catabolic enzymes, localized in the endoplasmic reticulu
95 s indicated by upregulated expression of the catabolic enzymes LYPLA1, LYPLA2, and GPCPD1.
96                                 The mannitol catabolic enzyme mannitol dehydrogenase (MTD) is a prime
97                 Conversely, we show that the catabolic enzyme mannitol dehydrogenase is induced in a
98 6, and Nos2), chemokines (Mcp1 and Mif), and catabolic enzymes (Mmp3, Mmp9, and Adamts4).
99 ), through pharmacological inhibition of its catabolic enzyme, monoacylglycerol lipase (MAGL), either
100            Inhibition of the endocannabinoid catabolic enzymes, monoacylglycerol lipase (MAGL) or fat
101                                          The catabolic enzyme myo-inositol oxygenase (MIOX) is expres
102 king PMA-induced expression of the polyamine catabolic enzyme N(1)-spermidine/spermine acetyltransfer
103 n level of the gene that encodes the primary catabolic enzyme of active vitamin D [25(OH)D-24-hydroxy
104 omocysteine has been proposed to inhibit the catabolic enzyme of ADMA, dimethylarginine dimethylamino
105                               DDAH1 is a key catabolic enzyme of asymmetric dimethylarginine (ADMA),
106                                              Catabolic enzymes of the ceramide and glycolipid pathway
107 s, type 1 and 2, as well as biosynthetic and catabolic enzymes of the endocannabinoids N-arachidonoyl
108 ytes and combined it with the specificity of catabolic enzymes of the sphingolipid pathway.
109 nephosphotransferase (PAF-CPT), and its main catabolic enzyme (PAF acetylhydrolase; PAF-AH), on U937
110 has been proposed that ancient expansions of catabolic enzyme paralogs broadened the spectrum of orga
111 gulated expression of genes for sphingolipid catabolic enzymes, pointing to additional mechanisms for
112 oleamine 2,3-dioxygenase (IDO), a tryptophan catabolic enzyme previously shown to have regulatory act
113 osis factor alpha [TNFalpha], and IL-6), and catabolic enzymes (procathepsin B and neutrophil elastas
114 atrix deposition, whilst enhancing selective catabolic enzyme production, suggesting its potential fo
115   Dioxane metabolism can be initiated by two catabolic enzymes, propane monooxygenase (PRM) and tetra
116 onoacylglycerol lipase (MAGL) is the pivotal catabolic enzyme responsible for signal termination in t
117 te phosphotransferase system (PTS) and other catabolic enzymes responsible for transport and cataboli
118 where the imbalance between biosynthetic and catabolic enzymes results in structural alterations and
119 on of the operon that encodes the L-rhamnose catabolic enzymes, rhaBAD, as well as the operon that en
120  Examination of chondroitin/dermatan sulfate catabolic enzymes showed that heparan sulfate and hepari
121 n nature have evolved new genes which encode catabolic enzymes specific for chlorinated aromatic subs
122           Maximal induction of the polyamine catabolic enzyme spermidine/spermine N(1)-acetyltransfer
123  enzymes and potently inducing the polyamine catabolic enzyme spermidine/spermine N1-acetyltransferas
124 nsive to analogue induction of the polyamine catabolic enzyme spermidine/spermine N1-acetyltransferas
125 sults in the superinduction of the polyamine catabolic enzyme spermidine/spermine N1-acetyltransferas
126 hesis and potently upregulates the polyamine catabolic enzyme spermidine/spermine N1-acetyltransferas
127             Rapid synthesis of the polyamine catabolic enzyme spermidine/spermine-N(1)-acetyltransfer
128 To test this, the responses of the polyamine catabolic enzymes spermidine/spermine acetyltransferase
129 ion of polyamines by overexpression of a key catabolic enzyme, spermidine/spermine N(1)-acetyltransfe
130 e most potent known inducer of the polyamine catabolic enzyme, spermidine/spermine N1-acetyltransfera
131                                The polyamine catabolic enzyme spermine oxidase (SMOX) is induced in c
132 pression levels of the gibberellic acid (GA) catabolic enzyme StGA2ox1.
133  for biochemically undefined observations in catabolic enzyme substrate specificity, the interplay be
134  of only two operons, both encoding pyruvate catabolic enzymes, suggesting an intimate relationship b
135  discovery of a novel IDO-related tryptophan catabolic enzyme termed IDO2 that is preferentially inhi
136  protein 43% identical to a mammalian valine catabolic enzyme that hydrolyzes beta-hydroxyisobutyryl-
137       Indoleamine 2,3 dioxygenase (IDO) is a catabolic enzyme that initiates the kynurenine pathway o
138        Spermine oxidase (SMO) is a polyamine catabolic enzyme that is highly inducible by inflammator
139        Adenosine deaminase (ADA) is a purine catabolic enzyme that manages levels of the biologically
140 ism by which bFGF controls the production of catabolic enzymes that are associated with excessive deg
141         We show, through misexpression of GA-catabolic enzymes that suppress GA accumulation, that GA
142 ceutical Co.'s KH-1060 (3), is recognized by catabolic enzymes, the selective biological profile of s
143                                  Targeting a catabolic enzyme to buy time for recombination is an ama
144  denitrificans did not produce extracellular catabolic enzymes to transform cholesterol.
145 ed to concentrate low levels of ethanolamine catabolic enzymes, to keep the level of toxic acetaldehy
146  genes that encode the tbu pathway's initial catabolic enzyme, toluene-3-monooxygenase, as well as Tb
147 ion of 589 curated metabolic gene functions (catabolic enzymes, transporters and transcriptional regu
148 uggests that coordinate targeting of the Trp catabolic enzymes tryptophan 2,3-dioxygenase (TDO) and I
149 peron contains three genes encoding probable catabolic enzymes, two of which (AgaF and AgaG) are thou
150 es encoding branched-chain amino acid (BCAA) catabolic enzymes was preserved in Klf6(PTKD) mice, with
151 erase (SSAT) gene, which encodes a polyamine catabolic enzyme, was induced by clinically relevant sul
152 expression of CYP26A1, a major retinoic acid catabolic enzyme, was up-regulated in Apc(MIN) mouse ade
153 atous degeneration by excessive secretion of catabolic enzymes, we examined the functional characteri
154          However, key polyamine anabolic and catabolic enzymes were upregulated, and there were corre
155 atch a broad specificity of hydroxycinnamate catabolic enzymes while responding to toxic thioester in
156 osine deaminase (ADA) is a ubiquitous purine catabolic enzyme whose expression is subject to developm
157 ofibroblasts and express excessive levels of catabolic enzymes, without altered levels of interstitia

 
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