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1                                     The bone catabolic actions of parathyroid hormone (PTH) are seen
2 their DNA binding sites, leading to a xylose catabolic activation independent of catabolite repressio
3  in the joint cavity, which can increase the catabolic activities of chondrocytes and damage cartilag
4 ion factors mediate the growth-promoting and catabolic activities of the lysosome and undergo a compl
5 iciency in resting liver is transformed into catabolic activities upon tissue loss.
6 tive remodelling by chondrocyte-mediated pro-catabolic activities.
7 sting-induced hypothermia due to exaggerated catabolic activity in brown adipocytes.
8 ryptophan was used as an index of tryptophan catabolic activity in this pathway.
9 gonia are prevented from responding to RA by catabolic activity of cytochrome P450 family 26 enzymes.
10                                          The catabolic activity of human microbiota led to the genera
11 to balance the benefits of the enhanced host catabolic activity with the risk of being eliminated by
12             How photoreceptors balance their catabolic and anabolic demands is poorly understood.
13 ng of specific nutrients to engage them into catabolic and anabolic processes, and contributes to tem
14 are in the center of the cellular control of catabolic and anabolic processes.
15 cesses, including upstream modulators of the catabolic and antibacterial pathway of autophagy.
16                           Acidic pH causes a catabolic and degenerate phenotype in NP cells which is
17 and TNF-alpha, induce aberrant expression of catabolic and degradative enzymes and inflammatory cytok
18 of anabolic genes and elevated expression of catabolic and inflammatory genes.
19 ondrocytes that increases gene expression of catabolic and inflammatory mediators.
20 vely impacts articular cartilage, triggering catabolic and inflammatory responses in chondrocytes.
21  energy homeostasis in the cell by promoting catabolic and inhibiting anabolic pathways.
22 tents of gene connectivity, are enriched for catabolic and muscle system processes respectively, and
23 uman IVD tissue and induced an inflammatory, catabolic and pro-angiogenic phenotype in bovine nucleus
24 th IL-1beta, a cytokine with known cartilage catabolic and pro-inflammatory effects.
25 r the identification of anabolic, transport, catabolic and regulatory portions of the cycloalternan p
26 nses energetic stress and, in turn, promotes catabolic and suppresses anabolic metabolism coordinatel
27 representation of endolysosomal, autophagic, catabolic, and mTOR-related proteins.
28 ulation represent much of the purpose of the catabolic arms of metabolism and then drive many anaboli
29             miRNAs contribute equally to the catabolic aspect of periodontal homeostasis as they affe
30 ations and the exoproteome of three aromatic-catabolic bacteria: Pseudomonas putida KT2440, Rhodoccoc
31 s, while PTs are especially characterized by catabolic/biosynthetic and transport processes including
32                              The majority of catabolic BMCs (metabolosomes) compartmentalize a common
33 etic (i.e., anabolic) and degradative (i.e., catabolic) branches of the endomembrane system.
34 rate, cyclohexanecarboxylate and benzoate as catabolic byproducts.
35 ism observed may indicate that mitochondrial catabolic capacity is a key constraint setting an upper
36  nitrogen starvation to address the roles of catabolic carbon recycling, acyl chain redistribution, a
37 in cartilage by regulating both anabolic and catabolic cellular activities.
38 at AGGF1 activates autophagy, a housekeeping catabolic cellular process, in endothelial cells (ECs),
39    Macroautophagy (hereafter autophagy) is a catabolic cellular self-eating process by which unwanted
40 mmune and nervous systems drive anorexia and catabolic changes in adipose tissue and skeletal muscle,
41 otes reactive oxygen species (ROS) to induce catabolic changes through stabilization of IkappaB-zeta,
42 s, MV-induced diaphragm inactivity initiates catabolic changes via rapid activation of Smad3 signalin
43  increased in skeletal muscle under multiple catabolic conditions, including cancer.
44 onsidered a promising therapeutic target for catabolic conditions.
45              Toxicokinetic interactions with catabolic cytochrome P450 (CYP) enzymes can inhibit chem
46                  To analyse the basis of the catabolic defect in amyotrophic lateral sclerosis we use
47 yntrophorhabdacaeae member) to uncover their catabolic diversity and flexibility.
48 dings enhance the understanding of microbial catabolic diversity during adaptive evolution in respons
49 fects suppressing osteoblastogenesis and pro-catabolic effects enhancing osteoclastogenesis, which dr
50 investigated the molecular mechanisms of the catabolic effects of CB(1) R blockade in the liver.
51 ecombinant Hsp70 and Hsp90 recapitulates the catabolic effects of tumor.
52  demonstrates that MCP-1 has a role in PTH's catabolic effects on bone including monocyte and macroph
53               To determine its role in PTH's catabolic effects, we continuously infused female wild-t
54 titution encodes an FAAH enzyme with reduced catabolic efficacy.
55 ard direct competition for the same limiting catabolic electron donor substrate with subsequent niche
56 s of serine, histidine, and methionine; (iv) catabolic end products of lignin (pyruvate and oxaloacet
57           The export of low-molecular-weight catabolic end-products is facilitated by polytopic trans
58 rely depleted of crucial enzymes involved in catabolic energy-converting pathways.
59 de (AEA) signaling through inhibition of its catabolic enzyme fatty acid amide hydrolase (FAAH) in th
60 type 1 (CRF1) potentiation of the anandamide catabolic enzyme fatty acid amide hydrolase.
61  x 10(-53)), a gene that encodes the primary catabolic enzyme for 1,25-dihydroxyvitamin D and 25-dihy
62 -molecule inhibitors of the tryptophan (Trp) catabolic enzyme indoleamine 2,3-dioxygenase (IDO) repre
63                                          The catabolic enzyme myo-inositol oxygenase (MIOX) is expres
64 pression levels of the gibberellic acid (GA) catabolic enzyme StGA2ox1.
65             Indoleamine 2,3-dioxygenase 1, a catabolic enzyme, and inhibitory ligands were employed a
66  mutants lacking Glo1, a Mrr1-independent MG catabolic enzyme.
67 ression of genes encoding putative cell wall catabolic enzymes (including those involved with pectin)
68  is consumed by this microorganism using the catabolic enzymes encoded by genes hpdH, hbdH and mmsA.
69  information exists on the quinate/shikimate catabolic enzymes found in these organisms.
70                                           GA catabolic enzymes include GA 2-oxidases that are classif
71 s, type 1 and 2, as well as biosynthetic and catabolic enzymes of the endocannabinoids N-arachidonoyl
72 uggests that coordinate targeting of the Trp catabolic enzymes tryptophan 2,3-dioxygenase (TDO) and I
73 atch a broad specificity of hydroxycinnamate catabolic enzymes while responding to toxic thioester in
74 gulated expression of genes for sphingolipid catabolic enzymes, pointing to additional mechanisms for
75   Dioxane metabolism can be initiated by two catabolic enzymes, propane monooxygenase (PRM) and tetra
76 gnalling, leading to subsequent induction of catabolic enzymes.
77 rgely layered structure consisting of mostly catabolic enzymes; (iii) an anabolic module with a simil
78               Treatment with P15-1 decreased catabolic events and stimulated anabolic events in artic
79  with HMWHA was more effective in inhibiting catabolic events and stimulating anabolic events than P1
80                                It stimulates catabolic events in articular chondrocytes and prevents
81 gest that P15-1 together with HMWHA inhibits catabolic events in articular chondrocytes via the inhib
82  identification of novel factors that reduce catabolic events in chondrocytes and enhances chondrogen
83 nflammatory properties of HMWHA and decrease catabolic events in interleukin-1beta (IL-1beta)-treated
84 , it can be presumed that PRF suppresses the catabolic events that are caused by osteoclastic bone re
85 ase expression of cytokines, chemokines, and catabolic factors that damage synovial tissues and can a
86 chanistic explanation for how increased BCAA catabolic flux can cause diabetes.
87 chondrial bioenergetics, biogenesis and fuel catabolic functions are distinct in cells harboring low
88 naling inhibits inflammatory stimuli-induced catabolic gene expression in human articular chondrocyte
89  triterpenoid biosynthetic and glucosinolate catabolic genes are up-regulated in jazQ independently o
90 hich controls the expression of many ectoine catabolic genes clusters.
91 mediation by flooding local populations with catabolic genes for petroleum hydrocarbon degradation.
92                                              Catabolic genes related to ECM degeneration were promote
93  in coordinated up-regulation of chlorophyll catabolic genes, impairment of chloroplast biogenesis, a
94 ulates the expression of multiple methionine catabolic genes, including SAM synthetase (Sam-S), as we
95            RNaseq identified eight candidate catabolic genes, sequence similarity networks, and genom
96  and fibrosis and causes activation of lipid catabolic genes.
97 vating C/EBPbeta, which then upregulates key catabolic genes.
98  may lead to relatively relaxed selection on catabolic genes.
99  conserved in diverse fungi that have GlcNAc catabolic genes.
100 ic strain, and the cloning of the riboflavin catabolic genes.
101     We find that S47 cells exhibit decreased catabolic glycolysis but increased use of the pentose ph
102  is a key regulator of autophagy, a critical catabolic homeostasis pathway that involves sequestratio
103  to the substantially elevated levels of the catabolic hormone cortisol.
104    Circulating concentrations of glucagon, a catabolic hormone that affects these metabolic pathways,
105 that Cyp26a1, which encodes a key enzyme for catabolic inactivation of RA required for tight control
106  producing N-gamma-ADABA but not the ectoine catabolic intermediate N-alpha-acetyl-l-2,4-diaminobutyr
107  to identify 3-hydroxyisobutyrate (3-HIB), a catabolic intermediate of the BCAA valine, as a new para
108            3-Hydroxyisobutyrate (3-HIB) is a catabolic intermediate of the BCAA valine.
109 e (C8:0-OH), putative hydrolysis products of catabolic intermediates for alpha-linolenic acid and lin
110 abolic organelles necessary for anabolic and catabolic lipid reactions whose numbers are highly dynam
111           Here, we use E. coli native lysine catabolic machinery for glutarate biosynthesis.
112 P-13, tumor necrosis factor-alpha, and other catabolic marker expression in OA chondrocytes.
113 nhibit ROS production and the suppression of catabolic markers including IL-6, COX-2, iNOS, MMP-3, MM
114                                 Autophagy, a catabolic mechanism for macromolecule and protein recycl
115         Autophagy, self-eating, is a pivotal catabolic mechanism that ensures homeostasis and surviva
116                                 Autophagy, a catabolic mechanism that involves degradation of cellula
117 hagy (hereafter referred to as autophagy), a catabolic membrane trafficking pathway that degrades cel
118 flux into the anabolic pathway and maintains catabolic metabolism for energy production, thus prevent
119 oduce the biological infrastructure, whereas catabolic metabolism generates energy to fuel all biolog
120 ted hyaluronan respond by switching to a pro-catabolic metabolism that includes enhanced production o
121 ls metabolically shift from an ATP-producing catabolic metabolism to a metabolism that supports anabo
122 ic metabolism while increasing oxidative and catabolic metabolism.
123 include the carboxysome for CO2 fixation and catabolic microcompartments found in many pathogenic mic
124 ed within the Staphylococcus aureus arginine-catabolic mobile element (ACME) that we hypothesized fun
125 e leukocidin (PVL), SCCmec IVa, the arginine catabolic mobile element (ACME), and a specific mutation
126 lular metabolic fluxes generally go from the catabolic module to the core for substantial interconver
127 sions among intermediate metabolites; (ii) a catabolic module, with a largely layered structure consi
128  protein regulates the expression of the hca catabolic operon in Acinetobacter and related bacterial
129 on in a transcriptional activator for xylose catabolic operons, either CRP or XylR, and these mutatio
130 eady state response of metabolic regulation (catabolic or anabolic) with respect to structural and in
131 lucose range, eventually making the response catabolic or unresponsive to increasing glucose levels.
132                 The lysosome is an essential catabolic organelle that consumes cellular biomass to re
133                           While evidence for catabolic oxygen respiration was limited to two phylogen
134 lism of Escherichia coli; (iii) the vanillin catabolic pathway (which is the converging point of majo
135  The fact that the genes responsible for the catabolic pathway are separately located on plasmid and
136 al profile after SCI and highlight the lipid catabolic pathway as an important macrophage function th
137 al profile after SCI and highlight the lipid catabolic pathway as an important macrophage function th
138 expression analysis establishes the vanillin catabolic pathway as the major contributor of NAD(P)H sy
139 ations of the first 6 metabolites in the Trp catabolic pathway by LC-MS-MS in the community-based Hor
140                Here we describe the complete catabolic pathway for carrageenans, major cell wall poly
141                                            A catabolic pathway for the enzymatic breakdown of aromati
142                               In contrast, a catabolic pathway for the stereospecific cleavage of bet
143 ish the production of GalOA or the full GalA catabolic pathway in Saccharomyces cerevisiae proved cha
144              Here, we show that the 2,6-DCBA catabolic pathway is unique and differs substantially fr
145 ing-opening lyase is involved in the further catabolic pathway proceeding via pimeloyl-CoA.
146 resistance mechanism in Mtb and an l-leucine catabolic pathway that proceeds via an unprecedented (R)
147 complete genes that encode the conserved IPU catabolic pathway were revealed, based on comparative an
148                         Autophagy is a major catabolic pathway whereby cytoplasmic constituents inclu
149 f the rate-limiting enzyme in the pyrimidine catabolic pathway, dihydropyrimidine dehydrogenase (DPYD
150   In the recently discovered bacterial L-AHG catabolic pathway, L-AHG is first oxidized by a NAD(P)(+
151 unctional comparisons to identify a putative catabolic pathway, thereby distinguishing RV1423 from a
152 ), the first intermediate of the fungal GalA catabolic pathway, which also has interesting properties
153 bioremediation requires knowledge of its BAM-catabolic pathway, which is currently restricted to the
154 ursor metabolite generated in the isoleucine catabolic pathway.
155 nel EcChiP for processing by the glucosamine catabolic pathway.
156 -ascorbate as sole carbon source via a novel catabolic pathway.
157 e hydrolase, the last enzyme in the tyrosine catabolic pathway.
158 e evolutionary scenario of the conserved IPU-catabolic pathway.
159                                The potential catabolic pathway/modification included ring-hydroxylati
160 as investigated in dependence of 2 different catabolic pathways (the Embden-Meyerhof-Parnas or the pe
161 n availability and specific transporters and catabolic pathways activated with increasing aerobiosis.
162                Key enzymes of such anaerobic catabolic pathways are corrinoid and Fe-S cluster-contai
163  of mutations, and that anabolic rather than catabolic pathways are more stringently required, likely
164 el ATP-dependent kinases that participate in catabolic pathways for four-carbon acid sugars.
165  that this pattern is caused by retention of catabolic pathways from the host during plastid secondar
166          Therapeutic interventions targeting catabolic pathways have, however, largely failed to pres
167                 The discovery of cholesterol catabolic pathways in Actinomycetes led us to the hypoth
168                   In analogy to anabolic and catabolic pathways in metabolism, there is mounting evid
169 luding proteins and amino acids; many of the catabolic pathways needed to assimilate these compounds
170   In response to low energy, AMPK stimulates catabolic pathways such as autophagy to enhance energy p
171 ge and understanding of the biosynthetic and catabolic pathways that are relevant to the complex trai
172 es the magnitude of mechanistically distinct catabolic pathways that ensure lysosomal clearance of a
173                 Autophagy refers to a set of catabolic pathways that together facilitate degradation
174 ars and fats can feed into many anabolic and catabolic pathways(1), how our bodies handle nutrients d
175 e converging point of majority of the lignin catabolic pathways) is coupled with the tetrahydrofolate
176  SIRT1 plays in modulating both anabolic and catabolic pathways, allow us to propose the hypothesis t
177  by oral microbes, specifically via arginine catabolic pathways, is an essential factor in maintainin
178 glycolysis, while memory T (TM) cells engage catabolic pathways, like fatty acid oxidation (FAO).
179 vating biosynthetic pathways and suppressing catabolic pathways, particularly that of macroautophagy.
180 sis is achieved via complex biosynthetic and catabolic pathways, whose exact activities remain to be
181 s during starvation and judiciously activate catabolic pathways.
182 ordinated activation of several anabolic and catabolic pathways.
183 cells that is tightly linked to anabolic and catabolic pathways.
184 spiration or limitations in uptake rates and catabolic pathways.
185 m muscle wasting due to a blockade in muscle catabolic pathways.
186 uster biosynthesis, transporters, as well as catabolic pathways.
187 sis is achieved via complex biosynthetic and catabolic pathways.
188 herefore, therapies targeted at reducing the catabolic phenotype may protect against degenerative joi
189 etic modifications that imparts a persistent catabolic phenotype to the FLS, despite their dissociati
190 firmed the presence of distinct anabolic and catabolic phenotypes, and identified differential expres
191 ocean, and is highest in the sediment.s DMSP catabolic potential is present throughout the trench wat
192  A wide range of therapeutics including anti-catabolic, pro-anabolic factors and chemo-attractants th
193 and biological processes, such as transport, catabolic process and small molecule metabolic process,
194                    Autophagy is an essential catabolic process frequently failing in neurodegeneratio
195                     Autophagy is an adaptive catabolic process functioning to promote cell survival i
196 IAA oxidation by DAO1 is the principal auxin catabolic process in Arabidopsis and that localized IAA
197                         Autophagy is a major catabolic process in eukaryotes with a key role in homeo
198 irect lipid sources for autophagy, a central catabolic process in homeostasis and stress response.
199  suggest that SIRT1 could be involved in the catabolic process of hypertrophy.
200  that LRRK2 can act to regulate the cellular catabolic process of macroautophagy, although the precis
201                Autophagy is an intracellular catabolic process prominent in starvation, aging and dis
202 utophagy ("autophagy") is the main lysosomal catabolic process that becomes activated under nutrient-
203 s a fundamental and evolutionarily conserved catabolic process that eradicates damaged and aging macr
204                    Autophagy is a multistage catabolic process that mediates stress responses.
205 ion in autophagy, an intracellular lysosomal catabolic process that regulates protein homeostasis and
206                               Autophagy is a catabolic process through which cytoplasmic components a
207                               Autophagy is a catabolic process whereby cytoplasmic components are deg
208 croenvironment and can activate autophagy, a catabolic process which provides nutrients during starva
209                     Selective autophagy is a catabolic process with which cellular material is specif
210 ic process, negative regulations of cellular catabolic process, and regulation of cellular protein lo
211              Autophagy, a membrane-dependent catabolic process, ensures survival of aging cells and d
212 nalling pathway, ubiquitin-dependent protein catabolic process, ion transport, abiotic and biotic str
213 teasome-mediated ubiquitin-dependent protein catabolic process, negative regulations of cellular cata
214 folding, response to stress, single-organism catabolic process, regulation of peptidase activity, and
215 calization to execute multiple steps in this catabolic process.
216 ains how CDK4 promotes anabolism by blocking catabolic processes (FAO) that are activated by AMPK.
217 on feedback loop that separates anabolic and catabolic processes across the Earth's 24-h light-dark c
218 , two proteins involved in mitochondrial RNA catabolic processes and both negatively correlated with
219 c intermediate acetyl-CoA links anabolic and catabolic processes and coordinates metabolism with cell
220 rocal effect of methotrexate on anabolic and catabolic processes and implicate AMPK activation as a m
221                                          The catabolic processes are strongly modified by the lipid c
222 onal protein targeting to membrane, and mRNA catabolic processes are the top biologic processes respo
223 al leaf senescence, mitochondria orchestrate catabolic processes by becoming increasingly central ene
224 WNT/beta-catenin signaling is a regulator of catabolic processes in cancer cells, which varies depend
225 reased expression of VEGF is associated with catabolic processes in chondrocytes and synovial cells.
226                 mTORC1 controls anabolic and catabolic processes in response to nutrients through the
227                     It balances anabolic and catabolic processes in response to nutrients, growth fac
228 cancers, their global impact on anabolic and catabolic processes remains unclear.
229 five protein complexes, utilizes energy from catabolic processes to synthesize ATP.
230 Strikingly, a strong upregulation of various catabolic processes was observed in the absence of autop
231                       Atrophy occurs through catabolic processes, namely the induction of autophagy,
232 mported amino acids in protein synthesis and catabolic processes.
233 ic processes and promoting energy-generating catabolic processes.
234 oordinates nutrient inputs with anabolic and catabolic processes.
235 ronment and the control of most anabolic and catabolic processes.
236 membrane-bound organelles mainly involved in catabolic processes.
237 tasis by suppressing anabolic and activating catabolic processes.
238 chondrial biogenesis and an increase in some catabolic processes.
239 notype and an imbalance between anabolic and catabolic processes.
240 raminidases 3 and 4, play important roles in catabolic processing of brain gangliosides by cleaving t
241 lism, lipid and fatty acid processing, lipid catabolic processing, and lipid localization.
242 g brain, and an increase in H(13)CO(3)(-), a catabolic product of KIC through the mitochondrial BCKDC
243               In addition, BCAAs and various catabolic products act as signaling molecules, activatin
244  show that at least three separate potential catabolic products of allyl-GSL or closely related compo
245 tential to form bioactive GAs in addition to catabolic products.
246                          The community-level catabolic profiles showed that the highest number of car
247     Faulty execution of lysosomal growth and catabolic programmes drives cancer, neurodegeneration an
248                                        A new catabolic property of Rhodotorula mucilaginosa (NCYC 65)
249 in the urea kinetic-based normalized protein catabolic rate (nPCR), an indicator of protein intake in
250 eatures that enable their persistence at low catabolic rates for millions of years, remain unknown.
251 th misleading information on how to quantify catabolic reaction energetics.
252 ling processes from dominance by anabolic to catabolic reaction processes.
253           We identified a novel mechanism of catabolic reaction where TWIST1 up-regulates MMP3 expres
254 ates to determine the energy yields of other catabolic reactions at environmentally relevant conditio
255 ses and the stimulation of energy-generating catabolic reactions by transcriptional reprogramming and
256 ules, which mediate hundreds of anabolic and catabolic reactions including energy metabolism.
257 ssure and chemical composition for microbial catabolic reactions, including a discussion of the effec
258 se phosphate pathway, favoring anabolic over catabolic reactions.
259            Macroautophagy/autophagy is a key catabolic recycling pathway that requires fine-tuned reg
260                                 Autophagy, a catabolic recycling process, has been implicated as a cr
261 review, we summarize current knowledge about catabolic reductive dehalogenases and the electron trans
262                                        While catabolic remodeling aligned with a microbiota dominated
263 4 host gene expression profiles, among which catabolic remodeling, associated with high expression of
264 atrix synthesis or degradation (anabolic and catabolic remodeling, respectively) was quantified by re
265                                              Catabolic remodelling of the cell surface trehalose myco
266 e utility of these tools by examining ADP1's catabolic repression regulation, creating a strain with
267  fructose, in addition to being under carbon catabolic repression.
268 CM)-treated C2C12 myotubes underwent a rapid catabolic response in a TLR4-dependent manner, including
269 by SGs indicates a role in IL-1beta-mediated catabolic response that could be therapeutically targete
270 en AKT and PDE3 is responsible for efficient catabolic response under low glucose condition; the cros
271 nduced activation of the C/EBPbeta-dependent catabolic response, which included upregulation of E3 li
272 f AM-ADSCs was more pronounced in preventing catabolic responses in activated chondrocytes.
273 ng nutrient stress-induced overactivation of catabolic responses in brown adipocytes.
274 tory, the immunosuppressive, and the protein catabolic responses individually, successful treatment o
275 SCs, AM hydrogels and AM-ADSCs inhibited the catabolic responses of IL-1beta and inhibited the Wnt/be
276 tic effect of AM with ADSC in preventing the catabolic responses of inflammation in stimulated chondr
277 tiated by age-related shifts in anabolic and catabolic responses that control bone homeostasis.
278                Deficiencies in several sugar catabolic routes were supported by severe retardation of
279 (PCM) around chondrocytes thereby decreasing catabolic signaling.
280                            The regulation of catabolic signalling via forkhead box O 1 and protein ub
281 composition, protein synthesis, anabolic and catabolic signalling, mitochondrial phenotype and gene e
282 as nonadecaneuropeptide (NDN) in response to catabolic signals.
283 e availability, resident species with a high catabolic similarity with the invader efficiently reduce
284 biquitination and proteasomal degradation, a catabolic source of asparagine.
285 c changes consistent with the induction of a catabolic state that was not rescued by inositol supplem
286 ficiency and uncontrolled diabetes lead to a catabolic state with decreased muscle strength, contribu
287 RNA methylation captured cells in a distinct catabolic state.
288 of events that maintains or prolongs the pro-catabolic state.
289 ays, shifting cartilage homeostasis toward a catabolic state.
290            They are widely known as terminal catabolic stations that rid cells of waste products and
291 (HX), and gelsolin (GSN), and tested against catabolic stimulation for their effects on glycosaminogl
292 n of a Microbacterium maritypicum riboflavin catabolic strain, and the cloning of the riboflavin cata
293                                              Catabolic stress can lead to changes in circulating acet
294 dings indicate that analytes associated with catabolic stress were altered in infants with HIE; howev
295 bserved activity within a complex eukaryotic catabolic system remains one of the most significant cha
296 opose that, by determining the fate of these catabolic systems, this hierarchical switch regulates th
297 hese responses were also linked to decreased catabolic (TNF-alpha, TWEAK/Fn14 axis; FOXO-1, Atrogin-1
298 ent signals to promote a transformation from catabolic to anabolic metabolism, cell growth, and cell
299 hich critically contributes to the supply of catabolic uridine and the generation of purine-2',3'-cyc
300 ible for ensuring ultrasensitive response in catabolic zone (glucose <4.5 mmol); the crosstalk betwee

 
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