ライフサイエンスコーパス: catabolism

1 ikely due to reduced need for fuel substrate catabolism.

2 te dehydrogenase complex (OADHc) in l-lysine catabolism.

3 eavage pathway responsible for 4-alkylphenol catabolism.

4 osynthesis during daylight to fuel nighttime catabolism.

5 osphatidylcholine utilization and fatty acid catabolism.

6 kynurenine (Kyn) pathway of tryptophan (Trp) catabolism.

7 way, Rv2498c, also participates in l-leucine catabolism.

8 as ADO deaminase, the enzyme involved in ADO catabolism.

9 e muscle attenuated LLC tumor-induced muscle catabolism.

10 to a better understanding of bacterial DMSP catabolism.

11 and intestine have roles in alpha-tocopherol catabolism.

12 es like Nuh, an enzyme involved in adenosine catabolism.

13 abundances for substrate uptake and initial catabolism.

14 d expression of genes involved in fatty acid catabolism.

15 t controls the balance between anabolism and catabolism.

16 in autophagy-lysosomal biogenesis and lipid catabolism.

17 ng of biochemical reactions involved in BCAA catabolism.

18 ation by reducing and/or counteracting their catabolism.

19 and transduction, metabolism, transport and catabolism.

20 anaerobic acetogenesis was central to their catabolism.

21 armacokinetic properties, particularly their catabolism.

22 ins, particularly LDL, by accelerating their catabolism.

23 derived from an intermediate of l-isoleucine catabolism.

24 egulates bile acid synthesis, transport, and catabolism.

25 enesis, fatty acid synthesis, and amino acid catabolism.

26 inflammatory milieu also stimulates protein catabolism.

27 l of energy resources via autophagy-mediated catabolism.

28 300 play pivotal roles in cell anabolism and catabolism.

29 hat both participate in MG resistance and MG catabolism.

30 counter CKD-induced abnormal muscle protein catabolism.

31 c acid (TCA) cycle, and amino acid synthesis/catabolism.

32 rbon catabolism flux redirection to tyrosine catabolism.

33 g membrane potential and accelerated protein catabolism.

34 olve the glucose-PTS or glucokinase in their catabolism.

35 phenotypes consistent with disrupted lysine catabolism.

36 rd glycolysis, glutaminolysis and methionine catabolism.

37 the brain, which drives anorexia and muscle catabolism.

38 istent with the enzyme disrupting fatty acid catabolism.

39 of peptides but has no effect on amino acid catabolism.

40 d its enzymatic activity in poly(ADP-ribose) catabolism.

41 with the subsequent reduction of fatty acid catabolism.

42 al substituted THIQs derived from amino acid catabolism.

43 VEN4, like human SAMHD1, is involved in dNTP catabolism.

44 cytokine, and the down-modulatory tryptophan catabolism.

45 el the core of ectoine and 5-hydroxy-ectoine catabolisms.

46 hree emergent co-culture properties: ethanol catabolism, a distinct volatile profile, and yeast popul

47 egulation, chromatin remodelling and protein catabolism according to Gene Ontology; and highlight the

48 e molecular mechanisms of 2,7-anhydro-Neu5Ac catabolism across bacterial species and a novel sialic a

49 -imaging techniques report glucose uptake or catabolism activity, yet do not trace the functional uti

50 T1) is the rate-limiting enzyme in polyamine catabolism and a primary genetic risk factor for suicida

51 Deletion of hepatocyte Bcl6 enhances lipid catabolism and ameliorates high-fat-diet-induced steatos

52 excess fatty acids (FAs) in perturbing BCAA catabolism and BCKA availability merits investigation.

53 on of chronic kidney disease, causes protein catabolism and bone demineralisation and is associated w

54 isk of disease progression and causes muscle catabolism and bone resorption.

55 nregulated while those associated with lipid catabolism and chitin turnover were significantly upregu

56 ion by heat of genes involved in chlorophyll catabolism and chloroplast protein turnover were subdued

57 study of Mtb enzymes initiating cholesterol catabolism and demonstrated their interrelation with hum

58 l conserved with plants, the pathways of TAG catabolism and downstream fatty acid beta-oxidation have

59 dissect the relationship between methionine catabolism and epigenetic regulation by SIN3, we sought

60 n of BCKAs is an indicator of defective BCAA catabolism and has been correlated with glucose intolera

61 nd rate-limiting step of branched amino acid catabolism and implicated in maple syrup urine disease,

62 R-276 prolongs high rates of amino acid (AA) catabolism and increases female fertility, suggesting th

63 shrinkage, consistent with enhanced protein catabolism and mitochondrial abnormalities.

64 sosomal and autophagic systems ensures basal catabolism and normal cell physiology, and failure of ei

65 in stressed cells by promoting intracellular catabolism and nutrient recycling.

66 the critical role of lysosomes in hepatic LD catabolism and provides insights into the mechanisms und

67 o cells in vivo, exhibit decreased glutamine catabolism and reduced reliance on glutamine anaplerosis

68 demonstrates that FIS1 mediates gibberellin catabolism and regulates fruit firmness, and it offers a

69 lly suppressed markers of hepatic amino acid catabolism and reversed the illness-induced hypoaminoaci

70 dicates that switching to a more specialized catabolism and scavenging lifestyle in the host allows f

71 in the expression of cytokinin biosynthesis, catabolism and signaling genes in response to infection

72 odern breeding on loci controlling raffinose catabolism and sugar transport.

73 moter region of genes involved in methionine catabolism and that this binding affects histone modific

74 PAI-1 concentrations and decreasing AT BCAA catabolism and thereby increasing plasma BCAA concentrat

75 bits de novo lipid synthesis, promotes lipid catabolism and thermogenesis, and protects against diet-

76 LBL also repressed limonene catabolism and triggered phenylpropanoid derivatives-rel

77 ATP levels, as a result of increased purine catabolism and urea cycle pathways.

78 n tumor cells abrogates tumor-induced muscle catabolism and wasting in cultured myotubes and in mice.

79 y genes, including some in ABA biosynthesis, catabolism and/or signalling, only ABA INSENSITIVE 3 is

80 sy1 amino acid sensor (amino acid uptake and catabolism) and partly Ssy1 independent (genes associate

81 sel acids (byproducts of aromatic amino acid catabolism) and this role is shared with at least one ad

82 pling, but instead is coupled with ascorbate catabolism, and controls the synthesis of the moss cutic

83 nergy use; lipid droplet assembly, lipolytic catabolism, and fatty acid compartmentalization; and ver

84 is linked with bone demineralization, muscle catabolism, and higher risks of CKD progression and mort

85 intake, increased energy expenditure, excess catabolism, and inflammation.

86 drolase (FAH) is the last enzyme in tyrosine catabolism, and mutations in the FAH gene are associated

87 associated with significant weight loss and catabolism, and negatively impacts quality of life (QL).

88 abolism and autophagy-mediated macromolecule catabolism; and (iii) activation of catabolism serves as

89 ism, fatty acid beta-oxidation, phospholipid catabolism, arachidonic acid and linoleic acid metabolis

90 However, the molecular determinants of its catabolism are poorly understood.

91 athways for endogenous H(2) S generation and catabolism are present in fASM, and are differentially s

92 es cerevisiae), in which polyP anabolism and catabolism are well-characterized.

93 bolism has been studied intensively, but its catabolism as a potentially important mechanism for the

94 , which may have implications in artemisinin catabolism as well as lignification in A. annua.

95 , which may have implications in artemisinin catabolism as well as lignification.

96 in skeletal muscle, supported by kynurenine catabolism, as part of the adaptations to endurance exer

97 s express the machinery for DA synthesis and catabolism, as well as all five DA receptors.

98 e to different stimuli modulating amino acid catabolism, as were cytokine secretion levels and regula

99 l-lysine, l-hydroxylysine, and l-tryptophan catabolism, associated with clinical presentations such

100 We also calculate DeltaG(r) for five example catabolisms at specific environmental conditions: aerobi

101 In turn, a BAT-specific defect in BCAA catabolism attenuates systemic BCAA clearance, BAT fuel

102 Despite intensive study, plant lysine catabolism beyond the 2-oxoadipate (2OA) intermediate re

103 poration into lignin polymers (synthesis) or catabolism (bioconversion), with both passive and transp

104 pes hadrus that encodes a composite inositol catabolism-butyrate biosynthesis pathway, the presence o

105 Further, Hsp70 and Hsp90 induce muscle catabolism by activating TLR4, and are responsible for e

106 ing insight into the mechanism of host lipid catabolism by an M. tuberculosis enzyme, augmenting our

107 r in brown adipocytes appears to drive lipid catabolism by promoting FoxO1 deacetylation independentl

108 and control the switch between anabolism and catabolism by regulating lysosomal biogenesis and autoph

109 results indicate that AHL4 suppresses lipid catabolism by repressing the expression of specific gene

110 Tryptophan catabolism by the enzymes indoleamine 2,3-dioxygenase 1

111 unds, a peptide antibiotic, and carbohydrate catabolism by using either mono-cultures or co-cultures.

112 t FF infants had higher levels of amino acid catabolism by-products and a low efficiency of amino aci

113 nformation generated during normal beta-cell catabolism can be delivered to the resident macrophage a

114 th biosynthesis, carbohydrate metabolism and catabolism, cellular protein modification, and response

115 dated computational model of heart's central catabolism, comprising glucose and fatty acid (FA) oxida

116 Here, we review evidence that Trp and Arg catabolism contributes to inflammatory processes that pr

117 rsisting inflammation, immunosuppression and catabolism contributes to many of these adverse clinical

118 ults indicate that branched-chain amino acid catabolism contributes to TAG metabolism by providing ca

119 othesis that if enzymes enabling cholesterol catabolism could be genetically engineered and introduce

120 y, we determined whether disruption of Abeta catabolism could trigger Abeta aggregation within neuron

121 nflammatory processes, including vitamin B-6 catabolism, could explain such findings.We investigated

122 E) synthesis, and to a moderate induction of catabolism (CsCYP707A, an ABA 8'-hydroxylase) and buildu

123 cessary and sufficient to increase glutamine catabolism, defining important determinants of glutamine

124 As it progresses, the massive macromolecular catabolism dismantles the chloroplasts and, consequently

125 This study investigated sucrose catabolism during cold-induced sweetening (CIS) and its

126 demonstrate that p16 represses hepatic lipid catabolism during fasting and may thus participate in th

127 siology (e.g. coordination of carbon uptake, catabolism, energy and redox production, and growth), wh

128 a HglS homolog coexpresses with known lysine catabolism enzymes, and mutants show phenotypes consiste

129 f lysosomal proteins, including sphingolipid catabolism enzymes, to the Golgi compartment, which may

130 Heme catabolism exerts physiological functions that impact he

131 effective detoxification system for acylate catabolism exists in DMSP-catabolizing Roseobacters.

132 ow that two different pathways for coumarate catabolism failed to function when initially transferred

133 of endogenous tyrosol through central carbon catabolism flux redirection to tyrosine catabolism.

134 rease in mitochondrial glucose and glutamine catabolism from generating damaging reactive oxygen spec

135 greater variety of pathways for carbohydrate catabolism, further illustrating temporal patterns of en

136 agenomes revealed enriched protein and mucin catabolism genes and depleted carbohydrate degradation g

137 Validated and predicted protein catabolism genes identified include a combination of est

138 Contemporaneous expression of sulfonate catabolism genes in heterotrophic bacteria highlights ac

139 l regulation of chlorophyll biosynthesis and catabolism genes.

140 However, L-serine catabolism has a minimal effect on its fitness in the he

141 Amino acid catabolism has been implicated in immunoregulatory mecha

142 ed lignin in plants, no pathway for syringol catabolism has been reported to date.

143 SAT1), the rate-limiting enzyme in polyamine catabolism, has broad regulatory roles due to near ubiqu

144 Yet, the genetics and structure of LA catabolism have remained unknown.

145 Strategies to counter sustained catabolism have therapeutic rationale.

146 1,2-dioxygenase the intermediary in tyrosine catabolism homogentisate accumulates and undergoes nonen

147 activity of enzymes involved in Trp and Arg catabolism (IDO1, IDO2, Trp 2,3-dioxygenase [TDO], argin

148 ncluded 3 transcripts involved in tryptophan catabolism (IDO1, KMO, KYNU) that play a pivotal role in

149 nockout of CEACAM6 alters ECM-cell adhesion, catabolism, immune environment, transmembrane transport

150 at in pericentral hepatocytes) and glutamine catabolism in (periportal) hepatocytes represents the hi

151 erase, we demonstrate that purine nucleotide catabolism in Arabidopsis (Arabidopsis thaliana) mainly

152 Mechanistically, active BCAA catabolism in BAT is mediated by SLC25A44, which transpo

153 erization of their pharmacokinetics (PK) and catabolism in both preclinical and clinical settings.

154 1 gene essential for reactive oxygen species catabolism in brain mitochondria, recapitulates these de

155 Mechanistically, glucose catabolism in CDCP1+ CSCs is routed to the oxidative pen

156 Fluxome calculations of central catabolism in diabetic hearts show that, in the presence

157 ays, we demonstrated that 2,7-anhydro-Neu5Ac catabolism in E. coli depended on YjhC and on the predic

158 e conducts the majority of regulated protein catabolism in eukaryotes.

159 Lipid catabolism in germinating seeds provides energy and subs

160 Lipid droplet (LD) catabolism in hepatocytes is mediated by a combination o

161 acid is a final breakdown product of purine catabolism in humans.

162 ata demonstrate that disruption of normal HA catabolism in Hyal2(-/-) mice causes increased HA, which

163 thereby the uric acid (UA) pathway of purine catabolism in macrophages, and pharmacologic targeting o

164 of rapamycin, suggesting reduced amino acid catabolism in MS patients.

165 Here, we report a critical role for proline catabolism in non-small cell lung cancer (NSCLC).

166 Prolongation of AA catabolism in P. falciparum-infected females also compro

167 trate increases glucose uptake and oxidative catabolism in primary adipocytes and white adipose tissu

168 sterol, the primary mechanism of cholesterol catabolism in the brain.

169 to describe compounds arising from microbial catabolism in the gastrointestinal tract.

170 Processes that induce Trp and Arg catabolism in the TME remain incompletely defined.

171 ation pathway to ensure DMSP functioning and catabolism in their cells.

172 balance of lipid metabolism, conversion, and catabolism in this study.

173 e-mediated enhancement of glucose uptake and catabolism in white adipose tissue may be a key contribu

174 ith the expression of genes involved in BCAA catabolism, in conjunction with an inverse relationship

175 nase (IDO), an enzyme involved in tryptophan catabolism, in macrophages and in the lungs of animals (

176 of transmethylation and polyamine synthesis/catabolism, including abnormalities in neurotransmitter

177 ated spermatogonia enriched for SSCs exhibit catabolism-independent RA insensitivity.

178 This was supported by an altered heme catabolism, indirectly reflecting in elevated unconjugat

179 rs that influence their production rates and catabolism inside the phagosome.

180 n that results from the shunting of arginine catabolism into alternative nitrogen repositories.

181 rate that mIL-6 promotes nutrient uptake and catabolism into myofibers during exercise in an osteocal

182 Human vitamin E (alpha-tocopherol) catabolism is a mechanism for regulating whole-body alph

183 In this study, we provide evidence that HA catabolism is disrupted in human intestinal microvascula

184 es robust evidence that increased vitamin B6 catabolism is independently associated with a higher ris

185 and often rate-limiting reaction in aromatic catabolism is O-aryl-demethylation of the abundant aroma

186 well understood, our understanding of their catabolism is only rudimentary.

187 the leucine infusion study indicate that KIC catabolism is upregulated through BCAT/BCKDC and further

188 tonia, PDE10A, a key enzyme in cAMP and cGMP catabolism, is downregulated in striatal projections to

189 GL) is involved in branched-chain amino acid catabolism leading to acetyl-CoA production.

190 protein biosynthesis and decrease in protein catabolism likely contribute to the attenuation of disus

191 glutaminase, the initial enzyme in glutamine catabolism, markedly blunts angiogenesis.

192 Therefore, new therapies that suppress heme catabolism may be beneficial in ameliorating the anemia

193 n of Th cell growth by SF through tryptophan catabolism may play an important role in preventing inap

194 rivation, HIF-1 activation down-modulates LD catabolism mediated by adipose triglyceride lipase (ATGL

195 ression of gene expression related to purine catabolism, methionine and S-adenosylmethionine biosynth

196 if this is due to increased muscular protein catabolism, obesity, and/or increased insulin resistance

197 nterest as a potential contributor to muscle catabolism observed with exposure to hypoxia at altitude

198 ues and measured fatty acid oxidation by the catabolism of (14)C-labeled palmitate to (14)CO(2).

199 A) are the key enzymes for the synthesis and catabolism of 5HT, respectively.

200 bioanalytical characterization of the PK and catabolism of a novel ADC.

201 e approaches include increasing or rerouting catabolism of alternative fuel sources to supplement the

202 generation of ADO depends on the sequential catabolism of ATP by two ecto-nucleotidases, CD39 (ATP -

203 n of unsaturated esters arising from partial catabolism of branched chain amino-acids.

204 tabolomics analysis revealed a defect in the catabolism of branched-chain amino acids in bkdE1alpha F

205 ctions driven by AMP deaminase 3 (Ampd3) and catabolism of branched-chain amino acids.

206 ol "housekeeping" enzyme responsible for the catabolism of canonical and noncanonical nucleoside trip

207 The presented platform combines the natural catabolism of charged amino acids with a catalytically e

208 siologically compatible bacteria, processive catabolism of complex substrates, and unidirectional int

209 ransferase (COMT) gene result in a different catabolism of dopamine in the PFC.

210 ed that soluble decorin evokes intracellular catabolism of endothelial VEGFA that is mechanistically

211 unts of heme released during the proteolytic catabolism of erythrocytic hemoglobin.

212 Microcompartment-mediated catabolism of ethanolamine, a host cell breakdown produc

213 ctivated receptor (PPAR)-alpha signaling and catabolism of fatty acids (FAs) when simultaneously subj

214 Catabolism of fatty acids stored in oil bodies is essent

215 wnregulated genes contribute to the cellular catabolism of glucose, amino acids and fatty acids.

216 In hyperoxia, anaplerotic catabolism of glutamine by Muller cells increased ammoni

217 nsmitter) produced endogenously by oxidative catabolism of heme, and the understanding of its spatial

218 evasion, and escape, while the importance of catabolism of host-derived proteins and peptides in vivo

219 ient metabolic networks for biosynthesis and catabolism of hydroxy-containing TAG.

220 In contrast, Akt suppresses lysosomal catabolism of ingested proteins when free amino acids ar

221 red for autophagosome- and lysosome-mediated catabolism of intracellular lipid droplets to impede the

222 en together, this work supports OMV-mediated catabolism of lignin-derived aromatic compounds as an ex

223 roxisomes is necessary for the synthesis and catabolism of lipids, the trafficking of cholesterol, an

224 dulating synaptic transmission by uptake and catabolism of major neurotransmitters.

225 way is unique and differs substantially from catabolism of other chlorobenzoates.

226 ine hydroxylase (PAH) is a key enzyme in the catabolism of phenylalanine, and mutations in this enzym

227 recently fixed carbon through the uptake and catabolism of phytoplankton metabolites.

228 de novo biosynthesis during infection and/or catabolism of preexisting host cell biomass, and the rel

229 we described a missing step in the D-lysine catabolism of Pseudomonas putida in which 2OA is convert

230 bsorption, phase II metabolism and microbial catabolism of quercetin-3-O-sophoroside, compared to tha

231 ent of cholesterol, 2) increased cancer cell catabolism of sphingomyelins to ceramide derivatives and

232 t behavior (sweet taste perception) and oral catabolism of sugar.

233 ies are hereditary disorders that affect the catabolism of sulfur-containing amino acids.

234 Elevated catabolism of the amino acids tryptophan (Trp) and argin

235 Emerging related forms of intracellular catabolism of the ER or contents, including ER-phagy by

236 Differential catabolism of the intravenous d6-alpha-tocopherol and or

237 The last step in the catabolism of the most abundant protein in pBM, collagen

238 les of subjects dosed with MEDI3726 revealed catabolism of the protein scaffold manifested by the mor

239 involved in degradation of arabinoxylan and catabolism of the released l-arabinose and d-xylose.

240 ysis is a metabolic pathway dedicated to the catabolism of the sulfosugar sulfoquinovose (SQ) into sm

241 phoryl transfer enzyme required for complete catabolism of trehalose and maltose, through the isomeri

242 is an enzymatic pathway responsible for the catabolism of triglycerides (TGs) that is complemented b

243 anch chain amino acids (BCAAs) and increased catabolism of tryptophan to the active kynurenine metabo

244 o ligands that are products of the microbial catabolism of tryptophan.

245 ombospondin motifs) family contribute to the catabolism of vascular proteoglycans.

246 irmed that mutants deficient in ethanolamine catabolism or in the type VII secretion system were atte

247 rt regulation mechanism in lignin synthesis, catabolism, or bioconversion requiring compound function

248 ss results in major physiological and carbon catabolism pathway changes, including an 80% reduction i

249 pecies and a novel sialic acid transport and catabolism pathway in E. coli.

250 strain that natively contains this coumarate catabolism pathway, Acinetobacter baumannii, is resistan

251 DH7A1 gene leading to blockade of the lysine catabolism pathway.

252 wledge of the role branched-chain amino acid catabolism plays in seed development and amino acid home

253 modulators of fatty acid synthesis (FAS) and catabolism (PPARalpha and CPT1)), hepatocellular injury

254 Catabolism, primarily in the lungs and secondarily syste

255 A subset of indole derivatives of tryptophan catabolism produced by E. tarda and other gut microbes a

256 evious studies show that aberrant tryptophan catabolism reduces maternal immune tolerance and adverse

257 l proteins linked to autophagy and lysosomal catabolism reflecting vesicular transport obstruction an

258 titutive mTORC1 signaling maintain lysosomal catabolism remain to be elucidated.

259 er, the spatiotemporal mechanisms for lignin catabolism remain unclear.

260 are best described as foam cells, with lipid catabolism representing the main biological process, and

261 ty, suggesting that timely termination of AA catabolism restricts mosquito investment into reproducti

262 uscle fuel metabolism that increases protein catabolism, resulting in exercise intolerance, muscle we

263 owed enrichment in proteins involved in BCAA catabolism, ROS metabolism, vesicle trafficking, and lip

264 molecule catabolism; and (iii) activation of catabolism serves as the mandatory switch and the drivin

265 ession of rate-limiting enzymes in polyamine catabolism (SMOX, SSAT) and depleted cellular natural po

266 r in AD, p < 0.001); (3) polyamine synthesis/catabolism (spermidine: higher in AD, p = 0.004); (4) ur

267 levels of metabolites involved in glutamine catabolism, such as glutamic acid, alanine, glycine, pyr

268 ersistent inflammation-immunosuppression and catabolism syndrome may require a more complementary app

269 sistent inflammation, immunosuppression, and catabolism syndrome observed in adult human surgical sep

270 ersistent inflammation-immunosuppression and catabolism syndrome," and it is proposed here that this

271 brosis, and branched-chain amino acid (BCAA) catabolism; systemic markers of inflammation; and plasma

272 ead to an altered model of purine nucleotide catabolism that includes an NSH heterocomplex as a centr

273 the autophagic process participates in lipid catabolism that supports OxPHOS in AML cells.

274 ma-, burn-, or cancer-induced hypermetabolic catabolism, the mediators are essentially unknown.

275 Without glutamine catabolism, there is near complete loss of TCA intermedi

276 Both inputs promote catabolism through bulk autophagy, but result in distinc

277 TOR complex 1 (TORC1) between anabolism and catabolism, thus controlling lifespan, development and a

278 diazotrophic bacteria tailor central carbon catabolism to accommodate the energy requirement for nit

279 Conversely, Utx deficiency skews lipid catabolism to enhance cholesterol/steroid hormone produc

280 ve shown that C. albicans co-opts amino acid catabolism to generate and excrete ammonia, which raises

281 n of the metabolic inputs that couple carbon catabolism to oxidative phosphorylation is a primary cau

282 ial intermediate of the proline and arginine catabolism, to glutamate.

283 directly or indirectly, to compromised sugar catabolism, to glycogen accumulation, and to distorted c

284 -released cachexins directly activate muscle catabolism via activating TLR4 on muscle cells independe

285 e-like mechanism combining lysine export and catabolism via aminoadipate.

286 orts previous studies that infer phosphonate catabolism via C-P lyase is an important adaptive strate

287 olism was assessed by the levels of arginine catabolism via the arginine deiminase pathway (ADS), aci

288 Catabolism was nevertheless more extensive for the nativ

289 sence of 0.25 M exogenous sucrose, increased catabolism was observed with increased concentrations of

290 elements (MGEs) previously linked to linuron catabolism were enriched in the heavy DNA-SIP fractions,

291 lyamine oxidase, a gene related to polyamine catabolism, when plants were exposed to Cd.

292 circulating IGF-I, but prednisolone induces catabolism, whereas infliximab may promote protein synth

293 e pentose phosphate pathway (PPP) for hexose catabolism, whereas species from the second group use mo

294 ketogenesis and glucocorticoid-driven muscle catabolism, which are prevented by increasing food intak

295 s, phenylacetate and gamma-aminobutyric acid catabolism, which were found to be important for resisti

296 les and up-regulated genes involved in lipid catabolism, while decreasing 241 exercise-responsive gen

297 Predation risk caused upregulation of lipid catabolism with high food, and downregulation with low f

298 nterpretation regarding dynamic synthesis or catabolism within metabolite pools.

299 d up-regulated markers of hepatic amino acid catabolism without affecting muscle wasting.

300 ly accepted model of plant purine nucleotide catabolism, xanthine can be generated in various ways in