ライフサイエンスコーパス: catabolism

1 and seed development was limited to leucine catabolism.

2 e as a coactivator of epidermal triglyceride catabolism.

3 s, markedly increasing glucose and glutamine catabolism.

4 GI-58) are limiting in cellular triglyceride catabolism.

5 ptake, de novo synthesis, and muscle protein catabolism.

6 ng enhanced potential abilities of microbial catabolism.

7 riptional regulation from stress response to catabolism.

8 bolic processes and environments beyond DMSP catabolism.

9 riggers auxin biosynthesis, conjugation, and catabolism.

10 chondrocyte hypertrophy and cartilage matrix catabolism.

11 he committed enzymatic step in homogentisate catabolism.

12 tabolic phenotype with lactate and glutamine catabolism.

13 proteins implicated in transcription and RNA catabolism.

14 ed cellular FAEE hydrolase activity and FAEE catabolism.

15 function, retinoid metabolism, and nicotine catabolism.

16 acids, reflective of lipid mobilization and catabolism.

17 armacokinetic properties, particularly their catabolism.

18 eads to a metabolic switch from anabolism to catabolism.

19 rFGF1 is independent of its effect on lipid catabolism.

20 ggesting that rFGF1 stimulates hepatic lipid catabolism.

21 gh His and makes Zn bioavailable through His catabolism.

22 rge set of genes responsible for cholesterol catabolism.

23 ins, particularly LDL, by accelerating their catabolism.

24 cterize putative hydrolases involved in FAEE catabolism.

25 compound Torin 2, which inhibits hemoglobin catabolism.

26 HIBCH is unique to valine catabolism.

27 agliflozin raises LDL levels through reduced catabolism.

28 sponsible for the rate-limiting step in BCAA catabolism.

29 genetic evidence for their function in BCAA catabolism.

30 (COMT), regulating catechol neurotransmitter catabolism.

31 ammonia-lyase in the first step of histidine catabolism.

32 derived from an intermediate of l-isoleucine catabolism.

33 than acidifying it, as occurs after dextrose catabolism.

34 ry peroxisomal fat oxidation, and amino acid catabolism.

35 ally ill patients are susceptible to protein catabolism.

36 egulates bile acid synthesis, transport, and catabolism.

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

38 inflammatory milieu also stimulates protein catabolism.

39 and transduction, metabolism, transport and catabolism.

40 as a consequence of increased IR and protein catabolism.

41 e surgical stress response and postoperative catabolism.

42 VC(R)-MMAE catabolite generated by lysosomal catabolism.

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

44 We have shown that amino acid catabolism allows the cell to neutralize the phagolysoso

45 nurenine, a metabolite related to tryptophan catabolism, also impairs memory CD4 T-cell survival and

46 f extracellular matrix degradation, collagen catabolism and angiogenesis in disease progression.

47 This BZR1 pattern requires local BR catabolism and auxin synthesis, as well as BR signaling.

48 directly, in concert with MMPs, in collagen catabolism and clearance and is an important factor in r

49 In livers of mice, FXR regulates amino acid catabolism and detoxification of ammonium via ureagenesi

50 e treated with SnPP exhibited decreased heme catabolism and diminished iron release as well as reduce

51 ta (PPARD) has essential roles in fatty acid catabolism and energy homeostasis as well as cell differ

52 A combined adaptive response of carbon-catabolism and enzyme production to locally available mo

53 cled may have important implications for the catabolism and function of Lp(a).

54 ration and viability, a shift towards matrix catabolism and increased expression of proinflammatory c

55 WNT-induced glutamine catabolism and ISR were beta-catenin independent, but re

56 as heat shock proteins, abscisic acid (ABA) catabolism and its signalling pathway, lipid metabolism

57 ic effects through increased LDL cholesterol catabolism and LDL-derived cholesterol fecal excretion a

58 ng implantation, we directly observe protein catabolism and macropinocytosis in situ by pancreatic ca

59 arrest, likely due to overly rapid galactose catabolism and metabolic overload.

60 factors FOXO3 and TFEB, which enhanced lipid catabolism and Mtb xenophagy.

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

62 signaling, a pathway involved in chondrocyte catabolism and OA.

63 enes involved in amino acid biosynthesis and catabolism and other cellular functions.

64 ule and Platelet Module, related to collagen catabolism and platelet function respectively.

65 l regulation to promote efficient fatty acid catabolism and prevent mitochondrial dysfunction.

66 xtracellular arginase, resulting in arginine catabolism and reduced levels of total brain arginine.

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

68 s mobilized from lean tissues during protein catabolism and results in acute increases in circulating

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

70 ith synaptic vulnerability, including valine catabolism and rho signalling pathways.

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

72 proteolysis, lipolysis and amino acid/lipid catabolism and significantly increases the cheese matura

73 It may be also due to in vivo catabolism and subsequent iodine loss as literature repo

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

75 evidence that the LDLR plays a role in Lp(a) catabolism and that this process can be modulated by PCS

76 apture of electrons generated from substrate catabolism and thus increase substrate-to-product yields

77 polarization was found to activate glutamine catabolism and UDP-GlcNAc-associated modules.

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

79 age-specific lipid metabolism and amino acid catabolism, and a dendritic-cell-specific program of reg

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

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

82 tty acid oxidation and membrane phospholipid catabolism, and impairs recruitment of Akt to the plasma

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

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

85 l of PPARalpha, the genes required for lipid catabolism are transcribed before birth so that the neon

86 while branched-chain amino acid and proline catabolism are very old mitochondrial functions particul

87 enrichment points to differences in protein catabolism as one major source of clock variation in hum

88 1 (Drp1), thus inhibiting insulin and Abeta catabolism as well as hyperactivating mitochondrial fiss

89 muscle wasting by directly activating muscle catabolism as well as stimulating an innate immune respo

90 activity of enzymes involved in Trp and Arg catabolism, as well as to investigate amino acid catabol

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

92 probably not caused by defective pyrimidine catabolism but by the accumulation of pyrimidine catabol

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

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

95 ed to validate the role of FXR in amino acid catabolism by gene expression and metabolomics studies.

96 ophs, mechanisms for how their organotrophic catabolism circumvents thermodynamic restrictions remain

97 ABA synthesis and catabolism, conjugation and deconjugation to glucose, an

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

99 vely, these results indicate that asparagine catabolism contributes to S Typhimurium virulence, provi

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

101 SAT1 is a rate-limiting enzyme in polyamine catabolism critically involved in the conversion of sper

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

103 t strongly induced both ABA biosynthesis and catabolism (CsNCED1, 9-cis-neoxanthin epoxycarotenoid di

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

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

106 atio (PAr), a proposed marker of vitamin B-6 catabolism during activated cellular immunity, as predic

107 Heme, a product of hemoglobin catabolism during certain intracellular pathogen infecti

108 idoxal + PLP), reflects increased vitamin B6 catabolism during inflammation.

109 well as improved metabolic capacity and fuel catabolism during prolonged elevated energy requirements

110 bolism, as well as to investigate amino acid catabolism effects on the immune system of multiple scle

111 Evidence of accelerated DHA catabolism (eg, activation of phospholipases and oxidati

112 ch glycogen synthesis is blocked, and xylose catabolism enabled through the introduction of xylose is

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

114 sion of glutamine transporters and glutamine catabolism enzymes.

115 Heme catabolism exerts physiological functions that impact he

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

117 ritical illness increases hepatic amino acid catabolism, explaining the illness-induced hypoaminoacid

118 Neu5Gc catabolism generates N-glycolylhexosamines, which are po

119 es revealed positive correlations among BCAA catabolism genes in stress, development, diurnal/circadi

120 further characterized one of the chlorophyll catabolism genes, Stay-green (SGR), and demonstrated tha

121 Inositol transporters and catabolism genes, which process sugars present in plants

122 ry chain oxidoreductases from central carbon catabolism (glycolysis and TCA cycle), and was controlle

123 hways in all major branches of biosynthesis, catabolism, gut microbiome activities, and xenobiotics.

124 peared to have stronger effects on liver fat catabolism (Hadh) and synthesis (Fasn) than exercise.

125 Amino acid catabolism has been implicated in immunoregulatory mecha

126 een isolated, the molecular mechanism of IPU catabolism has not been elucidated yet.

127 amine oxidase (hDAO), required for histamine catabolism, has multiple N-glycosylation sites, but thei

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

129 Strategies to counter sustained catabolism have therapeutic rationale.

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

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

132 2 metabolic programming by altering arginine catabolism, impairing polyamine biosynthesis and reducin

133 Further promoting FA catabolism improves the CD8(+) TILs' ability to slow tum

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

135 We show that reduced homogentisate catabolism in a soybean HGO mutant is an effective strat

136 ns revealed unique and specific l-malic acid catabolism in ABSA 1014 that was absent in UPSA 807.

137 proteins resembling enzymes involved in BCAA catabolism in animals, fungi, and bacteria as well as pr

138 y is the major route of L-tryptophan (L-Trp) catabolism in biology, leading ultimately to the formati

139 nzymes that participate in quinate/shikimate catabolism in different microbes.

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

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

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

143 ngs highlight the pivotal role of amino acid catabolism in muscle fatigue and type 2 diabetes pathoge

144 aling and MMP13 transcription, thus reducing catabolism in OA.

145 ses autophagy in AT and contributes to lipid catabolism in other cells, it was proposed that autophag

146 ation of a seven-gene operon that enables LA catabolism in Pseudomonas putida KT2440.

147 ative of activation, phagocytosis, and lipid catabolism in response to myelin damage.

148 suggests thatMtbrelies mainly on fatty acid catabolism in the host.

149 sults highlight the importance of amino acid catabolism in the modulation of the immunological respon

150 s the cou genes, encoding p-hydroxycinnamate catabolism in the soil bacterium Rhodococcus jostii RHA1

151 t into the integrity of the molecule and its catabolism in vivo.

152 mice expressing human APOC3 and enhances TRL catabolism in vivo.

153 OH) primarily through two steps of oxidative catabolism in which alcohol dehydrogenase (ADH) and alde

154 sidering the importance of the enzyme for TG catabolism in white adipose tissue (WAT).

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

156 on sources that do not produce NADH in their catabolism, including acetate and the amino acids glutam

157 d in amino acid and fatty acid transport and catabolism, indicating metabolic adaptation to a differe

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

159 Yolk catabolism initiates at cellularization in Drosophila me

160 preventing metabolic block during carbon co-catabolism inMtb.

161 bolism but by the accumulation of pyrimidine catabolism intermediates reaching toxic concentrations.

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

163 greater lipogenesis and reduced cholesterol catabolism into bile.

164 Tryptophan (Trp) catabolism into kynurenine (Kyn) contributes to immune d

165 synthesis of carotenoids, whereas carotenoid catabolism involves a multitude of nonenzymatic and enzy

166 The limiting step in intracellular glutamine catabolism involves its conversion to glutamate by gluta

167 The first step in glutamine catabolism is catalysis by the mitochondrial enzyme glut

168 In plants, amino acid catabolism is especially relevant in metabolic stress si

169 In mammals, hepatic lipid catabolism is essential for the newborns to efficiently

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

171 ains the transactivation domain when glucose catabolism is minimal.

172 erences in amino acid accumulation when BCAA catabolism is perturbed.

173 n these activities, a pathway for riboflavin catabolism is proposed.

174 produce and accumulate GA and 3HGA when Lys catabolism is stressed.

175 hes, we reveal that the capacity for choline catabolism is widespread in marine heterotrophs of the m

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

177 H) which disturb lysine (Lys) and tryptophan catabolism leading to neurotoxic accumulation of glutari

178 ipa), the enzyme required for lysosome lipid catabolism, leads to AT atrophy and severe hepatic steat

179 Hpd excision successfully reroutes tyrosine catabolism, leaving treated mice healthy and asymptomati

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

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

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

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

184 ellular membranes; these included nucleotide catabolism, membrane lipid breakdown and increased creat

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

186 in genes involved in vitamin D anabolism and catabolism might be of importance in VKH pathobiology.

187 ncoded and whether they harbored an arginine catabolism mobile element (ACME) locus.

188 tegic provision of specific nutrients, whose catabolism modulates conditions like pH or anoxia in the

189 ced stomatal opening is delayed in three TAG catabolism mutants (sdp1, pxa1, and cgi-58) and in stoma

190 These data imply that chondrocyte catabolism, not death, contributes to articular cartilag

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

192 Empagliflozin significantly reduced the catabolism of (3)H-cholesteryl oleate-labeled LDL inject

193 ixation as well as the aerobic and anaerobic catabolism of a variety of organic compounds.

194 THC and CBD inhibit the cellular uptake and catabolism of AEA by targeting FABPs.

195 Bacterial catabolism of aromatic compounds from various sources in

196 ism was reorganized to support the selective catabolism of both amino acids and fatty acids.

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

198 ferases (BCAT) are enzymes that initiate the catabolism of branched-chain amino acids (BCAA), such as

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

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

201 Finally, catabolism of chitin by the symbionts was also specifica

202 In contrast, the uptake and catabolism of cholesterol by Gram-negative species are p

203 al approaches to discover novel pathways for catabolism of d-threitol, l-threitol, and erythritol.

204 We investigated the compartmentation of the catabolism of dodecanedioate (DODA), azelate, and glutar

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

206 Inhibiting mTORC1 results in increased catabolism of endocytosed proteins and enhances cell pro

207 t can be obtained through the scavenging and catabolism of extracellular protein via macropinocytosis

208 s pancreatic cancer obtains amino acids from catabolism of extracellular protein.

209 acids through macropinocytosis and lysosomal catabolism of extracellular proteins.

210 or-stimulated macropinocytosis and lysosomal catabolism of extracellular proteins.

211 have opposing roles in regulating uptake and catabolism of extracellular proteins.

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

213 Catabolism of fatty acids stored in oil bodies is essent

214 ted pathway analysis revealed that increased catabolism of fixed carbon stores, metabolic signaling,

215 oC-III to lipoproteins and accelerated renal catabolism of free apoC-III.

216 Catabolism of galactose by Streptococcus pneumoniae alte

217 ybenzoic acid and catechol, derived from the catabolism of gallotannins, ellagitannins, flavan-3-ols

218 Metabolic blocks in processing and catabolism of gangliosides result in the development of

219 Catabolism of GlcNAc raises the ambient pH rather than a

220 a critical nodal role of PEPCKmt in linking catabolism of glucose and glutamine with anabolic pathwa

221 This glucose-induced excitation implies the catabolism of glucose, leading to a closure of ATP-sensi

222 of concept study showing that modulating the catabolism of glucosylceramide may be a therapeutic targ

223 ge disorders that result from defects in the catabolism of glycosaminoglycans.

224 nase-1 (HO-1), the rate-limiting step in the catabolism of heme into the bioactive signaling molecule

225 -acetyltransferase involved in the lysosomal catabolism of heparan sulphate.

226 uptake, as well as a role for CYP2E1 in the catabolism of hepatic retinoid.

227 ich may limit the efficient mobilization and catabolism of hepatic TAGs.

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

229 of enzymes and transporters involved in the catabolism of lactate and glutamine.

230 The bacterial catabolism of lignin and its breakdown products is of in

231 Although the lysosomal catabolism of lipid is necessary for normal ATM function

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

233 lieu, as exemplified by the distinct glucose catabolism of macrophages exposed to LPS/IFN-gamma or IL

234 rts sulfur and one-carbon metabolism and the catabolism of odd-chain fatty acids, branched-chain amin

235 ADMA is generated by the catabolism of proteins methylated on arginine residues b

236 PDE10A is a key enzyme in the catabolism of second messenger cAMP and cGMP, whose synt

237 yzing the terminal reaction in the oxidative catabolism of several metabolites.

238 rt is coupled with the initiation of HOC and catabolism of storage carbohydrates.

239 ation, early seedling growth is supported by catabolism of stored reserves of protein, oil or starch

240 enzyme that catalyzes the first step in the catabolism of the amino acid phenylalanine.

241 Because we observed rapid catabolism of the deoxynucleoside monophosphates to deox

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

243 The catabolism of these nutrients involves the action of 6-p

244 rea dissociation or myeloperoxidase-mediated catabolism of thiocyanate to free amino groups of protei

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

246 mab independently accelerated the fractional catabolism of VLDL-apoB (P<0.001 and P.032, respectively

247 Catabolism of yolk is initiated by acidification of the

248 interrogated the importance of IDE-mediated catabolism on insulin clearance in vivo.

249 Conversely, blockade of GABA catabolism or GABA uptake reduced NG2 cell numbers and i

250 uman osteosclerosis, inhibition of glutamine catabolism or Gcn2 deletion suppressed excessive bone fo

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

252 o an impaired A. baumannii phenylacetic acid catabolism pathway, which led to accumulation of phenyla

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

254 This elevation indicates increased protein catabolism, possibly as an alternate energy source given

255 Additionally, the catabolism profile of NicA2 was elucidated to assess the

256 ks the regulation of fatty acid flux to BCAA catabolism, providing a mechanistic explanation for how

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

258 mia (AML) and is linked to a reliance on fat catabolism regardless of external nutrient cues.

259 Carrageenan catabolism relies on a multifaceted carrageenan-induced

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

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

262 Hence, IAA conjugation and catabolism seem to regulate auxin levels in Arabidopsis

263 7, trauma patients showed increasing muscle catabolism: serine levels increased from 42.03 (31.20-54

264 no effect on monoamine oxidase A (serotonin catabolism), serotonin receptor 5-HT4, or mouse serotoni

265 ant similarity to a regulator of chlorophyll catabolism, SGR.

266 Tor metabolic sensing pathway regulates yolk catabolism, similar to Tor-dependent metabolic regulatio

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

268 cause of inflammation-immunosuppression and catabolism syndrome is currently unknown, but there is i

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

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

271 A central intermediate in purine catabolism, the inosine nucleobase hypoxanthine is also

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

273 accompanied by an increased ratio of glucose catabolism through glycolysis versus the tricarboxylic a

274 an important role in controlling pyrimidine catabolism through repression of DPYD expression, follow

275 te synthesis, suggesting involvement of BCAA catabolism through the IRG1/itaconate axis within the tr

276 we determined that WNT stimulates glutamine catabolism through the tricarboxylic acid (TCA) cycle an

277 -1 plays a critical role in regulating lipid catabolism to control the size of lipid droplets and pre

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

279 ES cells utilize both glucose and glutamine catabolism to maintain a high level of intracellular alp

280 ds on cooperativity of glucose and glutamine catabolism to meet biosynthetic demands.

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

282 naplerosis in culture rely less on glutamine catabolism to proliferate in vivo.

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

284 thus providing a novel link between protein catabolism, ureagenesis, and hepatic lipid metabolism.

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

286 tion on the peroxisomal versus mitochondrial catabolism was gathered from the labeling patterns of ac

287 rted for GS, inter-group differences in heme catabolism were explored.

288 Genes involved in carbon catabolism were expressed uniformly from the centre to t

289 ative pathways of respiration and amino acid catabolism were up-regulated in atg mutants.

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

291 tion is characterized by enhanced tryptophan catabolism, which contributes to immune suppression and

292 SMS deficiency leads to excessive spermidine catabolism, which generates toxic metabolites that cause

293 ing effector function by engaging fatty acid catabolism, which is promoted by fenofibrate and synergi

294 r the role of autophagy in hepatocellular LD catabolism while implicating the small GTPase Rab7 as a

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

296 lucidation of the molecular mechanism of IPU catabolism will enhance our understanding of the microbi

297 reveal a mechanism that coordinates glucose catabolism with L-2HG synthesis, and establish the fly a

298 trongly dependent on mitochondrial substrate catabolism, with availability of NADPH as a major rate-c

299 isinin (DHA) was found to disrupt hemoglobin catabolism within 1 hour of exposure, resulting in a tra

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