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1 Nigeria), using the gene ontology (GO) term "carbohydrate metabolism".
2 is (Arabidopsis thaliana) mutant impaired in carbohydrate metabolism.
3 AV1-/- mice is strictly dependent on hepatic carbohydrate metabolism.
4 ignaling, hexosamine biosynthesis, and lipid/carbohydrate metabolism.
5 nt, indicating that Atf4 regulates mammalian carbohydrate metabolism.
6 tive enzymes, suggesting a potential role in carbohydrate metabolism.
7 lating protein synthesis and degradation and carbohydrate metabolism.
8 ways, ranging from cell-cycle progression to carbohydrate metabolism.
9 hondrial proteins involved in fatty acid and carbohydrate metabolism.
10 ies, involves disturbances in both lipid and carbohydrate metabolism.
11 esses, including bile acid, cholesterol, and carbohydrate metabolism.
12 in cholesterol, bile acid, triglyceride, and carbohydrate metabolism.
13 cent to telomeres or function in vitamin and carbohydrate metabolism.
14 Escherichia coli, is important in regulating carbohydrate metabolism.
15 established roles in cholesterol, lipid, and carbohydrate metabolism.
16 and antibiotic tolerance, are responsive to carbohydrate metabolism.
17 es in redox responsive genes and in genes of carbohydrate metabolism.
18 on, serum proteins, amino acids, lipids, and carbohydrate metabolism.
19 ract with insulin to modulate its control of carbohydrate metabolism.
20 s are potent regulators of protein, fat, and carbohydrate metabolism.
21 and biogenesis, the cytoskeleton and energy/carbohydrate metabolism.
22 gy intake, energy expenditure, and lipid and carbohydrate metabolism.
23 diabetes mellitus is a metabolic disease of carbohydrate metabolism.
24 itive memory, the immune system, and fat and carbohydrate metabolism.
25 of these were involved in central lipid and carbohydrate metabolism.
26 ggested role in modulating sugar sensing and carbohydrate metabolism.
27 e ascorbate function with minimal effects on carbohydrate metabolism.
28 enotype that may be associated with impaired carbohydrate metabolism.
29 enes encoding proteins involved in lipid and carbohydrate metabolism.
30 y lipid sensors that regulate fatty acid and carbohydrate metabolism.
31 ide (NO) has an important role in regulating carbohydrate metabolism.
32 racted feeding temporally linked to enhanced carbohydrate metabolism.
33 in the control of host glucose disposal and carbohydrate metabolism.
34 Phosphorylases are key enzymes of carbohydrate metabolism.
35 for the S. solfataricus alpha-glucosidase in carbohydrate metabolism.
36 iquitous highly conserved enzyme involved in carbohydrate metabolism.
37 tly linking E. coli HPr to the regulation of carbohydrate metabolism.
38 s enhanced by moderate obesity, and abnormal carbohydrate metabolism.
39 ABC transporters, two-component systems, and carbohydrate metabolism.
40 acid utilization to the more oxygen-sparing carbohydrate metabolism.
41 es, anaerobic respiration, and cell wall and carbohydrate metabolism.
42 ns involved in transcriptional regulation or carbohydrate metabolism.
43 A-Ile-induced changes in limb fresh mass and carbohydrate metabolism.
44 system plays a key role in the regulation of carbohydrate metabolism.
45 ses support a role for the GxGYxYP domain in carbohydrate metabolism.
46 asive disease, upregulated genes involved in carbohydrate metabolism.
47 w of the quantitative programming of storage carbohydrate metabolism.
48 involved in translation, protein folding and carbohydrate metabolism.
49 androgenic effects and may disrupt lipid and carbohydrate metabolism.
50 thase kinase 3 (GSK3), a prominent enzyme in carbohydrate metabolism, also has a major role in brain
51 vides insights into thermal "fine-tuning" of carbohydrate metabolism and a warning that the physiolog
52 dative stress pathways, as well as decreased carbohydrate metabolism and amino acid biosynthesis in f
54 study provides a first genetic link between carbohydrate metabolism and BMI and demonstrates the pow
55 study, relationships among genes involved in carbohydrate metabolism and bud dormancy were examined a
56 indicated that many genes for amino acid and carbohydrate metabolism and cell cycle progression were
58 included metabolic intermediates in central carbohydrate metabolism and cofactors of peripheral meta
60 s of SREBP-1 leads to significant changes in carbohydrate metabolism and does not improve insulin res
62 ow oxygen include those encoding enzymes for carbohydrate metabolism and fermentation, pathways that
63 d to lipid metabolism, chloroplast function, carbohydrate metabolism and free radical detoxification,
64 a critical role in regulating both lipid and carbohydrate metabolism and FXR-controlled lipid homeost
65 transcriptional regulatory network involving carbohydrate metabolism and glucose homeostasis mediated
66 ptors (NRs) play a pivotal role in lipid and carbohydrate metabolism and have been highlighted as pot
67 ransketolase (TktA), are enzymes involved in carbohydrate metabolism and have not previously been sho
68 overexpression induced the reprogramming of carbohydrate metabolism and increased NADPH levels in a
70 nvestigated the effects of leptin on growth, carbohydrate metabolism and insulin signalling in fetal
72 tes pathways of cholesterol, fatty acid, and carbohydrate metabolism and may have therapeutic benefit
74 m, for example, may relate to alterations in carbohydrate metabolism and niche disruptions in mucosal
75 used to determine the rates of intermediary carbohydrate metabolism and oxygen use in five severely
76 quantitate the derangements in intermediary carbohydrate metabolism and oxygen use in severely septi
77 pression profiles of genes involved in major carbohydrate metabolism and photosynthesis in the flag l
78 coordination of cellulose biosynthesis with carbohydrate metabolism and photosynthesis is not well u
79 protein structure-function relationships in carbohydrate metabolism and recognition, carbon turnover
80 eleterious effects of PPARgamma mutations on carbohydrate metabolism and replicating the characterist
82 of the up-regulated proteins are involved in carbohydrate metabolism and some were photosynthesis or
83 a role in modulating insulin sensitivity and carbohydrate metabolism and that the eNOS isoform may pl
84 eas 4-nonylphenol deregulated genes from the carbohydrate metabolism and the ecdysone regulatory path
85 beta hexoses, which is essential for normal carbohydrate metabolism and the production of complex ol
86 ount of specific metabolites associated with carbohydrate metabolism and the shikimate pathway were a
87 involved in polysaccharide production and in carbohydrate metabolism and those in a region containing
88 rulence factor production in B. anthracis to carbohydrate metabolism and, for the first time, provide
89 transcripts involved in nutrient transport, carbohydrate metabolism, and cell cycle regulation, sugg
91 ) that encode proteins likely to function in carbohydrate metabolism, and four genes (orf1-4) that en
92 ian clock associated genes, DREBs, COP1-HY5, carbohydrate metabolism, and involvement of hormones (AB
93 ogen discrimination pathway, nonfermentative carbohydrate metabolism, and mitochondrial function.
94 cluding hypertension, dyslipidemia, impaired carbohydrate metabolism, and nonalcoholic fatty liver di
96 novel relationship between GPI, involved in carbohydrate metabolism, and PAP1, a lipogenic enzyme.
97 idative phosphorylation, electron transport, carbohydrate metabolism, and post-synaptic cytokinesis i
99 transport chain, tetrapyrrole biosynthesis, carbohydrate metabolism, and signaling lipid synthesis.
101 , cell wall maintenance (approximately 1/8), carbohydrate metabolism (approximately 1/10), and lipid
102 signal transduction, gland development, and carbohydrate metabolism are among the most prominent rap
103 ses and gene sequences for the regulation of carbohydrate metabolism are discussed, and a 4-fold role
104 n revealed the presence of genes involved in carbohydrate metabolism, aromatic carbon metabolism, and
105 any gene queried against our database.Taking carbohydrate metabolism as a test case, we observed that
106 splayed multiple defects in insulin-mediated carbohydrate metabolism as reflected by (i) decreased pe
107 ther previously unknown targets in lipid and carbohydrate metabolism as well as many putative target
108 was associated with alterations in bacterial carbohydrate metabolism, bacterial-host interactions, as
109 sphingolipids related to lipid, protein, and carbohydrate metabolism between male meat eaters, fish e
111 s not required for the maintenance of normal carbohydrate metabolism but is essential for the attainm
112 both Irs-1 and Irs-2 function in peripheral carbohydrate metabolism, but Irs-2 has the major role in
113 C/EBP beta influences the regulation of carbohydrate metabolism by altering the level of hepatic
116 at the effects of CBI on gene expression and carbohydrate metabolism can be neutralized by osmotic su
117 are part of pathways of kidney development, carbohydrate metabolism, cardiac septum development and
118 Among Gene Ontology categories related to carbohydrate metabolism, changes in starch and Suc metab
119 er, there were no significant differences in carbohydrate metabolism characteristics or lipid profile
120 DREBs) of molecular networks associated with carbohydrate metabolism, circadian clock, flowering, and
121 es (DEGs) involved in morphogenesis, primary carbohydrate metabolism, cold stimulation and blue-light
122 le genes found in this study are involved in carbohydrate metabolism, consistent with its role as a s
125 ty of genes involved in bile acid, lipid and carbohydrate metabolism, energy expenditure, and inflamm
126 ed in profound biochemical changes including carbohydrate metabolism, energy metabolism and glutathio
127 in the db/db nerve include lipid metabolism, carbohydrate metabolism, energy metabolism, peroxisome p
129 ing include those for putative enzymes and a carbohydrate metabolism enzyme, alkB2; this latter gene
131 arana extracts, after digestion in vitro, on carbohydrates-metabolism enzymes and to assess the bioac
132 significantly during fruit development, and carbohydrate metabolism (especially sugar synthesis) is
133 review, I focus primarily on alterations in carbohydrate metabolism, examining both the metabolic re
134 cription to our knowledge of a route feeding carbohydrate metabolism exclusively via D-erythrose 4-ph
135 or nuclear receptors in regulating lipid and carbohydrate metabolism, fibrosis, and inflammation.
136 ch may underlie persistent loss of oxidative carbohydrate metabolism following transient ischemia.
137 mes of plant-associated bacteria encode more carbohydrate metabolism functions and fewer mobile eleme
138 on of all solvent formation genes, sigF, and carbohydrate metabolism genes (similar to genes expresse
139 hus Msn2/4 exhibit a dual role in activating carbohydrate metabolism genes and stress response genes.
140 s used to determine the expression levels of carbohydrate metabolism genes at different phases of bud
141 irst evidence for the horizontal transfer of carbohydrate metabolism genes into ectomycorrhizal fungi
142 election were uncovered in genes controlling carbohydrate metabolism, glycoalkaloid biosynthesis, the
143 ways based on the proteomic analysis include carbohydrate metabolism (glycolysis/gluconeogenesis, pen
145 d enzymes of brush border membrane (BBM) and carbohydrate metabolism has been studied in rat kidney.
146 tain Gene Ontology groupings of genes (e.g., Carbohydrate Metabolism) have large amounts of high cons
147 nscriptional programs that control lipid and carbohydrate metabolism, immunity and inflammation, and
152 vement, heat tolerance, circadian clock, and carbohydrate metabolism in K. fedtschenkoi and other CAM
155 contrast, RSC binds to promoters involved in carbohydrate metabolism in response to transcriptional a
157 response by acting as a master regulator of carbohydrate metabolism in the infected animal, via JAK/
158 eins are likely to play an important role in carbohydrate metabolism in these abundant symbiotic spec
159 se data show that Ca(2+) signaling regulates carbohydrate metabolism in Toxoplasma and that the post-
160 e of Fru-2,6-P2 in the regulation of hepatic carbohydrate metabolism in vivo, Fru-2,6-P2 levels were
163 (body size and type, sex hormone status, and carbohydrate metabolism) in a cross-sectional population
164 ed by GLD4, several of which are involved in carbohydrate metabolism including GLUT1, a major glucose
165 in this class of mRNA are those involved in carbohydrate metabolism, including several mRNAs from th
166 we demonstrate that these strains differ in carbohydrate metabolism, including the ability to metabo
167 ined the regulation of processes involved in carbohydrate metabolism, including trehalose metabolism,
168 nt with a metabolic shift from fatty acid to carbohydrate metabolism, increased expression of extrace
169 e families within microbial ecosystems where carbohydrate metabolism is a major evolutionary driver.
170 s mature stalk and a considerable portion of carbohydrate metabolism is also devoted to cell wall syn
172 g other metabolic signatures, amino acid and carbohydrate metabolism is most prominent in undifferent
173 d skin substitutes may be increased if their carbohydrate metabolism is optimized by understanding wh
175 nal transduction, and the action of IGF-1 on carbohydrate metabolism is preserved in certain insulin-
178 PTS-mediated carbohydrate transport, but not carbohydrate metabolism, is required for production of a
179 ciated with nutrient storage (phaseolin) and carbohydrate metabolism (lectins) were significantly dow
182 here supports the notion that cellulose and carbohydrate metabolism may be coordinated via an osmose
183 te how changes in the flux of electrons from carbohydrate metabolism modulate the redox poise of the
184 s demonstrates significant activation of the carbohydrate metabolism network in experimental gingivit
185 analysis indicated that the major and minor carbohydrate metabolism, nitrogen metabolism, and ethyle
186 methods and opens new opportunities to study carbohydrate metabolism of algae under autotrophic, mixo
187 ransketolase reaction, being involved in the carbohydrate metabolism of many organisms, requires an i
188 The speculative function of this CDP in the carbohydrate metabolism of T. africanus TCF52B was also
190 e resting phase, indicating a preference for carbohydrate metabolism over fat oxidation in these mice
191 blocks from three major metabolic pathways: carbohydrate metabolism, peroxisomal beta-oxidation of f
192 enson cycle and other central pathways, leaf carbohydrate metabolism, photosynthetic gas exchange, an
194 expressed higher levels of genes involved in carbohydrate metabolism, priming them for anaerobic ener
195 number of genes including those involved in carbohydrate metabolism, quorum sensing, iron regulation
196 wed that Sko1 is conserved as a regulator of carbohydrate metabolism, redox metabolism, and glycerol
197 rboxylic acid cycle replenishment, disturbed carbohydrate metabolism, reduced phytosterol biosynthesi
198 t the Hadza GM is adapted for broad-spectrum carbohydrate metabolism, reflecting the complex polysacc
201 s to produce and tolerate organic acids from carbohydrate metabolism represents a major virulence fac
203 ticipated role for sweet taste in regulating carbohydrate metabolism, revealing a novel mechanism by
205 ge of genes, including genes associated with carbohydrate metabolism, signal transduction, and metabo
206 nthesis, Calvin cycle, photorespiration) and carbohydrate metabolism (starch synthesis/degradation),
208 effect of food (TEF), lipid concentrations, carbohydrate metabolism, subjective appetite, and gut ho
211 owever, these two taxa were less involved in carbohydrate metabolism than others and had few genes th
212 se superfamily comprises enzymes involved in carbohydrate metabolism that are found in all kingdoms o
213 are highly pleiotropic and affect aspects of carbohydrate metabolism that are not directly related to
214 mber of membrane transporters and enzymes of carbohydrate metabolism that are unique to Galdieria.
215 dings provide novel insights into the insect carbohydrate metabolism that governs glycogen and lipid
216 cycle and to identify changes in endogenous carbohydrate metabolism that occur when proliferative st
217 pression of genes involved in amino acid and carbohydrate metabolism, the stress response, and meiosi
218 t levels and activity of enzymes involved in carbohydrate metabolism throughout fruit development rev
220 pendent transcriptional repressor that links carbohydrate metabolism to epigenetic regulation by recr
221 es necessary to link the signal generated by carbohydrate metabolism to specific nuclear transcriptio
223 provides experimental evidence of the basic carbohydrate metabolism underlying the development of st
224 dance of phosphoproteins involved in primary carbohydrate metabolism upon Fe deficiency, complementin
227 (PACAP38), a critical mediator of lipid and carbohydrate metabolism, was also determined to be effic
228 dition to a battery of housekeeping genes of carbohydrate metabolism, we observed changes in hexose t
229 proximately 50% deficit in beta-cell mass on carbohydrate metabolism, we performed a approximately 50
231 nes associated with metabolic regulation and carbohydrate metabolism were differentially regulated be
234 ges, and genes related to photosynthesis and carbohydrates metabolism were highly expressed in mature
235 two of the mRNAs encode proteins involved in carbohydrate metabolism, whereas others encode proteins
236 ciated with ethylene, auxin, flavonoids, and carbohydrate metabolism; whereas, sub-network enrichment
237 icularly interesting are features related to carbohydrate metabolism, which include a minimalistic ge
238 involved in cell wall biogenesis and energy/carbohydrate metabolism, which is consistent with the st
239 Thus, Sol3p and Sol4p likely function in carbohydrate metabolism, while Sol1p and Sol2p appear to
240 ity, thus allowing co-ordinate regulation of carbohydrate metabolism with cell division processes.
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