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1 stration of the hormone is required for bone anabolism.
2 tease inhibitors did not prevent lean tissue anabolism.
3 as predictive of the extent of intracellular anabolism.
4 ANKL-OPG axis, without interfering with bone anabolism.
5 f a greater ability to utilize nutrients for anabolism.
6 s a novel pharmacologic approach to skeletal anabolism.
7 an osteogenic environment with enhanced PTH anabolism.
8 abecular bone mass and increased PTH-induced anabolism.
9 use oncogenic mutations constitutively drive anabolism.
10 e supporting this novel approach to skeletal anabolism.
11 protein beverages designed to enhance muscle anabolism.
12 ced cancer and the window of possible muscle anabolism.
13 s fatty acid oxidation while promoting lipid anabolism.
14 nase that is obligate for insulin-stimulated anabolism.
15 may provide pharmacological targets for bone anabolism.
16 atch the stoichiometric demands of microbial anabolism.
17 sphorylation of elements thought to increase anabolism.
18 F treatment, where it precedes activation of anabolism.
19 on networks, promote catabolism and suppress anabolism.
23 and mutations in genes involved in vitamin D anabolism and catabolism might be of importance in VKH p
25 tate mRNA levels of 14 genes involved in the anabolism and catabolism of reactive oxygen species (ROS
27 ke and utilization and direct the balance of anabolism and catabolism to ensure the appropriate use o
28 atic controls regulating the balance between anabolism and catabolism, favoring accelerated cartilage
33 essential reactions such as ATP production, anabolism and cellular oxidation-reduction (redox) regul
35 measurements, and in cellulo analysis of GAG anabolism and decorin glycosylation, we mapped the organ
36 es OS in the rat VP through elevation of ROS anabolism and diminution of antioxidant detoxification.
39 proline metabolism between yeast (cytosolic anabolism and mitochondrial catabolism) and humans (excl
41 x kg(-1) x d(-1) may enhance muscle protein anabolism and provide a means of reducing the progressiv
43 me Escherichia coli operons that function in anabolism and represses others involved in catabolism.
44 abundance, nutrient-sensing pathways engage anabolism and storage, whereas scarcity triggers homeost
46 d with anaplerotic central metabolism, lipid anabolism and the regeneration of oxidized cofactors.
47 ncrease the efficiency of EAA use for muscle anabolism and to lower the meal threshold for stimulatio
48 naling has been recognized in promoting bone anabolism, and application of strain has been shown to i
52 iofilm system, the dimensions of the zone of anabolism at the air interface ranged from 16 to 38 micr
53 s novel mechanism explains how CDK4 promotes anabolism by blocking catabolic processes (FAO) that are
54 ormonal regulation of amino acid and protein anabolism by coupling amino acid uptake and synthesis, a
56 plays an important role in PTH-induced bone anabolism by promoting T-cell production of Wnt10b and s
60 entails reprogramming photoreceptors towards anabolism by upregulating the mechanistic target of rapa
61 is decreased in the elderly, muscle protein anabolism can nonetheless be stimulated by increased ami
64 utrient oversupply and triacylglycerol (TAG) anabolism contribute to hepatic steatosis, little is kno
67 ovide a stimulatory effect on muscle protein anabolism, favoring the retention of lean muscle mass wh
68 ew of eukaryotic NAD+ biosynthesis, that all anabolism flows through nicotinic acid mononucleotide, w
72 Omega-3 (n-3) fatty acids stimulate protein anabolism in animals and might therefore be useful for t
73 signaling in osteocytes is critical for full anabolism in cortical bone, but tempers bone gain in can
77 hexia, but the potential for skeletal muscle anabolism in patients with advanced cancer is unproven.
78 hat aerobic exercise restores muscle protein anabolism in response to insulin by improving vasodilati
81 of an actual protein-rich food to stimulate anabolism in the young and the elderly has not been expl
83 metallothionein blockade on skeletal muscle anabolism in vitro and in vivo We found that concomitant
85 lude that exogenous HMB induces acute muscle anabolism (increased MPS and reduced MPB) albeit perhaps
88 t tomatidine stimulated mTORC1 signaling and anabolism, leading to accumulation of protein and mitoch
89 estrates adaptive responses, including lipid anabolism, metabolic reprogramming, increases in protein
90 r long term through microbial catabolism and anabolism, mostly due to uncoupled research on litter de
91 TORC1 senses amino acid abundance to promote anabolism, mTORC2 responds to declining glutamine catabo
93 g process in which mTORC1, the gatekeeper of anabolism, occupies a privileged regulatory position.
94 sed exposure to 5-FU and, in turn, increased anabolism of 5-FU to cytotoxic nucleotides, resulting in
95 may be feasible to measure the transport and anabolism of [18F]FU in tumors by kinetic modeling and P
96 activity of 5-fluorouracil (5-FU) and in the anabolism of its oral prodrug, capecitabine, through the
97 ction of OPP on Staphylococcus: OPP inhibits anabolism of many amino acids and highly downregulates t
99 central to an energy sensor that determines anabolism or catabolism depending on local sucrose avail
102 inding protein-3 as an index of nutrition or anabolism requires knowledge of its relationship to nonn
103 es the expression of genes involved in lipid anabolism, secretion, and redox metabolism, in response
104 s dispensable for BMP2 to induce the protein anabolism signature, which instead critically depends on
106 s and attenuated PTH-induced trabecular bone anabolism, supporting the positive function of macrophag
107 dioprotection, the balance of catabolism and anabolism, the concept of mitochondrial quality control,
108 by both IGF-1 and BMP-7 greatly potentiated anabolism through complementary and synergistic mechanis
109 ther iPTH induces Wnt10b production and bone anabolism through direct activation of the parathyroid h
110 cidate the complex role of periostin on bone anabolism, through the regulation of Sost, Wnt-beta-cate
111 entary pathways to ATF4 expression, allowing anabolism to be finely tuned to amino acid availability.
117 and parathyroid hormone (PTH)-dependent bone anabolism using murine models of targeted myeloid-lineag
119 proteins involved in lipid and carbohydrate anabolism was increased in the presence of ethanol, a re
122 e androgen receptor (AR) ligands that induce anabolism while having reduced effects in reproductive t
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