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1 PI3-kinase C2gamma and PI4-kinase IIIalpha (phospholipid metabolism).
2 with progression to T2D, implicating AA and phospholipid metabolism.
3 metabolism; alpha-linolenic metabolism; and phospholipid metabolism.
4 cond messengers derived from agonist-induced phospholipid metabolism.
5 duction in abundance of proteins involved in phospholipid metabolism.
6 ome editing validated its role in regulating phospholipid metabolism.
7 rging subcategory of PMDs involves defective phospholipid metabolism.
8 of phosphatidic acid as well as rewiring of phospholipid metabolism.
9 al regulator of cholesterol, fatty acid, and phospholipid metabolism.
10 istinct proteotoxic stress responses control phospholipid metabolism.
11 isorder is linked to highly altered membrane phospholipid metabolism.
12 p, and an inner membrane protein, Mdm31p, in phospholipid metabolism.
13 PI1, encoding a transcriptional repressor of phospholipid metabolism.
14 s to host cell glycolytic, nucleic acid, and phospholipid metabolism.
15 in mdm35Delta mitochondria failed to restore phospholipid metabolism.
16 ransferases suggests a role in mitochondrial phospholipid metabolism.
17 sstalk between the TLR signaling pathway and phospholipid metabolism.
18 ulated of a set of genes encoding enzymes of phospholipid metabolism.
19 ptor cells, it may have a role in surfactant phospholipid metabolism.
20 and has no significant consequence for bulk phospholipid metabolism.
21 ol and by signals generated by alteration of phospholipid metabolism.
22 contributor to the effects of gentamicin on phospholipid metabolism.
23 er cells, involving a specific modulation of phospholipid metabolism.
24 f, which is conserved in numerous enzymes of phospholipid metabolism.
25 t transformation and progression on membrane phospholipid metabolism.
26 a manner similar to other genes involved in phospholipid metabolism.
27 is associated with altered membrane choline phospholipid metabolism.
28 point for the generation of CSCs mediated by phospholipid metabolism.
29 f proteins that includes enzymes involved in phospholipid metabolism, a bacterial toxin, poxvirus env
30 se include altered calcium, cholesterol, and phospholipid metabolism; altered mitochondrial dynamics;
31 erappreciated role for gut microorganisms in phospholipid metabolism and a potential target for inhib
32 clear localization on lipin1beta function in phospholipid metabolism and adipogenic differentiation.
33 d cells from the animals exhibit deregulated phospholipid metabolism and an aberrant induction of pro
36 ing hypoxia-mediated chromatin regulation to phospholipid metabolism and ferroptosis resistance in ca
37 and useful for understanding the pathways of phospholipid metabolism and for elucidating the role of
38 s that are markers of neuronal viability and phospholipid metabolism and have also been implicated in
39 1 (Rsd1), which is genetically implicated in phospholipid metabolism and in the function of the actin
41 mitochondrial structure, with components of phospholipid metabolism and mitochondrial inner membrane
42 sults in profound alterations in hippocampal phospholipid metabolism and mitochondrial phospholipid h
43 e cancer is attributable to an alteration of phospholipid metabolism and not simply to increased cell
44 sm of anticancer action of EVs by disrupting phospholipid metabolism and survival signaling in cancer
45 products played a role in the regulation of phospholipid metabolism and the cellular levels of phosp
46 little is known about the regulators of MAM phospholipid metabolism and their connection to mitochon
47 eveal the intricate network of intracellular phospholipid metabolism and underscore the distinct regu
48 plsX (encoding a poorly understood enzyme of phospholipid metabolism) and pabC (encoding 4-amino-4-de
49 ons with lipid homeostasis, glucuronidation, phospholipid metabolism, and gastrointestinal motility.
52 roteins, heterotrimeric G proteins, inositol phospholipid metabolism, and protein serine/threonine ph
54 s been observed in many strains with altered phospholipid metabolism, and the relationship between ph
55 NPLA6 in photoreceptor survival and identify phospholipid metabolism as a potential therapeutic targe
56 This study identifies macropinocytosis and phospholipid metabolism as novel mechanisms of metabolic
57 iogenesis and breakdown, lipid oxidation and phospholipid metabolism, as well as cell-cell lipid tran
59 choline kinase by MN58b resulted in altered phospholipid metabolism both in cultured tumor cells and
60 diator serves as an intermediate in membrane phospholipid metabolism but is also produced in acute se
61 lubron appears to have no negative impact on phospholipid metabolism but rather enhances surfactant p
62 osphatase played a role in the regulation of phospholipid metabolism by inositol, as well as regulati
64 is determined, along with new insights into phospholipid metabolism, by in vitro and in vivo charact
66 HS) is an X-linked disorder of mitochondrial phospholipid metabolism caused by pathogenic variants in
67 mbrane surfaces and participates in cellular phospholipid metabolism during signal transduction and v
68 xamine the role of PKC alpha in keratinocyte phospholipid metabolism/eicosanoid production and cutane
69 serine-folate-glycine one carbon and serine-phospholipid metabolism, elevation of end products of ca
70 olved in signaling pathways (DEPDC4, GNG10), phospholipid metabolism (ENPP5, PLSCR2), beta-oxidation
72 o genes encoded putative enzymes involved in phospholipid metabolism, GdpD (which denotes glycerophos
73 ethotrexate and antimony, for ergosterol and phospholipid metabolism genes in resistance to miltefosi
74 ient cells. Our findings therefore implicate phospholipid metabolism in autophagosome biogenesis.
75 phosphatidylethanolamine, a critical step in phospholipid metabolism in both prokaryotes and eukaryot
76 ting lipid oxidation in liver and regulating phospholipid metabolism in brain of methionine-choline-d
79 pression of genes involved in fatty acid and phospholipid metabolism in dividing and ageing E. coli c
80 evidence that the IDH1-R132H mutation alters phospholipid metabolism in gliomas involving phosphoetha
82 lipid synthesis actively influences membrane phospholipid metabolism in logarithmically growing cells
83 ed to published evidence of altered cortical phospholipid metabolism in NBM-lesioned rats, suggest th
84 dings emphasize an important role for proper phospholipid metabolism in normal brain function and sug
87 ypotheses of abnormalities in fatty acid and phospholipid metabolism in regions associated with psych
88 ts support a role for PLC-delta1 and nuclear phospholipid metabolism in regulating cell cycle progres
89 ouracil, we find evidence for an increase in phospholipid metabolism in response to acetaminophen, an
90 p are three homologous proteins that control phospholipid metabolism in the mitochondrial intermembra
91 etogenesis and are required for ER-localized phospholipid metabolism in vegetative and reproductive g
93 sults suggest greater alteration of membrane phospholipid metabolisms in rapid cycling BD-I compared
95 ium of wild type cells results in changes in phospholipid metabolism, including an increase in phosph
96 nd plasma that impact both neutral lipid and phospholipid metabolism, including decreased triglycerid
97 ide expression that accompany alterations in phospholipid metabolism induced by inositol supplementat
98 hypothesis that this alteration in cellular phospholipid metabolism is an adaptive response to preve
99 ata suggest that cPLA2-mediated hypothalamic phospholipid metabolism is critical for controlling syst
102 he evidence from this pilot study shows that phospholipid metabolism is modulated by both conditions
103 the effects of inositol (a key regulator of phospholipid metabolism) led to predictions that show si
104 amily, have been predicted to be involved in phospholipid metabolism, lipid trafficking, membrane tur
106 m31p causes similar defects in mitochondrial phospholipid metabolism, mitochondrial morphology, and c
107 pase D (PLD) superfamily includes enzymes of phospholipid metabolism, nucleases, as well as ORFs of u
111 nesis, development, intracellular transport, phospholipid metabolism, protein biosynthesis, protein l
112 To test the hypothesis that skeletal muscle phospholipid metabolism regulates systemic glucose metab
114 lieve the requirement for Sec14p by altering phospholipid metabolism so as to expand the pool of diac
115 choline degradation pathways, subsequent to phospholipid metabolism, specifically links, and hence u
116 9-10.40 fold), and ppk (2.50-5.40 fold)) and phospholipid metabolism (SQD1 (1.85-2.79 fold), SQD2 (2.
117 decarboxylases (PSDs) are central enzymes in phospholipid metabolism that produce phosphatidylethanol
120 port, it has been demonstrated that enhanced phospholipid metabolism through PA in tumor cells can be
121 dy investigated their roles in gram-positive phospholipid metabolism through the analysis of conditio
123 ed choline kinase down-regulation on choline phospholipid metabolism was confirmed by the significant
125 cy influences myocardial Ca(2+) handling and phospholipid metabolism, which could compromise the hear
126 metabolic signaling networks that coordinate phospholipid metabolism with gene expression, we profile
127 nctional analyses indicate Sec14p integrates phospholipid metabolism with the membrane trafficking ac
128 al component of a regulatory pathway linking phospholipid metabolism with vesicle trafficking (the Se
129 tivity and decreased cholesteryl esters; (c) phospholipid metabolism, with increased phosphatidic aci