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1 emN, and desF (the latter encodes a putative fatty acid desaturase).
2 abditis elegans gene, fat-1, encoding an n-3 fatty acid desaturase.
3  coli to support the activities of the plant fatty acid desaturase.
4 re domain of OLE1, the S. cerevisiae Delta-9 fatty acid desaturase.
5 enzymes such as ribonucleotide reductase and fatty acid desaturase.
6 g a unique delta 9 14:0-acyl carrier protein fatty acid desaturase.
7 ated acyl-CoA precursors by Ole1p, a delta-9 fatty acid desaturase.
8  resembling those of metalloproteins such as fatty acid desaturases.
9 4 is the founding member of a novel class of fatty acid desaturases.
10 nserved histidine clusters characteristic of fatty acid desaturases.
11 uishes them from all known Delta12 or omega3 fatty acid desaturases.
12 scriptional network that upregulates delta-9 fatty acid desaturases.
13 at are characteristic of a group of membrane fatty acid desaturases.
14 fs that are characteristic of membrane-bound fatty acid desaturases.
15                                              Fatty acid desaturase 1 and 2 (FADS1 and FADS2) code for
16 ut also by the polymorphisms of coding genes fatty acid desaturase 1-3 for the desaturase enzymes tha
17 luding stearoyl-coenzyme A desaturase (SCD), fatty acid desaturases 1 and 2 (FADS1 and FADS2), and di
18 chemical pathway requiring repeated use of a fatty acid desaturase 2 (FADS2) protein to perform Delta
19                            Overexpression of fatty acid desaturase 2 (fads2), which metabolizes LA to
20 the transferrin (TF), hemochromatosis (HFE), fatty acid desaturase 2 (FADS2)/myelin regulatory factor
21 so observed for eSNPs in 3 additional genes: fatty acid desaturase 2 (FADS2; P = .002), N-acetyl-alph
22            Delta-6 desaturase, also known as fatty acid desaturase-2 (FADS2), is a component of a lip
23                                          The fatty acid desaturase-2 rs1535 variant, associated with
24 ces cerevisiae OLE1 gene encodes the Delta-9 fatty acid desaturase, a highly regulated integral membr
25 ers of oxidative stress, and a modulation of fatty acid desaturase activities and plasma and membrane
26  provides a rapid means of isolating variant fatty acid desaturase activities for modification of see
27  is the first study to demonstrate decreased fatty acid desaturase activity in humans with asthma.
28  Saccharomyces OLE1 gene encodes the Delta-9 fatty acid desaturase, an enzyme that converts saturated
29 ntial yeast chromosomal gene encoding delta9 fatty acid desaturase, an integral ER membrane protein a
30 -carrier protein synthetase, and two each to fatty acid desaturase and either desaturase or fatty acy
31 r protein thioesterase, or by suppression of fatty acid desaturases and elongases, resulted in new ov
32 led that tung FADX is grouped with delta(12) fatty acid desaturases and hydroxylases rather than conj
33                                     Membrane fatty acid desaturases are responsible for inserting dou
34                               We developed a fatty acid desaturase assay based on measurement of desa
35 rs to be unrelated to classic membrane bound fatty acid desaturases based on overall sequence conserv
36                                  In animals, fatty acid desaturases catalyze key reactions in the syn
37 X5 was shown to physically interact with the fatty acid desaturases CrDelta4FAD and CrFAD6, likely do
38 FATTY ACID DESATURASE7 (FAD7), SUPPRESSOR OF FATTY ACID DESATURASE DEFICIENCY1 (SFD1) and SFD2 genes
39 sor, we identified and cloned three putative fatty acid desaturases, designated SbDES1, SbDES2, and S
40 erver identified a low stringency match to a fatty acid desaturase domain in the N-terminal sequence
41 ein), encodes a member of the SUR4 family of fatty acid desaturases, enzymes involved in elongation o
42 results show that CrFAD7 is the only omega-3 fatty acid desaturase expressed in C. reinhardtii, and w
43  that members of the plant integral membrane fatty acid desaturase (FAD) family, FAD2, FAD3, FAD6, FA
44                 The embryo-specific Delta-12 fatty acid desaturase FAD2-1 gene was targeted because i
45 vities of the microsomal omega-6 and omega-3 fatty acid desaturases, FAD2 and FAD3.
46 endoplasmic reticulum (ER)-localized omega-3 fatty-acid desaturases (Fad3) increase the production of
47              Transgenic over-expression of a fatty acid desaturase (fad3C) gene of soybean driven by
48 ncestry participants, 31 SNPs in or near the fatty acid desaturase (FADS) 1 and 2 cluster were associ
49    Two of these steps are encoded for by the fatty acid desaturase (FADS) cluster (chromosome 11, 11q
50 ingle nucleotide polymorphisms (SNPs) in the fatty acid desaturase (FADS) gene affect the activity an
51        Minor alleles of polymorphisms in the fatty acid desaturase (FADS) gene cluster have been asso
52 ymorphisms (SNPs) rs1535 and rs174448 in the fatty acid desaturase (FADS) gene cluster have opposite
53                                              Fatty acid desaturase (FADS) genes and their variants ha
54      Genetic components, such as variants of fatty acid desaturase (FADS) genes, determine the compos
55 biosynthesis of LC-PUFAs is regulated by the fatty acid desaturase (FADS) genes, of which a human-spe
56 l-length genes coding for microsomal Delta12 fatty acid desaturases (FADs) from the two Santalaceae s
57 ple of such an event is the evolution of the fatty acid desaturases (FADS) genes, which have been cla
58         We identified pheromone-biosynthetic fatty acid desaturases (FADs) MsexD3, MsexD5, and MsexD6
59 tinct subset of nematode C-lectin (clec) and fatty acid desaturase (fat) genes.
60  We have isolated a cDNA encoding the Delta5-fatty acid desaturase from M. alpina via a polymerase ch
61                                     Further, fatty acid desaturases from different kingdoms and with
62  these processes, we have studied the Delta9 fatty acid desaturase gene OLE1 in Saccharomyces cerevis
63 e many lipid metabolism genes, including the fatty acid desaturase gene OLE1, which is essential for
64 3p, which direct transcription of the Delta9-fatty acid desaturase gene OLE1.
65 anisms is achieved by feedback regulation of fatty acid desaturase gene transcription through signall
66 eved through overexpressing a C. elegans n-3 fatty acid desaturase gene, mfat-1.
67 x-ray mutant, M23, with a known FAD2-1A (for fatty acid desaturase) gene deletion.
68 turated fatty acids and strongly express two fatty acid desaturase genes, omega3 FATTY ACID DESATURAS
69              It was found that a C. albicans fatty acid desaturase homolog (Ole2) and a multicopper o
70 tifies Delta-6 desaturase/FADS2 as the major fatty acid desaturase in human sebaceous glands and sugg
71 GF receptor, suggesting a possible role of a fatty acid desaturase in regulating biosynthetic process
72               ScOle1p is the only long chain fatty acid desaturase in Saccharomyces and its membrane
73 ory machinery governing the transcription of fatty acid desaturases in bacteria, yeasts and animals t
74                           The three putative fatty acid desaturases in the M. tuberculosis genome, de
75 phyll content suggests a role for plastidial fatty acid desaturases in thylakoid formation.
76 habditis elegans fat-1 gene encoding an n--3 fatty acid desaturase into mammalian cells can quickly a
77                                              Fatty acid desaturases introduce a double bond in a spec
78 nstrate here that Spr2 encodes a chloroplast fatty acid desaturase involved in JA biosynthesis.
79 DS) gene family contains nine genes encoding fatty acid desaturase-like proteins.
80 lentivirus-mediated expression of an omega-3 fatty acid desaturase, mfat-1, normalized blood glucose
81  Taking advantage of an Arabidopsis thaliana fatty acid desaturase mutant (fad5) that constitutively
82 to have temperature-related phenotypes (e.g. fatty acid desaturase mutants, uvh6).
83                       Introduction of the ER fatty acid desaturase mutation, fad2, and to a lesser ex
84 ene-specific activator, SWI5, and the Delta9 fatty acid desaturase of yeast, OLE1, as multicopy suppr
85 ist of Rsp5, which promotes synthesis of the fatty acids desaturase Ole1.
86              Regulation of expression of the fatty acid desaturase Ole1p was hitherto the only known
87 ycerol molecular species lacks the necessary fatty acid desaturase, or a component thereof.
88                                              Fatty acid desaturases regulate the unsaturation status
89  present results strongly suggest that these fatty acid desaturases represent key enzymes involved in
90 tearoyl-coenzyme A desaturase 1 is a delta-9 fatty acid desaturase that catalyzes the synthesis of mo
91 cOLE1, a gene that encodes scOle1p, a Delta9 fatty acid desaturase that forms cis-monounsaturated fat
92 the strongest signal located in a cluster of fatty acid desaturases that determine PUFA levels.
93                                            A fatty acid desaturase triple mutant that is defective in
94 nzymes function, whereas Ole1, the essential fatty acid desaturase, was resistant to iron depletion.
95  express the fat-1 gene encoding for omega-3 fatty acid desaturase, which leads to an increase in end
96 e OLE1 gene encodes a membrane-bound Delta-9 fatty acid desaturase, whose expression is regulated by
97 ae OLE1 gene encodes a membrane-bound Delta9 fatty-acid desaturase, whose expression is regulated thr

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