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1 ression in the absence of ydeO, an AraC/XylS regulator gene.
2 8-kb genetic region downstream from the alcR regulator gene.
3 an cystic fibrosis transmembrane conductance regulator gene.
4 utations in the CF transmembrane conductance regulator gene.
5 he cystic fibrosis transmembrane conductance regulator gene.
6 he cystic fibrosis transmembrane conductance regulator gene.
7 anscription factor PU.1 to key lymphoid fate regulator genes.
8 y silencing lineage-specifying developmental regulator genes.
9 fications of histone marks at several master regulator genes.
10 ne regulatory network among 87 transcription regulator genes.
11 mediately upstream of the fur (ferric uptake regulator) gene.
12 n the human interferon-related developmental regulator gene 1 (IFRD1) as a disease-causing candidate.
13 lated AMP kinase; and down-regulated silence regulator gene 1 and PGC-1alpha mRNA/proteins and hepati
14 nthetic genes and down-regulation of silence regulator gene 1, PGC-1alpha, adiponectin, and lipid deg
15 VI secretion-related gene, a transcriptional regulator gene, a guanine deaminase gene, and cviI.
16 mutations of the cystic fibrosis conductance regulator gene account for the chronic pancreatitis note
17    Mutations in the staphylococcal virulence regulator gene agr frequently occur during Staphylococcu
18 the function of the staphylococcal virulence regulator gene agr.
19                         The human autoimmune regulator gene (AIRE), responsible for autoimmune polygl
20 ted in mature mTEC expressing the autoimmune regulator gene (Aire).
21                      Recently, an autoimmune regulator gene (AIRE-1), which is located on chromosome
22 eatured higher basal expression of key PP(i) regulators, genes ALPL, progressive ankylosis protein (A
23  initial change in the expression of a given regulator gene and its potential target gene to estimate
24 nduced induction of a master transcriptional regulator gene and its protein expression critical to ne
25 he cystic fibrosis transmembrane conductance regulator gene and single nucleotide polymorphism in HLA
26 ssion of several type-A ARABIDOPSIS RESPONSE REGULATOR genes and a number of genes involved in cell w
27      Some evidence suggests that a number of regulator genes and gene clusters will likely be found t
28    The timing of transcription of two master regulator genes and two cell division genes is controlle
29 ssecting cross-interactions among multilevel regulators, genes and biological functions.
30 o a mixture of 17 Salmonella mutants lacking regulator genes, and their survival ratios were compared
31                         When superrepressed, regulator genes are anticipated either to block programs
32                      In contrast, epigenetic regulator genes are more frequently targeted by somatic
33 riptional activation of ARABIDOPSIS RESPONSE REGULATOR genes, ARR7 and ARR15, feedback repressors of
34 ing that Brachyury is not a notochord master regulator gene as strictly defined.
35 ription from the p1 promoter of the response-regulator gene bldM depended on bldN in vivo, and the bl
36 raembryonic lineages at promoters of lineage regulators, gene bodies, and DNA-methylation valleys.
37 a indicate that aberrations in the chromatin regulator gene BRPF1 cause histone H3 acetylation defici
38 romosomal translocations involving chromatin regulator genes can lead to the formation of fusion onco
39         Deletion of the main transcriptional regulator gene, cbbR, resulted in impaired growth on ben
40 ubisCO) along with a divergently transcribed regulator gene, cbbR.
41  detect gene amplification of the cell cycle regulator gene CCND1 in 88 examples of formalin-fixed, p
42  hepatic expression of the G(1)/S checkpoint regulator genes Ccnd1 and cMyc and increased expression
43 ng the expression of a fission yeast mitotic regulator gene, cdc25, under the control of a tetracycli
44 he cystic fibrosis transmembrane conductance regulator gene CFTR have empirical evidence that they ca
45 kb cystic fibrosis transmembrane conductance regulator gene ( CFTR ) and Escherichia coli lacZ .
46 an cystic fibrosis transmembrane conductance regulator gene ( CFTR ) and its murine homologue ( Cftr
47 he cystic fibrosis transmembrane conductance regulator gene (CFTR) are poorly understood.
48 he cystic fibrosis transmembrane conductance regulator gene (CFTR) encodes a transmembrane protein (C
49 he cystic fibrosis transmembrane conductance regulator gene (CFTR) in 1989 represents a landmark acco
50 ung disease mutation in the CF transmembrane regulator gene (CFTR) led to correction or partial corre
51 or cystic fibrosis transmembrane conductance regulator gene (CFTR) mutations or polymorphisms, were e
52 he cystic fibrosis transmembrane conductance regulator gene (CFTR) shows a tightly regulated pattern
53 he cystic fibrosis transmembrane conductance regulator gene (CFTR) that cause cystic fibrosis have be
54 he cystic fibrosis transmembrane conductance regulator gene (CFTR) that disturbs fluid homeostasis an
55 he cystic fibrosis transmembrane conductance regulator gene (Cftr) to test the hypothesis that SLC26A
56 an cystic fibrosis transmembrane conductance regulator gene (CFTR) transcription is tightly regulated
57 he cystic fibrosis transmembrane conductance regulator gene (CFTR), as well as genes involved in anti
58 an cystic fibrosis transmembrane conductance regulator gene (CFTR), in which an abbreviated polypyrim
59 he cystic fibrosis transmembrane conductance regulator gene (CFTR).
60 utations in the CF transmembrane conductance regulator gene (CFTR).
61 he cystic fibrosis transmembrane conductance regulator gene, CFTR.
62 , WT1 and TP53 (class III), and 5 epigenetic regulator genes (class IV), were analyzed in 206 childre
63 he cystic fibrosis transmembrane conductance regulator gene could be detected simultaneously in inter
64 entified early driver mutations in chromatin regulator genes (CREBBP, EZH2 and KMT2D (MLL2)), whereas
65 45], P = 4.54 x 10(-5) ), and the complement regulator gene CSMD1 (rs7002001; odds ratio 2.41 [95% co
66                           The carbon storage regulator gene, csrA, encodes a factor which negatively
67 t affect expression of eukaryotic cell cycle regulator genes CYCD3;1 and CDC2A but affects expression
68          An insertion mutation of the sensor-regulator gene eliminated the ability of uropathogenic E
69 of neighboring histidine kinase and response regulator genes, encoded on the same strand, was compile
70  The mtrR (multiple transferrable resistance Regulator) gene encodes a putative transcriptional repre
71 mline mutations in the WNT-signaling-pathway-regulator gene encoding APC, and we generated COs that e
72       As effector gene expression increases, regulator gene expression can
73 ce the expression of its own gene, such that regulator gene expression is repressible (like effector
74  in the same direction; uncoupling, in which regulator gene expression remains constant while effecto
75 h widespread homeostatic control of splicing regulator gene expression.
76 ime by binding to chromatin of the flowering regulator gene Flowering Locus C (FLC).
77        The RPGR (retinitis pigmentosa GTPase regulator) gene for RP3, the most frequent genetic subty
78 utation in the host's global transcriptional regulator gene fur.
79          Using a Vibrio cholerae iron uptake regulator gene (fur) as a probe, a 2.6-kb SalI/HindIII D
80 pathogenicity island (SPI) 1 transcriptional regulator genes hilA, C, and D and invF.
81 Lrp represses transcription of key virulence regulator genes--hilA, invF, and ssrA--in Salmonella pat
82 sults identify mtrA as an essential response regulator gene in M. tuberculosis which is differentiall
83 categories, 8 molecular networks, and 10 key regulator genes in confluency-induced differentiation of
84 ts provide a rationale for autoregulation of regulator genes in repressible gene circuits and lead to
85              This implicates putative master regulator genes in which multiple independent stop codon
86 ative stress response and pigment production Regulator) gene in Pseudomonas aeruginosa.
87 s several members of the B7 family of immune regulator genes, including butyrophilin-like 2 (BTNL2; O
88 ce of JAK2-V617F and mutations in epigenetic regulator genes, including EZH2 In this study, we show t
89 omplish metabolic processes, this network of regulator-gene interactions describes potential pathways
90                                            A regulator gene is adjacent to the operon of the sulfide-
91                      Such a subpopulation of regulator genes is expected to include, notably, genes g
92 ion alone, including the iron-sulfur cluster regulator gene, iscR, which was required for oxidative s
93 n the level of expression of the main myelin regulator gene Krox20/Egr2 and the myelin gene P0.
94 ta sets revealed the hematopoietic stem cell regulator gene latexin (LXN) to be commonly downregulate
95 howed that allele replacement of the NMB0595 regulator gene led to loss of virulence, sensitivity to
96  identified a novel maternal transcriptional regulator gene, lilliputian (lilli), which contains an H
97                     Deletion of the response regulator gene, lovR, results in severe attenuation of c
98                  Two new LysR-type symbiosis regulator genes, lsrA and lsrB, were identified in the s
99 lelic mutations in the lysosomal trafficking regulator gene (LYST), resulting in formation of giant l
100  Our analyses identified 41 consensus master regulator genes (MRs), the regulons of which comprised b
101 we constructed an flhD (the master flagellar regulator gene) mutant of Salmonella enterica serovar Ty
102                  Deletion of the sialic acid regulator gene nanR partially restored IBC formation in
103                          The global nitrogen regulator gene ntcA encodes a DNA-binding protein, NtcA,
104              The SKN7 two-component response regulator gene of Candida albicans was deleted, and the
105               osaC is linked to the response regulator gene osaB; expression analysis of the latter r
106       The independently transcribed response regulator gene, osaB, is essential for osmoadaptation; w
107 n rare and novel variants only in complement regulator genes (P<0.01), a distinction consistent with
108     A putative Lrp/AsnC-type transcriptional regulator (gene PA2082, here called kynR), is divergentl
109 is of a hybrid histidine kinase and response regulator gene pair, osaAB, involved in osmoadaptation i
110 defined two histidine kinase sensor-response regulator gene pairs important for S. aureus in vivo sur
111         A putative LysR-type transcriptional regulator gene, pcpM, and a maleylacetate reductase gene
112                   Two hypothetical LysR-type regulator genes, pcpM and pcpR, have been identified; pc
113 sociated only with mutations in the response regulator gene pleD that block the loss of motility.
114 tion is effected through control of both the regulator gene prpR and the prpBCDE operon itself.
115             These prophage-encoded secretion regulator genes (psr) are found exclusively on prophages
116 e gene (cph1) and its cotranscribed response regulator gene (rcp1) were significantly reduced and its
117             Mutation of the cognate response regulator gene rcsB restored full virulence to the rcsC
118        The transposon interrupted a response regulator gene (referred to as aoxR), which encodes an n
119 he cystic fibrosis transmembrane conductance regulator gene region across nine eutherian mammals reve
120 cence/immortalization and found that the key regulator genes represented six pathways: the cell cycle
121 se range of functions, including a number of regulators, genes required for glutamine synthesis, NADH
122 on efflux transporter gene and a PbrR family regulator gene, respectively.
123 aling molecules, including the redox-sensing regulator gene rex.
124 etected a GA insertion in the quorum-sensing regulator gene rhlR and, in addition, identified a novel
125 in R800, inactivation of the orphan response regulator gene ritR by allele replacement reduced pathog
126  associated with retinitis pigmentosa GTPase regulator gene (RPGR) mutations.
127 r of iron transport) for the orphan response regulator gene, rr489, is proposed.
128 ltogether, 18 molecular networks, and 39 key regulator genes, several of which were associated with e
129          In contrast, the flowering negative regulator gene SHORT VEGETATIVE PHASE (SVP) was up-regul
130 L and HMR) depends on the silent information regulator genes, SIR1, SIR2, SIR3, and SIR4.
131 fied a null allele of the silent information regulator gene SIR4 as a host mutant that allows for tra
132 ases (HDACs) 1 and 9, and Silent information regulator genes (sirtuins [SIRTs]) 6 and 7 were signific
133 d beta-cells activated expression of the EMT regulator gene Snail in a SMAD3/Stat3-dependent manner.
134  HIF-2alpha to a specific site in the master-regulator gene SOX9.
135 f target cell cytokine receptors, cell death regulator genes such as bcl-2 family members, Fas recept
136      We assayed histone modifications at key regulator genes (such as Nanog, Pou5f1 (also known as Oc
137                These include the cell growth regulator gene TGFbetaRII and the proapoptotic gene BAX.
138 often controlled by the protein product of a regulator gene that is directly involved in the control
139  interrogated the network to identify master regulator genes that mechanistically regulate brain regi
140 has been renamed the motility quorum-sensing regulator gene (the mqsR gene).
141 he cystic fibrosis transmembrane conductance regulator gene to human airway epithelia.
142 twork connecting loci enriched in cell cycle regulator genes to nuclear lamina that mediates the CTCF
143 cis-trans-regulated target genes, from trans-regulator genes to target genes, and from trans-eQTL to
144                  A putative His-Asp response regulator gene (trg1: transcriptional regulatory gene 1)
145 model, an insertion mutation in the response regulator gene, trxR, led to a significant reduction in
146 he cystic fibrosis transmembrane conductance regulator gene using SERRS active primers in an ARMS ass
147 charide synthesis and of the transcriptional regulator genes vpsR, vpsT, and hapR.
148                Transcription of the response regulator gene was induced by the presence of ethanolami
149 ions in the human hematopoietic cytoskeletal regulator gene WAS.
150 that ybbI (designated cueR for copper export regulator gene) was required for copper tolerance during
151 OPSIS RESPONSE REGULATOR5, a type-A response regulator gene, was upregulated at the time of shoot com
152 s containing unique DNA barcodes in place of regulator genes were mixed with the parental control, an
153 -rich CIM, and cytokinin-responsive response regulator genes were upregulated during incubation on cy
154                       The hurIR (heme uptake regulator) genes were previously identified upstream of
155 he cystic fibrosis transmembrane conductance regulator gene, which codes for a chloride channel, but
156 ing of the RPGR (retinitis pigmentosa GTPase regulator) gene, which has been shown to be mutated in 1
157  mutation that inactivates the etaR response regulator gene, while M7 is a wild-type revertant for et
158  in alginate production genes and a c-di-GMP regulator gene; while PA01 acquired mutations in PilT an
159 he cystic fibrosis transmembrane conductance regulator gene with respect to pancreatitis.

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