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1 ched normal samples (13 overexpressed and 28 underexpressed).
2 ulted in identification of one band that was underexpressed.
3 ger and, due to decreased mRNA stability, is underexpressed.
4 verexpressed while hundreds of others become underexpressed.
5 ke breast cancer (BLBC), in which ERalpha is underexpressed.
6 ematically and persistently overexpressed or underexpressed.
7 of identified miRNAs by miRNA profiling were underexpressed.
8 al responses in patients in which morgana is underexpressed.
9 -carbon metabolism, were hypermethylated and underexpressed.
10 X) activity in disorders where PGC-1alpha is underexpressed.
11 mean expression were designated as over- or underexpressed.
12 the monosomy 3 group, whereas two spots were underexpressed.
13 In comparison to MC, the genes were over- or underexpressed.
14 f these, 747 were overexpressed and 416 were underexpressed.
15 ng hormone receptor (GHRHR) and Homer-2 were underexpressed.
16 ly overexpressed, while p16 was consistently underexpressed.
17 s chlorophyll a/b binding protein (CAB) gene underexpressed 1 (cue1) mutant underexpresses light-regu
19 with or without VPF/VEGF overexpressed 9 and underexpressed 6 genes in comparison with their senescen
21 L8, IFIH1, NFKB1A, IL6, ISG15, and EGFR were underexpressed and ACTB, HSP90AA1, RAB7A, and RPS27A wer
22 ges, where IFN gamma-up-regulated genes were underexpressed and down-regulated genes were overexpress
25 re-examined the phenotype of three cue (cab-underexpressed) Arabidopsis mutants, defective in chloro
28 glycosylation was seen in proteins that were underexpressed based on the reversed-phase chromatogram
30 xpressed (17 were overexpressed, and 27 were underexpressed) between malignant high-grade astrocytoma
32 hsa-miR-203, hsa-miR-210, hsa-miR-205*) were underexpressed by > 2-fold in diseased vs. healthy gingi
36 y nodes of empirical networks with over- and underexpressed centrality relative to a null baseline.
37 ipt abundance in F1 hybrids (either over- or underexpressed compared to both parent species) did not
38 ct groups of genes that were either over- or underexpressed compared with normal thyroid, whereas the
40 urodegenerative disorders were significantly underexpressed during fetal life (N=46 genes, p=1.67x10-
42 e was used to estimate the cellular level of underexpressed FliK, which could partly restore function
43 rkedly elevated in the NSCLC cell lines that underexpressed gamma-catenin relative to those lines tha
44 ansgenic plants that either overexpressed or underexpressed GAST1 RNA exhibited no phenotypic differe
47 using microarray analysis, one-fifth of the underexpressed genes belonged to the kallikrein gene fam
49 ion at their transcription start sites while underexpressed genes featured hypomethylation at polycom
50 Semaphorin 3F (SEMA3F), is among the top 1% underexpressed genes in HNSCC, and that genomic loss of
52 alpha regulatory subunit, and IGFBP6, while underexpressed genes included NeuroD and nicotinic choli
53 ncluding 2 TET2-mutated cases, significantly underexpressed genes known to be downregulated in angioi
54 includes, at least in part, a collection of underexpressed genes that encode proteins that inhibit c
55 erexpressed genes and 13 of 28 clusters with underexpressed genes were concordant with previously rep
56 cDNAs were overexpressed and 303 cDNAs were underexpressed greater than 2-fold, compared with B10.RI
57 n oncogenic v-ras(Ha) gene, and RARalpha was underexpressed in a benign keratinocyte cell line carryi
58 elevance because the UBQLN1 gene is lost and underexpressed in a large percentage of human cancer cel
59 protein-tyrosine phosphatase 1B (PTP1B) was underexpressed in a panel of ovarian carcinoma-derived c
61 2 (NRF2) pathway signature was significantly underexpressed in AdCC of submandibular compared to paro
62 ent of a male-predominant transcript that is underexpressed in adult male hybrids of Drosophila pseud
65 Both cytosolic CK forms (CKM and CKB) were underexpressed in blood from asthmatics compared with co
68 on analysis, that miR-34a, a p53 target, was underexpressed in CD44(+) prostate cancer cells purified
69 that three miRNAs were overexpressed and 24 underexpressed in cervical cell lines containing integra
72 8 miRNAs are overexpressed and 28 miRNAs are underexpressed in cSCC compared to normal epidermis.
76 cantly more genes are overexpressed than are underexpressed in dystrophic muscle, with dystrophin und
78 A hemoglobin cluster was identified that was underexpressed in ERA patients but overexpressed in syst
79 osine monophosphate (cAMP) signaling and are underexpressed in GC-resistant or relapsed ALL patients.
80 rotein 45 (IIp45) we recently identified was underexpressed in glioblastoma multiforme, the most mali
81 one transcriptional regulator that was both underexpressed in GR(369-) larvae and consistently overe
82 ses, microRNA-218 (miR-218) was specifically underexpressed in HPV-positive cell lines, cervical lesi
83 The glucose transporter 1 (GLUT1) protein is underexpressed in human glioblastoma multiforme and is o
84 sed in synovial sarcoma cells but relatively underexpressed in human iPSC-derived cardiomyocytes, lev
86 t ZNF750 is exclusively deleted, mutated and underexpressed in human SCCs, and low ZNF750 expression
87 more, nine miRNAs were overexpressed and one underexpressed in integrated HPV-16 cell lines compared
89 PTEN encodes a lipid phosphatase that is underexpressed in many cancers owing to deletions, mutat
96 d concomitantly deleted, hypermethylated and underexpressed in multiple independent lung tumor data s
97 tic tissues, whereas FABP-1 is paradoxically underexpressed in NASH, suggesting a new potential mecha
98 oup (128%, P < 0.001), but was paradoxically underexpressed in NASH-mild versus SS (73%, P < 0.001),
100 actor early growth response gene 1 (EGR1) is underexpressed in non-small-cell lung cancer (NSCLC) com
103 ify two miRNAs, miR-15a and miR-16, that are underexpressed in ovarian cell lines and in primary ovar
106 th recent observations that these miRNAs are underexpressed in primary cancers support the idea that
107 us to identify 11 genes that were frequently underexpressed in prostate cancer and that co-localized
110 ctivation, metabolism, and survival that are underexpressed in resting memory T cells from MHC class
111 sets were found to be significantly over- or underexpressed in RPE, respectively, compared with retin
112 family, some of which phosphorylate pRb, are underexpressed in senescent cells, others are expressed
117 ysis revealed that 187 genes were relatively underexpressed in the absence of SigF in early stationar
118 P1) and 14-3-3final sigma, were consistently underexpressed in the adenocarcinomas, suggesting that t
124 of calcium-binding proteins, is known to be "underexpressed" in cultured breast carcinoma-derived cel
125 esults and find that CaN19 is also markedly "underexpressed" in several carcinoma-derived cell lines
126 erentially expressed (4 overexpressed and 12 underexpressed) in patients with cirrhotic-stage NASH.
127 e A2, and phospholipase D were significantly underexpressed, in breast cancer cells compared with HME
129 higher bacterial burdens than control mice, underexpressed indoleamine-2,3-dioxygenase (Ido1) in lun
130 1254 and 363 were overexpressed (>2-fold) or underexpressed (<0.5-fold), respectively, in the SP.
131 he transcriptional regulatory regions of the underexpressed metabolic genes, and we then hypothesized
133 ic homolog 4 (Smad4), whereas two frequently underexpressed miRNA families, miR-26 and miR-29, cooper
134 unctional overexpression of miR-31, the most underexpressed miRNA in serous ovarian cancer, repressed
135 SCC patients compared to HCs: 11 miRNAs were underexpressed (miRNA-136, miRNA-147, miRNA-1250, miRNA-
141 sis identified several genes that are either underexpressed or overexpressed in the Dd-STATb null str
144 eptors, such as those that are autoreactive, underexpressed, or that fail to promote positive selecti
147 s of cell growth, survival, and cycling, and underexpressed proinflammatory and apoptotic pathways, i
148 ted, or mutated proteins as well as over- or underexpressed proteins have been implicated in many dis
149 occurs either when alpha-tubulin is modestly underexpressed relative to beta-tubulin or when beta-tub
150 nd 93 genes that were significantly over- or underexpressed, respectively, compared with mature-DC.
153 with the risk allele, exon 5 is consistently underexpressed, thereby providing a mechanism by which t
154 Klf6, Klf9, Nid2, Ntn4, Per1, and Txnip) and underexpressed those associated with aggressive disease
156 genes overexpressed (PILRB, STS-1, SPRY1) or underexpressed (TSPAN16, ADAMTSL4) in p185BCR-ABL-positi
158 where hPepT1 expression was either over- or underexpressed, using an inducible adenovirus system or
159 ions of the neural tube where Pax-3 had been underexpressed were found subsequently to contain high c
160 genesis (50 genes overexpressed and 58 genes underexpressed) were modulated back to normal levels aft
162 ressed in dystrophic muscle, with dystrophin underexpressed, whereas other genes encoding muscle stru
163 Runx1, ephrin B2, cyclin D1, and Gata1 were underexpressed while P16/Ink4a, P21, GSK-3beta, Il-6, Ff
164 hich degrades HER2, is frequently mutated or underexpressed, while the client-protective co-chaperone