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1 nhibitory (E-I) balance as caused by channel underexpression.
2 he HCL surface that were dependent upon RhoH underexpression.
3 through this motif contributed to the global underexpression.
6 ort the cooperative relationship of sLe(x/a) underexpression and E-cadherin overexpression in the gen
9 so, there are two consequences: first, both underexpression and overexpression of protein complex su
11 es presenting concomitant cytidine deaminase underexpression and Tau upregulation open up new possibi
13 cell lines displayed corresponding over- or underexpression and up to 23-fold differences in cPLA2 a
14 ccording to overexpression, RNA interference underexpression, and promoter element mutation studies.
16 a, IL-1beta, IL-6, and IFN-beta, whereas p62 underexpression by small hairpin RNA markedly elevated t
17 lity resulting from either overexpression or underexpression (deletion) of Arf genes has previously b
21 to modulate its metabolism, and that FERMT2 underexpression impacts axonal growth, synaptic connecti
22 t cancer data sets revealed striking ANGPTL7 underexpression in cancerous compared to normal tissues.
25 evidence for a detrimental effect of FERMT2 underexpression in neurons and insight into how this may
26 in the D. pseudoobscura lineage and that its underexpression in sterile hybrid males may cause an ove
27 r AIRE and 7 of 16 TSAgs showed the expected underexpression in thymomas, levels were increased for f
28 Several of the proteins showing significant underexpression in tumor tissue were cytokeratins and ot
29 iptome sequencing revealed pathological gene underexpression induced by transcript disruptions in thr
30 essor with different modalities: (1) Morgana underexpression induces centrosome amplification and cyt
31 cyte differentiation and in myelination, its underexpression may be pivotal to, and upstream of, othe
33 ed 1924 differentially expressed genes, with underexpression of 1014 genes, 11 of which were within t
35 In addition, patients with HAP demonstrated underexpression of a type-I interferon signaling gene si
36 zed by overexpression of innate immunity and underexpression of adaptive immunity genes, whereas negl
38 is strongly induced in the TI after UUO, but underexpression of alpha8 integrin does not attenuate TI
39 xpression is of practical concern (e.g., the underexpression of an herbicide tolerance gene in crop p
40 ROt promoter is also responsive to over- and underexpression of AP-1, confirming the role of AP-1 in
41 d to have homozygous deletion or significant underexpression of ASF1a should be tested for high sensi
43 ny cortical systems must be accompanied with underexpression of bidirectionally connected inhibitory-
44 n markers CD23, CD25, CD69, and CD71 and the underexpression of CD22, Fcgamma receptor IIb, CD79b, an
46 xpression in resistant mites of CYP4DP24 and underexpression of CYP3012A6 and CYP4EP4 RNA interferenc
47 sistent expression of pluripotency genes and underexpression of developmental genes during differenti
48 nts with overexpression of UP genes also had underexpression of DOWN genes (correlation > .70 in both
49 and microRNA-expression signatures revealed underexpression of drug resistance and adverse outcome p
50 striking association of EGFR mutations with underexpression of DUSP4, a gene within a broad region o
53 ne-targeting mutation, mgR, which shows that underexpression of fibrillin-1 similarly leads to MFS-li
54 ic interaction between two genes whereby the underexpression of gene A combined with the overexpressi
56 d in monocarboxylate transport activity, and underexpression of genes involved in signal transduction
59 sence of pet sensitization but also with the underexpression of host gene expression of inflammatory
61 was to determine whether overexpression and underexpression of human heme oxygenase (HHO)-1 could be
64 tering revealed a striking pattern of global underexpression of intermediary metabolism transcripts i
67 d immunotherapeutic tar-gets (WT1, CD33) and underexpression of leukemia-associated (MLLT3, TAL1) and
68 pression of MGP in maturing chondrocytes and underexpression of MGP in proliferative and hypertrophic
69 ar, we observed overexpression of miR-21 and underexpression of miR-1 in the induced IL-13 transgenic
71 demonstrated overexpression of DOHH mRNA and underexpression of miR-331-3p and miR-642-5p in several
73 uated microRNA (miRNA) biogenesis and global underexpression of miRNAs; thus, targeting the miRNA bio
74 emble antigen-experienced lymphocytes in the underexpression of molecules that are down-regulated by
81 Finally, microarray analyses indicated that underexpression of PcsB may generate a signal that incre
82 revealed that loss of the PI4K2B allele and underexpression of PI4KIIbeta mRNA are associated with h
84 demonstrate excessive monocyte migration and underexpression of PLXNC1 in the lungs and circulation,
85 as hypermethylation, which should result in underexpression of PTEN or of KILLIN, a novel tumor supp
86 ory have demonstrated that overexpression or underexpression of PTHrP in the murine mammary gland lea
87 ently impacts the rate of senescence because underexpression of Rap1 or overexpression of the core hi
90 howed overexpression of ANXA2 and CDC42, and underexpression of SEMG2 proteins in primary infertility
91 is involved in trafficking of APP, and that underexpression of SORL1 leads to overproduction of Abet
92 ion were differentially expressed, including underexpression of stimulators of lymphocyte function an
93 microenvironmental effects, suggesting that underexpression of survival factors or overexpression of
97 laceable kind showed a consistent and robust underexpression of the deubiquitination gene ubiquitin c
99 ets and that its overexpression corrects the underexpression of the insulin gene and ameliorates gluc
100 airy cell leukemia (HCL) is characterized by underexpression of the intracellular signaling molecule
101 gh mice) or megakaryocyte lineage restricted underexpression of the transcription factor GATA-1 (GATA
104 te experimental evidence that both over- and underexpression of these channels can be epileptogenic,
109 e and the impact of PTP1B and TCPTP over- or underexpression on palmitate- or tunicamycin-induced ER
110 s in gene expression characterized by severe underexpression or overexpression of specific mRNAs.
112 ABL oncogene, and in this condition, morgana underexpression predicts a worse response to imatinib, t
114 n of PMSR4 lowered the sulfoxide content and underexpression resulted in an overall increase in conte
115 4EP4 in the susceptible population, to mimic underexpression seen in the resistant mites, prevented c
117 budgets that account for such local isotopic underexpression suggest that denitrification is responsi
120 scovered that insufficient NADPH due to GLS2 underexpression was responsible for the delayed metaboli
121 , hypermotility and flagellar gene over- and underexpression were not observed to affect the expressi