ライフサイエンスコーパス: underexpression

1 he HCL surface that were dependent upon RhoH underexpression.

2 through this motif contributed to the global underexpression.

3 Significant 3p underexpression and 22q overexpression were found in all

4 We find that 58% of underexpression and 28% of overexpression outliers have

5 ort the cooperative relationship of sLe(x/a) underexpression and E-cadherin overexpression in the gen

6 Underexpression and overexpression analyses demonstrate

7 otein expression of these genes in mice with underexpression and overexpression of PGC-1alpha.

8 so, there are two consequences: first, both underexpression and overexpression of protein complex su

9 es presenting concomitant cytidine deaminase underexpression and Tau upregulation open up new possibi

10 Both the gene underexpression and the leaf cell morphology phenotypes

11 cell lines displayed corresponding over- or underexpression and up to 23-fold differences in cPLA2 a

12 ccording to overexpression, RNA interference underexpression, and promoter element mutation studies.

13 Underexpression by knockout mutation and/or RNAi-mediate

14 a, IL-1beta, IL-6, and IFN-beta, whereas p62 underexpression by small hairpin RNA markedly elevated t

15 lity resulting from either overexpression or underexpression (deletion) of Arf genes has previously b

16 hibitory Bax binding partner as its over- or underexpression did not show any apoptosis defects.

17 ACE underexpression does not prevent cardiac hypertrophy or

18 Stable NGAL overexpression or underexpression had no effect on PaCa cell survival, via

19 t cancer data sets revealed striking ANGPTL7 underexpression in cancerous compared to normal tissues.

20 ed relatively reproducible overexpression or underexpression in individual tumors.

21 aberrant S-opsin overexpression and M-opsin underexpression in M cones.

22 in the D. pseudoobscura lineage and that its underexpression in sterile hybrid males may cause an ove

23 r AIRE and 7 of 16 TSAgs showed the expected underexpression in thymomas, levels were increased for f

24 Several of the proteins showing significant underexpression in tumor tissue were cytokeratins and ot

25 essor with different modalities: (1) Morgana underexpression induces centrosome amplification and cyt

26 cyte differentiation and in myelination, its underexpression may be pivotal to, and upstream of, othe

27 Notably, GPX3 hypermethylation and underexpression occur commonly in prostate, gastric, cer

28 ed 1924 differentially expressed genes, with underexpression of 1014 genes, 11 of which were within t

29 ized in 82 apparent transcription units) and underexpression of 19 genes.

30 In addition, patients with HAP demonstrated underexpression of a type-I interferon signaling gene si

31 zed by overexpression of innate immunity and underexpression of adaptive immunity genes, whereas negl

32 on of hsa-miR-155 leading to allele-specific underexpression of AGTR1.

33 is strongly induced in the TI after UUO, but underexpression of alpha8 integrin does not attenuate TI

34 xpression is of practical concern (e.g., the underexpression of an herbicide tolerance gene in crop p

35 ROt promoter is also responsive to over- and underexpression of AP-1, confirming the role of AP-1 in

36 d to have homozygous deletion or significant underexpression of ASF1a should be tested for high sensi

37 any diseases are caused by overexpression or underexpression of Bcl-x(L) homologues.

38 n markers CD23, CD25, CD69, and CD71 and the underexpression of CD22, Fcgamma receptor IIb, CD79b, an

39 An underexpression of collagen genes and of genes associate

40 sistent expression of pluripotency genes and underexpression of developmental genes during differenti

41 nts with overexpression of UP genes also had underexpression of DOWN genes (correlation > .70 in both

42 and microRNA-expression signatures revealed underexpression of drug resistance and adverse outcome p

43 striking association of EGFR mutations with underexpression of DUSP4, a gene within a broad region o

44 Over- or underexpression of EmbC resulted in reduced or increased

45 TG was high because of underexpression of fatty acid oxidative enzymes and thei

46 ne-targeting mutation, mgR, which shows that underexpression of fibrillin-1 similarly leads to MFS-li

47 ic interaction between two genes whereby the underexpression of gene A combined with the overexpressi

48 d in monocarboxylate transport activity, and underexpression of genes involved in signal transduction

49 These include a gross underexpression of genes preferentially expressed in fem

50 Underexpression of genes promoting cell proliferation wa

51 Extensive efforts to achieve underexpression of Hsc70-1 mRNA using a full-length anti

52 was to determine whether overexpression and underexpression of human heme oxygenase (HHO)-1 could be

53 This defect is characterized by the underexpression of IL-1 beta and multiple other cytokine

54 sufficient for enhanced mRNA degradation and underexpression of inflammatory mediators.

55 tering revealed a striking pattern of global underexpression of intermediary metabolism transcripts i

56 The marked underexpression of Ku70 and Ku86 starting at the adenoma

57 d immunotherapeutic tar-gets (WT1, CD33) and underexpression of leukemia-associated (MLLT3, TAL1) and

58 pression of MGP in maturing chondrocytes and underexpression of MGP in proliferative and hypertrophic

59 ar, we observed overexpression of miR-21 and underexpression of miR-1 in the induced IL-13 transgenic

60 Underexpression of miR-122 potentially contributes to al

61 demonstrated overexpression of DOHH mRNA and underexpression of miR-331-3p and miR-642-5p in several

62 Although underexpression of miR-9 in cancer cells is reported in

63 uated microRNA (miRNA) biogenesis and global underexpression of miRNAs; thus, targeting the miRNA bio

64 emble antigen-experienced lymphocytes in the underexpression of molecules that are down-regulated by

65 Overexpression of Skp2 coupled with underexpression of p27 are frequent characteristics of c

66 Overexpression of METII and underexpression of P2A-RS were confirmed in pooled and i

67 We observed dramatic underexpression of p57(KIP2) in BiCHM, identical to that

68 Underexpression of PcsB did not result in changes in the

69 Finally, microarray analyses indicated that underexpression of PcsB may generate a signal that incre

70 revealed that loss of the PI4K2B allele and underexpression of PI4KIIbeta mRNA are associated with h

71 ssion of PLA(2) and the cyclooxygenases, and underexpression of PLC-beta(1).

72 demonstrate excessive monocyte migration and underexpression of PLXNC1 in the lungs and circulation,

73 as hypermethylation, which should result in underexpression of PTEN or of KILLIN, a novel tumor supp

74 ory have demonstrated that overexpression or underexpression of PTHrP in the murine mammary gland lea

75 ently impacts the rate of senescence because underexpression of Rap1 or overexpression of the core hi

76 Over- and underexpression of RGS21 in 16HBE cells confirmed that R

77 is involved in trafficking of APP, and that underexpression of SORL1 leads to overproduction of Abet

78 ion were differentially expressed, including underexpression of stimulators of lymphocyte function an

79 microenvironmental effects, suggesting that underexpression of survival factors or overexpression of

80 The patients showed relative underexpression of SV3a and SV3b and overexpression of S

81 ns mothers by D. melanogaster males exhibits underexpression of Sxl in embryos.

82 trophils and Natural Killer (NK) cells, with underexpression of T- and B cell responses.

83 laceable kind showed a consistent and robust underexpression of the deubiquitination gene ubiquitin c

84 In addition, a synergistic underexpression of the gamma-protocadherin complex, loca

85 ets and that its overexpression corrects the underexpression of the insulin gene and ameliorates gluc

86 airy cell leukemia (HCL) is characterized by underexpression of the intracellular signaling molecule

87 gh mice) or megakaryocyte lineage restricted underexpression of the transcription factor GATA-1 (GATA

88 Underexpression of the transcriptional coactivator PGC-1

89 Conversely, underexpression of the wild-type fliK gene, achieved by

90 Western blots confirmed underexpression of those complex I-V subunits assessed a

91 We propose that the underexpression of Tip60 observed in many human tumors c

92 IF revealed possible concurrent underexpression of TSP2 in TSP1-null mice and of TSP1 in

93 Therefore this study shows that underexpression of tumor suppressor miR-375 could lead t

94 e and the impact of PTP1B and TCPTP over- or underexpression on palmitate- or tunicamycin-induced ER

95 s in gene expression characterized by severe underexpression or overexpression of specific mRNAs.

96 The pattern of expression, either underexpression or overexpression, was the same for 10 g

97 ABL oncogene, and in this condition, morgana underexpression predicts a worse response to imatinib, t

98 ors participate in GBM via drastic over- and underexpression, respectively.

99 n of PMSR4 lowered the sulfoxide content and underexpression resulted in an overall increase in conte

100 action, we carried out in vivo gce over- and underexpression studies.

101 budgets that account for such local isotopic underexpression suggest that denitrification is responsi

102 DNMT3A underexpression was also associated with adverse overall

103 Moreover, TIMP2 underexpression was frequent (41.8%; 23 of 55) in human

104 scovered that insufficient NADPH due to GLS2 underexpression was responsible for the delayed metaboli

105 , hypermotility and flagellar gene over- and underexpression were not observed to affect the expressi

106 ritical; overexpression causes toxicity, and underexpression would result in incomplete rescue.