ライフサイエンスコーパス: MDF

1 MDF during trophic transfer of MeHg leading to enrichmen

2 MDF encodes a putative RS domain protein with a predicte

3 MDF expression is modulated by osmotic and cold stress,

4 MDF expression is not defective in the bodenlos, pin1 or

5 MDF identifies patients at risk of relapse and poor outc

6 MDF is required for the correct splicing and expression

7 all ions that fall outside of the GSH adduct MDF template windows, the processed full scan MS chromat

8 ither uniquely by one MDF or randomly by all MDFs.

9 We analyzed MDF of end-induction bone marrow samples from a historic

10 Moreover, the sensitivities with FIGS and MDF were equal for all As species, allowing for the poss

11 In general, any MDF protein that is expressed also is present on transcr

12 249 patients were prospectively evaluated by MDF for RD, and presence of RD was correlated with disea

13 of target genes correlates with occupancy by MDF, in particular, herculin.

14 er abiotic reduction pathways, and combining MDF with the observed MIF allows the distinction from ph

15 y, the epsilon subunit gene becomes a common MDF target and begins to be expressed.

16 spindle assembly checkpoint (SAC) component MDF-1/MAD1 is required for the PGC arrest.

17 -1 or a second spindle checkpoint component, MDF-2, failed to arrest the cell cycle, exhibited chromo

18 ffects its binding to another SAC component, MDF-2/MAD2.

19 but the mass dependent isotope compositions (MDF; delta(202)Hg) were not (r(2) = 0.26, p = 0.16), ref

20 ase (RD) by multidimensional flow cytometry (MDF) in children treated on Children's Oncology Group AM

21 measured by multidimensional flow cytometry (MDF) is a key early prognostic indicator and is strongly

22 The MERISTEM-DEFECTIVE (MDF) Arabidopsis gene encodes an SR-related family prote

23 tions in the Arabidopsis MERISTEM-DEFECTIVE (MDF) gene lead to a loss of stem cell and meristematic a

24 Measurements of Hg isotopic mass-dependent (MDF) and mass-independent fractionation (MIF) in food we

25 indicating lower degrees of mass-dependent (MDF) and mass-independent Hg fractionation (MIF) (respec

26 the wear rate of sample after the different MDF pass numbers using the corresponding hardness magnit

27 appearance of myogenic determination factor (MDF) transcripts in developing chick limbs and other emb

28 The myogenic determination factors (MDFs) are transcriptional activators that target E boxes

29 of a single member of the MyoD gene family (MDF) is necessary and sufficient to establish the positi

30 raphene behave like massless Dirac fermions (MDFs) with linear energy-momentum dispersion (1, 2) , pr

31 as designed to apply the mass defect filter (MDF) approach to the screening and identification of rea

32 ates were filtered by mass defect filtering (MDF) and multiple-group comparison.

33 four functions: Marker Dependency Filtering (MDF) to correct for known dependency between omics marke

34 red to a standard miniature diffusion flame (MDF) atomizer.

35 Development of microbiota-directed foods (MDFs) that selectively increase the abundance of benefic

36 The measured enrichment factors for MDF and MIF (epsilon(202)Hg and E(199)Hg) ranged from 1.

37 haracterization of GEM (+/-0.3 per mille for MDF, +/-0.05 per mille for MIF, 2SD).

38 patterning, as splicing targets required for MDF function in the meristem.

39 y-derived metric (the Max-min Driving Force, MDF), which enables objective ranking of pathways by the

40 by application of multi-directional forging (MDF) as a well-known severe plastic deformation method.

41 Mass-dependent fractionation (MDF) and mass-independent fractionation (MIF) may cause

42 Mass-dependent fractionation (MDF) and mass-independent fractionation (MIF) of Hg isot

43 ish Hg isotope mass-dependent fractionation (MDF) during biotic methylation (-1.20 to +0.58 per thous

44 leads to both mass-dependent fractionation (MDF) of Hg isotopes and mass-independent fractionation (

45 this is due to mass-dependent fractionation (MDF) of up to -0.9 per thousand between IHg and MMHg.

46 ve equilibrium mass-dependent fractionation (MDF) with enrichment of heavier isotopes in the oxidized

47 sampling, the mass dependent fractionation (MDF, delta(202)Hg) of GEM taken up by the PAS was lower

48 atively narrow mass-dependent fractionation (MDF, delta(202)Hg; +/- 0.08 per thousand, 2SD) ranges (-

49 ependent and mass-independent fractionation (MDF and MIF) of methylmercury (MeHg) during trophic tran

50 with calculation of mean dominant frequency (MDF) and relative power of delta, theta, alpha and beta

51 e [MELD] >20, Maddrey discriminant function [MDF] >32) were randomized to receive methylprednisolone

52 gic complete remission at EOI1, 46 (24%) had MDF-detectable disease.

53 The difference in delta(202)Hg (MDF) and Delta(199)Hg (MIF) between fish tissues and foo

54 und that Hg mass dependent fractionation (Hg-MDF) values in sediments mostly reflect a mixing between

55 Seston presents intermediate Hg-MDF and odd Hg-MIF values falling between sediments and

56 dness and wear rate are improved by imposing MDF process.

57 Large variations in MDF and MIF are observed in fish and provide new insight

58 cipitation, have determined which individual MDFs reside at promoters of several receptor subunit gen

59 PGC arrest by two mechanisms, one involving MDF-2 and another that is independent of other SAC compo

60 West-Haven criteria) and various MMSE items, MDF showed no correlation with any of MMSE items as well

61 Fe(II) in open systems results in a kinetic MDF with a larger epsilon compared to other abiotic redu

62 te checkpoint mechanism in which a core Mad1(MDF-1)/Mad2(MDF-2) signal generated at kinetochores is i

63 s orchestrate the integration of a core Mad1(MDF-1)/Mad2(MDF-2)-based signal, with a largely independ

64 tically and physically with SAC protein MAD1/MDF-1, whose nuclear envelope accumulation requires NPP-

65 t mechanism in which a core Mad1(MDF-1)/Mad2(MDF-2) signal generated at kinetochores is integrated wi

66 e the integration of a core Mad1(MDF-1)/Mad2(MDF-2)-based signal, with a largely independent Mad3(SAN

67 mes from the fact that subtly elevating Mad2(MDF-2) levels bypasses the requirement for BUB-3 and Mad

68 etochore localization is independent of Mad2(MDF-2).

69 uence on the Hg isotope composition of MMHg (MDF) in sediments and aquatic organisms.

70 Expression of a non-phosphorylatable mutant MDF-1 partially suppressed the defect in the starvation-

71 The poplar leaves exhibited negative MDF (-3.18 to -1.22 per thousand) and small positive MIF

72 Non-MDF sample's surface shows spalling and delamination, wh

73 It is also shown that the application of MDF process changed the mechanism of wear.

74 We have analyzed expression of MDF and acetylcholine receptor subunits in cultured mous

75 lt2 double mutants have unaffected levels of MDF RNA, indicating that MDF acts upstream of PIN and PL

76 y defined as containing background levels of MDF transcripts which are thought to be nonfunctional.

77 The loss of MDF-2 or another SAC component also caused inappropriate

78 Overexpression of MDF leads to the activation of markers of embryonic iden

79 PDL-1 functions in a kinetochore receptor of MDF-1/MAD1 to induce SAC function.

80 n Bacteroides and control the selectivity of MDF components.

81 The phosphorylation status of MDF-1 affects its binding to another SAC component, MDF-

82 nowledge of both the bioactive components of MDFs and the mechanisms underlying microbe-microbe inter

83 ty of states consistent with the presence of MDFs.

84 tified 2 Akt kinase phosphorylation sites on MDF-1.

85 ive gene is occupied, either uniquely by one MDF or randomly by all MDFs.

86 n of stable oxidative metabolites with other MDF templates, and determination of metabolite molecular

87 This result is in contrast to net positive MDF (+0.4 to +0.8 per thousand) previously observed in l

88 lecular events and interactions that precede MDF expression in myogenic precursor cells.

89 mitotic delay and localizes the SAC protein MDF-1/MAD1 to the kinetochore facing away from the spind

90 s showed very similar Hg isotope signatures (MDF delta(202)Hg: -0.2 per thousand to -0.5 per thousand

91 ergence of a Dirac band structure supporting MDFs has been observed in AG using molecular (5) , atomi

92 naffected levels of MDF RNA, indicating that MDF acts upstream of PIN and PLT gene expression.

93 aused by mdf-1 hemizygosity, suggesting that MDF-1 causes the PGC arrest by two mechanisms, one invol

94 in L1 larvae lacking DAF-18, suggesting that MDF-1 regulates germ cell proliferation as a downstream

95 on-of-function allele of mdf-1 suggests that MDF-1 has a dual role during development.

96 The MDF offset occurred more during the sorption of GEM rath

97 Because the MDF offset was consistent across field studies and labor

98 types, that is not directly addressed by the MDF model.

99 uggests a unique pathway responsible for the MDF of Hg isotopes during methylation by this strain reg

100 se results demonstrate a requirement for the MDF-dependent pathway in regulating PIN/PLT- and WUS/CLV

101 scan by a triple quadrupole instrument, the MDF approach was more sensitive and selective in screeni

102 The GSH adduct screening capability of the MDF approach, together with the utility of accurate mass

103 tion energy, suggesting the emergence of the MDF linear dispersion in the AG.

104 while expressing the Pax3 gene and prior to MDF gene activation.

105 llowed a mass-dependent fractionation trend (MDF; Delta(33)S <= +/-0.2 mUr).

106 We propose a model in which MDF controls splicing in the root meristem to promote st

107 Therefore, while MDF family members act positively during myogenic differ

108 n addition, SPDL-1 coimmunoprecipitates with MDF-1/MAD1 in vivo.

109 Negative or zero MDF and MIF signatures are typical of geological Hg sour