ライフサイエンスコーパス: be depleted from

1 9 days of irradiation, the DOS concentration was depleted from 13 to 1 muM, together with a 9% decrea

2 th 5, 50, 200, and 500 mg/ml PLP, plasma MET was depleted from 50 microm to < or = 5 microm for 8, 24

3 distribution among daughter cells when clpA is depleted from a strain in which FtsZ is constitutivel

4 Human CSF samples were depleted from abundant proteins and subjected to au

5 units of eukaryotic chromatin, nucleosomes, are depleted from active regulatory elements throughout

6 aneous autoimmune thyroiditis (SAT), B cells were depleted from adult NOD.H-2h4 mice using anti-mouse

7 , and PIN7 display normal localization, PIN2 is depleted from apical membranes of epidermal cells and

8 thione (GSNO), an endogenous bronchodilator, is depleted from asthmatic airways, suggesting a protect

9 Glycogen granules were depleted from astrocytes and neurons in 0-min slice

10 obust expression of CXCL10, CXCR3(+) T cells were depleted from blood in the SIVmac239-infected anima

11 pe was not apparent when both MUS81 and SLX4 were depleted from Bloom's syndrome cells, suggesting th

12 However, HSCs were depleted from bone marrow when Scf was deleted from

13 rocess of ricin reduction; however, when PDI is depleted from cell fraction preparations ricin reduct

14 When cholesterol is depleted from cells expressing Gag, mobility is signi

15 The transcription that occurs when Pcf11 is depleted from cells or an extract is no longer sensit

16 When optineurin is depleted from cells using RNA interference, myosin VI

17 Both LATS1 and LATS2 were depleted from cells treated with the HSP90 inhibito

18 VGLUT1 was depleted from central terminals of transected myelin

19 und that the H2B ubiquitin E3 ligase, RNF20, was depleted from chromatin in differentiated myotubes,

20 When NK cells were depleted from control C57BL/6 mice, these mice did

21 rescent protein reporter suggests that auxin is depleted from crk5 root tips.

22 ing, whereas specific dendritic cell subsets were depleted from cultures with immune-magnetic beads.

23 Significantly, the export activity can be depleted from cytosol by preadsorption with a protein

24 nor naive P14 and LCMV-specific memory cells were depleted from day 2 LCMV-infected hosts by 16 h pos

25 changes in cardiomyocytes when Gata4 protein is depleted from developing zebrafish embryos.

26 milar results were observed when Sm proteins were depleted from egg extract: staining of the coiled b

27 When the Nup107-160 complex was depleted from extracts, the spindle checkpoint remai

28 Furthermore, we found that CrEB1 is depleted from flagella of the temperature-sensitive (

29 Xist is depleted from genes that escape XCI but may concentra

30 d and multilineage hematopoietic progenitors were depleted from grafts infected with either a molecul

31 T cells were depleted from granuloma cells by immune lysis, and

32 When CSB and NEIL1 are depleted from HeLa cells by short hairpin RNA knockd

33 These were depleted from HeLa cells to examine their effects o

34 AhR protein was depleted from Hepa-1 type I variants (that contain a

35 s of the SIINFEHL epitope, and such peptides are depleted from hsp90 preparations in hsp90-inhibited

36 antagonist of the IL1 receptor; macrophages were depleted from ilea of mice using clodronate-contain

37 When ENA-78 was depleted from IPF tissue specimens, tissue-derived a

38 When IL-8 or IP-10 was depleted from IPF tissue specimens, tissue-derived a

39 We found that CBP was depleted from its normal nuclear location and was pr

40 ochore outer domain, but not the inner core, are depleted from kinetochores and accumulate at spindle

41 cumulate multiple checkpoint proteins, which are depleted from kinetochores upon stable attachment, a

42 e to DNA damage, however, we find that SIRT6 is depleted from L1 loci, allowing the activation of the

43 and tomato (Solanum lycopersicum) that auxin is depleted from leaf axils during vegetative developmen

44 Platelets were depleted from MDR2-null mice by injection of an ant

45 ated protection, either CD4+ or CD8+ T cells were depleted from mice after the WEHI-3B/tmGM-CSF vacci

46 Kupffer and dendritic cells were depleted from mice by administration of clodronate,

47 Commensal bacteria were depleted from mice with antibiotics.

48 When PP2A-B55 delta was depleted from mitotic extracts, however, exit from m

49 When TDP-43 was depleted from mouse embryonic stem cells, these cryp

50 of STAT3 phosphorylation was lost when IL-6 was depleted from MSC conditioned media or the IL-6 rece

51 ditional knockout mouse in which the protein is depleted from muscle progenitors at embryonic day 8.5

52 Arginine, serine, and asparagine were depleted from mutant cultures during growth.

53 Human and mouse cardiac cells were depleted from myocytes and flow sorted to isolate c

54 cyte hypertrophic growth, PLCepsilon protein was depleted from neonatal rat ventricular myocytes (NRV

55 s were also observed when ribosomal proteins were depleted from neurons with established dendrites.

56 totic defects similar to those seen when pRB is depleted from non-transformed cells, but that the pre

57 lation (H3K79me), H3K4me, and H3K36me, which are depleted from OFF telomeres, are enriched at ON telo

58 horylated Cdk9 Thr-186 in vitro when 7SK RNA was depleted from P-TEFb.

59 However, when CD4(+) cells were depleted from P. carinii-infected IL-10 KO mice, th

60 When Tregs are depleted from PBMCs of viremic individuals, the effe

61 ls resolved neural infection, CD8(+) T cells were depleted from perforin-deficient or FasL-defective

62 Surprisingly, both DC subsets were depleted from peripheral and mesenteric lymph nodes

63 t one additional rate-limiting export factor is depleted from permeabilized cells by a preincubation

64 The axonal mRNAs accumulate at or are depleted from points of ligand stimulation along the

65 ith preference for poly-N-acetyllactosamine, was depleted from polarized MDCK cells.

66 ugh SUZ12, cause gene repression in cis, and are depleted from polycomb target genes activated during

67 Rhodopsin was depleted from primary cilia but gained access, witho

68 When NET37 is depleted from proliferating myoblasts by RNAi, myogen

69 imethylated histone H3 at lysine 4 (H3K4me2) is depleted from regions with DNA methylation and that t

70 In contrast, tau was depleted from RGC axons in the optic nerve of glauco

71 the POST to PRE state is observed when EF-G is depleted from ribosomes in the POST state or when tRN

72 When either CD4(+) or CD8(+)CD60(+) T cells were depleted from RS PBMC before culture with RA, no Ig

73 sing an anti-properdin mAb or when properdin was depleted from serum.

74 experiment grass pollen-specific antibodies were depleted from serum samples to determine the propor

75 tinue infinitely or until monomeric peptides are depleted from solution which results in an insoluble

76 ld be isolated from PICs, and activity could be depleted from such fractions with an antibody against

77 vation to mimic cerebral ischemia, GABA(A)Rs are depleted from synapses in dendrites, depending on th

78 nsities similar to those of free protein and are depleted from the bulk chromatin fractions.

79 aying engraftment, many other types of cells are depleted from the CD34-enriched grafts and immune re

80 fter glucose withdrawal show that most mRNAs are depleted from the cell coincident with their depleti

81 It is also apparent when neutrophils are depleted from the circulation.

82 t growth is restricted when brassinosteroids are depleted from the epidermis and brassinosteroids act

83 V-1 infection, more than 50% of CD4+ T cells are depleted from the gastrointestinal lamina propria.

84 an in-plane ferromagnetic phase as electrons are depleted from the interface.

85 results support a model in which nucleosomes are depleted from the LTR and transcribed region during

86 eukaryotic model of quiescence, proteasomes are depleted from the nucleus and accumulate in motile c

87 ree stages; (1) abundant protein backgrounds are depleted from the serum using magnetic bead coupled

88 but at low packing density the DNA segments are depleted from the surface owing to the local condens

89 clear subcellular fractions and PKC-delta to be depleted from the cytoskeleton.

90 ons, myopodin accumulates in the nucleus and is depleted from the cytoplasm.

91 int of clot formation, 80% of the fibrinogen is depleted from the fluid phase, whereas only 35% to 45

92 berrantly enters the degradative pathway and is depleted from the Golgi.

93 n aqueous solution, a PEG polymer suspension is depleted from the hot region and builds a concentrati

94 in, like Bub3 and other checkpoint proteins, is depleted from the kinetochore during chromosome align

95 Upon transcriptional induction, HP1alpha is depleted from the locus and the histone variant H3.3

96 MBNL1 is depleted from the muscle nucleoplasm because of seque

97 localized in the nuclei of migrating FBMNs, is depleted from the nuclei of Pk1b-deficient neurons.

98 1 (CrEB1) localizes to the flagellar tip and is depleted from the tips of the temperature-sensitive (

99 Surprisingly, we found that H4K16ac is depleted from the X even before the 30-cell stage in

100 The 6:2 FtSaAm was depleted from the aqueous phase in all but one soil,

101 is activity decreased extensively when TTase was depleted from the cell lysate by immunoprecipitation

102 Serotonin was depleted from the cortex by systemic administration

103 When Ca(2+) was depleted from the culture medium, occludin tyrosine

104 in LPL translation inhibition, the C subunit was depleted from the cytoplasmic extract of epinephrine

105 Specifically, Gnd(+) was depleted from the ELP/water interface and was found

106 nolamine kinase activity increased when zinc was depleted from the growth medium.

107 ositol synthase activity increased when zinc was depleted from the growth medium.

108 DMDS was depleted from the headspace during cocultivation wit

109 nhibitors of metalloproteinase or when MMP-9 was depleted from the inducing supernatants.

110 s, M130 concentrated in the tailing edge and was depleted from the leading half of the cell, where do

111 sely dispersed in the cytoplasm when calcium was depleted from the medium, and after calcium resupple

112 +) the cells accumulated [3H]Me-TCB until it was depleted from the medium, giving an internal concent

113 atrigel plugs in vivo was abolished when PLF was depleted from the medium.

114 in the oxygen gradient when the cholesterol was depleted from the plasma membrane.

115 When PABP was depleted from the reticulocyte lysate with anti-huma

116 We observed that a subset of shRNA vectors was depleted from the transduced cells after three weeks

117 normally arrayed at the apico-lateral apex, were depleted from the ADPKD cell plasma membrane.

118 When polyamines were depleted from the BAL fluids of infected animals, t

119 However, when Tregs were depleted from the CD4 T cells, the IFNgamma product

120 l, but was inhibited if ATP binding proteins were depleted from the cytosol.

121 uggesting that other checkpoint component(s) were depleted from the extract through their association

122 bination and repair proteins HsRad51 and XPA were depleted from the extracts using specific antibodie

123 Lymphocytes were depleted from the graft by selection of CD34-positi

124 When CD11b(+) Gr-1(high) cells were depleted from the liver with Gr-1 antibody treatmen

125 n glucose and other potential carbon sources were depleted from the medium.

126 ponse to p40 homodimer, CD4+ or CD8+ T cells were depleted from the MLC.

127 when nude-derived endogenous CD8(+) T cells were depleted from the nude recipients (intimal prolifer

128 production was restored when ganglion cells were depleted from the older cell population.

129 srupted and both polycystin-1 and E-cadherin were depleted from the plasma membrane as a result of th

130 nt, in which as few as 32.4% of CD4(+) cells were depleted from the spleen.

131 When platelets were depleted from the systemic circulation with an anti

132 ivation when CD8(+) T cells or CD45(+) cells were depleted from the TG cultures.

133 ice lacking both alphaDB and betaDB, and DBs are depleted from these synapses in mice lacking dystrop

134 Dystrophin is depleted from these synapses in mice lacking both alp

135 ns, indicating that the corepressor activity was depleted from these extracts through protein-protein

136 his decrease is not observed if CD8+ T cells were depleted from these mice.

137 pantophysin, and both GLUT4 and pantophysin were depleted from this vesicle population following tre

138 anti-tumor immune responses, mature B cells were depleted from wild-type adult mice using CD20 mAb p

139 When the checkpoint protein Xmad2 is depleted from Xenopus egg extracts, adding Xmad2 to i

140 are largely CD24(+) and CX3CR1(low) and can be depleted from Zbtb46-DTR mice, suggesting classical D