ライフサイエンスコーパス: low molecular mass

1 nd the amounts of APOBEC3G associated with a low molecular mass.

2 s of samples, especially those of relatively low-molecular mass.

3 favored basic and hydrophilic peptides with low molecular masses.

4 Low-molecular mass (10 kD) cytosolic acyl-coenzyme A-bin

5 neutralized by an antibody directed against low molecular mass, (14 kD) human synovial PLA2 and dith

6 proteins (sHSPs) are a ubiquitous family of low molecular mass (15-30 kDa) stress proteins that have

7 Centrin is a low molecular mass (20 kDa) protein that belongs to the

8 ve found that the production of total HA and low molecular mass 3-10 disaccharides of HA (o-HA) was i

9 se thrombin inhibitor, a potent and specific low molecular mass (3,530 Da) anticoagulant peptide, was

10 In contrast to selenoproteins, low molecular mass [75Se]compounds accumulated during HI

11 ells become permissive for HIV infection, as low molecular mass A3G is induced to assemble into high

12 riction block for HIV infection conferred by low molecular mass A3G.

13 Low molecular mass amelogenin-related polypeptides extra

14 reased permeability of the BBB to a range of low-molecular mass and high-molecular mass tracers.

15 profound functional effects of binding by a low-molecular-mass antibiotic to the megadalton ribosome

16 red in H+ media (H+LPS) expressed additional low-molecular-mass antigens, as determined by sodium dod

17 ast, unspecific elimination of ROS by use of low molecular mass antioxidant compounds was not success

18 Despite the relatively low molecular mass (approximately 400 Da) of these inhib

19 cid that results in more than 60wt% yield of low-molecular-mass aromatics.

20 monomer rapidly aggregates to form transient low molecular mass assemblies (<100 kDa) that are highly

21 lar mass band is phosphorylated, whereas the low molecular mass band is hypophosphorylated.

22 e high molecular mass band of 23 kDa and one low molecular mass band of 19 kDa.

23 ic cartilage exhibited CD44 fragmentation as low molecular mass bands, corresponding to the CD44-EXT

24 mbinations of the presence of any two of the low-molecular-mass bands (19, 25, 30, 32, and 37 kDa) or

25 Low molecular mass BAP sequences are less likely to be b

26 Numerous low molecular mass bioactive peptides (BAPs) can be gene

27 s on anion-exchange columns with inexpensive low molecular mass buffer components via HPLC gradient m

28 Numerous neurons release two transmitters of low molecular mass, but it is controversial whether they

29 Two low molecular mass c-type cytochromes were also characte

30 igands include S100/calgranulins, a class of low-molecular-mass, calcium-binding polypeptides, severa

31 e activity after in vitro treatment with the low molecular mass cell-permeable S-nitrosothiol S-nitro

32 both APOBEC3F and APOBEC3G were localized in low molecular mass complexes associated with viral rever

33 ich are converted into enzymatically active, low molecular mass complexes by RNase digestion.

34 t PA700-deficient cells but also accumulated low molecular mass complexes containing subunits of the

35 olecular-mass ribonucleoprotein complexes to low-molecular-mass complexes.

36 Low molecular mass compounds which would bind in the por

37 combination of beta-lapachone and taxol, two low molecular mass compounds.

38 ting term flavonolignan that is used for the low-molecular mass compounds composed of flavonoid and l

39 e results with those derived from studies on low-molecular-mass compounds to assess the validity of e

40 otein surface groups, we find the ability of low-molecular-mass compounds to model successfully prote

41 monolignols and hydroxystilbenes, as well as low-molecular-mass compounds, to obtain the mechanistic

42 vely different from those of polar groups in low-molecular-mass compounds.

43 may exist, particularly for the emerging and low molecular mass congeners.

44 th the 4.5- and 8-kD bands in immunoblots of low-molecular-mass, copper-binding proteins purified fro

45 fy MT proteins from Arabidopsis, we isolated low-molecular-mass, copper-binding, thiol-rich proteins

46 Many of these low molecular masses corresponded to molecular formulas

47 The low molecular mass cytosolic forms of guanylate kinase a

48 cteristics together with tubular presence of low molecular mass dextran provide clear evidence of fun

49 Using this approach, low-molecular-mass displacers with affinities higher tha

50 highly specific for the structurally unique low-molecular mass disulfide, mycothione, exhibiting Mic

51 Enhancers may be low molecular mass enhancers, such as glycerol, or other

52 roteins (including other hemolymph DAFPs) or low-molecular mass enhancers such as glycerol.

53 olitica has recently been shown to produce a low molecular mass envelope protein that contains an epi

54 inant peak at 1635 m/z, consistent with this low molecular mass estimate.

55 ate that a labile cationic zinc component of low molecular mass exists in the yeast mitochondrial mat

56 rk, we define the structure of both high and low molecular mass exopolysaccharide from R7A.

57 at a plant receptor-like kinase, EPR3, binds low molecular mass exopolysaccharide from strain R7A to

58 The low molecular mass exopolysaccharide produced by R7A is

59 romatic chemicals and/or provide a source of low-molecular-mass feedstocks suitable for downstream pr

60 capillaries has been investigated using the low molecular mass fluorescent dyes Lucifer Yellow and S

61 -resident naive CD4 T cells but resides in a low molecular mass form in nonpermissive, blood-derived

62 on of Mcb1 in cell extracts was present in a low-molecular-mass form free of the 26S complex.

63 me cells expressing the enzymatically active low-molecular-mass form of A3G, HIV-1 replication is res

64 pecific RNA fractions was observed, with the low-molecular-mass fraction exhibiting a much higher syn

65 xide-mediated fragmentation of hyaluronan to low molecular mass fragments.

66 ith control cells and that activation of the low-molecular-mass GTP-binding protein Rab27a, involved

67 number of signaling molecules, including the low-molecular mass GTPases.

68 es a high degree of sequence similarity with low-molecular-mass guanylate kinases.

69 that conversion of high molecular mass HA to low molecular mass HA facilitated GAS phagocytosis by ma

70 augmented levels of HA and the appearance of low molecular mass HA species in bronchial secretions.

71 polypeptides can serve as surrogates for the low molecular mass hapten digoxin.

72 odified residual lignin, especially for the (low molecular mass) hardwood lignosulfonate, revealing t

73 In the presence of low-molecular mass heparin ( approximately 3 kDa), we de

74 Low-molecular mass heparin-induced chemical shift pertur

75 lls, associated with increased expression of low molecular mass hyaluronan (sHA).

76 Recent studies found that elevated levels of low molecular mass hyaluronan are associated with inflam

77 o determine the role of the acetyl groups of low molecular mass hyaluronan in stimulating the product

78 lluar matrix, and lung injury can generate a low-molecular mass hyaluronan (HA) fragment that functio

79 Low molecular mass hyaluronans are known to induce infla

80 with LPS, lipoteichoic acid, CD40 ligand, or low molecular mass hyaluronic acid.

81 container cap are rapidly hydrogenolyzed to low molecular mass hydrocarbons.

82 id solution with methane, nitrogen and other low-molecular-mass hydrocarbons, is contained within Tit

83 sence in neonatal blood plasma of a soluble, low molecular mass inhibitory factor (<10 kDa) that we i

84 with the transfer and over-fragmentation of low molecular mass ions.

85 nsferrin and/or the presence of redox-active low molecular mass iron) and increased plasma thiol leve

86 trometry of flow-through solutions exhibited low-molecular-mass iron peaks that did not increase inte

87 Moreover, phosphorylation of the low molecular mass isoform of the protein (l-CaD) at the

88 d by selective inhibition of Tat activity by low molecular mass kinase inhibitors.

89 Further, HK and low molecular mass kininogen, but not factor XII, blocke

90 potential complex formation between Plg and low-molecular-mass kininogen (LK) and between LK and HK

91 We and others have shown that both high and low molecular mass kininogens are able to inhibit the th

92 olecules and report the discovery of a novel low-molecular-mass ligand for the von Hippel-Lindau (VHL

93 -free measurement of the binding kinetics of low molecular mass ligands with nanodisc-encapsulated me

94 h densities to allow the study of relatively low-molecular-mass ligands (2000-4000Da).

95 s A3G expression and leads to recruitment of low molecular mass (LMM) A3G, which functions as a post-

96 The low molecular mass (LMM) extract of Cichorium intybus va

97 Intratracheal administration of low molecular mass (LMM) hyaluronan (200 kDa) results in

98 Low molecular mass (LMM) RNAs as well as larger fragment

99 vity of tAFP is dependent on the presence of low molecular mass (LMM) species that copurify with tAFP

100 Low molecular mass (LMM) thiols is a diverse group of co

101 tion Hg(II)-complexes, combining either with low molecular mass (LMM) thiols like Cys, Hg(Cys)(Mem-RS

102 can be transformed in vitro into an active, low molecular mass (LMM) variant comparable with that of

103 n, however, that the preferred substrates of low-molecular mass (LMM) class B and C dd-peptidases con

104 horylated glycoproteins, lipids, and organic low-molecular mass (LMM) compounds.

105 wo groups, the high-molecular mass (HMM) and low-molecular mass (LMM) enzymes.

106 molecular-mass inactive A3G complexes to the low-molecular-mass (LMM) active A3G complexes.

107 coupled plasma mass spectrometer revealed a low-molecular-mass (LMM) Fe(II) pool consisting of two i

108 lex that converts to an enzymatically active low-molecular-mass (LMM) form after treatment with RNase

109 expressed either as an enzymatically active low-molecular-mass (LMM) form or as an enzymatically ina

110 Mitochondria are thought to export a low-molecular-mass (LMM) iron and/or sulfur species whic

111 ng are unestablished, but a nonproteinaceous low-molecular-mass (LMM) labile nickel pool (LNiP) is th

112 lysis, to determine the structure of the two low-molecular-mass LOS molecules (LOSI and LOSII) expres

113 Finally, 70 co-crystal structures of low molecular mass, low-affinity compounds with Pim1 hav

114 Initial results of an examination of the low molecular mass (< or =45 kDa) protein composition of

115 In this study, 23 low molecular mass (<3.5-kDa) peptides in the urea-solub

116 hances the partitioning into vacuoles of the low molecular mass metal chelator nicotianamine and lead

117 hase (NAS) catalyzes the biosynthesis of the low-molecular-mass metal chelator nicotianamine (NA) fro

118 , without using data derived from studies on low-molecular-mass model compounds.

119 Although a range of low molecular mass molecular single crystals has been sh

120 sign of a new generation of anti-aggregatory low-molecular mass molecules for therapeutic purposes.

121 a-synuclein exhibits a strong preference for low-molecular mass molecules, suggesting a pore-like mec

122 m-negative bacteria involved in transport of low-molecular-mass molecules.

123 However, low molecular mass (MW) molecules, including chemokines,

124 iotic processes and range in complexity from low molecular mass natural halocarbons (nHCs, mostly hal

125 The low molecular mass Neisseria gonorrhoeae PBP 4 (NG PBP 4

126 zation is associated with a reduction in the low molecular mass neurofilament mRNA levels.

127 lphaS-induced inclusions colocalize with the low-molecular-mass neurofilament subunit (NFL) or periph

128 oximately 34,000 compounds and identified 12 low-molecular-mass nonaminoglycosides with potential PTC

129 lation, characterization, and conjugation of low-molecular-mass O-SP-core (O-SPC) fragments.

130 contain novel VEGF receptors with relatively low molecular masses of approximately 120 and 130 kDa.

131 mass spectra of poorly soluble and insoluble low molecular mass oligomers (<4600 Da) of Nomex and Kev

132 anes, and show that binding of nonfibrillar, low molecular mass oligomers of Abeta40 to anionic, but

133 e of caveolin-1 expression, caveolin-2 forms low molecular mass oligomers that are retained at the le

134 coordination complexes that constitutes the low-molecular-mass (or labile) Cu pool were assumed.

135 illary electrophoresis (ICxCE) separation of low-molecular-mass organic acids as test analytes.

136 Immunology-based identity tests using low-molecular-mass organic compounds have historically b

137 ermal transformation of sols, comprised of a low molecular-mass organogelator (LMOG) and an organic l

138 an-3beta-yl N-(2-naphthyl)carbamate (CNC), a low-molecular-mass organogelator (LMOG), in n-octane and

139 A new class of low molecular-mass organogelators (LMOGs), N-alkyl perfl

140 deletion of both PBP 3 and PBP 4, the other low-molecular-mass PBP in N. gonorrhoeae, resulted in a

141 ance will lend insight into the role of this low-molecular-mass PBP whose function is poorly understo

142 nserved active site lysines in Class A and C low molecular mass PBPs.

143 reochemically, and as inhibitors of a set of low molecular mass PBPs: Escherichia coli (EC) PBP 5, Ne

144 erichia coli PBP4 is the archetypal class C, low molecular mass penicillin binding protein (LMM-PBP)

145 Escherichia coli low molecular mass penicillin-binding proteins (PBPs) in

146 nsertion in pbpG, which encodes the putative low-molecular-mass penicillin-binding protein 7/8 (PBP-7

147 idual or combined mutations in genes for the low-molecular-mass penicillin-binding proteins PBP3 and

148 ilisation in the efficient identification of low molecular mass peptide sequences in food protein hyd

149 hosphate, which has been shown to serve as a low molecular mass phosphate donor for certain response

150 ture of Ssu72 has some similarity to that of low-molecular-mass phosphotyrosine protein phosphatase,

151 t (iPLA2; bromoenol lactone) or of secretory low molecular mass PLA2.

152 They consist of telechelic, rubbery, low-molecular-mass polymers with ligand end groups that

153 , beta2, and beta5 by the inducible subunits low molecular mass polypeptide (LMP) 2 (beta1i), multica

154 ponents of the antigen processing machinery, low molecular mass polypeptide (LMP) 2 and transporter a

155 ve inhibitor of the immunoproteasome subunit low molecular mass polypeptide (LMP) 7 (beta5i) that att

156 The low molecular mass polypeptide (LMP2, LMP7, and MECL-1)

157 Low molecular mass polypeptide 2 (LMP-2 or beta(1i)) is

158 Expression of the low molecular mass polypeptide 2 (LMP2), which requires

159 ed the expression of the proteasomal subunit low molecular mass polypeptide 2 (LMP2).

160 Analysis of the Tap-1/low molecular mass polypeptide 2 bidirectional promoter

161 hat is influenced by the IFN-gamma-inducible low molecular mass polypeptide-2 (LMP2) subunit of the p

162 Despite a reduction in low molecular mass polypeptide-2 expression relative to

163 rization of PR-957, a selective inhibitor of low-molecular mass polypeptide-7 (LMP7, encoded by Psmb8

164 ntra-MHC-encoded subunits of the proteasome (low-molecular-mass polypeptide [Lmp]-2 and Lmp-7) reveal

165 AF-1 is a DNA-binding protein composed of low molecular mass polypeptides of 7-17 kDa that exists

166 b DNA fragments that are further degraded to low molecular mass products.

167 a B-cell derived NF-Y A:B:C complex with the low molecular mass protein fraction, NF-Y-associated fac

168 The submaxillary glands of boars contain a low molecular mass protein, pheromaxein, which is capabl

169 Low-molecular mass protein-7 (LMP7) is a proteolytic sub

170 Low molecular mass proteins (< 10 kDa) can be efficientl

171 Low molecular mass proteins are implicated in chemical c

172 Radiolabeling experiments revealed that low molecular mass proteins, particularly 20- and 8-kDa

173 ude potent inhibitors of MMP-9, particularly low molecular mass proteins.

174 is not well understood, although a group of low-molecular-mass proteins called rosettins have been d

175 The fact that the low-molecular-mass proteins do not affect contractility

176 aining CaD, CaP, and myosin RLC plus several low-molecular-mass proteins), all proteins used for rein

177 fied a group of four genes encoding putative low-molecular-mass proteins.

178 of flavodoxin to PsaC, PsaD, an unidentified low-molecular-mass PS I polypeptide, and a 15-kDa subuni

179 molecules, we detected a potent inhibitor in low molecular mass RNA (sRNA) preparations of eukaryotic

180 LCN) 2 belongs to the lipocalin subfamily of low-molecular mass-secreted proteins that bind small hyd

181 well as the presence of cosolutes including low molecular mass solutes and/or proteins.

182 hibit limited deaminase activity relative to low-molecular mass species prepared under RNA-depleted c

183 ttle effect on the action of DPP I towards a low molecular-mass substrate.

184 nd CP43, as well as most of their associated low molecular mass subunits, and the assembly factor Psb

185 face of stimulated neutrophils despite their low molecular mass, suggesting that the conformation and

186 It belongs to a subgroup of low molecular mass SWIB domain proteins, which in Arabid

187 In some cases the effects of low molecular mass synthetic MMP inhibitors and serum on

188 zed by a preponderance of phosphorylation of low molecular mass TCRzeta and the failure to phosphoryl

189 KCNE1 is a protein of low molecular mass that is known to regulate the chroman

190 produces and exports appreciable amounts of low molecular mass thiol (LMM-RSH) compounds reaching co

191 Mycothiol (MSH) is the major low-molecular-mass thiol in mycobacteria and is associat

192 glucopyranoside (GlcN-Ins), and is the major low-molecular-mass thiol in mycobacteria.

193 iol (MSH) (acetyl-Cys-GlcN-Ins) is the major low-molecular-mass thiol in Mycobacterium tuberculosis.

194 sured concentrations of MeHg, sulfide, eight low molecular mass thiols and thiol groups associated wi

195 inorganic mercury (Hg(II)), as controlled by low-molecular-mass thiols, and cell physiology govern Me

196 tinuum of glycogenin-containing species from low molecular mass to sizes significantly greater than 4

197 s of p-nitrophenyl phosphate (pNPP) with the low-molecular mass tyrosine phosphatase Stp1 and with th

198 Low molecular mass viscogens (ethane diol, glycerol, and

199 iral cores, but APOBEC3G was associated with low molecular mass, whereas APOBEC3F was still retained

200 hat Heliothis cecropin is a basic peptide of low molecular mass with bactericidal activity against Es

201 ctric points of Cx26 and Cx32, whereas their low molecular masses would not appreciably change connex