ライフサイエンスコーパス: Mueller

1 Mueller and Rose have proposed several age-structured de

2 Mueller matrix images of the unstained sections of mice

3 Mueller matrix imaging reveals radial oscillations in no

4 Mueller microscopes enable imaging of the optical anisot

5 Mueller-Hinton agar was the preferred medium, particular

6 Mueller-Wohlfahrt et al. introduced a new classification

7 rying reflective properties (described by 16 Mueller matrix elements m(ij)) with incident illuminatio

8 The resultant probe enables linear 3 x 3 Mueller matrix characterization of distal tissue.

9 We aim to demonstrate the use of a 3D Mueller matrix method to allow quick and easy clinical d

10 the realm of liquid biopsies, employing a 3D Mueller-matrix (MM) image reconstruction technique to an

11 first step towards the implementation of 3D Mueller matrix mapping for clinical analysis and diagnos

12 d lower MIC in tissue culture medium with 5% Mueller Hinton broth (MHB) and a 64-fold lower MIC in th

13 ty to easily switch its functionality from a Mueller to a Second Harmonic Generation (SHG) microscope

14 ely 12 mm apart (measured edge to edge) on a Mueller-Hinton agar plate that had been inoculated with

15 he different prostate tumour tissues using a Mueller matrix polarimeter set-up, based on the superpos

16 en two laboratory media (RPMI, cation adjust Mueller Hinton broth) and two physiological media (blood

17 h microdilution method using cation-adjusted Mueller-Hinton (MH) broth were 77.6% for minocycline and

18 microdilution using standard cation-adjusted Mueller-Hinton broth (BMD) and iron-depleted cation-adju

19 ere added to 4 separate 5-mL cation-adjusted Mueller-Hinton broth (CA-MHB) tubes, using various manuf

20 facturers (BBL and Difco) of cation-adjusted Mueller-Hinton broth (CA-MHB), and using three different

21 rinary Fastidious Medium and cation-adjusted Mueller-Hinton broth (CAMHB) + 1% chicken serum + 0.0025

22 Zinc concentrations in cation-adjusted Mueller-Hinton broth (caMHB) from different manufacturer

23 tested susceptible to SXT in cation-adjusted Mueller-Hinton broth (CAMHB) plus lysed horse blood and

24 For BMD, cation-adjusted Mueller-Hinton broth (CAMHB) requires iron depletion to

25 roth (BMD) and iron-depleted cation-adjusted Mueller-Hinton broth (ID-BMD), and agar dilution (AD) us

26 on (BMD) using iron-depleted cation-adjusted Mueller-Hinton broth (ID-CAMHB).

27 on with 2% NaCl-supplemented cation-adjusted Mueller-Hinton broth as specified by the NCCLS.

28 Cation-adjusted Mueller-Hinton broth containing 2.5% laked horse blood w

29 S) isolates in a panel using cation-adjusted Mueller-Hinton broth from three different manufacturers.

30 oth microdilution testing is cation-adjusted Mueller-Hinton broth supplemented with 2% lysed horse bl

31 s 10 antimicrobial agents in cation-adjusted Mueller-Hinton broth supplemented with 3% lysed horse bl

32 rinae tested did not grow in cation-adjusted Mueller-Hinton broth supplemented with 5% lysed horse bl

33 as performed with four 10-ml cation-adjusted Mueller-Hinton broth tubes per isolate, to which 0, 1, 2

34 n using two different media (cation-adjusted Mueller-Hinton broth with 5% oleic acid-albumin-dextrose

35 ilution method incorporating cation-adjusted Mueller-Hinton broth with 50 microg/ml calcium.

36 preparation of iron-depleted cation-adjusted Mueller-Hinton broth, and revised reading guidance to im

37 ethod includes iron-depleted cation-adjusted Mueller-Hinton broth, which eliminates variability in ce

38 e of BMD using iron-depleted cation-adjusted Mueller-Hinton broth.

39 with patient responses than cation-adjusted Mueller-Hinton broth.

40 f tazobactam and 2 brands of cation-adjusted Mueller-Hinton broth.

41 in 2016, using iron-depleted cation-adjusted Mueller-Hinton broth.

42 ueller-Hinton agar (MHA) and cation-adjusted Mueller-Hinton broth.

43 the inoculum and tubed 11-mL cation-adjusted Mueller-Hinton broth: 1 uL [tribe Proteeae (P-tribe) onl

44 n were 99.7 to 100% in three cation-adjusted Mueller-Hinton broths tested.

45 one diameters in millimeters on three agars (Mueller-Hinton agar supplemented with 2% dextrose and 0.

46 agar, Isosensitest agar, nutrient agar, and Mueller-Hinton agar for aerobes and brucella blood agar

47 ave model originally proposed by Baumann and Mueller.

48 g 2% glucose (RPG), Casitone agar (CAS), and Mueller-Hinton agar (MHA) and were read after incubation

49 th various growth factors were explored, and Mueller Hinton agar (MHA) supplemented with fetal bovine

50 between Sauvignon Blanc, Gewuerztraminer and Mueller-Thurgau grape pomace for the 3-mercaptohexan-1-o

51 f NG-Test Carba 5 from blood, MacConkey, and Mueller-Hinton agars with 110 isolates of Enterobacteral

52 from 95.2% to 100% for blood, MacConkey, and Mueller-Hinton agars.

53 With microdilution and Mueller-Hinton broth, agreement by interpretive category

54 g polarization ray tracing, full Stokes, and Mueller matrix imaging.

55 lum plated onto CHROMagar Candida as well as Mueller-Hinton agar to which 2% glucose and 0.5 microg/m

56 Two plated media (5% sheep blood Mueller-Hinton agar and Middlebrook 7H11 agar) were comp

57 n-house and commercially prepared HTM broth, Mueller-Hinton broth with 2% lysed horse blood and NAD,

58 tive, and a study of several crystallites by Mueller matrix microscopy shows that their optical activ

59 and circular birefringence, as determined by Mueller matrix microscopy, informs the cooperative organ

60 of an advanced experimental technique called Mueller polarimetry and state-of-the-art numerical simul

61 eptococcus suis tested on enriched chocolate Mueller-Hinton agar, susceptibility at > or =16 mm and r

62 stidious medium broth and enriched chocolate Mueller-Hinton agar.

63 for the disk diffusion testing is chocolate Mueller-Hinton agar.

64 h 6 mg/liter vancomycin (BHIA6V) (CDC/CLSI), Mueller-Hinton agar with 5 mg/liter teicoplanin (MHA5T)

65 lates tested in triplicate with 3 commercial Mueller-Hinton media across all sites, with 93% (604/648

66 lates were incubated in oxacillin-containing Mueller-Hinton broth, stained using the FASTEST total vi

67 ISA was performed with vancomycin-containing Mueller-Hinton agar (MHA) prepared in-house in place of

68 Conversely, Mueller cells and astrocytes, representing off-target ce

69 alculated from the elements of corresponding Mueller matrix pixel-wise.

70 strate a low cost wide field high definition Mueller polarimetric endoscope with minimal alterations

71 The results of BMD with Difco Mueller-Hinton broth were used as the standard for data

72 s SCHU S4 that had been cultivated in either Mueller-Hinton broth (MHB) or brain heart infusion (BHI)

73 The 16-element Mueller matrix provides the most complete description of

74 MD and MTS testing with both CLSI and EUCAST Mueller-Hinton Fastidious (MH-F).

75 e physical realizability of the experimental Mueller matrices in order to filter out non-physical dat

76 matrix, all calculated for the experimental Mueller matrix images (600 pixels x 700 pixels) of mouse

77 In contrast to C. jejuni harvested from Mueller-Hinton (MH) agar plates, C. jejuni harvested fro

78 In this report, a full Mueller scanning microscope based on spectral encoding o

79 l the information needed to produce the full Mueller matrix, which allows simultaneous display of all

80 pulse shape properties generated by a Geiger Mueller (GM) detector and its dependence on applied volt

81 A detailed analysis of Geiger Mueller counter deadtime dependence on operating voltage

82 re produced using a polarisation-holographic Mueller matrix method approach.

83 demonstrates that a polarisation-holographic Mueller matrix method can be applied to the assessment o

84 Imaging Mueller polarimetry has already proved its potential for

85 of pregnancy were performed with an imaging Mueller polarimeter at different time points of pregnanc

86 It supports the assumption that imaging Mueller polarimetry holds promise for the fast and accur

87 concentrations compared to colistin alone in Mueller-Hinton media and M9 media.

88 ed in Francisella research) to that grown in Mueller-Hinton broth (MHB; the most widely used F. tular

89 ofiles of uropathogenic clinical isolates in Mueller-Hinton media and in urine.

90 inally, growth of the LVS FTL_0325 mutant in Mueller-Hinton broth at 37 degrees C resulted in the app

91 ases were localized in microglia, but not in Mueller cells or astrocytes.

92 ct inoculation of the organisms suspended in Mueller-Hinton broth were within +/-1 dilution of those

93 interpretation and lot-to-lot variability in Mueller-Hinton agars were significant factors leading to

94 do not grow on routine AST media, including Mueller-Hinton agar (MHA) and cation-adjusted Mueller-Hi

95 In this issue of the JCI, Mueller and colleagues report their detailed kinetic and

96 experiment and theoretical simulation (Jones/Mueller calculus and time-dependent density-functional t

97 M., Burzenski, L., Mueller, C., Greiner, D.

98 uller, which was incorrectly given as Miryam Mueller.

99 ented with sheep blood (CHAB) or in modified Mueller-Hinton broth.

100 hat liquid domains form in asymmetric Montal-Mueller planar bilayers in which one leaflet's compositi

101 ayers contain an organic solvent, the Montal-Mueller or solvent-free technique, and a method for memb

102 derocol DD result variability using multiple Mueller-Hinton agar (MHA) brands.

103 In this issue of Neuron, Mueller-Steiner et al. manipulate the expression of cath

104 blue [for all isolates]) and nonsupplemented Mueller-Hinton (MH; molds only) agar.

105 illimeters, were obtained on nonsupplemented Mueller-Hinton agar at 16 to 48 h.

106 Stokes polarimeter may be adapted to obtain Mueller matrices and discuss various approaches for achi

107 + 0.5 mug/ml) with three different brands of Mueller-Hinton broth supplemented with 3% lysed horse bl

108 sent such a theory based on a combination of Mueller calculus and a Lorentz oscillator model.

109 However, the development of Mueller microscopes poses an instrumental challenge: the

110 The shelf life of Mueller-Hinton agar supplemented with 2% glucose and met

111 The current study identified the source of Mueller-Hinton broth as a variable in cefiderocol MIC de

112 A) include omitting serum supplementation of Mueller-Hinton broth, incubating tubes at 35 degrees C f

113 d their copolymers were analyzed in terms of Mueller matrix derived polarization parameters, namely,

114 s of Markovian models that includes those of Mueller and Rose and obtains a characterization of the p

115 f MSA containing oxacillin (MSA(Ox)), use of Mueller-Hinton agar containing oxacillin (MHA(Ox)), and

116 ial load time series data were enumerated on Mueller Hinton agar and colony forming unit data were mo

117 oplanin double-sided gradient test strips on Mueller-Hinton agar (MHA) with 5% sheep blood and a 0.5

118 oxitin Etests (AB Biodisk, Solna, Sweden) on Mueller-Hinton agar, an immunoassay for penicillin bindi

119 urella multocida and staphylococci tested on Mueller-Hinton agar, susceptibility at > or =19 mm and r

120 and E-test methods for agar-based testing on Mueller-Hinton agar supplemented with 2% glucose and 0.5

121 tes correlated with standard D-zone tests on Mueller-Hinton agar and with PCR for erm(A), erm(C), and

122 azole disk diffusion susceptibility tests on Mueller-Hinton agar supplemented with 2% glucose and 0.5

123 its for voriconazole disk diffusion tests on Mueller-Hinton agar with 2% glucose and 0.5 micro g of m

124 azole disk diffusion susceptibility tests on Mueller-Hinton agar with 2% glucose and 0.5 micro g of m

125 may be added before autoclaving the agar, or Mueller-Hinton agar plates may be flooded with a glucose

126 be added to the agar before autoclaving, or Mueller-Hinton agar plates may be flooded with a glucose

127 ed to beef and chicken juices (BJ and CJ) or Mueller Hinton broth (MHB) at 4 degrees C.

128 We used a partial Mueller matrix polarimeter to measure the corneal anisot

129 and 0.5 microg/ml methylene blue] and plain Mueller-Hinton [MH] agar), (ii) three incubation times (

130 over of simple stimuli-responsive polymers, Mueller matrix polarimetry offers an important advantage

131 y broth microdilution using freshly prepared Mueller-Hinton broth and by disk diffusion.

132 n (BHI) agar plate, and an in-house-prepared Mueller-Hinton (MH) agar plate, all incubated for 24 or

133 he logarithmic decomposition of the recorded Mueller matrices mapped the depolarization, linear retar

134 ificantly impacted by the brand of reference Mueller-Hinton broth base, and 14.6% of 117 A. urinae te

135 We measured the surface-reflectance Mueller matrix of live open ocean fish (lookdown, Selene

136 Peak increases in CFV during 20 s Mueller manoeuvres (40 +/- 3 %) were the same as control

137 Because a sample's Mueller matrix does not uniquely determine the linear, c

138 hyatt RM, Widen EM, Hassoun A, Oberfield SE, Mueller NT, Diaz D, Calafat AM, Perera FP, Rundle AG.

139 edominantly in patients with the most severe Mueller grade IV anaphylaxis (18.2% [24 of 132] vs 1.8%

140 Associated anaphylaxis severity (Mueller scale) was subsequently examined.

141 this regard, we have explored 4 x 4 spectral Mueller matrix measurement and its inverse analysis for

142 Through circular dichroism spectroscopy, Mueller matrix ellipsometry, and simulation using theore

143 For disk diffusion, standard Mueller-Hinton agar is recommended, presumably because i

144 All tests were conducted on standard Mueller-Hinton agar.

145 -BMD), and agar dilution (AD) using standard Mueller-Hinton agar were performed according to Clinical

146 The method is based on double Stokes-Mueller polarimetry and uses linear and circular inciden

147 xacin, and doxycycline on blood-supplemented Mueller-Hinton agar and to the inhibitory effects of met

148 es the use of lysed horse blood-supplemented Mueller-Hinton broth with incubation in 5% CO2 for 20 to

149 . (two species): (i) two media (supplemented Mueller-Hinton agar [2% dextrose and 0.5 microg/ml methy

150 The results demonstrate that Mueller matrix mapping of the depolarisation distributio

151 ron microscopy of normal retinas showed that Mueller cells, which synthesize a precursor of 11-cis-re

152 The Mueller calculus was used to model the polarization opti

153 the polarization properties by comparing the Mueller matrix under illumination at 450 nm and 589 nm.

154 ain approaches used in our laboratories (the Mueller-Rudin technique, in which the bilayers contain a

155 We find that increased media coverage of the Mueller investigation is immediately followed by Trump t

156 s followed by a reduction in coverage of the Mueller investigation-a finding that is consistent with

157 The potential applications of the Mueller polarimetric endoscope include wide field early

158 ould be classified as 3A or 3B, based on the Mueller-Wohlfarth (MW) classification.

159 the ventricular surface; in the retina, the Mueller radial glia were immunoreactive for Homer1, but

160 The optic train was modeled using the Mueller matrix representation and the combined sample pr

161 While the Mueller matrix offers the most chemical and physical ins

162 use of Fabry-Perot enhanced terahertz (THz) Mueller matrix ellipsometry to measure an electromagnon

163 ceptibility tests of Francisella tularensis, Mueller-Hinton broth with 2% Isovitalex is recommended.

164 lococci (half of which were S. aureus) using Mueller-Hinton agar from different manufacturers.

165 ditions were studied: agar dilution by using Mueller-Hinton (MH) medium (Difco) supplemented with eit

166 ); susceptibilities were determined by using Mueller-Hinton agar with oxacillin.

167 crodilution (BMD), disk diffusion (DD) using Mueller-Hinton agar (MHA) from three manufacturers, agar

168 2 isolates was tested by agar dilution using Mueller-Hinton sheep blood agar.

169 The performance of the Etest using Mueller-Hinton agar supplemented with glucose (2%) and m

170 as also performed on these 50 isolates using Mueller-Hinton agar (MHA) from three different manufactu

171 A similar method using Mueller-Hinton agar (5 microg of vancomycin per ml) gave

172 The disk diffusion method using Mueller-Hinton agar supplemented with glucose and methyl

173 erly NCCLS) broth microdilution method using Mueller-Hinton lysed horse blood broth, while a subset o

174 Disk diffusion testing was performed using Mueller-Hinton agar supplemented with 2% glucose and 0.5

175 Isolates were tested using Mueller-Hinton sheep blood agar plates incubated for 20

176 Potential in vivo Mueller matrix polarimetric tissue examinations in vario

177 helically twisted fibers were analyzed with Mueller matrix polarimetry.

178 ar containing 2% glucose (RPG agar) and with Mueller-Hinton agar containing 2% glucose and 0.5 microg

179 Etest IP plus IP-EDTA with Mueller-Hinton agar had a sensitivity of 94% (79 of 84)