ライフサイエンスコーパス: robin

1 logy and population genetics of the European Robin.

2 ments: constrained, unconstrained, and round robin.

3 s recently proposed by Tchetgen Tchetgen and Robins.

4 Cochrane's RoB 2.0 and ROBINS-1 tools assessed risk of bias.

5 QUADAS and ROBINS-1 tools were used to assess the quality of diagno

6 for nonrandomized studies of interventions (ROBINS-1).

7 was assessed with appropriate tools (RoB-2, ROBINS-1).

8 rted Repository Of BInders to Nucleic acids (ROBIN), a new library of nucleic acid binders identified

9 Allard et al. provide an overview of sea robins, a group of benthic fish that have evolved leg-li

10 may therefore affect migratory behaviour of robins, although large geographical variation in respons

11 The round-robin analyses of each database demonstrated similar res

12 Round-robin analysis and independent testing were performed to

13 ocols included independent testing and round-robin analysis.

14 esting that any differences in Cry4a between robin and chicken must stem from their ability to transm

15 n the solid state 1(2+) is a valence-trapped Robin and Day class II compound on the 10(-12) s infrare

16 (2)AlCl --> 2(IP(-))(IP)AlCl consistent with Robin and Day Class II mixed-valent behavior.

17 own to be valence trapped or Class II on the Robin and Day classification scheme.

18 n are Class II mixed-valent compounds in the Robin and Day classification, presenting an inherent ten

19 nearly a half-century before the proposal of Robin and Guze for the validation of psychiatric disorde

20 n system for MV systems introduced by Melvin Robin and Peter Day.

21 and two key reservoir species, the American robin and the house sparrow.

22 tion and average delay much lower than Round-Robin and threshold-based algorithms.

23 onal approaches of Load balancing like Round-Robin and Threshold-based load balancing fails in scalab

24 e tested by applying some of the criteria of Robins and Guze and Kendell.

25 refining them in accordance with the classic Robins and Guze strategy for validation of psychiatric d

26 John Feighner, a discussion group led by Eli Robins and including Sam Guze, George Winokur, Robert Wo

27 s and Lys, respectively, found in Cry4a from robins and other night-migratory passerines.

28 nectivity of the spinal cord between the sea robins and other vertebrates are striking.

29 an imputation variance estimator proposed by Robins and Wang (RW) in a scenario where the study exclu

30 is required for normal leg formation in sea robins, and for formation of enlarged central nervous sy

31 vertebrate and invertebrate cells, American robins, and two Culex species with WNV and/or SLEV.

32 f purified Cry4a from the migratory European robin are well characterized, but it is less clear what,

33 Sea robins are fish that possess specialized leg-like append

34 Our study establishes sea robins as a model organism for studying the evolution of

35 suggest some evolutionary trade-offs in sea robin C-start behavior compared with that of the goldfis

36 A round robin comparison was performed in order to test the perf

37 Using four-person round-robin conversation networks, we found that participants

38 Me))V}(2)(mu(4)-VN(4))] (5), conforming to a Robin-Day class I description.

39 es ranging from fully localized ([2-Co](4+); Robin-Day Class I) to fully delocalized ([1(CO2Me)-Co](3

40 tion of the bimolecular precursor complex as Robin-Day class II (localized) or class III (delocalized

41 e diagnostic (intervalence) NIR band reveals Robin-Day Class II behavior.

42 they have shown IVCT phenomena derived from Robin-Day Class II localized valency or even electronic

43 It shows a Hush-type Robin-Day class II mixed valence band in its optical spe

44 ahydrofuran, respectively, consistent with a Robin-Day class II mixed valence compound.

45 ns [Ru2-C2m-Ru2](-1) (m = 4-8) belong to the Robin-Day class II mixed valent ions and (ii) the electr

46 n the near-infrared region consistent with a Robin-Day class II system.

47 d in order to formulate a new definition for Robin-Day class II-III mixed valence compounds.

48 indicate a change from a charge delocalized, Robin-Day class II/III high spin state to a charge-local

49 measurements reveal the first observation of Robin-Day Class II/III mixed valency in a MOF.

50 ntal and computational analysis demonstrates Robin-Day Class III 6d-orbital valence delocalization in

51 ng occurs and, for the first time, IVCT in a Robin-Day Class III complex resulting from f-f transitio

52 refore, 2[B(Ar(F))4] meets the criteria of a Robin-Day class III mixed-valent compound.

53 ation, and computational analysis of a rare, Robin-Day Class III, singly reduced dinuclear Yb complex

54 neighboring sites, placing the system in the Robin-Day class III.

55 e MV systems close to the borderline between Robin-Day classes II and III.

56 This change in Robin-Day classification of the complex as a function of

57 sh formalism and found to be of class II (in Robin-Day classification) character with localized ferro

58 ent with class II compounds according to the Robin-Day classification.

59 tify the various D-br-D*(+) according to the Robin-Day classification.

60 es a single potential well) according to the Robin-Day classification.

61 NIR region and can be assigned as a Class 2 Robin-Day MV (mixed valence) system with weakly interact

62 , places these within class II or III of the Robin-Day system.

63 strongly coupled redox systems lying in the (Robin-Day) Class II category.

64 Using a round-robin design in each of six closed networks, we show tha

65 We propose an augmented round-robin design that accomplishes this.

66 idizations were carried out by using a round-robin design, and microarray data were analyzed with a t

67 mes of 19 F1 hybrid lines from a large round robin design, we independently attribute a robust cis-re

68 Utilizing a round-robin design, we present a quantitative description of v

69 allopatric wild-type populations in a round-robin design.

70 rize microsatellite markers for the European Robin, designing three multiplex panels to amplify 14 mi

71 We demonstrate that wild female robins' desire for particular foods changes over short t

72 Robins discusses reasons why national stereotypes are in

73 In his Perspective, Robins discusses Terracciano et al.'s finding that cultu

74 on time of activity onset in blackbirds and robins during both the pre- and post-breeding seasons: u

75 data extraction and quality assessment using ROBINS-E in duplicates.

76 of bias assessments were performed using the ROBINS-E tool.

77 The risk of bias was assessed using ROBINS-E tools and the certainty of the evidence by usin

78 Bias in Nonrandomized Studies-of Exposures (ROBINS-E) tool was used for critical appraisal of cohort

79 Bias In Non-randomised Studies of Exposures (ROBINS-E) tool.

80 The risk of bias was assessed with ROBINS-E, and the certainty of evidence (CoE) with GRADE

81 behaviour among populations of the European robin Erithacus rubecula across Europe.

82 that Cry4a from the night-migratory European robin (Erithacus rubecula) exhibits greater magnetic sen

83 e 4 (CRY4) from the night-migratory European robin (Erithacus rubecula) is magnetically sensitive in

84 ochrome 4a from the night-migratory European robin (Erithacus rubecula), ErCry4a, and to replace each

85 p) radicals in cryptochrome 4a from European robin (Erithacus rubecula, ErCry4a) and pigeon (Columba

86 When European robins, Erithacus rubecula, were exposed to the backgrou

87 uestion the generalizability of the Guze and Robins estimate.

88 ethods described here and used for the round robin experiment do not require specialized instrumentat

89 n occupational study, development of a round-robin experiment to validate BPA measurements in human s

90 ed on data from the remaining dog in a round-robin fashion.

91 Robin Fears and co-authors discuss evidence-informed reg

92 In this Policy Forum piece, Robin Feldman discusses how current legislation contribu

93 probe the genetic basis of trait gain in sea robin fish, which have evolved specialized leg-like appe

94 Sea robins, fish with legs, walk on the ocean bottom.

95 icial proficiency tests (International Round-Robins) for the Provisional Technical Secretariat/Prepar

96 apillae, and interspecies comparisons of sea robins from around the world demonstrate that papillae r

97 n a clade of small passerines (Tarsiger bush-robins) from the eastern edge of the Qinghai-Tibet Plate

98 ctivity in six passerine species (blackbird, robin, great tit, blue tit, dunnock and chaffinch) acros

99 r-Kupfer update and expansion of the classic Robins-Guze criteria for establishing psychiatric diagno

100 However, robins had comparable viremia and antibody responses reg

101 Although sea robins have a very different phylogenetic position, body

102 are ranked according to the results of round-robin, head-to-head comparisons using difference scores.

103 dinary DNA structure, originally proposed by Robin Holliday to explain genetic recombination in fungi

104 Interview with Robin Hopkins, who studies speciation and reinforcement

105 n Non-randomized Studies - of Interventions (ROBINS- I) tools and a specific tool for case reports/se

106 rvational studies was assessed regarding the ROBIN-I scale.

107 Risk of bias was evaluated using ROBINS-I (Risk Of Bias In Non-randomised Studies of Inte

108 Cochrane Collaboration's risk of bias, ROBINS-I and GRADE tools were used to assess quality and

109 Studies were assessed for bias using ROBINS-I and NIH Quality Assessment tool and assessed fo

110 n and quality assessment were performed with ROBINS-I and RoB-2 tools for observational studies and r

111 Risk of bias was assessed using ROBINS-I and RoB-2 tools.

112 bias in each study was determined using the ROBINS-I and RoB2 tools.

113 idence were assessed using Cochrane RoB-2 or ROBINS-I and the GRADE tool, respectively.

114 elines and risk of bias assessed through the ROBINS-I Cochrane tool by 2 independent reviewers.

115 A risk-of-bias evaluation that used ROBINS-I demonstrated notable bias in the confounder and

116 All included studies exhibited at least one ROBINS-I domain at high risk of bias, particularly relat

117 d using risk of Bias 2 tool for RCTs and the ROBINS-I for non-RCTs.

118 Risk of bias was evaluated using the ROBINS-I framework.

119 The risk of bias was evaluated using the ROBINS-I framework.

120 We assessed risk of bias using the ROBINS-I tool for observational studies and assessed cer

121 as assessment tool for randomized trials and ROBINS-I tool for observational studies.

122 We used the ROBINS-I tool to assess risk of bias.

123 The ROBINS-I tool was used to assess the risk of bias in non

124 The Cochrane Risk of Bias tool and ROBINS-I tool were used for assessing the risk of bias.

125 Based on the ROBINS-I tool, most studies (n = 8) had a serious risk o

126 ow or moderate risk of bias according to the ROBINS-I tool.

127 were assessed for the risk of bias using the ROBINS-I tool.

128 y of included studies was assessed using the Robins-I tool.

129 raised using the Cochrane Risk of Bias 2 and ROBINS-I tools.

130 as appraised using Cochrane Risk of Bias and ROBINS-I Tools.

131 We used a random-effects model, and ROBINS-I was used for the risk-of-bias analysis.

132 The Cochrane risk of bias tool 2 and ROBINS-I were used to assess risk of bias and GRADE eval

133 In Non-randomized Studies-of Interventions (ROBINS-I) and Strengthening the Reporting of Observation

134 in Non-randomized Studies of Interventions (ROBINS-I) and the Joanna Briggs Institute Critical Appra

135 the Risk of Bias of Non-Randomized Studies (ROBINS-I) assessed single-arm trials.

136 in non-randomized studies of interventions (ROBINS-I) for non-randomized studies of interventions.

137 in Non-randomized Studies-of Interventions (ROBINS-I) risk of bias assessment.

138 In Non-randomized Studies of Interventions (ROBINS-I) tool for observational studies.

139 n Non-Randomized Studies - of Interventions (ROBINS-I) tool was used to assess the risk of bias.

140 s in Non-randomized Studies of Intervention (ROBINS-I) tool.

141 In Non-randomized Studies-of Interventions (ROBINS-I) tool.

142 Bias in Non-Randomised Studies-Intervention (ROBINS-I).

143 be at serious or critical risk of bias using ROBINS-I.

144 individuate conceptually related items (e.g. robins, in particular, have red breasts).

145 The European Robin is a small passerine bird associated with woodland

146 The rotating ball inlet (ROBIN) is presented in a new design for on-line matrix-a

147 Methods and applications' by Robin J.

148 ural network (BP-ANN) was trained in a round-robin (leave-one-out) manner to predict biopsy outcome f

149 th the properties that typify concepts (e.g. robins, like all birds, have wings) as well as the prope

150 ponse to inbreeding in plants from 13 Ragged Robin (Lychnis flos-cuculi) populations.

151 r dimorphism in the reproductive benefits of robin memory performance suggests an additional role for

152 Bobbi Pritt and Robin Patel of the Mayo Clinic, where S. pyogenes NAATs

153 barachnoid space and infiltrated the Virchow-Robin (perivascular) space.

154 males in a caching songbird, the New Zealand robin (Petroica longipes).

155 igate whether and how wild male North Island robins (Petroica longipes) respond to changes in their m

156 In our experiments, wild male robins preferentially shared the larvae type that their

157 study these predictions in the northern sea robin, Prionotus carolinus, a percomorph fish.

158 sociated ascending spinal systems in the sea robin, Prionotus carolinus.

159 In 1970, Guze and Robins published a meta-analysis of suicide in patients

160 the proposed algorithm is better than Round Robin, Random Allocation, and Threshold Based algorithms

161 ergy and has less processing time than Round-Robin, Random Offloading, and Threshold-Based techniques

162 e second putative CxNV1 segment, the 0.8-kb "Robin" RNA.

163 pping disease-associated mutations in Pierre Robin sequence (PRS) patients regulate SOX9 expression a

164 h craniofacial variation and disease (Pierre Robin sequence (PRS)).

165 ction by the tongue, resembling human Pierre Robin sequence (PRS)-like cleft secondary palate.

166 a human craniofacial disorder called Pierre Robin sequence (PRS).

167 est derivatives phenocopies the human Pierre Robin sequence and highlights the interconnection of pal

168 defects similar to those seen in the Pierre Robin Sequence in humans.

169 SLC35B3 (cleft palate only), CASC20 (Pierre Robin Sequence) and CHRM2 (non-syndromic cleft palate on

170 bases upstream of SOX9 (EC1.45) cause Pierre Robin sequence, a craniofacial disorder characterised by

171 , talipes equinovarus, atrial septal defect, Robin sequence, and persistent left superior vena cava.

172 showed higher myopia and incidence of Pierre Robin sequence, and similar rates of RD and systemic man

173 We also conducted the first GWAS of Pierre Robin Sequence, despite the small sample size (n cases =

174 pectrum of skeletal abnormalities, including Robin sequence, hypoplastic scapulae, and a missing pair

175 ft palate, mimicking the phenotype of Pierre Robin sequence.

176 ith opposing effects on cleft lip and Pierre Robin sequence.

177 e of the most common malformation sequences, Robin sequence.

178 in a family with a mild acampomelic CD with Robin sequence.

179 rve as a mouse model for the human disorder, Robin sequence.

180 th wild birds, including jays, sparrows, and robins, serving as vertebrate hosts.

181 MRI revealed dilated atypical Virchow-Robin space (VRS).

182 vascular spaces (PVS), also known as Virchow-Robin space, has significant clinical value, but there r

183 s CNS microvessels, pia, subpia, and Virchow-Robin space.

184 Markedly enlarged Virchow-Robin spaces throughout the striatum appear occasionally

185 vity to CNS microvessels, subpia and Virchow-Robin spaces was described in patients with NMO [called

186 time, new subcortical infarcts, new Virchow-Robin spaces, 1 standard deviation lower total brain vol

187 ical infarcts, cerebral microbleeds, Virchow-Robin spaces, and total brain parenchyma volume.

188 and specific features like enlarged Virchow-Robin spaces, this review then explores clinical aspects

189 seasons: urban populations of blackbird and robin started their daily activity earlier than their fo

190 The fin rays of the pectoral fin of the sea robins (teleostei) are specialized chemosensory organs h

191 e investigation with 144 patterns of a round robin test using 18 feline APOBEC3Z3 genes, an antiviral

192 We performed an international round-robin testing of module performance to confirm the measu

193 During round-robin testing, the neural network estimate of pulmonary

194 , 0.923]) was wider than that with the round-robin tests.

195 but also achieve remarkable success in round-robin tournaments and evolutionary interactions.

196 Accordingly, American robins (Turdus migratorius), two species of mosquitoes,

197 It is especially notable because sea robins utilize the chemosensory input from the fin rays

198 In 1984, Barry Marshall and Robin Warren proposed a role for bacterial infections in

199 Experiments with robins wearing frosted goggles have revealed a tantalisi

200 Two American robins were also seropositive.

201 Robins were disoriented when exposed to a vertically ali

202 Robins were efficiently coinfected, with no impact of co

203 rlings, rock pigeons, swallows, and American robins were the most commonly captured birds.

204 g that this already may be true for American robins, which are arriving 14 days earlier than they did

205 with two prominent celebrity suicide events: Robin Williams during 2014 and Kate Spade and Anthony Bo