ライフサイエンスコーパス: corpora

1 rends of continuity and change in historical corpora.

2 , or in the equivalent transcription of oral corpora.

3 to their own systems and train models on new corpora.

4 nt Dirichlet allocation used to analyze text corpora.

5 spectrum of languages that allow us to rank corpora.

6 veral models trained on different individual corpora.

7 traction methods requires manually annotated corpora.

8 rage of semantic types annotated in existing corpora.

9 rkup is also among the largest of comparable corpora.

10 e largest gold-standard annotated biomedical corpora.

11 these were implanted to replace the excised corpora.

12 contingencies are important for large-scale corpora.

13 1.7%, as tested on the gold-standard ITI-TXM corpora.

14 f the medulla with stromal proliferation and corpora albicantia.

15 zyme was isolated from a cDNA library of the corpora allata (CA) from reproductively active Diplopter

16 uvenile hormone biosynthesis by the isolated corpora allata (CA) of adult female A. aegypti.

17 The regulation of JH synthesis by the corpora allata (CA), a pair of endocrine glands with ner

18 ctors of disease, but the minute size of the corpora allata (CA), the glands that synthesize JH, has

19 attaching themselves to the primordia of the corpora allata (CA).

20 tically ablating the JH-producing organ, the corpora allata (CA).

21 e cuticular hydrocarbon profiles showed that corpora allata ablation caused a delay in production of

22 e hormone biosynthesis in adult lepidopteran corpora allata and was subsequently shown to have cardio

23 Innervation of the corpora allata by YXFGLamide-immunoreactive processes wa

24 etamorphosis of Drosophila melanogaster, the corpora allata cells, which produce JH, were killed usin

25 CYP15A1 gene is expressed selectively in the corpora allata of D. punctata, at the time of maximal JH

26 Expressed sequence tags from the corpora allata of the cockroach Diploptera punctata yiel

27 ids appears to be a metabolic pathway in the corpora allata that may play a role in the suppression o

28 ent through mechanisms such as inhibition of corpora allata, as seen in Orthoptera and Blattaria.

29 ar organs, the crustacean homologs of insect corpora allata, produce precursors of juvenile hormone w

30 analysis of females genetically lacking the corpora allata, the glands that produce JH, showed that

31 1 was isolated as an EST in a library of the corpora allata-corpora cardiaca of the mosquito Aedes ae

32 reproduction in insects, is produced by the corpora allata.

33 urohemal endings in the corpora cardiaca and corpora allata.

34 bodies, the subesophageal ganglion, and the corpora allata.

35 Corpora amylacea (CA) are a frequent microscopic finding

36 Accumulation of numerous 7F3-positive corpora amylacea in the memory and motor system subdivis

37 hould be made by incorporating out-of-domain corpora and domain-specific lexicons, we believe that th

38 m that outperforms systems trained on single corpora and exceeds previously reported results on two e

39 package for preparing medical message board corpora and extracting patient mentions and statistics f

40 he annotation process using two named entity corpora and show that our approach can reduce the number

41 arts of speech for each of the four language corpora, and accounts for approximately 50% of the varia

42 Biomedical corpora annotated with event-level information represent

43 Manually annotated corpora are critical for the training and evaluation of

44 The evaluation resources (manually annotated corpora) are also available through the website: http://

45 cy of the system against the CRAFT and ShARe corpora as reference standards and compared it to MMTx,

46 owever, the nature of the annotated training corpora, as well as the training process itself, can lim

47 tter results on the GENIA Event and BioInfer corpora, both of which contain more varied and complex e

48 ntrol participants were reciprocally thinner corpora callosa (18.6%; P < .003 and P < .001, respectiv

49 ominent features were dysmorphic and thicker corpora callosa compared with familial noncarriers and p

50 The very preterm subjects with damaged corpora callosa had significantly different activation p

51 ransfer with nine very preterm subjects with corpora callosa of normal appearance on structural MRI,

52 At 4-week cuprizone treatment, the corpora callosa of wildtype (WT) mice had robust Oil Red

53 antly more Oil Red O+ staining in the Axl-/- corpora callosa than in the WT indicating a lag in the c

54 Corpora callosa were measured for area, length and thick

55 In Axl-/- corpora callosa, 5-week post-cuprizone withdrawal, the n

56 l, indicative of axonal damage in the Axl-/- corpora callosa.

57 total, shows that learning from overlapping corpora can produce a single, corpus-independent, wide c

58 , by targeted cell ablation, that Drosophila corpora cardiaca (CC) cells of the ring gland are also e

59 he brain and their neurohemal endings in the corpora cardiaca and corpora allata.

60 oblasts as progenitors of the neurosecretory Corpora cardiaca cells, which are homologous to the gluc

61 rdiac recurrent nerve, hypocerebral ganglion/corpora cardiaca complex, crop duct, and crop.

62 Intrinsic cells of the corpora cardiaca contain pburs transcripts and pburs-lik

63 he dAkh gene is expressed exclusively in the corpora cardiaca from late embryos to adult stages.

64 as an EST in a library of the corpora allata-corpora cardiaca of the mosquito Aedes aegypti.

65 cells that innervate the corpus allatum and corpora cardiaca of the ring gland, an endocrine organ w

66 s of the larval and adult visual system, the corpora cardiaca, and subsets of cells in the developing

67 kinetic hormone (AKH)-producing cells of the corpora cardiaca, and we demonstrate that AKH signalling

68 ssage could not be detected in the fat body, corpora cardiaca, or brain, but trace levels of expressi

69 Absence of the corpora cardiaca, the endocrine gland innervated by neur

70 five Lem-MIPs in preparations of the AMe and corpora cardiaca.

71 re that employs aspiration of blood from the corpora cavernosa and irrigation with a dilute epinephri

72 Thus, aspiration of the corpora cavernosa followed by irrigation with dilute epi

73 A biopsy of the corpora cavernosa on both sides revealed a carcinoma har

74 is necessary to increase blood flow into the corpora cavernosa that leads to penile tumescence.

75 l as NADPH CYP reductase were present in rat corpora cavernosa, which was confirmed by immunohistoche

76 oduct metabolized by CYP epoxygenases in rat corpora cavernosa.

77 ontaining the eNOS gene (AdCMVeNOS) into the corpora cavernosum of the aged rat.

78 Our results indicate that text corpora contain recoverable and accurate imprints of our

79 idated TaggerOne with multiple gold-standard corpora containing both mention- and concept-level annot

80 iled analysis of three open access bio-event corpora containing negation information (i.e., GENIA Eve

81 Although combined use of several such corpora could potentially allow an extraction system to

82 The bioengineered corpora demonstrated structural and functional parameter

83 ftp://ftp.ebi.ac.uk/pub/software/textmining/corpora/diseases and can serve as a benchmark to other s

84 In particular, most event-annotated corpora do not deal adequately with coreference.

85 y, but is prone to false-positives on larger corpora due to noun modifiers.

86 ere we use four large and divergent language corpora (English, Spanish, Russian and Greek) and a comp

87 n analytical tool to structure large textual corpora for data mining.

88 . protein and cell line) trained on standard corpora, for which performance is roughly state of the a

89 ed the SVM classifier first on gold standard corpora from GENIA and find it achieved 82% precision an

90 red using the three GO sub-ontologies in the corpora (function, process and component).

91 cted with two independent, time-stamped text corpora (Google books Ngrams and the New York Times), we

92 Urethral plate elevation from the corpora has previously been reported to reduce bending,

93 evaluation of 100,000 words spread across 24 corpora in 10 languages diverse in origin and culture, w

94 and relatedness measures computed from text corpora in three domains (Clinical Notes, PubMed Central

95 An evaluation using seven event annotated corpora, including 65 event types in total, shows that l

96 ndations were adherent in most instances for corpora lutea (88%), simple cysts (56%), and cysts sugge

97 zyme 20alpha-hydroxysteroid dehydrogenase in corpora lutea (CL) inactivated of Lgr5.

98 f ischemic necrosis were demonstrated in the corpora lutea (CLs) of treated animals.

99 C/EBP beta-deficient ovaries lack corpora lutea and fail to down-regulate expression of th

100 le infertility with abnormal ovaries lacking corpora lutea and increase in luteinizing hormone levels

101 ing washed mitochondria isolated from bovine corpora lutea and purified recombinant His-tag StAR prot

102 in wild type recipients, significantly more corpora lutea containing un-ovulated oocytes were presen

103 aphase II oocytes can be retrieved from, and corpora lutea form in, ovaries of aged Bax-/- females fo

104 ning, we identified individual follicles and corpora lutea in intact ovaries.

105 increase in NUR77 mRNA was observed in mice corpora lutea just before parturition at a time when 20a

106 ncreased fertility based on ovulated egg and corpora lutea numbers.

107 Analysis of PKC delta activity in corpora lutea obtained during pregnancy by both the IC k

108 sessed the activation status of PKC delta in corpora lutea obtained when the corpus luteum is exposed

109 ithelial and granulosa cells and also in the corpora lutea of GREKO(-/-) mice.

110 munohistochemical analyses demonstrated that corpora lutea of p27(Kip1), p21(Cip1) double-null mice s

111 support development and maintain functional corpora lutea through the production of estrogen.

112 ssion was evaluated in ovarian follicles and corpora lutea utilizing immunohistochemical techniques a

113 70, inhibition of endometrial maturation and corpora lutea was observed.

114 o found to be severely subfertile, and fewer corpora lutea were found to form in response to exogenou

115 Corpora lutea were present in all groups.

116 No corpora lutea were present.

117 In the ovaries of macrophage-depleted mice, corpora lutea were profoundly abnormal, with elevated Pt

118 ed imaging of the ovary revealed cyst walls, corpora lutea, and ovarian medulla.

119 nsplants displayed normal estrous cycles and corpora lutea, despite DHT treatment, implying extraovar

120 contrast, progesterone, which is secreted by corpora lutea, increased SLA and beta(2)m in luminal epi

121 n mice on lower P:C (1:8), and the number of corpora lutea, indicative of recent ovulations, was grea

122 In normally developing corpora lutea, macrophages were intimately juxtaposed wi

123 ibit defects in luteinization, with numerous corpora lutea, some of which contain central trapped, fu

124 Similar to corpora lutea, the lesions were highly vascularized, alt

125 turation of secondary ovarian follicles into corpora lutea, which express high levels of p27, was mar

126 of follicle maturation, most notably around corpora lutea, without significantly affecting follicula

127 egenerating antral follicles, and absence of corpora lutea.

128 xhibited a marked reduction in the number of corpora lutea.

129 produced fewer oocytes and also showed fewer corpora lutea.

130 ntation-promoting activity has been found in corpora lutea.

131 e, whereas they undergo differentiation into corpora lutea.

132 ary to VEGF expression in both follicles and corpora lutea.

133 tions of follicles, they ovulate and develop corpora lutea.

134 wing preovulatory follicles as well as early corpora lutea.

135 was weak in atretic follicles and regressing corpora lutea.

136 o ovulate and develop numerous inappropriate corpora lutea.

137 educed numbers of large antral follicles and corpora lutea.

138 rrested folliculogenesis and failure to form corpora lutea.

139 and atrophic reproductive tracts with absent corpora lutea.

140 her percentage of antral follicles and fewer corpora lutea; follicles progressed to the antral stage

141 r, the lack of training data (i.e. annotated corpora) makes it difficult for machine learning-based n

142 our system on each of the three open access corpora mentioned above.

143 However, the lack of adequate specialized corpora needed to train statistical models currently lim

144 Here, using parsed corpora of 37 diverse languages, we show that overall de

145 We use time series derived from large corpora of annotated texts dating from the 12th to 21st

146 information that can be obtained from large corpora of naturally occurring texts.

147 sed temporal topic models to transform large corpora of news articles into temporal topic trends.

148 h precision and recall on several evaluation corpora of PubMed abstracts.

149 summary of rich biological information from corpora of users' interests.

150 The paragraph spaces of five text corpora, of different genres and intended audiences, in

151 need to either select a subset of compatible corpora or semantic types, or to merge results from seve

152 have been routinely investigated in written corpora, or in the equivalent transcription of oral corp

153 analyze two very large, sequence-containing corpora: over 7.75 million Medline abstracts and 9000 fu

154 and 0.88 based on the BioNLP-ST and Genia-MK corpora, respectively, making considerable improvements

155 ources are freely available at http://bionlp-corpora.sourceforge.net/CRAFT/index.shtml.

156 ng text mining applications exist, including corpora, structured test suites, and post hoc judging.

157 We introduced three new corpora suggesting named-entity recognition (NER) to be

158 The manually annotated corpora, supporting resources, and evaluation tools for

159 identifying meaningful categories in textual corpora that span long historic durees, where terms, con

160 rage by allowing several different annotated corpora to be used during training.

161 al websites, which substantially extends the corpora used in previous work.

162 classify sequence patterns from within large corpora using an n-gram Markov model (MM).

163 On filtering the corpora using GO evidence codes we found that the value

164 ation scheme for enriching biomedical domain corpora with causality relations.

165 propose a method for learning from multiple corpora with partial semantic annotation overlap, and im

166 he-art event extraction system from multiple corpora with partial semantic annotation overlap.

167 little research into learning from multiple corpora with partially overlapping semantic annotation s