Bioimaging最新文献

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Time-resolved identification of individual mononucleotide molecules in aqueous solution with pulsed semiconductor lasers 脉冲半导体激光在水溶液中单个单核苷酸分子的时间分辨鉴定
Bioimaging Pub Date : 2001-05-11 DOI: 10.1002/1361-6374(199803)6:1<14::AID-BIO3>3.0.CO;2-O
Markus Sauer, Jutta Arden-Jacob, Karl H Drexhage, Florian Göbel, Ulrike Lieberwirth, Klaus Mühlegger, Ralph Müller, Jürgen Wolfrum, Christoph Zander
{"title":"Time-resolved identification of individual mononucleotide molecules in aqueous solution with pulsed semiconductor lasers","authors":"Markus Sauer,&nbsp;Jutta Arden-Jacob,&nbsp;Karl H Drexhage,&nbsp;Florian Göbel,&nbsp;Ulrike Lieberwirth,&nbsp;Klaus Mühlegger,&nbsp;Ralph Müller,&nbsp;Jürgen Wolfrum,&nbsp;Christoph Zander","doi":"10.1002/1361-6374(199803)6:1<14::AID-BIO3>3.0.CO;2-O","DOIUrl":"10.1002/1361-6374(199803)6:1<14::AID-BIO3>3.0.CO;2-O","url":null,"abstract":"<p>We applied a short-pulse diode laser emitting at 640 nm with a repetition rate of 56 MHz in combination with a confocal microscope to study bursts of fluorescence photons from individual differently labeled mononucleotide molecules in water. Two newly synthesized dyes, an oxazine dye (MR121) and a rhodamine dye (JA53), and two commercially available dyes, a carbocyanine dye (Cy5) and a bora-diaza-indacene dye (Bodipy630/650), were used as fluorescent labels. The time-resolved fluorescence signals of individual mononucleotiode molecules in water were analyzed and identified by a maximum likelihood estimator (MLE). Taking only those single molecule transits which contain more than 30 collected photoelectrons, the two labeled mononucleotide molecules, Cy5-dCTP and Bodipy-dUTP, can be identified by time-resolved fluorescence spectroscopy with a probability of correct classification of greater than 99%. Our results show that at least three differently labeled mononucleotide molecules can be identified in a common aqueous solution. We obtain an overall classification probability of 90% for the time-resolved identification of Cy5-dCTP, MR121-dUTP and Bodipy-dUTP molecules via their characteristic fluorescence lifetimes of 1.05 ± 0.33 ns (Cy5-dCTP), 2.07 ± 0.59 ns (MR121-dUTP) and 3.88 ± 1.71 ns (Bodipy-dUTP).</p>","PeriodicalId":100176,"journal":{"name":"Bioimaging","volume":"6 1","pages":"14-24"},"PeriodicalIF":0.0,"publicationDate":"2001-05-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/1361-6374(199803)6:1<14::AID-BIO3>3.0.CO;2-O","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"81059938","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 46
Improvement in imaging in confocal fluorescent microscopes using multiple detectors 多探测器共聚焦荧光显微镜成像技术的改进
Bioimaging Pub Date : 2001-05-11 DOI: 10.1002/1361-6374(199809)6:3<126::AID-BIO2>3.0.CO;2-L
R Gauderon, C J R Sheppard
{"title":"Improvement in imaging in confocal fluorescent microscopes using multiple detectors","authors":"R Gauderon,&nbsp;C J R Sheppard","doi":"10.1002/1361-6374(199809)6:3<126::AID-BIO2>3.0.CO;2-L","DOIUrl":"10.1002/1361-6374(199809)6:3<126::AID-BIO2>3.0.CO;2-L","url":null,"abstract":"<p>Imaging performance in a confocal fluorescent microscope can be improved by using multiple detectors. The use of a large detector radius in a confocal fluorescent microscope, while giving a strong signal for lower spatial frequencies, results in negative components at some higher frequencies. Using this fact, effects of a simple detector array consisting of the difference signal between small and large detectors are considered. The effects on the transverse and axial variation of the three-dimensional optical transfer functions (OTFs) of the confocal fluorescent microscope are considered. The results show that the resulting OTFs are boosted, resulting in a better resolution.</p>","PeriodicalId":100176,"journal":{"name":"Bioimaging","volume":"6 3","pages":"126-129"},"PeriodicalIF":0.0,"publicationDate":"2001-05-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/1361-6374(199809)6:3<126::AID-BIO2>3.0.CO;2-L","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"86727463","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 10
Determination of pore networks and water content distributions from 3-D computed tomography images of a clay soil 黏土三维计算机断层成像中孔隙网络和含水量分布的测定
Bioimaging Pub Date : 2001-05-11 DOI: 10.1002/1361-6374(199712)5:4<194::AID-BIO3>3.0.CO;2-3
Anton W J Heijs, Jacqueline de Lange
{"title":"Determination of pore networks and water content distributions from 3-D computed tomography images of a clay soil","authors":"Anton W J Heijs,&nbsp;Jacqueline de Lange","doi":"10.1002/1361-6374(199712)5:4<194::AID-BIO3>3.0.CO;2-3","DOIUrl":"10.1002/1361-6374(199712)5:4<194::AID-BIO3>3.0.CO;2-3","url":null,"abstract":"<p>Knowledge of flow in porous media can be improved by analyzing three-dimensional (3-D) images of the water distribution in a soil. We report on such a study using computed tomography (CT) scanning of a clay soil sample first in dry conditions. Then, after an infiltration experiment, by scanning the sample again in wet conditions. We used test phantoms to determine the optimal scanning parameters to obtain images with a bimodal gray value distribution with high contrast and small standard deviation. We also determined the effect of slice thickness and reconstruction algorithm on the restoration and segmentation of the images. For a good 3-D representation of the pore space we scanned the slices adjacently at an axial resolution of 1 mm and a pixel size of 0.27 × 0.27 mm<sup>2</sup>. The high contrast between air in the pores and the clay background allowed a global thresholding for the segmentation whereby the connectivity and topology of the pore networks is conserved. From the difference between the images of the dry sample and the wet sample we determined the water content distribution. We used the image data for measurements of the water distribution to study the relation between the structure of the pore networks and water flow.</p>","PeriodicalId":100176,"journal":{"name":"Bioimaging","volume":"5 4","pages":"194-204"},"PeriodicalIF":0.0,"publicationDate":"2001-05-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/1361-6374(199712)5:4<194::AID-BIO3>3.0.CO;2-3","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84487345","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 7
Efficient suppression of diffusing photons using polarising annular objectives for microscopic imaging through turbid media. Bioimaging 6:92–97 1998 利用偏振环形物镜对混浊介质显微成像的有效抑制扩散光子。生物成像,6:92-97 1998
Bioimaging Pub Date : 2001-05-11 DOI: 10.1002/1361-6374(199809)6:3<150::AID-BIO5>3.0.CO;2-R
S P Schilders, X S Gan, M Gu
{"title":"Efficient suppression of diffusing photons using polarising annular objectives for microscopic imaging through turbid media. Bioimaging 6:92–97 1998","authors":"S P Schilders,&nbsp;X S Gan,&nbsp;M Gu","doi":"10.1002/1361-6374(199809)6:3<150::AID-BIO5>3.0.CO;2-R","DOIUrl":"10.1002/1361-6374(199809)6:3<150::AID-BIO5>3.0.CO;2-R","url":null,"abstract":"","PeriodicalId":100176,"journal":{"name":"Bioimaging","volume":"6 3","pages":"150"},"PeriodicalIF":0.0,"publicationDate":"2001-05-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/1361-6374(199809)6:3<150::AID-BIO5>3.0.CO;2-R","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"84780008","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
The effect of spatial filtering on the performance of time-of-flight imaging systems 空间滤波对飞行时间成像系统性能的影响
Bioimaging Pub Date : 2001-05-11 DOI: 10.1002/1361-6374(199706)5:2<71::AID-BIO4>3.0.CO;2-M
M C Pitter, J G Walker
{"title":"The effect of spatial filtering on the performance of time-of-flight imaging systems","authors":"M C Pitter,&nbsp;J G Walker","doi":"10.1002/1361-6374(199706)5:2<71::AID-BIO4>3.0.CO;2-M","DOIUrl":"https://doi.org/10.1002/1361-6374(199706)5:2<71::AID-BIO4>3.0.CO;2-M","url":null,"abstract":"<p>The results of a Monte Carlo computer simulation of photon transport through biological tissue are presented. A comparison is made of the performance, in terms of resolution for a given signal-to-noise ratio, of spatial filtering, time-of-flight imaging and a combination of these approaches. The results show that a careful choice of time gate and aperture dimensions can significantly improve the performance of time-gated optical imaging systems.</p>","PeriodicalId":100176,"journal":{"name":"Bioimaging","volume":"5 2","pages":"71-81"},"PeriodicalIF":0.0,"publicationDate":"2001-05-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/1361-6374(199706)5:2<71::AID-BIO4>3.0.CO;2-M","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"137819671","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Comparison between time-correlated single photon counting and fluorescence correlation spectroscopy in single molecule identification 时间相关单光子计数与荧光相关光谱在单分子鉴定中的比较
Bioimaging Pub Date : 2001-05-11 DOI: 10.1002/1361-6374(199803)6:1<3::AID-BIO2>3.0.CO;2-M
Jörg Enderlein, Malte Köllner
{"title":"Comparison between time-correlated single photon counting and fluorescence correlation spectroscopy in single molecule identification","authors":"Jörg Enderlein,&nbsp;Malte Köllner","doi":"10.1002/1361-6374(199803)6:1<3::AID-BIO2>3.0.CO;2-M","DOIUrl":"10.1002/1361-6374(199803)6:1<3::AID-BIO2>3.0.CO;2-M","url":null,"abstract":"<p>Currently, two methods of detection and identification of single molecules are widely used: fluorescence correlation spectroscopy (FCS) and time-correlated single photon counting (TCSPC). We present a thorough theoretical analysis of the error rates for identifying single molecules according to their diffusion coefficients (using FCS), and to their fluorescence lifetimes (using TCSPC). In most cases, the error rate using TCSPC is much lower. TCSPC is thus proven to be more versatile for analyzing single molecule events. The study is significant for a broad range of ultra-sensitive fluorescence detection applications.</p>","PeriodicalId":100176,"journal":{"name":"Bioimaging","volume":"6 1","pages":"3-13"},"PeriodicalIF":0.0,"publicationDate":"2001-05-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/1361-6374(199803)6:1<3::AID-BIO2>3.0.CO;2-M","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"85013944","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 11
Confocal microscopy of single molecules of the green fluorescent protein 绿色荧光蛋白的单分子共聚焦显微镜
Bioimaging Pub Date : 2001-05-11 DOI: 10.1002/1361-6374(199803)6:1<54::AID-BIO7>3.0.CO;2-8
G Jung, J Wiehler, W Göhde, J Tittel, Th Basché, B Steipe, C Bräuchle
{"title":"Confocal microscopy of single molecules of the green fluorescent protein","authors":"G Jung,&nbsp;J Wiehler,&nbsp;W Göhde,&nbsp;J Tittel,&nbsp;Th Basché,&nbsp;B Steipe,&nbsp;C Bräuchle","doi":"10.1002/1361-6374(199803)6:1<54::AID-BIO7>3.0.CO;2-8","DOIUrl":"10.1002/1361-6374(199803)6:1<54::AID-BIO7>3.0.CO;2-8","url":null,"abstract":"<p>Single molecule detection has been extended into life sciences by use of strongly fluorescent labels. The green fluorescent protein (GFP) as a self-fluorescent biomolecule has attracted considerable attention. Here, single molecules of the GFP-mutant Glu222Gln are immobilized in a polyvinylalcohol matrix and detected by confocal fluorescence microscopy. Although this mutant stabilizes one of both conformers of the wild-type GFP, the investigation of its fluorescence dynamics reveals strong signal fluctuations. This fluorescence behaviour is—at least partly—caused by reversible photochemical changes of the protein framework, that can relax into the fluorescent state on different timescales. Thus, this protein appears particularly appropriate for studying the microheterogeneity of the macromolecule GFP on a single molecule level.</p>","PeriodicalId":100176,"journal":{"name":"Bioimaging","volume":"6 1","pages":"54-61"},"PeriodicalIF":0.0,"publicationDate":"2001-05-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/1361-6374(199803)6:1<54::AID-BIO7>3.0.CO;2-8","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"73554994","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 43
Heavy metal contrast enhancement for the selective detection of gold particles in electron microscopical sections using electron spectroscopic imaging 利用电子光谱成像技术在电子显微切片中选择性检测金颗粒的重金属对比度增强
Bioimaging Pub Date : 2001-05-11 DOI: 10.1002/1361-6374(199809)6:3<130::AID-BIO3>3.0.CO;2-Z
Ansgar Haking, Helmut Troester, Karsten Richter, Annett Burzlaff, Herbert Spring, Michael F Trendelenburg
{"title":"Heavy metal contrast enhancement for the selective detection of gold particles in electron microscopical sections using electron spectroscopic imaging","authors":"Ansgar Haking,&nbsp;Helmut Troester,&nbsp;Karsten Richter,&nbsp;Annett Burzlaff,&nbsp;Herbert Spring,&nbsp;Michael F Trendelenburg","doi":"10.1002/1361-6374(199809)6:3<130::AID-BIO3>3.0.CO;2-Z","DOIUrl":"10.1002/1361-6374(199809)6:3<130::AID-BIO3>3.0.CO;2-Z","url":null,"abstract":"<p>In ultrathin sections for electron microscopy the evaluation of images generated with immunocytochemical or <i>in situ</i> hybridization techniques can become difficult if the colloidal gold label is very small and the underlying structure shows a strong heavy metal contrast caused by conventional uranium/lead staining. Normally, the problem is overcome by analyzing specimens at higher magnifications or by enlarging the gold grains in a secondary process called silver enhancement. We present a method to visualize the small gold particles with electron spectroscopic imaging (ESI). Three energy-filtered images acquired at energy losses of 0, 45 and 120 eV are analyzed by digital image treatment so as to allow the optical separation of the Au-markers from the image background. This protocol can be adapted for applications related to the automated counting of the label.</p>","PeriodicalId":100176,"journal":{"name":"Bioimaging","volume":"6 3","pages":"130-137"},"PeriodicalIF":0.0,"publicationDate":"2001-05-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/1361-6374(199809)6:3<130::AID-BIO3>3.0.CO;2-Z","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"76034188","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Real-time endoscopic fluorescence imaging for early cancer detection in the gastrointestinal tract 实时内镜荧光成像用于胃肠道早期癌症的检测
Bioimaging Pub Date : 2001-05-11 DOI: 10.1002/1361-6374(199812)6:4<151::AID-BIO1>3.0.CO;2-G
Haishan Zeng, Alan Weiss, Richard Cline, Calum E MacAulay
{"title":"Real-time endoscopic fluorescence imaging for early cancer detection in the gastrointestinal tract","authors":"Haishan Zeng,&nbsp;Alan Weiss,&nbsp;Richard Cline,&nbsp;Calum E MacAulay","doi":"10.1002/1361-6374(199812)6:4<151::AID-BIO1>3.0.CO;2-G","DOIUrl":"10.1002/1361-6374(199812)6:4<151::AID-BIO1>3.0.CO;2-G","url":null,"abstract":"<p>The utility of autofluorescence imaging for early lung cancer detection has been previously demonstrated. The aim of this work is to extend the use of real-time autofluorescence imaging to the early cancer detection in the esophagus, stomach, and colon. A prototype fluorescence imaging system for the gastrointestinal (GI) tract was developed which produces real-time video images of tissue autofluorescence. It consists of a filtered mercury arc lamp light source, two intensified charge coupled device (ICCD) cameras, a fiber optic endoscope, and a computer-based control console. The system is capable of working with three different imaging modalities: (1) conventional white light imaging mode; (2) light induced fluorescence (LIF) imaging mode based on the fluorescence imaging of two wavelength bands (green and red); and (3) light induced fluorescence and reflectance (LIFR) imaging mode based on the combination of a green band fluorescence image and a red–near-IR reflectance image. The imaging wavelength bands were selected based on <i>in vivo</i> fluorescence spectroscopic studies. The fluorescence images (both LIF image and LIFR image) clearly delineate the abnormal tissue areas for biopsy. Early cancer sites are better visualized under fluorescence imaging than under conventional white light examination. Initial clinical tests demonstrated the usefulness of the imaging prototype system for early cancer detection in the GI tract.</p>","PeriodicalId":100176,"journal":{"name":"Bioimaging","volume":"6 4","pages":"151-165"},"PeriodicalIF":0.0,"publicationDate":"2001-05-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1002/1361-6374(199812)6:4<151::AID-BIO1>3.0.CO;2-G","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"78138944","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 75
Techniques for single molecule sequencing 单分子测序技术
Bioimaging Pub Date : 2001-05-11 DOI: 10.1002/1361-6374(199709)5:3<139::AID-BIO8>3.0.CO;2-%23
Klaus Dörre, Susanne Brakmann, Michael Brinkmeier, Kyung-Tae Han, Katja Riebeseel, Petra Schwille, Jens Stephan, Timm Wetzel, Markus Lapczyna, Michael Stuke, Raoul Bader, Michael Hinz, Hartmut Seliger, Johan Holm, Manfred Eigen, Rudolf Rigler
{"title":"Techniques for single molecule sequencing","authors":"Klaus Dörre,&nbsp;Susanne Brakmann,&nbsp;Michael Brinkmeier,&nbsp;Kyung-Tae Han,&nbsp;Katja Riebeseel,&nbsp;Petra Schwille,&nbsp;Jens Stephan,&nbsp;Timm Wetzel,&nbsp;Markus Lapczyna,&nbsp;Michael Stuke,&nbsp;Raoul Bader,&nbsp;Michael Hinz,&nbsp;Hartmut Seliger,&nbsp;Johan Holm,&nbsp;Manfred Eigen,&nbsp;Rudolf Rigler","doi":"10.1002/1361-6374(199709)5:3<139::AID-BIO8>3.0.CO;2-%23","DOIUrl":"https://doi.org/10.1002/1361-6374(199709)5:3<139::AID-BIO8>3.0.CO;2-%23","url":null,"abstract":"<p>A method is described that demonstrates a new technique for rapid and high-throughput single molecule sequencing. This sequencing technique is based on the successive enzymatic degradation of fluorescently labeled single DNA molecules, and the detection and identification of the released monomer molecules according to their sequential order in a microstructured channel.</p><p>The detection technique is evolved from confocal fluorescence microscopy, with two different laser sources to excite the individual mononucleotides that are either labeled with tetramethylrhodamine (TMR) or Cyanine5 (Cy5). The handling of DNA which is immobilized on carrier beads, and the detection of the cleaved monomers is performed in optically transparent and biochemically inert microstructures (glass or PMMA) with detection channels of 7 μ × 10 μm.</p><p>The projected rate of sequencing is ≈100 bases min<sup>−1</sup>, dependent solely on the rate of the enzymatic DNA cleavage.</p>","PeriodicalId":100176,"journal":{"name":"Bioimaging","volume":"5 3","pages":"139-152"},"PeriodicalIF":0.0,"publicationDate":"2001-05-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/1361-6374%28199709%295%3A3%3C139%3A%3AAID-BIO8%3E3.0.CO%3B2-%23","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"137670534","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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