Regional function-structure relationships in lungs of an elastase murine model of emphysema
Changes in lung function and structure were studied using hyperpolarized (3)He MRI in an elastase-induced murine model of emphysema. The combined analysis of the apparent diffusion coefficient (ADC) and fractional ventilation (R) were used to distinguish emphysematous changes and also to develop a m...
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creator | ISHII, Masaru EMAMI, Kiarash KUZMA, Nicholas KADLECEK, Stephen PODOLIN, Patricia L RIZI, Rahim R YI XIN BARULIC, Amy KOTZER, Charles J LOGAN, Gregory A CHIA, Elaine MACDUFFIE-WOODBURN, John P JIANLIANG ZHU PICKUP, Stephen |
description | Changes in lung function and structure were studied using hyperpolarized (3)He MRI in an elastase-induced murine model of emphysema. The combined analysis of the apparent diffusion coefficient (ADC) and fractional ventilation (R) were used to distinguish emphysematous changes and also to develop a model for classifying sections of the lung into diseased and normal. Twelve healthy male BALB/c mice (26 ± 2 g) were randomized into healthy and elastase-induced mice and studied ∼8-11 wk after model induction. ADC and R were measured at a submillimeter planar resolution. Chord length (L(x)) data were analyzed from histology samples from the corresponding imaged slices. Logistic regression was applied to estimate the probability that an imaged pixel came from a diseased animal, and bootstrap methods (1,000 samples) were used to compare the regression results for the morphological and imaging results. Multivariate ANOVA (MANOVA) was used to analyze transformed ADC (ADC(BC)), and R (R(BC)) data and also to control for the experiment-wide error rate. MANOVA and ANOVA showed that elastase induced a statistically measureable change in the average transformed L(x) and ADC(BC) but not in the average R(BC). Marginal mean analysis demonstrated that ADC(BC) was on average 0.19 [95% confidence interval (CI): 0.16, 0.22] higher in the emphysema group, whereas R(BC) was on average 0.05 (95% CI: 0.04, 0.06) lower. Logistic regression supported the hypothesis that ADC(BC) and R(BC), together, were better at differentiating normal from diseased tissue than either measurement alone. The odds ratios for ADC(BC) and R(BC) were 7.73 (95% CI: 5.23, 11.42) and 9.14 × 10(-5) (95% CI: 3.33 × 10(-5), 25.06 × 10(-5)), respectively. Using a 50% probability cutoff, this model classified 70.6% of pixels correctly. The sensitivity and specificity of this model at the 50% cutoff were 74.9% and 65.2%, respectively. The area under the receiver operating characteristic curve was 0.76 (95% CI: 0.74, 0.78). The regression model presented can be used to map MRI data to disease probability maps. These probability maps present a future possibility of using both measurements in a more clinically feasible method of diagnosing this disease. |
doi_str_mv | 10.1152/japplphysiol.01181.2010 |
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The combined analysis of the apparent diffusion coefficient (ADC) and fractional ventilation (R) were used to distinguish emphysematous changes and also to develop a model for classifying sections of the lung into diseased and normal. Twelve healthy male BALB/c mice (26 ± 2 g) were randomized into healthy and elastase-induced mice and studied ∼8-11 wk after model induction. ADC and R were measured at a submillimeter planar resolution. Chord length (L(x)) data were analyzed from histology samples from the corresponding imaged slices. Logistic regression was applied to estimate the probability that an imaged pixel came from a diseased animal, and bootstrap methods (1,000 samples) were used to compare the regression results for the morphological and imaging results. Multivariate ANOVA (MANOVA) was used to analyze transformed ADC (ADC(BC)), and R (R(BC)) data and also to control for the experiment-wide error rate. MANOVA and ANOVA showed that elastase induced a statistically measureable change in the average transformed L(x) and ADC(BC) but not in the average R(BC). Marginal mean analysis demonstrated that ADC(BC) was on average 0.19 [95% confidence interval (CI): 0.16, 0.22] higher in the emphysema group, whereas R(BC) was on average 0.05 (95% CI: 0.04, 0.06) lower. Logistic regression supported the hypothesis that ADC(BC) and R(BC), together, were better at differentiating normal from diseased tissue than either measurement alone. The odds ratios for ADC(BC) and R(BC) were 7.73 (95% CI: 5.23, 11.42) and 9.14 × 10(-5) (95% CI: 3.33 × 10(-5), 25.06 × 10(-5)), respectively. Using a 50% probability cutoff, this model classified 70.6% of pixels correctly. The sensitivity and specificity of this model at the 50% cutoff were 74.9% and 65.2%, respectively. The area under the receiver operating characteristic curve was 0.76 (95% CI: 0.74, 0.78). The regression model presented can be used to map MRI data to disease probability maps. These probability maps present a future possibility of using both measurements in a more clinically feasible method of diagnosing this disease.</description><identifier>ISSN: 8750-7587</identifier><identifier>EISSN: 1522-1601</identifier><identifier>DOI: 10.1152/japplphysiol.01181.2010</identifier><identifier>PMID: 21940853</identifier><identifier>CODEN: JAPHEV</identifier><language>eng</language><publisher>Bethesda, MD: American Physiological Society</publisher><subject>Analysis of Variance ; Animals ; Biological and medical sciences ; Disease Models, Animal ; Emphysema ; Fundamental and applied biological sciences. Psychology ; Logistic Models ; Lung - pathology ; Lung - physiology ; Lungs ; Male ; Mice ; Mice, Inbred BALB C ; NMR ; Nuclear magnetic resonance ; Pancreatic Elastase - toxicity ; Physiology ; Pulmonary Emphysema - chemically induced ; Pulmonary Emphysema - pathology ; Pulmonary Emphysema - physiopathology ; Random Allocation ; Rodents</subject><ispartof>Journal of applied physiology (1985), 2012-01, Vol.112 (1), p.135-148</ispartof><rights>2015 INIST-CNRS</rights><rights>Copyright American Physiological Society Jan 2012</rights><rights>Copyright © 2012 the American Physiological Society 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c539t-d09188f851b9de39fff71d7a7dd6e73c32c57986d0f39f84d270d8e9ae4696e33</citedby><cites>FETCH-LOGICAL-c539t-d09188f851b9de39fff71d7a7dd6e73c32c57986d0f39f84d270d8e9ae4696e33</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,315,781,785,886,3040,27929,27930</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=25476525$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21940853$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>ISHII, Masaru</creatorcontrib><creatorcontrib>EMAMI, Kiarash</creatorcontrib><creatorcontrib>KUZMA, Nicholas</creatorcontrib><creatorcontrib>KADLECEK, Stephen</creatorcontrib><creatorcontrib>PODOLIN, Patricia L</creatorcontrib><creatorcontrib>RIZI, Rahim R</creatorcontrib><creatorcontrib>YI XIN</creatorcontrib><creatorcontrib>BARULIC, Amy</creatorcontrib><creatorcontrib>KOTZER, Charles J</creatorcontrib><creatorcontrib>LOGAN, Gregory A</creatorcontrib><creatorcontrib>CHIA, Elaine</creatorcontrib><creatorcontrib>MACDUFFIE-WOODBURN, John P</creatorcontrib><creatorcontrib>JIANLIANG ZHU</creatorcontrib><creatorcontrib>PICKUP, Stephen</creatorcontrib><title>Regional function-structure relationships in lungs of an elastase murine model of emphysema</title><title>Journal of applied physiology (1985)</title><addtitle>J Appl Physiol (1985)</addtitle><description>Changes in lung function and structure were studied using hyperpolarized (3)He MRI in an elastase-induced murine model of emphysema. The combined analysis of the apparent diffusion coefficient (ADC) and fractional ventilation (R) were used to distinguish emphysematous changes and also to develop a model for classifying sections of the lung into diseased and normal. Twelve healthy male BALB/c mice (26 ± 2 g) were randomized into healthy and elastase-induced mice and studied ∼8-11 wk after model induction. ADC and R were measured at a submillimeter planar resolution. Chord length (L(x)) data were analyzed from histology samples from the corresponding imaged slices. Logistic regression was applied to estimate the probability that an imaged pixel came from a diseased animal, and bootstrap methods (1,000 samples) were used to compare the regression results for the morphological and imaging results. Multivariate ANOVA (MANOVA) was used to analyze transformed ADC (ADC(BC)), and R (R(BC)) data and also to control for the experiment-wide error rate. MANOVA and ANOVA showed that elastase induced a statistically measureable change in the average transformed L(x) and ADC(BC) but not in the average R(BC). Marginal mean analysis demonstrated that ADC(BC) was on average 0.19 [95% confidence interval (CI): 0.16, 0.22] higher in the emphysema group, whereas R(BC) was on average 0.05 (95% CI: 0.04, 0.06) lower. Logistic regression supported the hypothesis that ADC(BC) and R(BC), together, were better at differentiating normal from diseased tissue than either measurement alone. The odds ratios for ADC(BC) and R(BC) were 7.73 (95% CI: 5.23, 11.42) and 9.14 × 10(-5) (95% CI: 3.33 × 10(-5), 25.06 × 10(-5)), respectively. Using a 50% probability cutoff, this model classified 70.6% of pixels correctly. The sensitivity and specificity of this model at the 50% cutoff were 74.9% and 65.2%, respectively. The area under the receiver operating characteristic curve was 0.76 (95% CI: 0.74, 0.78). The regression model presented can be used to map MRI data to disease probability maps. These probability maps present a future possibility of using both measurements in a more clinically feasible method of diagnosing this disease.</description><subject>Analysis of Variance</subject><subject>Animals</subject><subject>Biological and medical sciences</subject><subject>Disease Models, Animal</subject><subject>Emphysema</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Logistic Models</subject><subject>Lung - pathology</subject><subject>Lung - physiology</subject><subject>Lungs</subject><subject>Male</subject><subject>Mice</subject><subject>Mice, Inbred BALB C</subject><subject>NMR</subject><subject>Nuclear magnetic resonance</subject><subject>Pancreatic Elastase - toxicity</subject><subject>Physiology</subject><subject>Pulmonary Emphysema - chemically induced</subject><subject>Pulmonary Emphysema - pathology</subject><subject>Pulmonary Emphysema - physiopathology</subject><subject>Random Allocation</subject><subject>Rodents</subject><issn>8750-7587</issn><issn>1522-1601</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkV1LHDEUhkOp6Gr7F9qh4OWs-ZhMkhtBRG1BKJR65UWI-djNkkmmyYzgv29GV2uvzuG8z3lzyAvAVwTXCFF8tlPjGMbtU_EprCFCHK0xRPADWFUVt6iH6CNYcUZhyyhnR-C4lB2EqOsoOgRHGIkOckpW4P6X3fgUVWjcHPVU27ZMedbTnG2TbVDLqGz9WBofmzDHTWmSa1RsqlYmVWwzzNnHWpKxYdHssBxmB_UJHDgViv28ryfg7vrq9-X39vbnzY_Li9tWUyKm1kCBOHecogdhLBHOOYYMU8yY3jKiCdaUCd4b6KrIO4MZNNwKZbte9JaQE3D-4jvOD4M12sYpqyDH7AeVn2RSXv6vRL-Vm_QoCRaww7AafNsb5PRntmWSuzTn-ilFCkQ5FJiwCrEXSOdUSrbu7QEE5RKKfB-KfA5FLqHUzS_v73vbe02hAqd7QBWtgssqal_-cbRjPcWU_AUyM5wx</recordid><startdate>20120101</startdate><enddate>20120101</enddate><creator>ISHII, Masaru</creator><creator>EMAMI, Kiarash</creator><creator>KUZMA, Nicholas</creator><creator>KADLECEK, Stephen</creator><creator>PODOLIN, Patricia L</creator><creator>RIZI, Rahim R</creator><creator>YI XIN</creator><creator>BARULIC, Amy</creator><creator>KOTZER, Charles J</creator><creator>LOGAN, Gregory A</creator><creator>CHIA, Elaine</creator><creator>MACDUFFIE-WOODBURN, John P</creator><creator>JIANLIANG ZHU</creator><creator>PICKUP, Stephen</creator><general>American Physiological Society</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7TS</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope><scope>5PM</scope></search><sort><creationdate>20120101</creationdate><title>Regional function-structure relationships in lungs of an elastase murine model of emphysema</title><author>ISHII, Masaru ; EMAMI, Kiarash ; KUZMA, Nicholas ; KADLECEK, Stephen ; PODOLIN, Patricia L ; RIZI, Rahim R ; YI XIN ; BARULIC, Amy ; KOTZER, Charles J ; LOGAN, Gregory A ; CHIA, Elaine ; MACDUFFIE-WOODBURN, John P ; JIANLIANG ZHU ; PICKUP, Stephen</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c539t-d09188f851b9de39fff71d7a7dd6e73c32c57986d0f39f84d270d8e9ae4696e33</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Analysis of Variance</topic><topic>Animals</topic><topic>Biological and medical sciences</topic><topic>Disease Models, Animal</topic><topic>Emphysema</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Logistic Models</topic><topic>Lung - pathology</topic><topic>Lung - physiology</topic><topic>Lungs</topic><topic>Male</topic><topic>Mice</topic><topic>Mice, Inbred BALB C</topic><topic>NMR</topic><topic>Nuclear magnetic resonance</topic><topic>Pancreatic Elastase - toxicity</topic><topic>Physiology</topic><topic>Pulmonary Emphysema - chemically induced</topic><topic>Pulmonary Emphysema - pathology</topic><topic>Pulmonary Emphysema - physiopathology</topic><topic>Random Allocation</topic><topic>Rodents</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>ISHII, Masaru</creatorcontrib><creatorcontrib>EMAMI, Kiarash</creatorcontrib><creatorcontrib>KUZMA, Nicholas</creatorcontrib><creatorcontrib>KADLECEK, Stephen</creatorcontrib><creatorcontrib>PODOLIN, Patricia L</creatorcontrib><creatorcontrib>RIZI, Rahim R</creatorcontrib><creatorcontrib>YI XIN</creatorcontrib><creatorcontrib>BARULIC, Amy</creatorcontrib><creatorcontrib>KOTZER, Charles J</creatorcontrib><creatorcontrib>LOGAN, Gregory A</creatorcontrib><creatorcontrib>CHIA, Elaine</creatorcontrib><creatorcontrib>MACDUFFIE-WOODBURN, John P</creatorcontrib><creatorcontrib>JIANLIANG ZHU</creatorcontrib><creatorcontrib>PICKUP, Stephen</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Physical Education Index</collection><collection>Toxicology Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Journal of applied physiology (1985)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>ISHII, Masaru</au><au>EMAMI, Kiarash</au><au>KUZMA, Nicholas</au><au>KADLECEK, Stephen</au><au>PODOLIN, Patricia L</au><au>RIZI, Rahim R</au><au>YI XIN</au><au>BARULIC, Amy</au><au>KOTZER, Charles J</au><au>LOGAN, Gregory A</au><au>CHIA, Elaine</au><au>MACDUFFIE-WOODBURN, John P</au><au>JIANLIANG ZHU</au><au>PICKUP, Stephen</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Regional function-structure relationships in lungs of an elastase murine model of emphysema</atitle><jtitle>Journal of applied physiology (1985)</jtitle><addtitle>J Appl Physiol (1985)</addtitle><date>2012-01-01</date><risdate>2012</risdate><volume>112</volume><issue>1</issue><spage>135</spage><epage>148</epage><pages>135-148</pages><issn>8750-7587</issn><eissn>1522-1601</eissn><coden>JAPHEV</coden><abstract>Changes in lung function and structure were studied using hyperpolarized (3)He MRI in an elastase-induced murine model of emphysema. The combined analysis of the apparent diffusion coefficient (ADC) and fractional ventilation (R) were used to distinguish emphysematous changes and also to develop a model for classifying sections of the lung into diseased and normal. Twelve healthy male BALB/c mice (26 ± 2 g) were randomized into healthy and elastase-induced mice and studied ∼8-11 wk after model induction. ADC and R were measured at a submillimeter planar resolution. Chord length (L(x)) data were analyzed from histology samples from the corresponding imaged slices. Logistic regression was applied to estimate the probability that an imaged pixel came from a diseased animal, and bootstrap methods (1,000 samples) were used to compare the regression results for the morphological and imaging results. Multivariate ANOVA (MANOVA) was used to analyze transformed ADC (ADC(BC)), and R (R(BC)) data and also to control for the experiment-wide error rate. MANOVA and ANOVA showed that elastase induced a statistically measureable change in the average transformed L(x) and ADC(BC) but not in the average R(BC). Marginal mean analysis demonstrated that ADC(BC) was on average 0.19 [95% confidence interval (CI): 0.16, 0.22] higher in the emphysema group, whereas R(BC) was on average 0.05 (95% CI: 0.04, 0.06) lower. Logistic regression supported the hypothesis that ADC(BC) and R(BC), together, were better at differentiating normal from diseased tissue than either measurement alone. The odds ratios for ADC(BC) and R(BC) were 7.73 (95% CI: 5.23, 11.42) and 9.14 × 10(-5) (95% CI: 3.33 × 10(-5), 25.06 × 10(-5)), respectively. Using a 50% probability cutoff, this model classified 70.6% of pixels correctly. The sensitivity and specificity of this model at the 50% cutoff were 74.9% and 65.2%, respectively. The area under the receiver operating characteristic curve was 0.76 (95% CI: 0.74, 0.78). The regression model presented can be used to map MRI data to disease probability maps. These probability maps present a future possibility of using both measurements in a more clinically feasible method of diagnosing this disease.</abstract><cop>Bethesda, MD</cop><pub>American Physiological Society</pub><pmid>21940853</pmid><doi>10.1152/japplphysiol.01181.2010</doi><tpages>14</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Analysis of Variance Animals Biological and medical sciences Disease Models, Animal Emphysema Fundamental and applied biological sciences. Psychology Logistic Models Lung - pathology Lung - physiology Lungs Male Mice Mice, Inbred BALB C NMR Nuclear magnetic resonance Pancreatic Elastase - toxicity Physiology Pulmonary Emphysema - chemically induced Pulmonary Emphysema - pathology Pulmonary Emphysema - physiopathology Random Allocation Rodents |
title | Regional function-structure relationships in lungs of an elastase murine model of emphysema |
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