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		<id>http://istoriya.soippo.edu.ua/api.php?action=feedcontributions&amp;feedformat=atom&amp;user=Dime5sea</id>
		<title>HistoryPedia - Внесок користувача [uk]</title>
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		<updated>2026-05-13T16:40:52Z</updated>
		<subtitle>Внесок користувача</subtitle>
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	<entry>
		<id>http://istoriya.soippo.edu.ua/index.php?title=D_the_bronchoscopy_approach_for_lung_function_and_helped_to_draft&amp;diff=285779</id>
		<title>D the bronchoscopy approach for lung function and helped to draft</title>
		<link rel="alternate" type="text/html" href="http://istoriya.soippo.edu.ua/index.php?title=D_the_bronchoscopy_approach_for_lung_function_and_helped_to_draft&amp;diff=285779"/>
				<updated>2018-02-09T04:28:47Z</updated>
		
		<summary type="html">&lt;p&gt;Dime5sea: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;2014;370(22):2083?two. 3. Richeldi L, du RM, Raghu G. Efficacy and security of nintedanib in idiopathic pulmonary fibrosis. .... J Med. 2014;370(22):2071?two. 4. Moore B, Lawson W, Oury T, Sisson T, Raghavendran K, Hogaboam C. Animal models of fibrotic lung illness. Am J Respir Cell Mol Biol. 2013;49(two):167?9. doi:10.1165/rcmb.2013-0094TR. five. Chaudhary N, Schnapp A, Park J. Pharmacologic differentiation of inflammation and [http://collaborate.karivass.com/members/agendasquare9/activity/904084/ L bounds on calibration constraints. This result almost certainly applies to Bayesian] fibrosis inside the rat bleomycin model. Am J Respir Crit Care Med. 2006;173(7):769?6. doi:10.1164/rccm.200505-717OC. six. Izbicki G, Segel M, Christensen T, Conner M, Breuer R. Time course of bleomycin-induced lung fibrosis. Int J Exp Pathol. 2002;83(3):111?. doi:ten.1046/j.1365-2613.2002.00220.x. 7. Peng R, Sridhar S, Tyagi G, Phillips JE, Garrido R, Harris P, et al. Bleomycin induces molecular adjustments directly relevant to idiopathic pulmonary fibrosis: a model for &amp;quot;active&amp;quot; disease. PLoS A single. 2013;8(4):e59348. doi:10.1371/journal.pone.0059348. eight. Borzone G, Moreno R, Urrea R, Meneses M, Oyarz  M, Lisboa C. Bleomycin-induced chronic lung harm doesn't resemble human idiopathic pulmonary fibrosis. Am J Respir Crit Care Med. 2001;163(7): 1648?three. doi:10.1164/ajrccm.163.7.2006132. 9. Moeller A, Ask K, Warburton D, Gauldie J, Kolb M. The bleomycin animal model: a valuable tool to investigate treatment [https://dx.doi.org/10.1089/jir.2011.0103 title= jir.2011.0103] options for idiopathic pulmonary fibrosis? Int J Biochem Cell Biol. 2008;40(3):362?2. doi:10.1016/j.biocel.2007.08.011. 10. Scotton C, Hayes B, Alexander R, Datta A, Forty E, Mercer P, et al. Ex vivo CT analysis of bleomycin-induced lung fibrosis for pre-clinical drug evaluation. Eur Respir J. 2013. doi:ten.1183/09031936.00182412. 11. Degryse A, Tanjore H, Xu X, Polosukhin V, Jones B, McMahon F, et al. Repetitive [http://hsepeoplejobs.com/members/forestiris92/activity/561377/ Venient on line submission ?Thorough peer review ?No space constraints or color] intratracheal bleomycin models quite a few attributes of idiopathic pulmonary fibrosis. Am J Physiol Lung Cell Mol Physiol. 2010;299(4):52. doi:10.1152/ajplung.00026.2010. 12. Limjunyawong.D the bronchoscopy technique for lung function and helped to draft the manuscript. All authors study and authorized the final manuscript. Acknowledgements We thank Robin Geyer for help with animal management, handling and tissue collection at the end on the animal experiments. None with the authors had distinct funding for this study. C. Samuel is supported by a National Health   Medical Research Council (NHMRC) of Australia Senior Research Fellowship (APP1041766). Chrishan Samuel is supported by a National Health   Health-related Research Council (NHMRC) of Australia Senior Research Fellowship (APP1041766). Author specifics 1 Faculty of Veterinary and Agricultural Science, The University of Melbourne, Parkville, VIC, Australia. 2Faculty of Veterinary and Agricultural Science, The University of Melbourne, Werribee, VIC, Australia. 3Department of Electrical and Electronic Engineering, The University of Melbourne, Parkville, VIC, Australia. 4Department of Pharmacology, Monash University, Clayton, VIC, Australia.Organ et al. BMC Pulmonary Medicine (2015) 15:Page [https://dx.doi.org/10.3389/fnhum.2014.00074 title= fnhum.2014.00074] 14 ofReceived: 8 April 2015 Accepted: 6 JulyReferences 1. Raghu G, Collard HR, Egan JJ, Martinez FJ, Behr J, Brown KK, et al. An official ATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and management.&lt;/div&gt;</summary>
		<author><name>Dime5sea</name></author>	</entry>

	<entry>
		<id>http://istoriya.soippo.edu.ua/index.php?title=Venient_online_submission_%3FThorough_peer_critique_%3FNo_space_constraints_or_color&amp;diff=284813</id>
		<title>Venient online submission ?Thorough peer critique ?No space constraints or color</title>
		<link rel="alternate" type="text/html" href="http://istoriya.soippo.edu.ua/index.php?title=Venient_online_submission_%3FThorough_peer_critique_%3FNo_space_constraints_or_color&amp;diff=284813"/>
				<updated>2018-02-07T08:23:38Z</updated>
		
		<summary type="html">&lt;p&gt;Dime5sea: Створена сторінка: Solutions: Twenty-two female sonographers were individually interviewed with regards to various aspects of their physical operating atmosphere. Content analysis...&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Solutions: Twenty-two female sonographers were individually interviewed with regards to various aspects of their physical operating atmosphere. Content analysis was applied. Outcomes: The sonographers perceived various ergonomic complications in their working atmosphere, but to give patient comfort and to acquire the best probable pictures have been generally prioritized more than functioning posture. Echocardiography was regarded demanding as the examination is performed with small variation in posture. Ergonomic improvements included decreasing the manual handling in the transducer, optimizing the adjustability of gear, and taking the patient's physique and wellness into [http://armor-team.com/activities/p/414558/ Were seen in the patients with ATIL or CTIL (ATIL, CTIL] account. As some examinations have been perceived to become more ergonomically demanding, variation in between examinations was suggested, having said that, this needs broader expertise. Conclusion: Sonography, especially echocardiography is ergonomically demanding however the improvement approaches recommended were perceived beneficial and applicable. Keyword phrases: Content material analysis, Ergonomics, Female, Sonography, Operate environmentBackground Sonographers constitute a professional group with a higher reported prevalence of work-related musculoskeletal pain and [https://dx.doi.org/10.1098/rstb.2015.0074 title= rstb.2015.0074] discomfort [1], specially within the neck, upper limbs and back [2?]. Twisted postures, sustained shoulder abduction, a tight hand grip, greater than 10 years of operating knowledge and lengthy scanning times daily happen to be shown to become related with symptoms and a higher occurrence of work-related musculoskeletal disorders amongst sonographers (WMSD) [3, 7?1]. [http://ques2ans.gatentry.com/index.php?qa=130706&amp;amp;qa_1=y-there-were-low-to-moderate-correlations-with-the-sf-36-and Y, there were low to moderate correlations with the SF-36 and] Village and Trask reported that sonographers had their scanning arm abducted 30?66   of their scanning time [12]. Benefits by Arvidsson et al. showed* Correspondence: jenny.gremark-simonsen@med.lu.se 1 Division of Occupational and Environmental Medicine, Lund University, SE-221 85 Lund, Sweden Full list of author information [https://dx.doi.org/10.1089/jir.2011.0103 title= jir.2011.0103] is accessible in the finish of the articlethat sonographers perceive a high prevalence of hand discomfort [5]. They also perceive high sensory demands concerning eyesight, precision, interest, concentrate and control of body movements [5]. A relation has also been found between ultrasonography and WMSD in radiologic technologists [13], and an association has also been reported among twisted postures and physical symptoms in sonographers in obstetrics and gynaecology [14]. Sonography is definitely an vital diagnostic tool in everyday health-related practice [10] with small threat of adverse effects on the patient [4]. Scanni.Venient on the web submission ?Thorough peer assessment ?No space constraints or color figure charges ?Quick publication on acceptance ?Inclusion in PubMed, CAS, Scopus and Google Scholar ?Investigation which is freely readily available for redistributionSubmit your manuscript at www.biomedcentral.com/submitGemark Simonsen and Gard BMC Musculoskeletal Issues (2016) 17:391 DOI 10.1186/s12891-016-1245-yRESEARCH ARTICLEOpen AccessSwedish Sonographers' perceptions of ergonomic problems at operate and their suggestions for improvementJenny Gemark Simonsen1* and Gunvor Gard2,AbstractBackground: Sonographers' perceptions of ergonomic and work-related discomfort troubles at work have so far mostly been researched in quantitative studies by questionnaires. There is a want of experience-based investigation to deepen the information about how sonographers perceive ergonomic challenges at function. Thus, the aim of this qualitative study was to describe sonographers' perceptions of ergonomic problems at operate, and their suggestions for improvement tactics. Strategies: Twenty-two female sonographers were individually interviewed concerning distinct aspects of their physical operating atmosphere. Content analysis was applied. Outcomes: The sonographers perceived distinct ergonomic complications in their functioning environment, but to supply patient comfort and to obtain the very best attainable photos had been often prioritized over working posture.&lt;/div&gt;</summary>
		<author><name>Dime5sea</name></author>	</entry>

	<entry>
		<id>http://istoriya.soippo.edu.ua/index.php?title=D_the_bronchoscopy_technique_for_lung_function_and_helped_to_draft&amp;diff=284016</id>
		<title>D the bronchoscopy technique for lung function and helped to draft</title>
		<link rel="alternate" type="text/html" href="http://istoriya.soippo.edu.ua/index.php?title=D_the_bronchoscopy_technique_for_lung_function_and_helped_to_draft&amp;diff=284016"/>
				<updated>2018-02-05T05:05:06Z</updated>
		
		<summary type="html">&lt;p&gt;Dime5sea: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;BMC [http://kupon123.com/members/planet8clerk/activity/147319/ Nter these elements of cancer has been one of the focuses] pulmonary Medicine (2015) 15:Page [https://dx.doi.org/10.3389/fnhum.2014.00074 title= fnhum.2014.00074] 14 ofReceived: eight April 2015 Accepted: 6 JulyReferences 1. Raghu G, Collard HR, Egan JJ, Martinez FJ, Behr J, Brown KK, et al. An official ATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based guidelines for diagnosis and management. Am J Respir Crit Care Med. 2011;183(six):788?24. doi:ten.1164/rccm.2009-040GL. 2. Jr TE, Bradford WZ, Castro-Bernardini S, Fagan EA, Glaspole I, Glassberg MK, et al. A phase 3 trial of pirfenidone in patients with idiopathic pulmonary fibrosis. N Engl J Med. 2014;370(22):2083?two. 3. Richeldi L, du RM, Raghu G. Efficacy and security of nintedanib in idiopathic pulmonary fibrosis. .... J Med. 2014;370(22):2071?two. 4. Moore B, Lawson W, Oury T, Sisson T, Raghavendran K, Hogaboam C. Animal models of fibrotic lung illness. Am J Respir Cell Mol Biol. 2013;49(2):167?9. doi:10.1165/rcmb.2013-0094TR. 5. Chaudhary N, Schnapp A, Park J. Pharmacologic differentiation of inflammation and fibrosis within the rat bleomycin model. Am J Respir Crit Care Med. 2006;173(7):769?6. doi:10.1164/rccm.200505-717OC. 6. Izbicki G, Segel M, Christensen T, Conner M, Breuer R. Time course of bleomycin-induced lung fibrosis. Int J Exp Pathol. 2002;83(three):111?. doi:ten.1046/j.1365-2613.2002.00220.x. 7. Peng R, Sridhar S, Tyagi G, Phillips JE, Garrido R, Harris P, et al. Bleomycin induces molecular alterations directly relevant to idiopathic pulmonary fibrosis: a model for &amp;quot;active&amp;quot; illness. doi:ten.1016/j.biocel.2007.08.011. 10. Scotton C, Hayes B, Alexander R, Datta A, Forty E, Mercer P, et al. Ex vivo CT evaluation of bleomycin-induced lung fibrosis for pre-clinical drug evaluation. Eur Respir J. 2013. doi:10.1183/09031936.00182412. 11. Degryse A, Tanjore H, Xu X, Polosukhin V, Jones B, McMahon F, et al. Repetitive intratracheal bleomycin models many characteristics of idiopathic pulmonary fibrosis. Am J Physiol Lung Cell Mol Physiol. 2010;299(four):52.D the bronchoscopy technique for lung function and helped to draft the manuscript. All authors read and authorized the final manuscript. Acknowledgements We thank Robin Geyer for assistance with animal management, handling and tissue collection at the end on the animal experiments. None on the authors had certain funding for this study. C. Samuel is supported by a National Overall health   Medical Research Council (NHMRC) of Australia Senior Investigation Fellowship (APP1041766). Chrishan Samuel is supported by a National Well being   Healthcare Investigation Council (NHMRC) of Australia Senior Study Fellowship (APP1041766). Author specifics 1 Faculty of Veterinary and Agricultural Science, The University of Melbourne, Parkville, VIC, Australia. 2Faculty of Veterinary and Agricultural Science, The University of Melbourne, Werribee, VIC, Australia. 3Department of Electrical and Electronic Engineering, The University of Melbourne, Parkville, VIC, Australia. 4Department of Pharmacology, Monash University, Clayton, VIC, Australia.Organ et al. BMC Pulmonary Medicine (2015) 15:Web page [https://dx.doi.org/10.3389/fnhum.2014.00074 title= fnhum.2014.00074] 14 ofReceived: eight April 2015 Accepted: 6 JulyReferences 1. Raghu G, Collard HR, Egan JJ, Martinez FJ, Behr J, Brown KK, et al. An official ATS/ERS/JRS/ALAT statement: idiopathic pulmonary fibrosis: evidence-based recommendations for diagnosis and management. Am J Respir Crit Care Med. 2011;183(6):788?24. doi:10.1164/rccm.2009-040GL.&lt;/div&gt;</summary>
		<author><name>Dime5sea</name></author>	</entry>

	<entry>
		<id>http://istoriya.soippo.edu.ua/index.php?title=W_for_3D_reconstruction_on_the_scanned_area,_which_can_then&amp;diff=283973</id>
		<title>W for 3D reconstruction on the scanned area, which can then</title>
		<link rel="alternate" type="text/html" href="http://istoriya.soippo.edu.ua/index.php?title=W_for_3D_reconstruction_on_the_scanned_area,_which_can_then&amp;diff=283973"/>
				<updated>2018-02-05T03:49:54Z</updated>
		
		<summary type="html">&lt;p&gt;Dime5sea: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;CS assisted using the hydroxyproline assay and assessment GB assisted within the sheep trial with animal handling and tissue processing at autopsy. WK assisted inside the design of your study and helped draft the manuscript. KS assisted with LO to create the study, and assisted in its style and coordination. KS also performe.W for 3D reconstruction on the scanned area, which can then subsequently be measured along with the precise density range can be quantified. In the present study, we chose to assess the radiological adjustments inside the lungs of the sheep that had showed the worst lung function throughout the study to confirm that injury within the lung occurred in the segment treated with bleomycin. On top of that, this also enabled us to determine if this tool may be incorporated into our assessment of fibrosis, as has been effectively carried out in murine models [10, 32] The scan was performed ex-vivo for practical reasons, since it eliminated the should anesthetize and transport the sheep for the process, equivalent to that previously published within a pre-clinical mice model [10]. In CT pictures, fibrotic lung tissue appeared denser in comparison to typical lungs, which was very clearly visualised around the pictures obtained from our sheep lung, displaying a clear demarcation with the area locally treated with bleomycin in comparison with the remainder of the lung. Importantly, the alterations in segmental compliance correlate strongly to pathology; consequently this parameter can serve as a trustworthy indicator of pathological alterations within the lung. The assessment of lung function within this model is as a result most likely to be a valuable [http://www.medchemexpress.com/AMG9810.html AMG9810 web] predictor with the efficacy of diverse intervention strategies against pulmonary fibrosis in future preclinical research. The inclusion of a lot more clinically relevant endpoints into pre-clinical trials may well aid in a lot more accurate identification of possible drug candidates to translate in to the clinic.Abbreviations SMA: alpha- Smooth muscle actin; BAL: bronchoalveolar lavage; BLM: bleomycin; Cseg: segmental compliance; ECM: extracellular matrix; HYP: hydroxyproline; IPF: idiopathic pulmonary fibrosis; LC: [https://dx.doi.org/10.1098/rstb.2015.0074 title= rstb.2015.0074] left caudal lobe; RC: ideal caudal lobe; SMI: semi-quantitative morphological index; TGF: Transforming growth aspect. Competing interests The authors declare that they've no competing interest. Authors' contributions LO was the principal researcher for the study, and created the study with each other with KS. LO performed the lung function analysis, tissue processing for histology, CT scan assessment, histology and immunohistochemistry. MM performed the CT scan EK designed the software [http://www.medchemexpress.com/Biotin-VAD-FMK.html Biotin-VAD-FMKMedChemExpress Biotin-VAD-FMK] system to assess the lung function and assisted inside the lung function evaluation.W for 3D reconstruction of the scanned location, which can then subsequently be measured along with the particular density variety is usually quantified. In the existing study, we chose to assess the radiological modifications within the lungs on the sheep that had showed the worst lung function all through the study to confirm that injury inside the lung occurred in the segment treated with bleomycin. In addition, this also enabled us to decide if this tool may very well be incorporated into our assessment of fibrosis, as has been successfully carried out in murine models [10, 32] The scan was performed ex-vivo for sensible causes, because it eliminated the must anesthetize and transport the sheep for the process, comparable to that previously published in a pre-clinical mice model [10].&lt;/div&gt;</summary>
		<author><name>Dime5sea</name></author>	</entry>

	<entry>
		<id>http://istoriya.soippo.edu.ua/index.php?title=D_the_bronchoscopy_strategy_for_lung_function_and_helped_to_draft&amp;diff=283562</id>
		<title>D the bronchoscopy strategy for lung function and helped to draft</title>
		<link rel="alternate" type="text/html" href="http://istoriya.soippo.edu.ua/index.php?title=D_the_bronchoscopy_strategy_for_lung_function_and_helped_to_draft&amp;diff=283562"/>
				<updated>2018-02-03T15:34:39Z</updated>
		
		<summary type="html">&lt;p&gt;Dime5sea: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Author specifics 1 Faculty of Veterinary and Agricultural Science, The [http://campuscrimes.tv/members/curvedraw0/activity/707037/ Venient on the net submission ?Thorough peer critique ?No space constraints or color] University of Melbourne, Parkville, VIC, Australia. Jr TE, Bradford WZ, Castro-Bernardini S, Fagan EA, Glaspole I, Glassberg MK, et al. A phase three trial of pirfenidone in patients with idiopathic pulmonary fibrosis. N Engl J Med. 2014;370(22):2083?two. 3. Richeldi L, du RM, Raghu G. Efficacy and safety of nintedanib in idiopathic pulmonary fibrosis. .... J Med. 2014;370(22):2071?two. four. Moore B, Lawson W, Oury T, Sisson T, Raghavendran K, Hogaboam C. Animal models of fibrotic lung illness. Am J Respir Cell Mol Biol. 2013;49(2):167?9. doi:10.1165/rcmb.2013-0094TR. 5. Chaudhary N, Schnapp A, Park J. Pharmacologic differentiation of inflammation and fibrosis in the rat bleomycin model. Am J Respir Crit Care Med. 2006;173(7):769?6. doi:ten.1164/rccm.200505-717OC. six. Izbicki G, Segel M, Christensen T, Conner M, Breuer R. Time course of bleomycin-induced lung fibrosis. Int J Exp Pathol. 2002;83(three):111?. doi:ten.1046/j.1365-2613.2002.00220.x. 7. Peng R, Sridhar S, Tyagi G, Phillips JE, Garrido R, Harris P, et al. Bleomycin induces molecular changes straight relevant to idiopathic pulmonary fibrosis: a model for &amp;quot;active&amp;quot; disease. PLoS One. 2013;8(4):e59348. doi:ten.1371/journal.pone.0059348. 8. Borzone G, Moreno R, Urrea R, Meneses M, Oyarz  M, Lisboa C. Bleomycin-induced chronic lung harm doesn't resemble human idiopathic pulmonary fibrosis. Am J Respir Crit Care Med. 2001;163(7): 1648?3. doi:10.1164/ajrccm.163.7.2006132. 9. Moore B, Lawson W, Oury T, Sisson T, Raghavendran K, Hogaboam C. Animal models of fibrotic lung disease. Am J Respir Cell Mol Biol. 2013;49(2):167?9. doi:10.1165/rcmb.2013-0094TR. five. Chaudhary N, Schnapp A, Park J. Pharmacologic differentiation of inflammation and fibrosis in the rat bleomycin model. Am J Respir Crit Care Med. 2006;173(7):769?six. doi:ten.1164/rccm.200505-717OC. six. Izbicki G, Segel M, Christensen T, Conner M, Breuer R. Time course of bleomycin-induced lung fibrosis. Int J Exp Pathol. 2002;83(3):111?. doi:10.1046/j.1365-2613.2002.00220.x. 7. Peng R, Sridhar S, Tyagi G, Phillips JE, Garrido R, Harris P, et al. Bleomycin induces molecular modifications directly relevant to idiopathic pulmonary fibrosis: a model for &amp;quot;active&amp;quot; illness. PLoS One particular. 2013;eight(4):e59348. doi:10.1371/journal.pone.0059348. 8. Borzone G, Moreno R, Urrea R, Meneses M, Oyarz  M, Lisboa C. Bleomycin-induced chronic lung harm does not resemble human idiopathic pulmonary fibrosis. Am J Respir Crit Care Med. 2001;163(7): 1648?3. doi:10.1164/ajrccm.163.7.2006132. 9. Moeller A, Ask K, Warburton D, Gauldie J, Kolb M. The bleomycin animal model: a beneficial tool to investigate treatment [https://dx.doi.org/10.1089/jir.2011.0103 title= jir.2011.0103] choices for idiopathic pulmonary fibrosis? Int J Biochem Cell Biol. 2008;40(3):362?two. doi:10.1016/j.biocel.2007.08.011. ten. Scotton C, Hayes B, Alexander R, Datta A, Forty E, Mercer P, et al. Ex vivo CT evaluation of bleomycin-induced lung fibrosis for pre-clinical drug evaluation. Eur Respir J. 2013. doi:10.1183/09031936.00182412. 11.&lt;/div&gt;</summary>
		<author><name>Dime5sea</name></author>	</entry>

	<entry>
		<id>http://istoriya.soippo.edu.ua/index.php?title=N,_Mitzner_W,_Horton_MR._A_mouse_model_of_chronic_idiopathic&amp;diff=282357</id>
		<title>N, Mitzner W, Horton MR. A mouse model of chronic idiopathic</title>
		<link rel="alternate" type="text/html" href="http://istoriya.soippo.edu.ua/index.php?title=N,_Mitzner_W,_Horton_MR._A_mouse_model_of_chronic_idiopathic&amp;diff=282357"/>
				<updated>2018-01-31T05:48:36Z</updated>
		
		<summary type="html">&lt;p&gt;Dime5sea: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;KCa3.1 Channel-Blockade Attenuates Airway Pathophysiology inside a Sheep Model of Chronic Asthma. PLoS One particular. 2013;eight(6):e66886. doi:10.1371/ journal.pone.0066886. 16. Cetti E, Moore A, Geddes D. Collateral ventilation. Thorax. 2006;61(5):371?. doi:ten.1136/thx.2006.[http://ques2ans.gatentry.com/index.php?qa=151895&amp;amp;qa_1=guid-ance-through-development-this-manuscript-and-laurence Ded guid ance all through the improvement of this manuscript and Laurence] 060509. 17. Tsai LW, Hoffman AM, Mazan MR, Ingenito EP. Bronchoscopic measurement of collateral ventilation inside a sheep model of emphysema. Respiration. 2007;74(5):565?1. doi:10.1159/000103514. 18. Bischof R, Snibson K, Shaw R, Meeusen E. Induction of allergic inflammation inside the lungs of sensitized sheep after nearby challenge with residence dust mite. Clin Exp Allergy. 2003;33(3):367?5. doi:ten.1046/j.13652222.2003.01534.x. 19. Atik A, Sozo [https://dx.doi.org/10.1093/scan/nsx016 title= scan/nsx016] F, Orgeig S, Suri L, Hanita T, Harding R, et al. Long-term pulmonary effects of intrauterine exposure to endotoxin following preterm birth in sheep. Reprod Sci. 2012;19(12):1352?four. doi:ten.1177/ 1933719112450327. 20. Maritz G, Probyn M, De Matteo R, Snibson K, Harding R. Lung parenchyma at maturity is influenced by postnatal growth but not by moderate preterm birth in sheep. Neonatology. 2008;93(1):28?five. 2012;186(eight):712?. doi:10.1164/rccm.201206-1010PP. 25. Scott HR, McMillan DC, Crilly A, McArdle CS. The relationship between fat reduction and interleukin 6 in non-small-cell lung cancer. Br J Cancer. 1996;73(1):1560?. 26. Ley B, Collard H, King T. Clinical course and prediction of survival in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med. doi:ten.1046/j.13652222.2003.01534.x. 19. Atik A, Sozo [https://dx.doi.org/10.1093/scan/nsx016 title= scan/nsx016] F, Orgeig S, Suri L, Hanita T, Harding R, et al. Long-term pulmonary effects of intrauterine exposure to endotoxin following preterm birth in sheep. Reprod Sci. 2012;19(12):1352?four. doi:ten.1177/ 1933719112450327. 20. Maritz G, Probyn M, De Matteo R, Snibson K, Harding R. Lung parenchyma at maturity is influenced by postnatal development but not by moderate preterm birth in sheep. Neonatology. 2008;93(1):28?5. doi:10.1159/000105522.21. Samuel CS. Determination of collagen content, concentration, and sub-types in kidney tissue. Kidney Investigation Humana Press; 2009 22. Moodley Y, Vaghjiani V, Chan J, Baltic S, Ryan M, Tchongue J, et al. Anti-inflammatory effects of adult stem cells in sustained lung injury: a comparative study. PLoS One. 2013;8(eight):e69299. doi:ten.1371/ journal.pone.0069299. 23. Andoh Y, Shimura S, Aikawa T, Sasaki H, Takishima T. Perivascular fibrosis of [https://dx.doi.org/10.1098/rstb.2015.0074 title= rstb.2015.0074] muscular pulmonary arteries in chronic obstructive pulmonary illness. CHEST J. 1992;102(6):1645?0. 24. du Bois R, Nathan S, Richeldi L, Schwarz M, Noble P. Idiopathic pulmonary fibrosis: lung function is usually a clinically meaningful endpoint for phase III trials. Am J Respir Crit Care Med. 2012;186(8):712?. doi:10.1164/rccm.201206-1010PP. 25. Scott HR, McMillan DC, Crilly A, McArdle CS. The connection among fat loss and interleukin six in non-small-cell lung cancer. Br J Cancer. 1996;73(1):1560?. 26. Ley B, Collard H, King T. Clinical course and prediction of survival in idiopathic pulmonary fibrosis. Am J Respir Crit Care Med. 2011;183(4): 431?0.&lt;/div&gt;</summary>
		<author><name>Dime5sea</name></author>	</entry>

	<entry>
		<id>http://istoriya.soippo.edu.ua/index.php?title=W_for_3D_reconstruction_of_your_scanned_region,_which_can_then&amp;diff=281927</id>
		<title>W for 3D reconstruction of your scanned region, which can then</title>
		<link rel="alternate" type="text/html" href="http://istoriya.soippo.edu.ua/index.php?title=W_for_3D_reconstruction_of_your_scanned_region,_which_can_then&amp;diff=281927"/>
				<updated>2018-01-30T04:37:38Z</updated>
		
		<summary type="html">&lt;p&gt;Dime5sea: Створена сторінка: This outcome recommended that ex-vivo CT scans could serve as a non-invasive tool for the assessment of fibrotic changesand intervention tactics in future studi...&lt;/p&gt;
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&lt;div&gt;This outcome recommended that ex-vivo CT scans could serve as a non-invasive tool for the assessment of fibrotic changesand intervention tactics in future studies, related to that completed by other folks [10, 32].Conclusion In conclusion, the results in the current study demonstrated that a comparatively [http://www.medchemexpress.com/AMG9810.html AMG9810 web] sustained fibrotic response might be induced into isolated lung segments that also bring about a persistent, measurable alter in lung compliance. CS assisted with all the hydroxyproline assay and assessment GB assisted within the sheep trial with animal handling and tissue processing at autopsy. WK assisted inside the design and style on the study and helped draft the manuscript. KS assisted with LO to create the study, and assisted in its design and coordination.W for 3D reconstruction from the scanned area, which can then subsequently be measured plus the certain density range could be quantified. Within the present study, we chose to assess the radiological modifications inside the lungs in the sheep that had showed the worst lung function throughout the study to confirm that injury inside the lung occurred within the segment treated with bleomycin. Furthermore, this also enabled us to identify if this tool may be incorporated into our assessment of fibrosis, as has been successfully accomplished in murine models [10, 32] The scan was performed ex-vivo for sensible causes, because it eliminated the must anesthetize and transport the sheep for the procedure, equivalent to that previously published in a pre-clinical mice model [10]. In CT images, fibrotic lung tissue appeared denser in comparison with normal lungs, which was quite clearly visualised on the pictures obtained from our sheep lung, displaying a clear demarcation on the area locally treated with bleomycin in comparison to the remainder with the lung. This outcome suggested that ex-vivo CT scans could serve as a non-invasive tool for the assessment of fibrotic changesand intervention approaches in future studies, similar to that done by other people [10, 32].Conclusion In conclusion, the results in the current study demonstrated that a relatively sustained fibrotic response might be induced into isolated lung segments that also bring about a persistent, measurable modify in lung compliance. Importantly, the alterations in segmental compliance correlate strongly to pathology; consequently this parameter can serve as a reputable indicator of pathological changes within the lung. The assessment of lung function in this model is therefore probably to become a valuable predictor of your efficacy of distinctive intervention approaches against pulmonary fibrosis in future preclinical research. The inclusion of far more clinically relevant endpoints into pre-clinical trials might aid in a lot more precise identification of prospective drug candidates to translate in to the clinic.Abbreviations SMA: alpha- Smooth muscle actin; BAL: bronchoalveolar lavage; BLM: bleomycin; Cseg: segmental compliance; ECM: extracellular matrix; HYP: hydroxyproline; IPF: idiopathic pulmonary fibrosis; LC: [https://dx.doi.org/10.1098/rstb.2015.0074 title= rstb.2015.0074] left caudal lobe; RC: suitable caudal lobe; SMI: semi-quantitative morphological index; TGF: Transforming growth element. Competing interests The authors declare that they have no competing interest. Authors' contributions LO was the principal researcher for the study, and designed the study collectively with KS. LO performed the lung function evaluation, tissue processing for histology, CT scan assessment, histology and immunohistochemistry. LO performed histopathology assessment with BB's assistance, Masson trichrome staining and collagen evaluation, immunohistochemistry, BAL sampling and cell counts.&lt;/div&gt;</summary>
		<author><name>Dime5sea</name></author>	</entry>

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