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Comparison between effects of pressure support and pressure-controlled ventilation on lung and diaphragmatic damage in experimental emphysema.

Intensive care medicine experimental

Padilha GA, Horta LF, Moraes L, Braga CL, Oliveira MV, Santos CL, Ramos IP, Morales MM, Capelozzi VL, Goldenberg RC, de Abreu MG, Pelosi P, Silva PL, Rocco PR.
PMID: 27761886
Intensive Care Med Exp. 2016 Dec;4(1):35. doi: 10.1186/s40635-016-0107-0. Epub 2016 Oct 19.

BACKGROUND: In patients with emphysema, invasive mechanical ventilation settings should be adjusted to minimize hyperinflation while reducing respiratory effort and providing adequate gas exchange. We evaluated the impact of pressure-controlled ventilation (PCV) and pressure support ventilation (PSV) on pulmonary...

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Padilha GA, Horta LF, Moraes L, et al. Comparison between effects of pressure support and pressure-controlled ventilation on lung and diaphragmatic damage in experimental emphysema. Intensive Care Med Exp. 2016;4(1):35doi: 10.1186/s40635-016-0107-0.
Padilha, G. A., Horta, L. F., Moraes, L., Braga, C. L., Oliveira, M. V., Santos, C. L., Ramos, I. P., Morales, M. M., Capelozzi, V. L., Goldenberg, R. C., de Abreu, M. G., Pelosi, P., Silva, P. L., & Rocco, P. R. (2016). Comparison between effects of pressure support and pressure-controlled ventilation on lung and diaphragmatic damage in experimental emphysema. Intensive care medicine experimental, 4(1), 35. https://doi.org/10.1186/s40635-016-0107-0
Padilha, Gisele de A, et al. "Comparison between effects of pressure support and pressure-controlled ventilation on lung and diaphragmatic damage in experimental emphysema." Intensive care medicine experimental vol. 4,1 (2016): 35. doi: https://doi.org/10.1186/s40635-016-0107-0
Padilha GA, Horta LF, Moraes L, Braga CL, Oliveira MV, Santos CL, Ramos IP, Morales MM, Capelozzi VL, Goldenberg RC, de Abreu MG, Pelosi P, Silva PL, Rocco PR. Comparison between effects of pressure support and pressure-controlled ventilation on lung and diaphragmatic damage in experimental emphysema. Intensive Care Med Exp. 2016 Dec;4(1):35. doi: 10.1186/s40635-016-0107-0. Epub 2016 Oct 19. PMID: 27761886; PMCID: PMC5071308.
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Protein Crystallography at Ultra-Short Wavelengths: Feasibility Study of Anomalous-Dispersion Experiments at the Xenon K-edge.

Journal of synchrotron radiation

Schiltz M, Kvick A, Svensson OS, Shepard W, de La Fortelle E, Prangé T, Kahn R, Bricogne G, Fourme R.
PMID: 16699242
J Synchrotron Radiat. 1997 Sep 01;4:287-97. doi: 10.1107/S0909049597008571.

A protein crystallography experiment at the xenon K-edge (lambda = 0.358 A) has been successfully carried out at the materials science beamline (BL2/ID11) of the ESRF. The samples used in this methodological study were crystals of porcine pancreatic elastase,...

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Schiltz M, Kvick A, Svensson OS, et al. Protein Crystallography at Ultra-Short Wavelengths: Feasibility Study of Anomalous-Dispersion Experiments at the Xenon K-edge. J Synchrotron Radiat. 1997;4:287-97doi: 10.1107/S0909049597008571.
Schiltz, M., Kvick, A., Svensson, O. S., Shepard, W., de La Fortelle, E., Prangé, T., Kahn, R., Bricogne, G., & Fourme, R. (1997). Protein Crystallography at Ultra-Short Wavelengths: Feasibility Study of Anomalous-Dispersion Experiments at the Xenon K-edge. Journal of synchrotron radiation, 4287-97. https://doi.org/10.1107/S0909049597008571
Schiltz, M, et al. "Protein Crystallography at Ultra-Short Wavelengths: Feasibility Study of Anomalous-Dispersion Experiments at the Xenon K-edge." Journal of synchrotron radiation vol. 4 (1997): 287-97. doi: https://doi.org/10.1107/S0909049597008571
Schiltz M, Kvick A, Svensson OS, Shepard W, de La Fortelle E, Prangé T, Kahn R, Bricogne G, Fourme R. Protein Crystallography at Ultra-Short Wavelengths: Feasibility Study of Anomalous-Dispersion Experiments at the Xenon K-edge. J Synchrotron Radiat. 1997 Sep 01;4:287-97. doi: 10.1107/S0909049597008571. PMID: 16699242.
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Structure of native pancreatic elastase from North Atlantic salmon at 1.61 A resolution.

Acta crystallographica. Section D, Biological crystallography

Berglund GI, Willassen NP, Hordvik A, Smalås AO.
PMID: 15299762
Acta Crystallogr D Biol Crystallogr. 1995 Nov 01;51:925-37. doi: 10.1107/S0907444995004835.

The crystal structure of native salmon pancreatic elastase (SPE) has been solved by molecular-replacement methods, and refined by conventional conjugate-gradient methods and simulated-annealing techniques. The final R value is 17.2% for 21 389 reflections between 8.0 and 1.61 A,...

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Berglund GI, Willassen NP, Hordvik A, et al. Structure of native pancreatic elastase from North Atlantic salmon at 1.61 A resolution. Acta Crystallogr D Biol Crystallogr. 1995;51:925-37doi: 10.1107/S0907444995004835.
Berglund, G. I., Willassen, N. P., Hordvik, A., & Smalås, A. O. (1995). Structure of native pancreatic elastase from North Atlantic salmon at 1.61 A resolution. Acta crystallographica. Section D, Biological crystallography, 51925-37. https://doi.org/10.1107/S0907444995004835
Berglund, G I, et al. "Structure of native pancreatic elastase from North Atlantic salmon at 1.61 A resolution." Acta crystallographica. Section D, Biological crystallography vol. 51 (1995): 925-37. doi: https://doi.org/10.1107/S0907444995004835
Berglund GI, Willassen NP, Hordvik A, Smalås AO. Structure of native pancreatic elastase from North Atlantic salmon at 1.61 A resolution. Acta Crystallogr D Biol Crystallogr. 1995 Nov 01;51:925-37. doi: 10.1107/S0907444995004835. PMID: 15299762.
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Influence of SPK with Enteric Drainage on the Pancreatic Exocrine Function in Diabetic Patients with Uremia.

International journal of endocrinology

Pei G, Lv W, Li X, Zhang G, Zhang J.
PMID: 29138633
Int J Endocrinol. 2017;2017:3709306. doi: 10.1155/2017/3709306. Epub 2017 Aug 24.

OBJECTIVE: This study aimed to determine the use of fecal elastase in evaluating the effect of simultaneous pancreas-kidney transplantation with enteric drainage on the pancreatic exocrine function of diabetic patients with uremia.METHODS: A total of 19 patients with simultaneous...

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Pei G, Lv W, Li X, et al. Influence of SPK with Enteric Drainage on the Pancreatic Exocrine Function in Diabetic Patients with Uremia. Int J Endocrinol. 2017;2017:3709306doi: 10.1155/2017/3709306.
Pei, G., Lv, W., Li, X., Zhang, G., & Zhang, J. (2017). Influence of SPK with Enteric Drainage on the Pancreatic Exocrine Function in Diabetic Patients with Uremia. International journal of endocrinology, 20173709306. https://doi.org/10.1155/2017/3709306
Pei, Guanghui, et al. "Influence of SPK with Enteric Drainage on the Pancreatic Exocrine Function in Diabetic Patients with Uremia." International journal of endocrinology vol. 2017 (2017): 3709306. doi: https://doi.org/10.1155/2017/3709306
Pei G, Lv W, Li X, Zhang G, Zhang J. Influence of SPK with Enteric Drainage on the Pancreatic Exocrine Function in Diabetic Patients with Uremia. Int J Endocrinol. 2017;2017:3709306. doi: 10.1155/2017/3709306. Epub 2017 Aug 24. PMID: 29138633; PMCID: PMC5613707.
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Exocrine Dysfunction Correlates with Endocrinal Impairment of Pancreas in Type 2 Diabetes Mellitus.

Indian journal of endocrinology and metabolism

Prasanna Kumar HR, Gowdappa HB, Hosmani T, Urs T.
PMID: 29535950
Indian J Endocrinol Metab. 2018 Jan-Feb;22(1):121-125. doi: 10.4103/ijem.IJEM_139_17.

BACKGROUND: Diabetes mellitus (DM) is a chronic abnormal metabolic condition, which manifests elevated blood sugar level over a prolonged period. The pancreatic endocrine system generally gets affected during diabetes, but often abnormal exocrine functions are also manifested due to...

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Prasanna Kumar HR, Gowdappa HB, Hosmani T, et al. Exocrine Dysfunction Correlates with Endocrinal Impairment of Pancreas in Type 2 Diabetes Mellitus. Indian J Endocrinol Metab. 2018;22(1):121-125doi: 10.4103/ijem.IJEM_139_17.
Prasanna Kumar, H. R., Gowdappa, H. B., Hosmani, T., & Urs, T. (2018). Exocrine Dysfunction Correlates with Endocrinal Impairment of Pancreas in Type 2 Diabetes Mellitus. Indian journal of endocrinology and metabolism, 22(1), 121-125. https://doi.org/10.4103/ijem.IJEM_139_17
Prasanna Kumar, H R, et al. "Exocrine Dysfunction Correlates with Endocrinal Impairment of Pancreas in Type 2 Diabetes Mellitus." Indian journal of endocrinology and metabolism vol. 22,1 (2018): 121-125. doi: https://doi.org/10.4103/ijem.IJEM_139_17
Prasanna Kumar HR, Gowdappa HB, Hosmani T, Urs T. Exocrine Dysfunction Correlates with Endocrinal Impairment of Pancreas in Type 2 Diabetes Mellitus. Indian J Endocrinol Metab. 2018 Jan-Feb;22(1):121-125. doi: 10.4103/ijem.IJEM_139_17. PMID: 29535950; PMCID: PMC5838891.
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Bruising as the first sign of exocrine pancreatic insufficiency in infancy.

Medicine and pharmacy reports

Szabo CE, Man OI, Şerban RS, Kiss E, Lazăr CF.
PMID: 31086851
Med Pharm Rep. 2019 Apr;92(2):200-204. doi: 10.15386/mpr-1231. Epub 2019 Apr 25.

Exocrine pancreatic insufficiency is an important cause of chronic malnutrition, secondary to maldigestion-malabsorption, which can be caused in children especially by cystic fibrosis, but also by other much rarer diseases. The case of a 6 months and 3 weeks...

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Szabo CE, Man OI, Şerban RS, et al. Bruising as the first sign of exocrine pancreatic insufficiency in infancy. Med Pharm Rep. 2019;92(2):200-204doi: 10.15386/mpr-1231.
Szabo, C. E., Man, O. I., Şerban, R. S., Kiss, E., & Lazăr, C. F. (2019). Bruising as the first sign of exocrine pancreatic insufficiency in infancy. Medicine and pharmacy reports, 92(2), 200-204. https://doi.org/10.15386/mpr-1231
Szabo, Csilla Enikő, et al. "Bruising as the first sign of exocrine pancreatic insufficiency in infancy." Medicine and pharmacy reports vol. 92,2 (2019): 200-204. doi: https://doi.org/10.15386/mpr-1231
Szabo CE, Man OI, Şerban RS, Kiss E, Lazăr CF. Bruising as the first sign of exocrine pancreatic insufficiency in infancy. Med Pharm Rep. 2019 Apr;92(2):200-204. doi: 10.15386/mpr-1231. Epub 2019 Apr 25. PMID: 31086851; PMCID: PMC6510358.
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Development of a Model for Abdominal Aortic Aneurysms in Swine.

The Journal of surgical research

De Leo N, Melillo A, Zhang P, Badach J, Miller H, Lin A, Williamson J, Ghobrial G, Gaughan J, Krishnadoss V, Noshadi I, Brown SA, Carpenter JP.
PMID: 34289418
J Surg Res. 2021 Jul 18;268:79-86. doi: 10.1016/j.jss.2021.05.047. Epub 2021 Jul 18.

INTRODUCTION: Producing a reliable large-animal model of AAA has proven challenging. We sought to create a reproducible swine model of AAA using enzymatic degradation of the aortic wall.METHODS: Twelve male Yorkshire swine received periadventitial injections of type 1 collagenase...

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De Leo N, Melillo A, Zhang P, et al. Development of a Model for Abdominal Aortic Aneurysms in Swine. J Surg Res. 2021;268:79-86doi: 10.1016/j.jss.2021.05.047.
De Leo, N., Melillo, A., Zhang, P., Badach, J., Miller, H., Lin, A., Williamson, J., Ghobrial, G., Gaughan, J., Krishnadoss, V., Noshadi, I., Brown, S. A., & Carpenter, J. P. (2021). Development of a Model for Abdominal Aortic Aneurysms in Swine. The Journal of surgical research, 26879-86. https://doi.org/10.1016/j.jss.2021.05.047
De Leo, Nicholas, et al. "Development of a Model for Abdominal Aortic Aneurysms in Swine." The Journal of surgical research vol. 268 (2021): 79-86. doi: https://doi.org/10.1016/j.jss.2021.05.047
De Leo N, Melillo A, Zhang P, Badach J, Miller H, Lin A, Williamson J, Ghobrial G, Gaughan J, Krishnadoss V, Noshadi I, Brown SA, Carpenter JP. Development of a Model for Abdominal Aortic Aneurysms in Swine. J Surg Res. 2021 Jul 18;268:79-86. doi: 10.1016/j.jss.2021.05.047. Epub 2021 Jul 18. PMID: 34289418.
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Translating mouse models of abdominal aortic aneurysm to the translational needs of vascular surgery.

JVS-vascular science

Busch A, Bleichert S, Ibrahim N, Wortmann M, Eckstein HH, Brostjan C, Wagenhäuser MU, Goergen CJ, Maegdefessel L.
PMID: 34778850
JVS Vasc Sci. 2021 Mar 03;2:219-234. doi: 10.1016/j.jvssci.2021.01.002. eCollection 2021.

INTRODUCTION: Abdominal aortic aneurysm (AAA) is a condition that has considerable socioeconomic impact and an eventual rupture is associated with high mortality and morbidity. Despite decades of research, surgical repair remains the treatment of choice and no medical therapy...

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Busch A, Bleichert S, Ibrahim N, et al. Translating mouse models of abdominal aortic aneurysm to the translational needs of vascular surgery. JVS Vasc Sci. 2021;2:219-234doi: 10.1016/j.jvssci.2021.01.002.
Busch, A., Bleichert, S., Ibrahim, N., Wortmann, M., Eckstein, H. H., Brostjan, C., Wagenhäuser, M. U., Goergen, C. J., & Maegdefessel, L. (2021). Translating mouse models of abdominal aortic aneurysm to the translational needs of vascular surgery. JVS-vascular science, 2219-234. https://doi.org/10.1016/j.jvssci.2021.01.002
Busch, Albert, et al. "Translating mouse models of abdominal aortic aneurysm to the translational needs of vascular surgery." JVS-vascular science vol. 2 (2021): 219-234. doi: https://doi.org/10.1016/j.jvssci.2021.01.002
Busch A, Bleichert S, Ibrahim N, Wortmann M, Eckstein HH, Brostjan C, Wagenhäuser MU, Goergen CJ, Maegdefessel L. Translating mouse models of abdominal aortic aneurysm to the translational needs of vascular surgery. JVS Vasc Sci. 2021 Mar 03;2:219-234. doi: 10.1016/j.jvssci.2021.01.002. eCollection 2021. PMID: 34778850; PMCID: PMC8577080.
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Progression and Regression of Abdominal Aortic Aneurysms in Mice.

Current medical science

Ding YC, Zhang XJ, Zhang JX, Zhai ZY, Zhang MX, Jiang BH.
PMID: 34643880
Curr Med Sci. 2021 Oct;41(5):901-908. doi: 10.1007/s11596-021-2425-z. Epub 2021 Oct 13.

OBJECTIVE: Abdominal aortic aneurysm (AAA) is a significant medical problem with a high mortality rate. Nevertheless, the underlying mechanism for the progression and regression of AAA is unknown.METHODS: Experimental model of AAA was first created by porcine pancreatic elastase...

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Ding YC, Zhang XJ, Zhang JX, et al. Progression and Regression of Abdominal Aortic Aneurysms in Mice. Curr Med Sci. 2021;41(5):901-908doi: 10.1007/s11596-021-2425-z.
Ding, Y. C., Zhang, X. J., Zhang, J. X., Zhai, Z. Y., Zhang, M. X., & Jiang, B. H. (2021). Progression and Regression of Abdominal Aortic Aneurysms in Mice. Current medical science, 41(5), 901-908. https://doi.org/10.1007/s11596-021-2425-z
Ding, Yu-Chao, et al. "Progression and Regression of Abdominal Aortic Aneurysms in Mice." Current medical science vol. 41,5 (2021): 901-908. doi: https://doi.org/10.1007/s11596-021-2425-z
Ding YC, Zhang XJ, Zhang JX, Zhai ZY, Zhang MX, Jiang BH. Progression and Regression of Abdominal Aortic Aneurysms in Mice. Curr Med Sci. 2021 Oct;41(5):901-908. doi: 10.1007/s11596-021-2425-z. Epub 2021 Oct 13. PMID: 34643880.
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Evaluation of Circulating Endothelial Progenitor Cells in Abdominal Aortic Aneurysms after Endovascular Aneurysm Repair.

International journal of stem cells

Wu W, Zhang J, Shao L, Huang H, Meng Q, Shen Z, Teng X.
PMID: 34711694
Int J Stem Cells. 2021 Oct 31; doi: 10.15283/ijsc21027. Epub 2021 Oct 31.

BACKGROUND AND OBJECTIVES: Circulating endothelial progenitor cells (EPCs) participate in vascular repair and predict cardiovascular outcomes. The aim of this study was to investigate the correlation between EPCs and abdominal aortic aneurysms (AAAs).METHODS AND RESULTS: Patients (age 67±9.41 years)...

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Wu W, Zhang J, Shao L, et al. Evaluation of Circulating Endothelial Progenitor Cells in Abdominal Aortic Aneurysms after Endovascular Aneurysm Repair. Int J Stem Cells. 2021;doi: 10.15283/ijsc21027.
Wu, W., Zhang, J., Shao, L., Huang, H., Meng, Q., Shen, Z., & Teng, X. (2021). Evaluation of Circulating Endothelial Progenitor Cells in Abdominal Aortic Aneurysms after Endovascular Aneurysm Repair. International journal of stem cells, . https://doi.org/10.15283/ijsc21027
Wu, Weihua, et al. "Evaluation of Circulating Endothelial Progenitor Cells in Abdominal Aortic Aneurysms after Endovascular Aneurysm Repair." International journal of stem cells vol. (2021). doi: https://doi.org/10.15283/ijsc21027
Wu W, Zhang J, Shao L, Huang H, Meng Q, Shen Z, Teng X. Evaluation of Circulating Endothelial Progenitor Cells in Abdominal Aortic Aneurysms after Endovascular Aneurysm Repair. Int J Stem Cells. 2021 Oct 31; doi: 10.15283/ijsc21027. Epub 2021 Oct 31. PMID: 34711694.
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Establishing the blood reference interval of pancreatic elastase-1: A prospective study.

Journal of gastroenterology and hepatology

Chi SF, Lai CY, Dong WT, Wang JM, Wang YY, Yang SS, Lin JT, Lee TY.
PMID: 34498301
J Gastroenterol Hepatol. 2021 Sep 08; doi: 10.1111/jgh.15685. Epub 2021 Sep 08.

BACKGROUND AND AIM: Pancreatic elastase-1 (PE-1) has been investigated in pancreatic disorders. However, the reference interval (RI) of PE-1 in blood remains unconfirmed. We aimed to establish the blood RI of PE-1 in an adult population.METHODS: In this prospective...

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Chi SF, Lai CY, Dong WT, et al. Establishing the blood reference interval of pancreatic elastase-1: A prospective study. J Gastroenterol Hepatol. 2021;doi: 10.1111/jgh.15685.
Chi, S. F., Lai, C. Y., Dong, W. T., Wang, J. M., Wang, Y. Y., Yang, S. S., Lin, J. T., & Lee, T. Y. (2021). Establishing the blood reference interval of pancreatic elastase-1: A prospective study. Journal of gastroenterology and hepatology, . https://doi.org/10.1111/jgh.15685
Chi, Su-Fen, et al. "Establishing the blood reference interval of pancreatic elastase-1: A prospective study." Journal of gastroenterology and hepatology vol. (2021). doi: https://doi.org/10.1111/jgh.15685
Chi SF, Lai CY, Dong WT, Wang JM, Wang YY, Yang SS, Lin JT, Lee TY. Establishing the blood reference interval of pancreatic elastase-1: A prospective study. J Gastroenterol Hepatol. 2021 Sep 08; doi: 10.1111/jgh.15685. Epub 2021 Sep 08. PMID: 34498301.
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Fluorescence Determination of Peptidase Activity Based on the Quenching of a Fluorophore-Labelled Peptide by Graphene Oxide.

The protein journal

Le DV.
PMID: 33856620
Protein J. 2021 Oct;40(5):682-688. doi: 10.1007/s10930-021-09985-6. Epub 2021 Apr 15.

In this study, a fluorescence detection strategy is reported for the peptidase activity assay, which is based on fluorescence resonance energy transfer (FRET) from a fluorophore-labelled peptide to graphene oxide (GO). By the hydrolysis of the peptide, the fluorophore-labelled...

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Le DV. Fluorescence Determination of Peptidase Activity Based on the Quenching of a Fluorophore-Labelled Peptide by Graphene Oxide. Protein J. 2021;40(5):682-688doi: 10.1007/s10930-021-09985-6.
Le, D. V. (2021). Fluorescence Determination of Peptidase Activity Based on the Quenching of a Fluorophore-Labelled Peptide by Graphene Oxide. The protein journal, 40(5), 682-688. https://doi.org/10.1007/s10930-021-09985-6
Le, Dinh-Vu. "Fluorescence Determination of Peptidase Activity Based on the Quenching of a Fluorophore-Labelled Peptide by Graphene Oxide." The protein journal vol. 40,5 (2021): 682-688. doi: https://doi.org/10.1007/s10930-021-09985-6
Le DV. Fluorescence Determination of Peptidase Activity Based on the Quenching of a Fluorophore-Labelled Peptide by Graphene Oxide. Protein J. 2021 Oct;40(5):682-688. doi: 10.1007/s10930-021-09985-6. Epub 2021 Apr 15. PMID: 33856620.
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Showing 1 to 12 of 73 entries