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Effects of Toasting Time on Digestive Hydrolysis of Soluble and Insoluble 00-Rapeseed Meal Proteins.

Journal of the American Oil Chemists' Society

Salazar-Villanea S, Bruininx EMAM, Gruppen H, Carré P, Quinsac A, van der Poel AFB.
PMID: 28392576
J Am Oil Chem Soc. 2017;94(4):619-630. doi: 10.1007/s11746-017-2960-8. Epub 2017 Feb 11.

Thermal damage to proteins can reduce their nutritional value. The effects of toasting time on the kinetics of hydrolysis, the resulting molecular weight distribution of 00-rapeseed meal (RSM) and the soluble and insoluble protein fractions separated from the RSM...

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Salazar-Villanea S, Bruininx EMAM, Gruppen H, et al. Effects of Toasting Time on Digestive Hydrolysis of Soluble and Insoluble 00-Rapeseed Meal Proteins. J Am Oil Chem Soc. 2017;94(4):619-630doi: 10.1007/s11746-017-2960-8.
Salazar-Villanea, S., Bruininx, E. M. A. M., Gruppen, H., Carré, P., Quinsac, A., & van der Poel, A. F. B. (2017). Effects of Toasting Time on Digestive Hydrolysis of Soluble and Insoluble 00-Rapeseed Meal Proteins. Journal of the American Oil Chemists' Society, 94(4), 619-630. https://doi.org/10.1007/s11746-017-2960-8
Salazar-Villanea, Sergio, et al. "Effects of Toasting Time on Digestive Hydrolysis of Soluble and Insoluble 00-Rapeseed Meal Proteins." Journal of the American Oil Chemists' Society vol. 94,4 (2017): 619-630. doi: https://doi.org/10.1007/s11746-017-2960-8
Salazar-Villanea S, Bruininx EMAM, Gruppen H, Carré P, Quinsac A, van der Poel AFB. Effects of Toasting Time on Digestive Hydrolysis of Soluble and Insoluble 00-Rapeseed Meal Proteins. J Am Oil Chem Soc. 2017;94(4):619-630. doi: 10.1007/s11746-017-2960-8. Epub 2017 Feb 11. PMID: 28392576; PMCID: PMC5364235.
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Technology for noninvasive mechanical ventilation: looking into the black box.

ERJ open research

Farré R, Navajas D, Montserrat JM.
PMID: 27730162
ERJ Open Res. 2016 Mar 11;2(1). doi: 10.1183/23120541.00004-2016. eCollection 2016 Jan.

Current devices for providing noninvasive respiratory support contain sensors and built-in intelligence for automatically modifying ventilation according to the patient's needs. These devices, including automatic continuous positive airway pressure devices and noninvasive ventilators, are technologically complex and offer a...

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Farré R, Navajas D, Montserrat JM. Technology for noninvasive mechanical ventilation: looking into the black box. ERJ Open Res. 2016;2(1)doi: 10.1183/23120541.00004-2016.
Farré, R., Navajas, D., & Montserrat, J. M. (2016). Technology for noninvasive mechanical ventilation: looking into the black box. ERJ open research, 2(1), . https://doi.org/10.1183/23120541.00004-2016
Farré, Ramon, et al. "Technology for noninvasive mechanical ventilation: looking into the black box." ERJ open research vol. 2,1 (2016). doi: https://doi.org/10.1183/23120541.00004-2016
Farré R, Navajas D, Montserrat JM. Technology for noninvasive mechanical ventilation: looking into the black box. ERJ Open Res. 2016 Mar 11;2(1). doi: 10.1183/23120541.00004-2016. eCollection 2016 Jan. PMID: 27730162; PMCID: PMC5005145.
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STAT3 as a new autophagy regulator.

JAK-STAT

Jonchère B, Bélanger A, Guette C, Barré B, Coqueret O.
PMID: 24069557
JAKSTAT. 2013 Jul 01;2(3):e24353. doi: 10.4161/jkst.24353. Epub 2013 Aug 15.

Signal transducers and activators of transcription 3 (STAT3) proteins are cytoplasmic transcription factors that translocate into the nucleus to induce transcription following growth factor or cytokine stimulation. Besides their normal functions, these proteins play an important role in cancer...

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Jonchère B, Bélanger A, Guette C, et al. STAT3 as a new autophagy regulator. JAKSTAT. 2013;2(3):e24353doi: 10.4161/jkst.24353.
Jonchère, B., Bélanger, A., Guette, C., Barré, B., & Coqueret, O. (2013). STAT3 as a new autophagy regulator. JAK-STAT, 2(3), e24353. https://doi.org/10.4161/jkst.24353
Jonchère, Barbara, et al. "STAT3 as a new autophagy regulator." JAK-STAT vol. 2,3 (2013): e24353. doi: https://doi.org/10.4161/jkst.24353
Jonchère B, Bélanger A, Guette C, Barré B, Coqueret O. STAT3 as a new autophagy regulator. JAKSTAT. 2013 Jul 01;2(3):e24353. doi: 10.4161/jkst.24353. Epub 2013 Aug 15. PMID: 24069557; PMCID: PMC3772109.
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The expanding role of the bile acid receptor farnesoid X in the intestine and its potential clinical implications.

Acta chirurgica Belgica

Ceulemans LJ, Canovai E, Verbeke L, Pirenne J, Farré R.
PMID: 27684270
Acta Chir Belg. 2016 Jun;116(3):156-163. doi: 10.1080/00015458.2016.1215953. Epub 2016 Aug 10.

Knowledge about the role of farnesoid X receptor (FXR) in the intestine is rapidly expanding. In pre-clinical animal models of inflammatory bowel disease and bile duct ligation, FXR activation has proven to directly target the three pillars of intestinal...

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Ceulemans LJ, Canovai E, Verbeke L, et al. The expanding role of the bile acid receptor farnesoid X in the intestine and its potential clinical implications. Acta Chir Belg. 2016;116(3):156-163doi: 10.1080/00015458.2016.1215953.
Ceulemans, L. J., Canovai, E., Verbeke, L., Pirenne, J., & Farré, R. (2016). The expanding role of the bile acid receptor farnesoid X in the intestine and its potential clinical implications. Acta chirurgica Belgica, 116(3), 156-163. https://doi.org/10.1080/00015458.2016.1215953
Ceulemans, Laurens J, et al. "The expanding role of the bile acid receptor farnesoid X in the intestine and its potential clinical implications." Acta chirurgica Belgica vol. 116,3 (2016): 156-163. doi: https://doi.org/10.1080/00015458.2016.1215953
Ceulemans LJ, Canovai E, Verbeke L, Pirenne J, Farré R. The expanding role of the bile acid receptor farnesoid X in the intestine and its potential clinical implications. Acta Chir Belg. 2016 Jun;116(3):156-163. doi: 10.1080/00015458.2016.1215953. Epub 2016 Aug 10. PMID: 27684270.
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Self-Probing Spectroscopy of the SF6 Molecule: A Study of the Spectral Amplitude and Phase of the High Harmonic Emission.

The journal of physical chemistry. A

Manschwetus B, Lin N, Rothhardt J, Guichard R, Auguste T, Camper A, Breger P, Caillat J, Géléoc M, Ruchon T, Taïeb R, Carré B, Salières P.
PMID: 25812633
J Phys Chem A. 2015 Jun 11;119(23):6111-22. doi: 10.1021/acs.jpca.5b00446. Epub 2015 Apr 10.

We present characterizations of the attosecond pulse train produced in the high harmonic generation (HHG) from SF6 molecules irradiated by a strong pulsed laser field at 800 nm. At harmonic order 17, we observe a minimum in the amplitude...

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Manschwetus B, Lin N, Rothhardt J, et al. Self-Probing Spectroscopy of the SF6 Molecule: A Study of the Spectral Amplitude and Phase of the High Harmonic Emission. J Phys Chem A. 2015;119(23):6111-22doi: 10.1021/acs.jpca.5b00446.
Manschwetus, B., Lin, N., Rothhardt, J., Guichard, R., Auguste, T., Camper, A., Breger, P., Caillat, J., Géléoc, M., Ruchon, T., Taïeb, R., Carré, B., & Salières, P. (2015). Self-Probing Spectroscopy of the SF6 Molecule: A Study of the Spectral Amplitude and Phase of the High Harmonic Emission. The journal of physical chemistry. A, 119(23), 6111-22. https://doi.org/10.1021/acs.jpca.5b00446
Manschwetus, Bastian, et al. "Self-Probing Spectroscopy of the SF6 Molecule: A Study of the Spectral Amplitude and Phase of the High Harmonic Emission." The journal of physical chemistry. A vol. 119,23 (2015): 6111-22. doi: https://doi.org/10.1021/acs.jpca.5b00446
Manschwetus B, Lin N, Rothhardt J, Guichard R, Auguste T, Camper A, Breger P, Caillat J, Géléoc M, Ruchon T, Taïeb R, Carré B, Salières P. Self-Probing Spectroscopy of the SF6 Molecule: A Study of the Spectral Amplitude and Phase of the High Harmonic Emission. J Phys Chem A. 2015 Jun 11;119(23):6111-22. doi: 10.1021/acs.jpca.5b00446. Epub 2015 Apr 10. PMID: 25812633.
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Draft Genome Sequences of Mycoplasma auris and Mycoplasma yeatsii, Two Species of the Ear Canal of Caprinae.

Genome announcements

Dordet-Frisoni E, Baranowski E, Barré A, Blanchard A, Breton M, Couture C, Dupuy V, Gaurivaud P, Jacob D, Lemaitre C, Manso-Silván L, Nikolski M, Nouvel LX, Poumarat F, Sirand-Pugnet P, Thébault P, Theil S, Thiaucourt F, Citti C, Tardy F.
PMID: 23766401
Genome Announc. 2013 Jun 13;1(3). doi: 10.1128/genomeA.00280-13.

We report here the draft genome sequences of Mycoplasma auris and Mycoplasma yeatsii, two species commonly isolated from the external ear canal of Caprinae.

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Dordet-Frisoni E, Baranowski E, Barré A, et al. Draft Genome Sequences of Mycoplasma auris and Mycoplasma yeatsii, Two Species of the Ear Canal of Caprinae. Genome Announc. 2013;1(3)doi: 10.1128/genomeA.00280-13.
Dordet-Frisoni, E., Baranowski, E., Barré, A., Blanchard, A., Breton, M., Couture, C., Dupuy, V., Gaurivaud, P., Jacob, D., Lemaitre, C., Manso-Silván, L., Nikolski, M., Nouvel, L. X., Poumarat, F., Sirand-Pugnet, P., Thébault, P., Theil, S., Thiaucourt, F., Citti, C., & Tardy, F. (2013). Draft Genome Sequences of Mycoplasma auris and Mycoplasma yeatsii, Two Species of the Ear Canal of Caprinae. Genome announcements, 1(3), . https://doi.org/10.1128/genomeA.00280-13
Dordet-Frisoni, Emilie, et al. "Draft Genome Sequences of Mycoplasma auris and Mycoplasma yeatsii, Two Species of the Ear Canal of Caprinae." Genome announcements vol. 1,3 (2013). doi: https://doi.org/10.1128/genomeA.00280-13
Dordet-Frisoni E, Baranowski E, Barré A, Blanchard A, Breton M, Couture C, Dupuy V, Gaurivaud P, Jacob D, Lemaitre C, Manso-Silván L, Nikolski M, Nouvel LX, Poumarat F, Sirand-Pugnet P, Thébault P, Theil S, Thiaucourt F, Citti C, Tardy F. Draft Genome Sequences of Mycoplasma auris and Mycoplasma yeatsii, Two Species of the Ear Canal of Caprinae. Genome Announc. 2013 Jun 13;1(3). doi: 10.1128/genomeA.00280-13. PMID: 23766401; PMCID: PMC3707572.
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Draft Genome Sequences of Mycoplasma alkalescens, Mycoplasma arginini, and Mycoplasma bovigenitalium, Three Species with Equivocal Pathogenic Status for Cattle.

Genome announcements

Manso-Silván L, Tardy F, Baranowski E, Barré A, Blanchard A, Breton M, Couture C, Citti C, Dordet-Frisoni E, Dupuy V, Gaurivaud P, Jacob D, Lemaitre C, Nikolski M, Nouvel LX, Poumarat F, Thébault P, Theil S, Thiaucourt F, Sirand-Pugnet P.
PMID: 23766408
Genome Announc. 2013 Jun 13;1(3). doi: 10.1128/genomeA.00348-13.

We report here the draft genome sequences of Mycoplasma alkalescens, Mycoplasma arginini, and Mycoplasma bovigenitalium. These three species are regularly isolated from bovine clinical specimens, although their role in disease is unclear.

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Manso-Silván L, Tardy F, Baranowski E, et al. Draft Genome Sequences of Mycoplasma alkalescens, Mycoplasma arginini, and Mycoplasma bovigenitalium, Three Species with Equivocal Pathogenic Status for Cattle. Genome Announc. 2013;1(3)doi: 10.1128/genomeA.00348-13.
Manso-Silván, L., Tardy, F., Baranowski, E., Barré, A., Blanchard, A., Breton, M., Couture, C., Citti, C., Dordet-Frisoni, E., Dupuy, V., Gaurivaud, P., Jacob, D., Lemaitre, C., Nikolski, M., Nouvel, L. X., Poumarat, F., Thébault, P., Theil, S., Thiaucourt, F., & Sirand-Pugnet, P. (2013). Draft Genome Sequences of Mycoplasma alkalescens, Mycoplasma arginini, and Mycoplasma bovigenitalium, Three Species with Equivocal Pathogenic Status for Cattle. Genome announcements, 1(3), . https://doi.org/10.1128/genomeA.00348-13
Manso-Silván, Lucía, et al. "Draft Genome Sequences of Mycoplasma alkalescens, Mycoplasma arginini, and Mycoplasma bovigenitalium, Three Species with Equivocal Pathogenic Status for Cattle." Genome announcements vol. 1,3 (2013). doi: https://doi.org/10.1128/genomeA.00348-13
Manso-Silván L, Tardy F, Baranowski E, Barré A, Blanchard A, Breton M, Couture C, Citti C, Dordet-Frisoni E, Dupuy V, Gaurivaud P, Jacob D, Lemaitre C, Nikolski M, Nouvel LX, Poumarat F, Thébault P, Theil S, Thiaucourt F, Sirand-Pugnet P. Draft Genome Sequences of Mycoplasma alkalescens, Mycoplasma arginini, and Mycoplasma bovigenitalium, Three Species with Equivocal Pathogenic Status for Cattle. Genome Announc. 2013 Jun 13;1(3). doi: 10.1128/genomeA.00348-13. PMID: 23766408; PMCID: PMC3707579.
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Feynman's path-integral approach for intense-laser-atom interactions.

Science (New York, N.Y.)

Salières P, Carré B, Le Déroff L, Grasbon F, Paulus GG, Walther H, Kopold R, Becker W, Milosević DB, Sanpera A, Lewenstein M.
PMID: 11340197
Science. 2001 May 04;292(5518):902-5. doi: 10.1126/science.108836.

Atoms interacting with intense laser fields can emit electrons and photons of very high energies. An intuitive and quantitative explanation of these highly nonlinear processes can be found in terms of a generalization of classical Newtonian particle trajectories, the...

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Salières P, Carré B, Le Déroff L, et al. Feynman's path-integral approach for intense-laser-atom interactions. Science. 2001;292(5518):902-5doi: 10.1126/science.108836.
Salières, P., Carré, B., Le Déroff, L., Grasbon, F., Paulus, G. G., Walther, H., Kopold, R., Becker, W., Milosević, D. B., Sanpera, A., & Lewenstein, M. (2001). Feynman's path-integral approach for intense-laser-atom interactions. Science (New York, N.Y.), 292(5518), 902-5. https://doi.org/10.1126/science.108836
Salières, P, et al. "Feynman's path-integral approach for intense-laser-atom interactions." Science (New York, N.Y.) vol. 292,5518 (2001): 902-5. doi: https://doi.org/10.1126/science.108836
Salières P, Carré B, Le Déroff L, Grasbon F, Paulus GG, Walther H, Kopold R, Becker W, Milosević DB, Sanpera A, Lewenstein M. Feynman's path-integral approach for intense-laser-atom interactions. Science. 2001 May 04;292(5518):902-5. doi: 10.1126/science.108836. PMID: 11340197.
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On the Spreading of Glycerol Trioleate.

Journal of colloid and interface science

Shanahan ME, Carré A.
PMID: 11237460
J Colloid Interface Sci. 2001 Mar 01;235(1):197-199. doi: 10.1006/jcis.2000.7342.

Spreading of liquids can often successfully be described by either hydrodynamic or molecular kinetics theories. The natural wetting of small, sessile drops of glycerol trioleate on smooth, flat, solid surfaces may be expected to comply with the former model,...

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Shanahan ME, Carré A. On the Spreading of Glycerol Trioleate. J Colloid Interface Sci. 2001;235(1):197-199doi: 10.1006/jcis.2000.7342.
Shanahan, M. E., & Carré, A. (2001). On the Spreading of Glycerol Trioleate. Journal of colloid and interface science, 235(1), 197-199. https://doi.org/10.1006/jcis.2000.7342
Shanahan, Martin E. R., and Carré, Alain. "On the Spreading of Glycerol Trioleate." Journal of colloid and interface science vol. 235,1 (2001): 197-199. doi: https://doi.org/10.1006/jcis.2000.7342
Shanahan ME, Carré A. On the Spreading of Glycerol Trioleate. J Colloid Interface Sci. 2001 Mar 01;235(1):197-199. doi: 10.1006/jcis.2000.7342. PMID: 11237460.
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Identification of disinfection by-products of selected triazines in drinking water by LC-Q-ToF-MS/MS and evaluation of their toxicity.

Journal of mass spectrometry : JMS

Brix R, Bahi N, Lopez de Alda MJ, Farré M, Fernandez JM, Barceló D.
PMID: 19034890
J Mass Spectrom. 2009 Mar;44(3):330-7. doi: 10.1002/jms.1509.

During the development of an on-line solid phase extraction-liquid chromatography-ultraviolet detection (SPE-LC-UV) analytical method for determination of eight selected triazines; ametryn, atrazine, cyanazine, metrybuzine, prometryn, propazin, simazine, and terbutryn, in drinking water, it was observed that the retention times...

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Brix R, Bahi N, Lopez de Alda MJ, et al. Identification of disinfection by-products of selected triazines in drinking water by LC-Q-ToF-MS/MS and evaluation of their toxicity. J Mass Spectrom. 2009;44(3):330-7doi: 10.1002/jms.1509.
Brix, R., Bahi, N., Lopez de Alda, M. J., Farré, M., Fernandez, J. M., & Barceló, D. (2009). Identification of disinfection by-products of selected triazines in drinking water by LC-Q-ToF-MS/MS and evaluation of their toxicity. Journal of mass spectrometry : JMS, 44(3), 330-7. https://doi.org/10.1002/jms.1509
Brix, Rikke, et al. "Identification of disinfection by-products of selected triazines in drinking water by LC-Q-ToF-MS/MS and evaluation of their toxicity." Journal of mass spectrometry : JMS vol. 44,3 (2009): 330-7. doi: https://doi.org/10.1002/jms.1509
Brix R, Bahi N, Lopez de Alda MJ, Farré M, Fernandez JM, Barceló D. Identification of disinfection by-products of selected triazines in drinking water by LC-Q-ToF-MS/MS and evaluation of their toxicity. J Mass Spectrom. 2009 Mar;44(3):330-7. doi: 10.1002/jms.1509. PMID: 19034890.
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Bronchial responses to substance P after antigen challenge in the guinea-pig: in vivo and in vitro studies.

Mediators of inflammation

Boichot E, Lagente V, Gall GL, Carré C, Mencia-Huerta JM, Braquet P, Lockhart A, Frossard N.
PMID: 18475463
Mediators Inflamm. 1992;1(3):207-12. doi: 10.1155/S0962935192000322.

The effect of antigen challenge on the airway responses to substance P and on the epithelial neutral endopeptidase (NEP) activity was investigated in aerosol sensitized guinea-pigs. In vivo, bronchial responses to aerosolized substance P were similar to the responses...

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Boichot E, Lagente V, Gall GL, et al. Bronchial responses to substance P after antigen challenge in the guinea-pig: in vivo and in vitro studies. Mediators Inflamm. 1992;1(3):207-12doi: 10.1155/S0962935192000322.
Boichot, E., Lagente, V., Gall, G. L., Carré, C., Mencia-Huerta, J. M., Braquet, P., Lockhart, A., & Frossard, N. (1992). Bronchial responses to substance P after antigen challenge in the guinea-pig: in vivo and in vitro studies. Mediators of inflammation, 1(3), 207-12. https://doi.org/10.1155/S0962935192000322
Boichot, E, et al. "Bronchial responses to substance P after antigen challenge in the guinea-pig: in vivo and in vitro studies." Mediators of inflammation vol. 1,3 (1992): 207-12. doi: https://doi.org/10.1155/S0962935192000322
Boichot E, Lagente V, Gall GL, Carré C, Mencia-Huerta JM, Braquet P, Lockhart A, Frossard N. Bronchial responses to substance P after antigen challenge in the guinea-pig: in vivo and in vitro studies. Mediators Inflamm. 1992;1(3):207-12. doi: 10.1155/S0962935192000322. PMID: 18475463; PMCID: PMC2365335.
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Polyamines, hydroxycinnamoylputrescines, and root formation in leaf explants of tobacco cultivated in vitro: effects of the suicide inhibitors of putrescine synthesis.

Plant physiology

Burtin D, Martin-Tanguy J, Paynot M, Carré M, Rossin N.
PMID: 16667631
Plant Physiol. 1990 Aug;93(4):1398-404. doi: 10.1104/pp.93.4.1398.

In vitro formation of roots is obtained directly, without intermediate growth of callus, from foliar explants of a tobacco (Nicotiana tabacum) plant cultured on Murashige and Skoog medium containing IAA. Auxin-induced root formation was accompanied by significant changes in...

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Burtin D, Martin-Tanguy J, Paynot M, et al. Polyamines, hydroxycinnamoylputrescines, and root formation in leaf explants of tobacco cultivated in vitro: effects of the suicide inhibitors of putrescine synthesis. Plant Physiol. 1990;93(4):1398-404doi: 10.1104/pp.93.4.1398.
Burtin, D., Martin-Tanguy, J., Paynot, M., Carré, M., & Rossin, N. (1990). Polyamines, hydroxycinnamoylputrescines, and root formation in leaf explants of tobacco cultivated in vitro: effects of the suicide inhibitors of putrescine synthesis. Plant physiology, 93(4), 1398-404. https://doi.org/10.1104/pp.93.4.1398
Burtin, D, et al. "Polyamines, hydroxycinnamoylputrescines, and root formation in leaf explants of tobacco cultivated in vitro: effects of the suicide inhibitors of putrescine synthesis." Plant physiology vol. 93,4 (1990): 1398-404. doi: https://doi.org/10.1104/pp.93.4.1398
Burtin D, Martin-Tanguy J, Paynot M, Carré M, Rossin N. Polyamines, hydroxycinnamoylputrescines, and root formation in leaf explants of tobacco cultivated in vitro: effects of the suicide inhibitors of putrescine synthesis. Plant Physiol. 1990 Aug;93(4):1398-404. doi: 10.1104/pp.93.4.1398. PMID: 16667631; PMCID: PMC1062686.
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