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IFNγ producing CD8.

Oncoimmunology

Buferne M, Chasson L, Grange M, Mas A, Arnoux F, Bertuzzi M, Naquet P, Leserman L, Schmitt-Verhulst AM, Auphan-Anezin N.
PMID: 25949872
Oncoimmunology. 2015 Mar 06;4(2):e974959. doi: 10.4161/2162402X.2014.974959. eCollection 2015 Feb.

Tumors with reduced expression of MHC class I (MHC-I) molecules may be unrecognized by tumor antigen-specific CD8

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Buferne M, Chasson L, Grange M, et al. IFNγ producing CD8. Oncoimmunology. 2015;4(2):e974959doi: 10.4161/2162402X.2014.974959.
Buferne, M., Chasson, L., Grange, M., Mas, A., Arnoux, F., Bertuzzi, M., Naquet, P., Leserman, L., Schmitt-Verhulst, A. M., & Auphan-Anezin, N. (2015). IFNγ producing CD8. Oncoimmunology, 4(2), e974959. https://doi.org/10.4161/2162402X.2014.974959
Buferne, Michel, et al. "IFNγ producing CD8." Oncoimmunology vol. 4,2 (2015): e974959. doi: https://doi.org/10.4161/2162402X.2014.974959
Buferne M, Chasson L, Grange M, Mas A, Arnoux F, Bertuzzi M, Naquet P, Leserman L, Schmitt-Verhulst AM, Auphan-Anezin N. IFNγ producing CD8. Oncoimmunology. 2015 Mar 06;4(2):e974959. doi: 10.4161/2162402X.2014.974959. eCollection 2015 Feb. PMID: 25949872; PMCID: PMC4404920.
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Carbo-quinoids: stability and reversible redox-proaromatic character towards carbo-benzenes.

Angewandte Chemie (International ed. in English)

Cocq K, Maraval V, Saffon-Merceron N, Saquet A, Poidevin C, Lepetit C, Chauvin R.
PMID: 25612252
Angew Chem Int Ed Engl. 2015 Feb 23;54(9):2703-6. doi: 10.1002/anie.201407889. Epub 2015 Jan 21.

The carbo-mer of the para-quinodimethane core is stable within in a bis(9-fluorenylidene) derivative. Oxidation of this carbo-quinoid with MnO2 in the presence of SnCl2 and ethanol affords the corresponding p-bis(9-ethoxy-fluoren-9-yl)-carbo-benzene. The latter can be in turn converted back into...

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Cocq K, Maraval V, Saffon-Merceron N, et al. Carbo-quinoids: stability and reversible redox-proaromatic character towards carbo-benzenes. Angew Chem Int Ed Engl. 2015;54(9):2703-6doi: 10.1002/anie.201407889.
Cocq, K., Maraval, V., Saffon-Merceron, N., Saquet, A., Poidevin, C., Lepetit, C., & Chauvin, R. (2015). Carbo-quinoids: stability and reversible redox-proaromatic character towards carbo-benzenes. Angewandte Chemie (International ed. in English), 54(9), 2703-6. https://doi.org/10.1002/anie.201407889
Cocq, Kévin, et al. "Carbo-quinoids: stability and reversible redox-proaromatic character towards carbo-benzenes." Angewandte Chemie (International ed. in English) vol. 54,9 (2015): 2703-6. doi: https://doi.org/10.1002/anie.201407889
Cocq K, Maraval V, Saffon-Merceron N, Saquet A, Poidevin C, Lepetit C, Chauvin R. Carbo-quinoids: stability and reversible redox-proaromatic character towards carbo-benzenes. Angew Chem Int Ed Engl. 2015 Feb 23;54(9):2703-6. doi: 10.1002/anie.201407889. Epub 2015 Jan 21. PMID: 25612252.
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Thyroid-stimulating hormone binding to cultured thyroid cells.

FEBS letters

Lissitzky S, Fayet G, Verrier B, Hennen G, Jaquet P.
PMID: 11946899
FEBS Lett. 1973 Jan 01;29(1):20-24. doi: 10.1016/0014-5793(73)80006-7.

No abstract available.

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Lissitzky S, Fayet G, Verrier B, et al. Thyroid-stimulating hormone binding to cultured thyroid cells. FEBS Lett. 1973;29(1):20-24doi: 10.1016/0014-5793(73)80006-7.
Lissitzky, S., Fayet, G., Verrier, B., Hennen, G., & Jaquet, P. (1973). Thyroid-stimulating hormone binding to cultured thyroid cells. FEBS letters, 29(1), 20-24. https://doi.org/10.1016/0014-5793(73)80006-7
Lissitzky, S, et al. "Thyroid-stimulating hormone binding to cultured thyroid cells." FEBS letters vol. 29,1 (1973): 20-24. doi: https://doi.org/10.1016/0014-5793(73)80006-7
Lissitzky S, Fayet G, Verrier B, Hennen G, Jaquet P. Thyroid-stimulating hormone binding to cultured thyroid cells. FEBS Lett. 1973 Jan 01;29(1):20-24. doi: 10.1016/0014-5793(73)80006-7. PMID: 11946899.
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Guidelines for reporting results of quality of life assessments in clinical trials.

Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation

Staquet M, Berzon R, Osoba D, Machin D.
PMID: 8973129
Qual Life Res. 1996 Oct;5(5):496-502. doi: 10.1007/BF00540022.

Clinical trials involving quality of life measurement published in the literature suffer from important weaknesses due to the lack of information on numerous topics. The psychometric properties of the instruments are often lacking as well as data on the...

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Staquet M, Berzon R, Osoba D, et al. Guidelines for reporting results of quality of life assessments in clinical trials. Qual Life Res. 1996;5(5):496-502doi: 10.1007/BF00540022.
Staquet, M., Berzon, R., Osoba, D., & Machin, D. (1996). Guidelines for reporting results of quality of life assessments in clinical trials. Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation, 5(5), 496-502. https://doi.org/10.1007/BF00540022
Staquet, M, et al. "Guidelines for reporting results of quality of life assessments in clinical trials." Quality of life research : an international journal of quality of life aspects of treatment, care and rehabilitation vol. 5,5 (1996): 496-502. doi: https://doi.org/10.1007/BF00540022
Staquet M, Berzon R, Osoba D, Machin D. Guidelines for reporting results of quality of life assessments in clinical trials. Qual Life Res. 1996 Oct;5(5):496-502. doi: 10.1007/BF00540022. PMID: 8973129.
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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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[Evolution of extreme prematurity in a "haut-normand" level-3 center: comparison between 1997 and 2000].

Archives de pediatrie : organe officiel de la Societe francaise de pediatrie

Adde-Michel C, Staquet P, Arsac M, Marret S.
PMID: 15596345
Arch Pediatr. 2004 Dec;11(12):1512-3. doi: 10.1016/j.arcped.2004.09.025.

No abstract available.

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Adde-Michel C, Staquet P, Arsac M, et al. Evolution de la grande prématurité dans un centre de niveau 3 haut-normand: comparaison 1997-2000. [Evolution of extreme prematurity in a "haut-normand" level-3 center: comparison between 1997 and 2000]. Arch Pediatr. 2004;11(12):1512-3doi: 10.1016/j.arcped.2004.09.025.
Adde-Michel, C., Staquet, P., Arsac, M., & Marret, S. (2004). Evolution de la grande prématurité dans un centre de niveau 3 haut-normand: comparaison 1997-2000. [Evolution of extreme prematurity in a "haut-normand" level-3 center: comparison between 1997 and 2000]. Archives de pediatrie : organe officiel de la Societe francaise de pediatrie, 11(12), 1512-3. https://doi.org/10.1016/j.arcped.2004.09.025
Adde-Michel, C, et al. "Evolution de la grande prématurité dans un centre de niveau 3 haut-normand: comparaison 1997-2000." [Evolution of extreme prematurity in a "haut-normand" level-3 center: comparison between 1997 and 2000]. Archives de pediatrie : organe officiel de la Societe francaise de pediatrie vol. 11,12 (2004): 1512-3. doi: https://doi.org/10.1016/j.arcped.2004.09.025
Adde-Michel C, Staquet P, Arsac M, Marret S. Evolution de la grande prématurité dans un centre de niveau 3 haut-normand: comparaison 1997-2000. [Evolution of extreme prematurity in a "haut-normand" level-3 center: comparison between 1997 and 2000]. Arch Pediatr. 2004 Dec;11(12):1512-3. doi: 10.1016/j.arcped.2004.09.025. French. PMID: 15596345.
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Bronchopulmonary and pressor effects of big-endothelin-1 in the guinea-pig.

Neurochemistry international

Pons F, Touvay C, Lagente V, Mencia-Huerta JM, Braquet P.
PMID: 20504729
Neurochem Int. 1991;18(4):481-3. doi: 10.1016/0197-0186(91)90143-2.

Injection of 1 nmol/kg Big-endothelin-1 (ET-1) into anaesthetized and ventilated guinea-pigs did not evoke significant changes in pulmonary inflation pressure and mean arterial blood pressure. In contrast, injection of 1 nmol/kg ET-1 induced marked and rapid bronchoconstrictor and pressor...

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Pons F, Touvay C, Lagente V, et al. Bronchopulmonary and pressor effects of big-endothelin-1 in the guinea-pig. Neurochem Int. 1991;18(4):481-3doi: 10.1016/0197-0186(91)90143-2.
Pons, F., Touvay, C., Lagente, V., Mencia-Huerta, J. M., & Braquet, P. (1991). Bronchopulmonary and pressor effects of big-endothelin-1 in the guinea-pig. Neurochemistry international, 18(4), 481-3. https://doi.org/10.1016/0197-0186(91)90143-2
Pons, F, et al. "Bronchopulmonary and pressor effects of big-endothelin-1 in the guinea-pig." Neurochemistry international vol. 18,4 (1991): 481-3. doi: https://doi.org/10.1016/0197-0186(91)90143-2
Pons F, Touvay C, Lagente V, Mencia-Huerta JM, Braquet P. Bronchopulmonary and pressor effects of big-endothelin-1 in the guinea-pig. Neurochem Int. 1991;18(4):481-3. doi: 10.1016/0197-0186(91)90143-2. PMID: 20504729.
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Ionization constants of ginkgolide B in aqueous solution.

Analytical chemistry

Zekri O, Boudeville P, Genay P, Perly B, Braquet P, Jouenne P, Burgot JL.
PMID: 21619206
Anal Chem. 1996 Aug 01;68(15):2598-604. doi: 10.1021/ac950939g.

The thermodynamic ionization constants (pK(a)(1), pK(a)(2), and pK(a)(3)) of ginkgolide B (9H-1,7a-(epoxymethano)-1H,6aH-cyclopenta[c]furo[2,3-b]furo-[3',2':3,4]cyclopenta[1,2-d]furan-5,9,12-(4H)-trione, 3-tert-butylhexahydro-4,7b,11-trihydroxy-8-methyl-) in aqueous solution have been settled by pH-metric and NMR studies. The three macroscopic pK(a) values as well as the water solubility and the water/n-octanol partition...

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Zekri O, Boudeville P, Genay P, et al. Ionization constants of ginkgolide B in aqueous solution. Anal Chem. 1996;68(15):2598-604doi: 10.1021/ac950939g.
Zekri, O., Boudeville, P., Genay, P., Perly, B., Braquet, P., Jouenne, P., & Burgot, J. L. (1996). Ionization constants of ginkgolide B in aqueous solution. Analytical chemistry, 68(15), 2598-604. https://doi.org/10.1021/ac950939g
Zekri, O, et al. "Ionization constants of ginkgolide B in aqueous solution." Analytical chemistry vol. 68,15 (1996): 2598-604. doi: https://doi.org/10.1021/ac950939g
Zekri O, Boudeville P, Genay P, Perly B, Braquet P, Jouenne P, Burgot JL. Ionization constants of ginkgolide B in aqueous solution. Anal Chem. 1996 Aug 01;68(15):2598-604. doi: 10.1021/ac950939g. PMID: 21619206.
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Assessment of procalcitonin to predict outcome in hypothermia-treated patients after cardiac arrest.

Critical care research and practice

Stammet P, Devaux Y, Azuaje F, Werer C, Lorang C, Gilson G, Max M.
PMID: 22110909
Crit Care Res Pract. 2011;2011:631062. doi: 10.1155/2011/631062. Epub 2011 Oct 26.

Objective. Determine the potential of procalcitonin (PCT) to predict neurological outcome after hypothermia treatment following cardiac arrest. Methods. Retrospective analysis of patient data over a 2-year period. Mortality and neurological outcome of survivors were determined 6 months after cardiac...

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Stammet P, Devaux Y, Azuaje F, et al. Assessment of procalcitonin to predict outcome in hypothermia-treated patients after cardiac arrest. Crit Care Res Pract. 2011;2011:631062doi: 10.1155/2011/631062.
Stammet, P., Devaux, Y., Azuaje, F., Werer, C., Lorang, C., Gilson, G., & Max, M. (2011). Assessment of procalcitonin to predict outcome in hypothermia-treated patients after cardiac arrest. Critical care research and practice, 2011631062. https://doi.org/10.1155/2011/631062
Stammet, Pascal, et al. "Assessment of procalcitonin to predict outcome in hypothermia-treated patients after cardiac arrest." Critical care research and practice vol. 2011 (2011): 631062. doi: https://doi.org/10.1155/2011/631062
Stammet P, Devaux Y, Azuaje F, Werer C, Lorang C, Gilson G, Max M. Assessment of procalcitonin to predict outcome in hypothermia-treated patients after cardiac arrest. Crit Care Res Pract. 2011;2011:631062. doi: 10.1155/2011/631062. Epub 2011 Oct 26. PMID: 22110909; PMCID: PMC3205599.
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Toxic Epidermal Necrolysis and Graft-versus-Host Reaction: Revisiting a Puzzling Similarity.

ISRN dermatology

Piérard GE, Hermanns-Lê T, Paquet P, Rousseau AF, Delvenne P, Piérard-Franchimont C.
PMID: 23862070
ISRN Dermatol. 2013 Jun 03;2013:651590. doi: 10.1155/2013/651590. Print 2013.

Drug-induced toxic epidermal necrolysis (TEN) and acute cutaneous graft-versus-host reaction (GVHR) under immunopreventive therapy share some histopathological resemblance. So far, there are no serum biomarkers and no immunohistochemical criteria distinguishing with confidence and specificity the skin lesions of TEN...

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Piérard GE, Hermanns-Lê T, Paquet P, et al. Toxic Epidermal Necrolysis and Graft-versus-Host Reaction: Revisiting a Puzzling Similarity. ISRN Dermatol. 2013;2013:651590doi: 10.1155/2013/651590.
Piérard, G. E., Hermanns-Lê, T., Paquet, P., Rousseau, A. F., Delvenne, P., & Piérard-Franchimont, C. (2013). Toxic Epidermal Necrolysis and Graft-versus-Host Reaction: Revisiting a Puzzling Similarity. ISRN dermatology, 2013651590. https://doi.org/10.1155/2013/651590
Piérard, G E, et al. "Toxic Epidermal Necrolysis and Graft-versus-Host Reaction: Revisiting a Puzzling Similarity." ISRN dermatology vol. 2013 (2013): 651590. doi: https://doi.org/10.1155/2013/651590
Piérard GE, Hermanns-Lê T, Paquet P, Rousseau AF, Delvenne P, Piérard-Franchimont C. Toxic Epidermal Necrolysis and Graft-versus-Host Reaction: Revisiting a Puzzling Similarity. ISRN Dermatol. 2013 Jun 03;2013:651590. doi: 10.1155/2013/651590. Print 2013. PMID: 23862070; PMCID: PMC3686138.
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Intense pulsed-light therapy for proliferative haemangiomas of infancy.

Case reports in dermatological medicine

Caucanas M, Paquet P, Henry F, Piérard-Franchimont C, Reginster MA, Piérard GE.
PMID: 23198171
Case Rep Dermatol Med. 2011;2011:253607. doi: 10.1155/2011/253607. Epub 2011 Dec 27.

Infantile haemangioma therapy has long been a wait-and-see policy. Since recent development of laser and light therapy, pulsed dye laser has been successfully used for treating superficial haemangiomas. Few studies have been published about treatment with intense pulsed light...

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Caucanas M, Paquet P, Henry F, et al. Intense pulsed-light therapy for proliferative haemangiomas of infancy. Case Rep Dermatol Med. 2011;2011:253607doi: 10.1155/2011/253607.
Caucanas, M., Paquet, P., Henry, F., Piérard-Franchimont, C., Reginster, M. A., & Piérard, G. E. (2011). Intense pulsed-light therapy for proliferative haemangiomas of infancy. Case reports in dermatological medicine, 2011253607. https://doi.org/10.1155/2011/253607
Caucanas, Marie, et al. "Intense pulsed-light therapy for proliferative haemangiomas of infancy." Case reports in dermatological medicine vol. 2011 (2011): 253607. doi: https://doi.org/10.1155/2011/253607
Caucanas M, Paquet P, Henry F, Piérard-Franchimont C, Reginster MA, Piérard GE. Intense pulsed-light therapy for proliferative haemangiomas of infancy. Case Rep Dermatol Med. 2011;2011:253607. doi: 10.1155/2011/253607. Epub 2011 Dec 27. PMID: 23198171; PMCID: PMC3505945.
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Cytotoxic activity against resistant human tumor-cell lines by 2 synthetic demethylpodophyllotoxin derivatives - a single stereoisomeric change prevents cell-death by apoptosis.

International journal of oncology

Morimoto H, Robin J, Broquet C, Menciahuerta J, Braquet P, Bonavida B.
PMID: 21573473
Int J Oncol. 1993 Dec;3(6):1061-6. doi: 10.3892/ijo.3.6.1061.

The podophyllotoxin derivative, etoposide, is currently being used in patients with variant malignant diseases. However, studies show resistance to etoposide develops, and thus new agents to overcome resistance are needed. The present study investigated the cytotoxic properties of two...

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Morimoto H, Robin J, Broquet C, et al. Cytotoxic activity against resistant human tumor-cell lines by 2 synthetic demethylpodophyllotoxin derivatives - a single stereoisomeric change prevents cell-death by apoptosis. Int J Oncol. 1993;3(6):1061-6doi: 10.3892/ijo.3.6.1061.
Morimoto, H., Robin, J., Broquet, C., Menciahuerta, J., Braquet, P., & Bonavida, B. (1993). Cytotoxic activity against resistant human tumor-cell lines by 2 synthetic demethylpodophyllotoxin derivatives - a single stereoisomeric change prevents cell-death by apoptosis. International journal of oncology, 3(6), 1061-6. https://doi.org/10.3892/ijo.3.6.1061
Morimoto, H, et al. "Cytotoxic activity against resistant human tumor-cell lines by 2 synthetic demethylpodophyllotoxin derivatives - a single stereoisomeric change prevents cell-death by apoptosis." International journal of oncology vol. 3,6 (1993): 1061-6. doi: https://doi.org/10.3892/ijo.3.6.1061
Morimoto H, Robin J, Broquet C, Menciahuerta J, Braquet P, Bonavida B. Cytotoxic activity against resistant human tumor-cell lines by 2 synthetic demethylpodophyllotoxin derivatives - a single stereoisomeric change prevents cell-death by apoptosis. Int J Oncol. 1993 Dec;3(6):1061-6. doi: 10.3892/ijo.3.6.1061. PMID: 21573473.
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Showing 1 to 12 of 121 entries