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See detailp-[18F]MPPF, 5-HT1A antagonist: comparison to [3H]8-OH-DPAT with autoradiography
Plenevaux, Alain ULg; Weissmann, D.; Lemaire, Christian ULg et al

in Society for Neuroscience / Abstracts (1999)

p-MPPF 4-(2’-methoxyphenyl)-1-[2’-[N-(2’’-pyridinyl)-p-fluorobenzamido] ethyl]piperazine is the para-fluorobenzoyl analog of the highly selective 5-HT1A antagonist WAY-100635. The one step procedure used ... [more ▼]

p-MPPF 4-(2’-methoxyphenyl)-1-[2’-[N-(2’’-pyridinyl)-p-fluorobenzamido] ethyl]piperazine is the para-fluorobenzoyl analog of the highly selective 5-HT1A antagonist WAY-100635. The one step procedure used to label p-MPPF with fluorine-18 (cyclotron produced positron emitter of 110 min half-life) leads to a radiopharmaceutical compound easily prepared on a large scale. The preliminary evaluations conducted in rats and cats are good reason to consider p-[18F]MPPF as an interesting reversible radioligand to study the 5-HT1A receptor family in humans with positron emission tomography (PET). In this paper we report a careful comparison between p-[18F]MPPF and [3H]8-OH-DPAT with autoradiography and quantitative densitometry in the same animal. All experiments were conducted in Sprague Dawley male rats. For p-[18F]MMPF, the results were obtained ex-vivo after an intravenous injection of high specific activity radioligand (0.8-1.5 Ci/µmol) in vigil (no anesthesia), free moving and unstressed animals. For the purpose, permanent cannulation of the posterior vena cava were realized at least four days in advance. The [3H]8-OH-DPAT results were obtained in vitro on adjacent coronal sections to the one used for the p-[18F]MPPF autoradiography. Quantitative densitometry was employed to compare the values obtained in relevant brain structures (frontal cortex, lateral septum, hippocampus, dorsal raphe, entorhinal cortex and cerebellum). The plot of the p-[18F]MPPF values obtained for each structure against the [3H]8-OH-DPAT results displayed a significant linear correlation. These results demonstrate that from a qualitative as well as quantitative point of view, the binding of p-[18F]MPPF is totally comparable to the one of [3H]8-OH-DPAT. Supported by grants from INSERM/CGRI and FNRS Belgium. [less ▲]

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See detailp-[18F]MPPF, a fluoro analog of WAY-100635 for visualisation of 5-HT1A receptors in cat.
Le Bars, D.; Ginovart, N.; Hassoun, W. et al

in Journal of Labelled Compounds & Radiopharmaceuticals (1999), 42

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See detailLe p-[18F]MPPF: un nouveau ligand pour l'étude par TEP des récepteurs 5-HT1A
Ginovart, Nathalie; Le Bars, Didier; Lemaire, Christian ULg et al

Poster (1997, May 25)

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See detailP-doped titania xerogels as efficient UV-visible photocatalysts
Bodson, Céline ULg; Pirard, Sophie ULg; PIRARD, Arlette ULg et al

in Journal of Materials Science and Chemical Engineering (2014), 2

In the present study, sol-gel process is used to synthesize P-doped TiO2 xerogels by the cogelation method of a functionalized P alkoxide, (NH2-(CH2)2-NH-(CH2)2-P(O)-(OC2H5)2) with Ti(OC3H7)4 in either 2 ... [more ▼]

In the present study, sol-gel process is used to synthesize P-doped TiO2 xerogels by the cogelation method of a functionalized P alkoxide, (NH2-(CH2)2-NH-(CH2)2-P(O)-(OC2H5)2) with Ti(OC3H7)4 in either 2-methoxyethanol or isopropanol. The phosphorus-doping improved the thermal stability of titania and decreased the phase transformation of anatase into rutile. This modification by phosphorus shifted the absorption edge of titania to the visible region as proved by Diffuse reflectance measurements, and thus offers the possibility to produce visible light effective TiO2 photocatalyst. The excellent photocatalytic activity of P-doped TiO2 xerogels compared to pure TiO2 could be explained by its high surface area and small TiO2-anatase crystallite size. From these results, it was proved by using three different models that phosphorus intrinsically influences the photocatalytic activity. [less ▲]

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See detailp-mode Oscillations of alpha Cen A
Thoul, Anne ULg; Scuflaire, Richard ULg; Vatovez, B. et al

in Astrophysics & Space Science (2003), 284

Models of alpha Cen A & B have been computed using the masses determined by Pourbaix et al. (2002) and the data derived from the spectroscopic analysis of Neuforge and Magain (1997). The seismological ... [more ▼]

Models of alpha Cen A & B have been computed using the masses determined by Pourbaix et al. (2002) and the data derived from the spectroscopic analysis of Neuforge and Magain (1997). The seismological data obtained by Bouchy and Carrier (2001, 2002) do help improve our knowledge of the evolutionary status of the system. All the constraints are satisfied with a model which gives an age of about 6 Gyr for the binary. [less ▲]

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See detailP. Colon. Inv. 4781 verso: vente d'une esclave
Straus, Jean ULg

in Zeitschrift für Papyrologie und Epigraphik (1993), 98

Edition du contrat de vente d'une esclave. Papyrus grec d'Egypte. Ptolémaïs Euergétis, 3 décmebre 65

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See detailP. H. Liotta, the Graveyard of Fallen Monuments
Delville, Michel ULg

in Sentence: A Journal of Prose Poetics (2008), 7

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See detailLe P. Vindob. L 150 et les "glossaires" virgiliens
Rochette, Bruno ULg

in Chronique d'Egypte : Bulletin Périodique de la Fondation Egyptologique Reine Elisabeth (1989), 64(127-128), 231-234

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See detailLa P.E.B. expliquée
Delnoy, Michel ULg

in Delnoy, Michel; Hauglustaine, Jean-Marie; Levaux, Jean-Baptiste (Eds.) La P.E.B. expliquée (2009)

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See detailP.E.T.R.A.E. : une banque de données des inscriptions grecques et latines
Denooz, Joseph ULg

in Archéo-log (1988), 3

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See detailP.ParisBnF inv. Suppl. gr. 1385. Un nouveau papyrus homérique
Carlig, Nathan ULg

Scientific conference (2012, February 17)

Description, édition, identification et commentaire du P.ParisBnF inv. Suppl. gr. 1385 (inédit), conservé à la Bibliothèque nationale de France et contenant un passage de l'Iliade d'Homère, réunion avec ... [more ▼]

Description, édition, identification et commentaire du P.ParisBnF inv. Suppl. gr. 1385 (inédit), conservé à la Bibliothèque nationale de France et contenant un passage de l'Iliade d'Homère, réunion avec un autre fragment de papyrus provenant de la même entité bibliologique et présentation des outils de la papyrologie littéraire, notamment informatiques (Base de données Mertens-Pack³ et Leuven Database of Ancient Books). [less ▲]

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See detailP.Pintaudi 7. Wartetexte
Marganne, Marie-Hélène ULg

in Minutoli, Diletta (Ed.) Inediti offerti a Rosario Pintaudi per il suo 65° compleanno (P.Pintaudi) (2012)

Edition of the Greek papyrus P. Leodiensis inv. 1 (P.Pintaudi 7)

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See detailP1 incompatibility in pigeon breeders
Radermecker, Maurice ULg; Bruwier, M.; Bury, Jean et al

in Clinical Allergy (1980), 10

Pigeon breeders of the P2 blood phenotype may develop anti-P1 haemagglutinins as a consequence of natural immunization to pigeon dust. The half-life of labelled P1 erythrocytes was determined in two P2 ... [more ▼]

Pigeon breeders of the P2 blood phenotype may develop anti-P1 haemagglutinins as a consequence of natural immunization to pigeon dust. The half-life of labelled P1 erythrocytes was determined in two P2 pigeon breeders otherwise compatible except for the presence of anti-P1 antibodies and in four compatible controls without anti-P1. The half-life of tagged cells was within the normal range in one breeder but significantly reduced in the other, indicating that P1 incompatibility may occur in vivo. Since anti-P1 antibodies are found in about 20% of P2 pigeon breeders, it is suggested that this group may be prone to developing an incompatibility to transfused P1 red cells. [less ▲]

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See detailp21(WAF1) gene promoter is epigenetically silenced by CTIP2 and SUV39H1.
Cherrier, Thomas ULg; Suzanne, S.; Redel, L. et al

in Oncogene (2009), 28(38), 3380-9

Mainly regulated at the transcriptional level, the cellular cyclin-dependent kinase inhibitor, CDKN1A/p21(WAF1) (p21), is a major cell cycle regulator of the response to DNA damage, senescence and tumor ... [more ▼]

Mainly regulated at the transcriptional level, the cellular cyclin-dependent kinase inhibitor, CDKN1A/p21(WAF1) (p21), is a major cell cycle regulator of the response to DNA damage, senescence and tumor suppression. Here, we report that COUP-TF-interacting protein 2 (CTIP2), recruited to the p21 gene promoter, silenced p21 gene transcription through interactions with histone deacetylases and methyltransferases. Importantly, treatment with the specific SUV39H1 inhibitor, chaetocin, repressed histone H3 lysine 9 trimethylation at the p21 gene promoter, stimulated p21 gene expression and induced cell cycle arrest. In addition, CTIP2 and SUV39H1 were recruited to the silenced p21 gene promoter to cooperatively inhibit p21 gene transcription. Induction of p21(WAF1) gene upon human immunodeficiency virus 1 (HIV-1) infection benefits viral expression in macrophages. Here, we report that CTIP2 further abolishes Vpr-mediated stimulation of p21, thereby indirectly contributing to HIV-1 latency. Altogether, our results suggest that CTIP2 is a constitutive p21 gene suppressor that cooperates with SUV39H1 and histone methylation to silence the p21 gene transcription. [less ▲]

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