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Peer Reviewed
See detailIsolation and purification of bovine immunoglobins : use of Sephacryl S-300 filtration avoids protein precipitation steps.
Collard, Alfred; Pivont, P.; Portetelle, Daniel ULg et al

in Annales de Recherches Vétérinaires = Annals of Veterinary Research (1984), 15

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See detailIsolation and Purification of Panarine, a Quaternary Alkaloid from a Venezuelian Curare
Quetin-Leclercq, Joëlle; Angenot, Luc ULg; Dupont, Léon et al

in Phytochemistry (1988), 27(12), 4002-4004

High Speed Counter Current Chromatography (HSCCC) has been used to isolate and purify two quaternary alkaloids from a sample of curare prepared by the Panare Indians of Estado Bolivar, Venezuela. One of ... [more ▼]

High Speed Counter Current Chromatography (HSCCC) has been used to isolate and purify two quaternary alkaloids from a sample of curare prepared by the Panare Indians of Estado Bolivar, Venezuela. One of the compounds is the known base Macusine B. The other one is a new but related base named panarine. Its structure has been established unequivocally by spectral and X-ray cristallographic analysis. [less ▲]

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See detailIsolation and Radioimmunoassay Formation of Equine Osteocalcin- Preliminary Results
Carstanjen, B; Sulon, J; Banga-Mboko, H et al

in Biotechnologie, Agronomie, Société et Environnement = Biotechnology, Agronomy, Society and Environment [=BASE] (2002), 6(1), 8-9

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See detailIsolation and radioimmunoassay of a bovine pregnancy specific protein.
Beckers, Jean-François ULg; Wouters-Ballman, P.; Ectors, F.

in Theriogenology (1988, January), 29(1), 219

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See detailIsolation and sequence analysis of the rat prolactin structural gene
Martial, Joseph ULg; Cooke, N. E.

in MacLeod, Robert; Scapagnini, Umberto (Eds.) Central and peripheral regulation of prolactin function (1980)

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See detailIsolation and sequencing of Myo-Inositol Phosphate Synthase cDNA from common bean (Phaseolus vulgaris L.)
Abid, Ghassen ULg; Baudoin, Jean-Pierre ULg; Jacquemin, Jean-Marie et al

Conference given outside the academic context (2009)

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See detailIsolation and structure of akagerine: a new type of indole alkaloid
Angenot, Luc ULg; Dideberg, Otto; Dupont, Léon

in Tetrahedron Letters (1975), (16), 1357-1358

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See detailIsolation and structure of sungucine, a new type of bisindoline alkaloid
Lamotte, Josette ULg; Dupont, Léon; Dideberg, Otto et al

in Tetrahedron Letters (1979), (43), 4227-4228

From the roots of Strychnos icaja BAILLON, an unsymmetrical dimeric alkaloid has been isolated and called sungucine. Its original structure has been established by X-Ray diffraction; UV,IR,MS and NMR data ... [more ▼]

From the roots of Strychnos icaja BAILLON, an unsymmetrical dimeric alkaloid has been isolated and called sungucine. Its original structure has been established by X-Ray diffraction; UV,IR,MS and NMR data are also given. [less ▲]

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See detailIsolation and use of a porcine FSH to improve the quality of superovulation in cattle.
Beckers, Jean-François ULg

in Theriogenology (1987, January), 27(1), 213

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See detailIsolation from a multigene family of the active human gene of the metastasis-associated multifunctional protein 37LRP/p40 at chromosome 3p21.3.
Jackers, Pascale ULg; Minoletti, Fabiola; Belotti, Dorina et al

in Oncogene (1996), 13(3), 495-503

The 37 kD precursor of the 67 kD laminin receptor (37LRP) is a polypeptide whose expression is consistently upregulated in aggressive carcinoma. Interestingly, the 37LRP appears to be a multifunctional ... [more ▼]

The 37 kD precursor of the 67 kD laminin receptor (37LRP) is a polypeptide whose expression is consistently upregulated in aggressive carcinoma. Interestingly, the 37LRP appears to be a multifunctional protein involved in the translational machinery and has also been identified as p40 ribosome-associated protein. Although highly conserved cDNAs corresponding to this polypeptide have been isolated from several species including vertebrates, invertebrates, plants and prokaryotes, characterization of any of the corresponding active genes has never been reported. In this study, we have cloned an intron-containing fragment which permitted us to isolate the active 37LRP/p40 human gene. This gene contains seven exons and six introns. Ribonuclease protection experiments suggest multiple transcription start sites. The promoter area does not bear a TATA box but contains four Sp1 sites. The first intron is also GC rich containing five Sp1 sites. Intron 4 contains the full sequence of the small nuclear RNA E2 and two Alu sequences are found in intron 3. Fluorescent in situ hybridization localized the 37LRP/p40 active gene on chromosome 3 in the locus 3p21.3 which, interestingly, is a hot spot for genetic alterations in several cancers and particularly in small cell lung carcinoma. [less ▲]

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See detailIsolation in an ovine pregnancy specific protein
Zoli, AP; Beckers, Jean-François ULg; Ectors, F

in Theriogenology (1990), 33(1), 366

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See detailIsolation of a bovine chorionic gonadotrophin (bCG)
Beckers, Jean-François ULg; Dewulf, M.; Verstegen, J. et al

in Theriogenology (1988, January), 29(1), 218

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See detailIsolation of a glycoprotein E-deleted bovine herpesvirus type 1 strain in the field
Dispas, M.; Schynts, F.; Lemaire, Mylène et al

in Veterinary Record : Journal of the British Veterinary Association (2003), 153(7), 209-212

During a field trial to evaluate the efficacy of repeated vaccinations with bovine herpesvirus type 1 (BHV-1) marker vaccines, a glycoprotein E (gE)-negative BHV-1 strain was isolated from the nasal ... [more ▼]

During a field trial to evaluate the efficacy of repeated vaccinations with bovine herpesvirus type 1 (BHV-1) marker vaccines, a glycoprotein E (gE)-negative BHV-1 strain was isolated from the nasal secretions of two cows, eight months after vaccination with a gE-negative live-attenuated vaccine, initially given intranasally, then intramuscularly. The strain isolated was characterised using immunofluorescence, restriction analysis and PCR. All the techniques used identified the isolated virus as a gE-negative BHV-1 phenotypically and genotypically identical to the Za strain used as a control. [less ▲]

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See detailIsolation of a Microsporum canis gene family encoding three subtilisin-like proteases expressed in vivo
Descamps, Frédéric; Brouta, Frédéric; Monod, Michel et al

in Journal of Investigative Dermatology (2002), 119(4), 830-835

Microsporum canis is the main agent of dermatophytosis in dogs and cats and is responsible for frequent zoonosis. The pathogenesis of the disease remains largely unknown, however. Among potential fungal ... [more ▼]

Microsporum canis is the main agent of dermatophytosis in dogs and cats and is responsible for frequent zoonosis. The pathogenesis of the disease remains largely unknown, however. Among potential fungal virulence factors are secreted keratinolytic proteases, whose molecular characterization would be an important step towards the understanding of dermatophytic infection pathogenesis. M. canis secretes a 31.5 kDa keratinolytic subtilisin-like protease as the major component in a culture medium containing cat keratin as the sole nitrogen source. Using a probe corresponding to a gene's internal fragment, which was obtained by polymerase chain reaction, the entire gene encoding this protease named SUB3 was cloned from a M. canis lambdaEMBL3 genomic library. Two closely related genes, termed SUB1 and SUB2, were also cloned from the library using as a probe the gene coding for Aspergillus fumigatus 33 kDa alkaline protease (ALP). Deduced amino acid sequence analysis revealed that SUB1, SUB2, and SUB3 are secreted proteases and show large regions of identity between themselves and with subtilisin-like proteases of other filamentous fungi. Interestingly, mRNA of SUB1, SUB2, and SUBS were detected by reverse transcriptase nested-polymerase chain reaction from hair of experimentally infected guinea pigs. These results show that SUB1, SUB2, and SUB3 encode a family of subtilisin-like proteases and strongly suggest that these proteases are produced by M. canis during the invasion of keratinized structures. This is the first report describing the isolation of a gene family encoding potential virulence-related factors in dermatophytes. [less ▲]

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See detailIsolation of an amylolytic chrysophyte, Poterioochromonas sp. from the digestive tract of the termite R. santonensis
Tarayre, Cédric ULg; Bauwens, Julien ULg; Brasseur, Catherine ULg et al

in Biotechnologie, Agronomie, Société et Environnement = Biotechnology, Agronomy, Society and Environment [=BASE] (2014), 18(1),

The aim of this work was the isolation and cultivation of amylolytic protists living in the digestive tract of the termite Reticulitermes santonensis (Feytaud). A chrysophyte identified as ... [more ▼]

The aim of this work was the isolation and cultivation of amylolytic protists living in the digestive tract of the termite Reticulitermes santonensis (Feytaud). A chrysophyte identified as Poterioochromonas sp. was isolated in a special medium containing rice grains as a source of carbon and nitrogen. Then, the protist was grown in a medium containing starch as a carbon source, tryptone, and a phosphate buffer at different pH values (5, 6 and 7). Yeast extract was added or not. Ciprofloxacin was used to avoid the bacterial development. Other antibiotics were also tested but showed an inhibitive effect on the growth of Poterioochromonas sp. Yeast extract allowed reaching 1.9 (pH 5), 2.3 (pH 6) and 2.2 (pH 7) times higher final cell concentrations, and 2.8 (pH 5), 2.8 (pH 6) and 2.2 (pH 7) times higher biomass yields. The starch concentration did not decrease in the medium until 3 and 4 days of culture, with and without yeast extract, respectively. Eight days of culture were necessary for hydrolyzing the starch completely, with and without yeast extract. Maltose and maltotriose were detected in the culture media and were hydrolyzed progressively. Maximal maltose concentrations were 0.68, 0.66 and 0.51 g.l-1 in the medium containing yeast extract. Maltotriose concentrations were only 0.17, 0.14 and 0.12 g.l-1. Other glucose oligomers were also detected but in lower quantities. It was determined that the protist developed a weak amylase activity, particularly at a weakly acidic pH (5-6). Such a pH also allowed a better growth of the protist. A maximal amylase activity of 112 nkat.l-1 was measured with yeast extract at pH 5. No other enzymatic activity (protease, cellulase or xylanase) was detected except amylase. The degradation products of starch which were obtained by enzymatic hydrolysis allow the identification of α-amylase, amyloglucosidase and possibly β-amylase activities. [less ▲]

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See detailIsolation of an n-alkylated benzylamine derivative from Pseudomonas putida BTP1 as elicitor of induced systemic resistance in bean
Ongena, MARC ULg; Jourdan, Emmanuel ULg; Schafer, M. et al

in Molecular Plant-Microbe Interactions (2005), 18(6), 562-569

Root treatment of Phaseolus vulgaris with the nonpathogenic Pseudomonas putida BTP1 led to significant reduction of the disease caused by the pathogen Botrytis cinerea on leaves. The molecular determinant ... [more ▼]

Root treatment of Phaseolus vulgaris with the nonpathogenic Pseudomonas putida BTP1 led to significant reduction of the disease caused by the pathogen Botrytis cinerea on leaves. The molecular determinant of P putida BTP1 mainly responsible for the induced systemic resistance (ISR) was isolated from cell-free culture fluid after growth of the strain in the iron-poor casamino acid medium. Mass spectrometry analyses performed on both the bacterial product and synthetic analogues revealed a polyalkylated benzylamine structure, with the quaternary ammonium substituted by methyl, ethyl, and C-13 aliphatic groups responsible for the relative hydrophobicity of the molecule. The specific involvement of the N-alkylated benzylamine derivative (NABD) in ISR elicitation was first evidenced by testing the purified compound that mimicked the protective effect afforded by crude supernatant samples. The evidence was supported by the loss of elicitor activity of mutants impaired in NABD biosynthesis. Our experiments also showed that other iron-regulated metabolites secreted by the strain are not involved in ISR stimulation. Thus, these results indicate a wider variety of Pseudomonas determinants for ISR than reported to date. [less ▲]

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See detailIsolation of bacteriocin-producing lactic acid bacteria from fermented fish product in Senegal.
Dortu, C.; Roblain, D.; Totte, A. et al

Poster (2003, May)

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See detailIsolation of bacteriocin-producing lactic acid bacteria from fermented fish product in Senegal.
Dortu, C.; Roblain, D.; Totte, A. et al

Poster (2003, August)

Detailed reference viewed: 1 (0 ULg)