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See detailIDENTIFICATION OF PLACENTAL HUMAN GROWTH-HORMONE AS THE GROWTH HORMONE-V GENE-EXPRESSION PRODUCT
Frankenne, Francis ULg; Scippo, Marie-Louise ULg; Van Beeumen, Jos et al

in Journal Of Clinical Endocrinology And Metabolism (1990), 71(1), 15-18

Detailed reference viewed: 4 (1 ULg)
See detailIdentification of plasma growth hormone binding proteins (GHBPs) in cattle
Devolder, Anne; Renaville, Robert ULg; Massart, Serge et al

Poster (1992)

Detailed reference viewed: 6 (0 ULg)
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See detailIdentification of pollutant gases with a multisensorial arrange.
Negri, Martin; Reich, S.; Fernandez, D. et al

in Weimar, Udo (Ed.) proceedings of ISOEN 99 (1999)

Detailed reference viewed: 27 (7 ULg)
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See detailIdentification of Post-Transplant Anti-Alpha 5 (Iv) Collagen Alloantibodies in X-Linked Alport Syndrome
Dehan, Pierre ULg; Van den Heuvel, L. P.; Smeets, H. J. et al

in Nephrology Dialysis Transplantation (1996), 11(10), 1983-8

X-linked Alport syndrome (AS) is a heritable disorder which is associated with mutations in the type IV collagen alpha 5 (IV) chain gene (COL4A5) located on chromosome X. Following renal transplantation ... [more ▼]

X-linked Alport syndrome (AS) is a heritable disorder which is associated with mutations in the type IV collagen alpha 5 (IV) chain gene (COL4A5) located on chromosome X. Following renal transplantation, an average of 6% of male AS patients develop anti-GBM nephritis. We studied the specificity of the antibodies against type IV collagen in the serum of a patient with COL4A5 partial deletion. The specificity of these alloantibodies was determined against collagenase-digested GBM, as well as against recombinant non-collagenous (NC1) domains of the type IV collagen alpha 1(IV)-alpha 6(IV) chains expressed in escherichia coli. Immunoblotting and ELISA demonstrated that these antibodies bound specifically to the NC1 domain of alpha 5(IV) collagen. There was no binding to the NC1 domain of the other chains, including the Goodpasture antigen. Competitive ELISA confirmed the results obtained by ELISA and immunoblotting. This patient developed alloantibodies directed against antigens present in the grafted kidney, but absent from his Alport kidney. The pathogenesis of post-transplantation glomerulonephritis in the Alport patient studied is thus similar to that of Goodpasture syndrome, with the exception that the pathogenic antibodies are targeted to another alpha chain of type IV collagen. [less ▲]

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See detailIdentification of Potential Biomarkers of Human Peripheral Blood Mononuclear Cell intoxication by dioxins
Brenez, Cécile; Cellier, Nicolas; Gerkens, Pascal et al

in Organohalogen Compounds (2005), 67

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See detailIdentification of pregnancy-associated glycoprotein 1 (PAG-1) in zebu (Bos indicus) placenta
Melo de Sousa, Noelita ULg; Remy, Benoit; El Amiri, Bouchra et al

in Theriogenology (2001), 55(1), 327

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See detailIdentification of pregnancy-associated glycoproteins and alpha-fetoprotein in fallow deer (Dama dama) placenta
Bériot, Mathilde ULg; Tchimbou Njanjo, Aline Flora ULg; Barbato, Olimpia et al

in Acta Veterinaria Scandinavica (2014), 56(4), 1-11

Background: This paper describes the isolation and characterization of pregnancy-associated glycoproteins (PAG) from fetal cotyledonary tissue (FCT) and maternal caruncular tissue (MCT) collected from ... [more ▼]

Background: This paper describes the isolation and characterization of pregnancy-associated glycoproteins (PAG) from fetal cotyledonary tissue (FCT) and maternal caruncular tissue (MCT) collected from fallow deer (Dama dama) pregnant females. Proteins issued from FCT and MCT were submitted to affinity chromatographies by using Vicia villosa agarose (VVA) or anti-bovine PAG-2 (R#438) coupled to Sepharose 4B gel. Finally, they were characterized by SDSPAGE and N-terminal microsequencing. Results: Four distinct fallow deer PAG (fdPAG) sequences were identified and submitted to Swiss-Prot database. Comparison of fdPAG with PAG sequences identified in other ruminant species exhibited 64 to 83% identity. Additionally, alpha-fetoprotein was identified in fetal and maternal tissues. Conclusion: Our results demonstrate the efficacy of VVA and bovine PAG-2 affinity chromatographies for the isolation of PAG molecules expressed in deer placenta. This is the first report giving four specific amino acid sequences of PAG isolated from feto-maternal junction (FCT and MCT) in the Cervidae family. [less ▲]

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See detailIdentification of protein biomarkers associated with cardiac ischemia by a proteomic approach.
Fillet, Marianne ULg; Deroyer, Céline ULg; COBRAIVILLE, G. et al

in Biomarkers : biochemical indicators of exposure, response, and susceptibility to chemicals (2013), 18(7), 614-24

Angina is chest pain induced by ischemia of the heart muscle, generally due to obstruction or spasm of the coronary arteries. People that suffer from average to severe cases of angina have an increased ... [more ▼]

Angina is chest pain induced by ischemia of the heart muscle, generally due to obstruction or spasm of the coronary arteries. People that suffer from average to severe cases of angina have an increased percentage of death before the age of 55, usually around 60%. Therefore, prevention of major complications, optimizing diagnosis, prognosis and therapeutics are of primary importance. The main objective of this study was to uncover biomarkers by comparing serum protein profiles of patients suffering from stable or unstable angina and controls. We identified by non-targeted proteomic approach and confirmed by the means of independent techniques, the differential expression of several proteins indicating significantly increased vascular inflammation response, disturbance in the lipid metabolism and in atherogenic plaques stability. [less ▲]

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See detailIdentification of protein networks involved in the disease course of experimental autoimmune encephalomyelitis, an animal model of multiple sclerosis.
Vanheel, Annelies; Daniels, Ruth; Plaisance, Stephane et al

in PLoS ONE (2012), 7(4), 35544

A more detailed insight into disease mechanisms of multiple sclerosis (MS) is crucial for the development of new and more effective therapies. MS is a chronic inflammatory autoimmune disease of the ... [more ▼]

A more detailed insight into disease mechanisms of multiple sclerosis (MS) is crucial for the development of new and more effective therapies. MS is a chronic inflammatory autoimmune disease of the central nervous system. The aim of this study is to identify novel disease associated proteins involved in the development of inflammatory brain lesions, to help unravel underlying disease processes. Brainstem proteins were obtained from rats with MBP induced acute experimental autoimmune encephalomyelitis (EAE), a well characterized disease model of MS. Samples were collected at different time points: just before onset of symptoms, at the top of the disease and following recovery. To analyze changes in the brainstem proteome during the disease course, a quantitative proteomics study was performed using two-dimensional difference in-gel electrophoresis (2D-DIGE) followed by mass spectrometry. We identified 75 unique proteins in 92 spots with a significant abundance difference between the experimental groups. To find disease-related networks, these regulated proteins were mapped to existing biological networks by Ingenuity Pathway Analysis (IPA). The analysis revealed that 70% of these proteins have been described to take part in neurological disease. Furthermore, some focus networks were created by IPA. These networks suggest an integrated regulation of the identified proteins with the addition of some putative regulators. Post-synaptic density protein 95 (DLG4), a key player in neuronal signalling and calcium-activated potassium channel alpha 1 (KCNMA1), involved in neurotransmitter release, are 2 putative regulators connecting 64% of the identified proteins. Functional blocking of the KCNMA1 in macrophages was able to alter myelin phagocytosis, a disease mechanism highly involved in EAE and MS pathology. Quantitative analysis of differentially expressed brainstem proteins in an animal model of MS is a first step to identify disease-associated proteins and networks that warrant further research to study their actual contribution to disease pathology. [less ▲]

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See detailIdentification of Psf, the Polypyrimidine Tract-Binding Protein-Associated Splicing Factor, as a Developmentally Regulated Neuronal Protein
Chanas-Sacre, Grazyna; Mazy-Servais, Cécile; Wattiez, Ruddy et al

in Journal of Neuroscience Research (1999), 57(1), 62-73

The polypyrimidine tract-binding protein-associated splicing factor (PSF), which plays an essential role in mammalian spliceosomes, has been found to be expressed by differentiating neurons in developing ... [more ▼]

The polypyrimidine tract-binding protein-associated splicing factor (PSF), which plays an essential role in mammalian spliceosomes, has been found to be expressed by differentiating neurons in developing mouse brain. The sequence of a fragment of mouse PSF was found to be remarkably similar to that of human PSF. Both the expression of PSF mRNA in cortex and cerebellum and PSF immunoreactivity in all brain areas were high during embryonic and early postnatal life and almost disappeared in adult tissue, except in the hippocampus and olfactory bulb where various neuronal populations remained PSF-immunopositive. Double-labeling experiments with anti-PSF antibody and anti-neurofilaments or anti-glial fibrillary acidic protein antibodies on sections of cortex, hippocampus, and cerebellum indicate that PSF is expressed by differentiating neurons but not by astrocytic cells. In vitro, mouse PSF was found to be expressed by differentiating cortical and cerebellar neurons. Radial glia or astrocyte nuclei were not immunopositive; however, oligodendrocytes differentiating in vitro were found to express PSF. The restricted expression of PSF suggests that this splicing factor could be involved in the control of neuronal-specific splicing events occurring at particular stages of neuronal differentiation and maturation. [less ▲]

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See detailIdentification of Pythium species inducing common bean (Phaseolus vulgaris L.) root rot symptoms and development of backcrosses to improve the level of varietal resistance to this disease
Nzungize Rusagara, John ULg

Doctoral thesis (2012)

The common bean (Phaseolus vulgaris L.) is the most important food legume grown worldwide. It is a prioritary crop in various countries of East Africa and is grown mainly by small farmers for home ... [more ▼]

The common bean (Phaseolus vulgaris L.) is the most important food legume grown worldwide. It is a prioritary crop in various countries of East Africa and is grown mainly by small farmers for home consumption, the excess being sold in markets. Important yield losses of common bean induced by root rot diseases have been identified in several countries in East Africa including Rwanda. This is partly explained by the intensification of the cultivation of beans, the absence of rotations, the practice of continuous cultivation of this legume, and decline in soil fertility. Although bean root rot symptoms are caused by a number of soil borne pathogens depending on environmental conditions, Pythium spp. are the fungal pathogens most frequently associated with severe epidemics in eastern Africa. Studies on root rot have indicated that continuous cropping of beans, a common practice in eastern Africa, exacerbates the problem. This work was undertaken to improve the varietal resistance of common bean to limit the damages caused by Pythium in Rwanda. An analysis of the diversity of Pythium species associated with root rot was conducted through collect of samples of common bean plants throughout the country and through the characterization of the Pythium species causing root rot. The collected samples were used to isolate 96 typical Pythium colonies which were classified into 16 Pythium species according to their respective molecular sequences of the ribosomal ITS fragments. Molecular characterization using the ITS-DNA sequences was also carried out on samples isolated on infected beans roots. The study of the distribution of each species identified within the samples analyzed, revealed that Pythium vexans is the most widespread taxon in the different common bean producing areas in Rwanda. Pathogenicity tests of the 16 identified Pythium species were performed on a set of 10 common bean varieties. The results showed that all identified Pythium species were pathogenic to common bean: they all induce symptoms of root rot under controlled conditions. However, the common bean varieties used in this investigation showed differences in their reaction to inoculation with the 16 Pythium species. At the end of this work of the characterization of Pythium species isolated in Rwanda, a scheme for improving varietal resistance has been implemented. It is based on a backcross protocol assisted by molecular marker (PYAA 19800). Recurrent parents are composed of three common bean varieties traditionally grown in Rwanda while the two donor parents are a resistant variety of the Mesoamerican gene pool and a resistant variety of Andean pool. The progeny obtained after the backcrossing program was subjected to the pathogenicity trials by inoculating with a strain of Pythium ultimum in controlled conditions in order to verify the effectiveness of this improvement protocol. These trials have shown that in the offspring all the individuals showing the presence of the marker gene were also resistant to Pythium with very low levels of severity at the end of inoculation tests. [less ▲]

Detailed reference viewed: 111 (7 ULg)
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See detailIdentification of radial glial cells within the developing murine central nervous system using a new immunohistochemical marker
Misson, Jean-Paul ULg; Yamamoto, M.; Edwards, M. A. et al

in Neuroscience (1988)

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See detailIdentification of radial glial cells within the developing murine central nervous system:studies based upon a new immunohistochemical marker
Misson, Jean-Paul ULg; Edwards, Michael; Yamamoto, Miyuki et al

in Developmental Brain Research (1988), 44

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See detailIdentification of radial glial growth cones
Misson, Jean-Paul ULg; Evrard, P.; Gadisseux, J.-F. et al

in Neuroscience (1988)

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See detailIdentification of residues within human glycoprotein VI involved in the binding to collagen: evidence for the existence of distinct binding sites.
Lecut, Christelle ULg; Arocas, Veronique; Ulrichts, Hans et al

in Journal of Biological Chemistry (2004), 279(50), 52293-9

Glycoprotein VI (GPVI) has a crucial role in platelet responses to collagen. Still, little is known about its interaction with its ligands. In binding assays using soluble or cell-expressed human GPVI, we ... [more ▼]

Glycoprotein VI (GPVI) has a crucial role in platelet responses to collagen. Still, little is known about its interaction with its ligands. In binding assays using soluble or cell-expressed human GPVI, we observed that (i) collagen, and the GPVI-specific ligands collagen-related peptides (CRP) and convulxin, competed with one another for the binding to GPVI and (ii) monoclonal antibodies directed against the extracellular part of the human receptor displayed selective inhibitory properties on GPVI interaction with its ligands. Monoclonal antibody 9E18 strongly reduced the binding of GPVI to collagen/CRP, 3F8 inhibited its interaction with convulxin, whereas 9O12 prevented all three interactions. These observations suggest that ligand-binding sites are distinct, exhibiting specific features but at the same time also sharing some common residues participating in the recognition of these ligands. The epitope of 9O12 was mapped by phage display, along with molecular modeling of human GPVI, which allowed the identification of residues within GPVI potentially involved in ligand recognition. Site-directed mutagenesis revealed that valine 34 and leucine 36 are critical for GPVI interaction with collagen and CRP. The loop might thus be part of a collagen/CRP-binding site. [less ▲]

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See detailIdentification of responders to teriparatide therapy by procollagen Type I N-Propeptide (P1NP) using the least significant change approach
Eastell, R.; Chen, P.; Krege, J. H. et al

in Osteoporosis International (2005, March), 16(Suppl.3), 5

Detailed reference viewed: 11 (0 ULg)