Search Results - "Poncin, J"

A novel gene overexpressed in the prostate of castrated rats: hormonal regulation, relationship to apoptosis and to acquired prostatic cell androgen independence by Bruyninx, M, Hennuy, B, Cornet, A, Houssa, P, Daukandt, M, Reiter, E, Poncin, J, Closset, J, Hennen, G

“…We have identified a novel complementary DNA (cDNA) corresponding to a gene overexpressed in the rat ventral prostate after castration. This cDNA displays…”
Get full text

On the distribution of silicic acid as a frontal zone tracer in the Indian sector of the Southern Ocean by Prego, R., Park, Y. H., Barciela, M. C., Morvan, J., Poncin, J., Tréguer, P.

“…The subantarctic frontal zone surveyed during the April-May 1991 SUZIL cruise in the Crozet-Kerguelen-Amsterdam area shows a strong horizontal (north to south)…”
Get full text

Confirmation and refinement of the genetic localization of the Coffin-Lowry syndrome locus in Xp22.1-p22.2 by BIANCALANA, V, BRIARD, M. L, GILBENKRANTZ, S, KAPLAN, J, MATHIEU, M, PIUSSAN, C, PONCIN, J, SCHINZEL, A, OUDET, C, HANAUER, A

“…The Coffin-Lowry syndrome (CLS) is an X-linked inherited disease of unknown pathogenesis characterized by severe mental retardation, typical facial and digital…”
Get full text

Prenatal diagnosis of cystic fibrosis using linked DNA probes by Schwartz, M, Super, M, Schmidtke, J, Buys, C, Farrall, M, Halley, D, Krawczak, M, Poncin, J E, Loukopoulos, D, Devoto, M

“…This paper presents data collected in Europe on 107 prenatal diagnoses of cystic fibrosis (CF) using linked DNA markers. To date, 38 children have been born…”
Get more information

Parental origin and germline mosaicism of deletions and duplications of the dystrophin gene : a European study by VAN ESSEN, A. J, ABBS, S, FERRARI, M, FERLINI, A, GALLUZZI, G, GRIMM, T, GRUBBEN, C, JEANPIERRE, M, KÄÄRIÄINEN, H, LIECHTI-GALLATI, S, MELIS, M. A, VAN OMMEN, G.-J. B, BAIGET, M, PONCIN, J. E, SCHEFFER, H, SCHWARTZ, M, SPEER, A, STUHRMANN, M, VERELLEN-DUMOULIN, C, WILCOX, D. E, TEN KATE, L. P, BAKKER, E, BOILEAU, C, VAN BROECKHOVEN, C, BUSHBY, K, CLARKE, A, CLAUSTRES, M, COVONE, A. E

“…Knowledge about the parental origin of new mutations and the occurrence of germline mosaicism is important for estimating recurrence risks in Duchenne (DMD)…”
Get full text

Prevalence of the delta F508 deletion of the cystic fibrosis gene in Belgian patients by Cochaux, P, van Geffel, R, Baran, D, Poncin, J, Vassart, G

“…A sample of 107 Belgian cystic fibrosis patients has been tested for the presence of the delta F508 deletion. We have shown that 166 (78%) of the CF…”
Get full text

Évaluation de la mesure rapide de la créatinine par le StatSensor (Nova Biomedical) by Cavalier, E., Poncin, J., Musso, G., Haleng, J.

“…Il existe un risque de développer une insuffisance rénale aiguë après injection d’un produit de contraste iodé, d’autant plus grand que le patient présente une…”
Get full text

Somatic MEN1 gene mutation does not contribute significantly to sporadic pituitary tumorigenesis by Poncin, J, Stevenaert, A, Beckers, A

“…Pituitary adenomas are a common manifestation of multiple endocrine neoplasia type 1 (MEN1) but most of them occur sporadically. There are only a few well…”
Get full text

The noncatalytic triad of α-amylases: A novel structural motif involved in conformational stability by Marx, Jean-Claude, Poncin, Johan, Simorre, Jean-Pierre, Ramteke, Pramod W., Feller, Georges

“…Chloride‐activated α‐amylases contain a noncatalytic triad, independent of the glycosidic active site, perfectly mimicking the catalytic triad of…”
Get full text

Geographic distribution and regional origin of 272 cystic fibrosis mutations in European populations by Estivill, Xavier, Bancells, Consol, Ramos, Cristina

“…The geographic distribution of 272 cystic fibrosis (CF) mutations has been studied by assessing the origin of 27,177 CF chromosomes from 29 European countries…”
Get full text

Linkage relationships and allelic associations of the cystic fibrosis locus and four marker loci by SCHMIDTKE, J, KRAWCZAK, M, FREY, D, FRYBURG, K, HALLEY, D, HUNDRIESER, J, LADANYI, L, LIBAERS, I, LISSENS, W, MÄCHLER, M, MALIK, N. J, MORREAU, J, SCHWARTZ, M, NEUBAUER, V, OOSTRA, B, PAPE, B, PONCIN, J. E, SCHINZEL, A, SIMON, P, TREFZ, F. K, TÜMMLER, B, VASSART, G, VOSS, R, ALKAN, M, BONDUELLE, M, BÜHLER, E, CHEMKE, M, DARNEDDE, T, DOMAGK, J, ENGEL, W

“…The linkage relationships between the cystic fibrosis (CF) locus and four marker loci (MET-H, MET-D, D7S8 and D7S16), allelic associations between these loci…”
Get full text

Cloning and structure analysis of the rat apolipoprotein A-I cDNA by PONCIN, J. E, MARTIAL, J. A, GIELEN, J. E

“…Apolipoprotein A-I, the major protein in mammalian high-density lipoprotein, acts as a cofactor for lecithin-cholesterol acyltransferase during the formation…”
Get full text

Mutation analysis of the MEN1 gene in Belgian patients with multiple endocrine neoplasia type 1 and related diseases by Poncin, Jacques, Abs, Roger, Velkeniers, Brigitte, Bonduelle, Maryse, Abramowicz, Marc, Legros, Jean-Jacques, Verloes, Alain, Meurisse, Michel, Van Gaal, Luc, Verellen, Christine, Koulischer, Lucien, Beckers, Albert

“…Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant disorder characterized by tumors in parathyroids, enteropancreatic endocrine tissues,…”
Get full text

Paternal Uniparental Disomy for Chromosome 1 Revealed by Molecular Analysis of a Patient with Pycnodysostosis by Gelb, Bruce D., Willner, Judith P., Dunn, Teresa M., Kardon, Nataline B., Verloes, Alain, Poncin, Jacques, Desnick, Robert J.

“…Molecular analysis of a patient affected by the autosomal recessive skeletal dysplasia, pycnodysostosis (cathepsin K deficiency; MIM 265800), revealed…”
Get full text

Characterization and reduction of interferences in flow-injection analysis for the in situ determination of nitrate and nitrite in sea water by Daniel, Anne, Birot, Dominique, Lehaitre, Michel, Poncin, Jacques

“…The aim of this work is to improve the precision and the sensitivity of nitrite and nitrate determination by flow-injection analysis (FIA) for an in situ…”
Get full text

APC mutations in human colorectal adenomas: analysis of the mutation cluster region with temperature gradient gel electrophoresis and clinicopathological features by Mulkens, Judith, Poncin, Jacques, Arends, Jan Willem, de Goeij, Anton F. P. M.

“…To date, the earliest mutations in colorectal adenomas have been found in the adenomatous polyposis coli (APC) gene, considered the ‘gatekeeper’ in…”
Get full text

Optimizing the APC gene mutation analysis in archival colorectal tumor tissue by Poncin, J, Mulkens, J, Arends, J W, de Goeij, A

“…Critical steps in the methodology of mutation analysis on routinely fixed, paraffin-embedded samples have been evaluated, including extraction and purification…”
Get more information

Luteinizing Hormone Increases the Abundance of Various Transcripts, Independently of the Androgens, in the Rat Prostate by Reiter, Eric, Poncin, Jacques, Hennuy, Benoit, Bruyninx, Marc, Klug, Marc, Cornet, Anne, Closset, Jean, Hennen, Georges

“…Differential display analysis was carried out to find, in the rat prostate, genes that could be regulated by Luteinizing Hormone (LH), independently of the…”
Get full text

China's Green Frenzy by Poncin, Jacques

Get full text

242 breakpoints in the 200-kb deletion-prone P20 region of the DMD gene are widely spread by Blonden, L A, Grootscholten, P M, den Dunnen, J T, Bakker, E, Abbs, S, Bobrow, M, Boehm, C, van Broeckhoven, C, Baumbach, L, Chamberlain, J

“…Using whole cosmids as probes, we have mapped 242 DMD/BMD deletion breakpoints located in the major deletion hot spot of the DMD gene. Of these, 113…”
Get more information