References of "Pasleau, Françoise"
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See detailExpression transitoire du promoteur c-erbB2 dans les cellules épithéliales mammaires normales et tumorales en culture.
Grooteclaes, Madeleine; Pasleau, Françoise ULg; Dijkmans, Huguette et al

Conference (1992, February)

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See detailCloning and sequencing the upstream regulatory region of the c-erbB2 gene, an adenocarcinoma specific oncogene.
Dijkmans, H.; Pasleau, Françoise ULg; Gol-Winkler, R.

Conference (1991, September)

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See detailHalf-life of the c-erbB2 mRNA synthesized in human mammary adenocarcinoma cell lines.
Pasleau, Françoise ULg; Grooteclaes, M.; Gol-Winkler, R.

Poster (1991, June)

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See detailCloning and sequencing the upstream regulatory regions of the c-erbB2 gene.
Pasleau, Françoise ULg; Dijkmans, H.; Bertrand, B. et al

in Archives Internationales de Physiologie, de Biochimie et de Biophysique (1990), 98(B40),

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See detailLes oncogènes dans les cancers du sein.
Gol-Winkler, Rose; Pasleau, Françoise ULg; Dijkmans, Huguette

Conference (1990)

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See detailTowards the design and the synthesis of an artificial alpha/beta protein.
Goraj, K.; Gohimont, C.; Pasleau, Françoise ULg et al

Conference (1988, February)

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See detailExpression of a synthetic gene encoding human insulin-like growth factor I in cultured mouse fibroblasts.
Bayne, M. L.; Cascieri, M. A.; Kelder, B. et al

in Proceedings of the National Academy of Sciences of the United States of America (1987), 84

A synthetic gene encoding human insulin-like growth factor I (hIGF-I) was assembled and inserted into an expression vector containing the cytomegalovirus immediate early (CMV-IE) transcriptional ... [more ▼]

A synthetic gene encoding human insulin-like growth factor I (hIGF-I) was assembled and inserted into an expression vector containing the cytomegalovirus immediate early (CMV-IE) transcriptional regulatory region and portions of the bovine growth hormone gene. The recombinant plasmid encodes a 97 amino acid fusion protein containing the first 27 amino acids of the bovine growth hormone precursor and the 70 amino acids of hIGF-I. This plasmid, when transiently introduced into cultured mouse fibroblasts, directs synthesis of the fusion protein, subsequent proteolytic removal of the bovine growth hormone signal peptide, and secretion of hIGF-I into the culture medium. Conditioned medium from transfected cells inhibits binding of 125I-labeled IGF-I to type I IGF receptors on human placental membranes and to acid-stable human serum carrier proteins. The recombinant hIGF-I produced is biologically active, as monitored by the stimulation of DNA synthesis in vascular smooth muscle cells. [less ▲]

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See detailA comparison of bovine growth hormone expression directed by bGH genomic or intronless DNA in transiently transfected eukaryotic cells.
Pasleau, Françoise ULg; Leung, F. C.; Kopchick, J. J.

in Gene. (1987), 57

Two recombinant DNA plasmids were constructed with identical transcriptional and translational regulatory elements controlling expression of the bovine growth hormone (bGH) gene or the bGH gene lacking ... [more ▼]

Two recombinant DNA plasmids were constructed with identical transcriptional and translational regulatory elements controlling expression of the bovine growth hormone (bGH) gene or the bGH gene lacking introns. Transient expression of these plasmids in cultured eukaryotic cells, monitored by assaying secretion of bGH into the culture medium, was employed to examine the relative importance of introns in the expression of this gene. The bGH gene lacking introns is expressed more efficiently than the bGH gene in avian and mammalian cells. [less ▲]

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See detailLocation of transcriptional and regulatory sequences within the prolactin family genes
Belayew, A.; Bellefroid, Eric J.; Berwaer, M. et al

in Müller, E. E.; McLeod, R. M. (Eds.) Neuroendocrine Perspectives (1986)

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See detailLocalisation des séquences régulatrices de la transcription. Application aux gènes de la famille prolactine.
Belayew, A.; Bellefroid, Eric J.; Berwaer, M. et al

in Annales d'Endocrinologie (1986), 47

We are studying nucleotide sequences responsible for the regulation of eukaryotic gene expression. Our test system comprises the human genes coding for prolactin (hPRL), growth hormone (hGH-N) and ... [more ▼]

We are studying nucleotide sequences responsible for the regulation of eukaryotic gene expression. Our test system comprises the human genes coding for prolactin (hPRL), growth hormone (hGH-N) and placental lactogen (hCS-B). We have cloned these genes and are searching within their sequences for in vitro binding sites of the human glucocorticoid receptor on the hGH-N and hCS-B genes; the in vivo activity of such DNA sequences by assaying hybrid gene expression in transfected cells; in vivo "enhancer" activity of different hPRL gene fragments linked to a marker gene and transfected in cultured cells. [less ▲]

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See detailLocation of transcriptional regulatory sequences within the prolactin family genes.
Belayew, A.; Bellefroid, Eric J.; Berwaer, M. et al

in Neuroendocrine Perspectives. (1986)

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See detailExpression of the bovine growth hormone in cultured rodent cells.
Kopchick, J. J.; Pasleau, Françoise ULg; Leung, F. C.

in Basic Life Sciences (1986), 37

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See detailExpression of avian retroviral-bovine growth hormone recombinant DNA in rat GH3 cells.
Kopchick, John J.; Leung, Frederic C.; Pasleau, Françoise ULg

Conference (1985, June)

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