Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Karine Chantrel-Groussard"'
Autor:
Havouis R, François Gaboriau, Pierre Brissot, N. Pasdeloup, Jean-Louis Pierre, Hanspeter Nick, Gérard Lescoat, Karine Chantrel-Groussard
Publikováno v:
European Journal of Pharmacology. 541:129-137
By comparing the antiproliferative effect of the iron chelators ICL670A and O-trensox in the human hepatoma cell line HUH7 and human hepatocyte cultures, we have shown that ICL670A decreased cell viability, inhibited DNA replication and induced DNA f
Autor:
Alain Houlgatte, Karine Chantrel-Groussard, Pierre Teillac, S. Guimard, Philippe Berthon, R. Thuret, Alain Latil, Abdel-Rahmène Azzouzi, Olivier Cussenot, Jean-Marie Villette
Publikováno v:
British Journal of Cancer
We investigated whether genetic lesions such as loss of heterozygosity (LOH) are detected in prostatic cells obtained by prostatic massage during early diagnosis of prostate cancer (CaP) and discussed their clinical relevance. Blood and first urine v
Autor:
Nicole Pasdeloup, Karine Chantrel-Groussard, François Gaboriau, Pascal Loyer, Gérard Lescoat, Robert C. Hider, Pierre Brissot, Nafissa Rakba
Publikováno v:
Biochemical Pharmacology. 67:1479-1487
The present study analyzes the iron mobilization, the cytoprotective, and the antiproliferative effects of the lipophilic hydroxypyridinone CP411, in comparison with the hydrophilic chelator CP20 or deferiprone used in the treatment of iron overload.
Autor:
Karine Chantrel-Groussard, B. Guillonneau, Vincent Joulin, Guy Vallancien, Alain Latil, Pierre Validire, Olivier Cussenot, Gaëlle Fromont
Publikováno v:
Journal of Urology. 170:1394-1397
Loss of heterozygosity (LOH) is the most consistent genetic alteration in prostate cancer (CaP), frequently associated with advanced cancer and metastasis. We performed LOH analysis on 6 chromosomal regions of interest in localized CaP to obtain an o
Autor:
Karine Chantrel-Groussard, Serge Romana, Arnold Munnich, Agnès Rötig, Jean Weissenbach, Dominique Chretien, Gabor Gyapay, Sophie Lebon, Damien Sanlaville, Pascale de Lonlay, Claude Mugnier, Paule Bénit, Safa Saker, Pierre Rustin, Noman Kadhom
Publikováno v:
ResearcherID
The mapping and identification of respiratory chain deficiency genes is particularly tedious owing to the large number of genes encoding catalytic subunits and involved in respiratory chain (RC) assembly and maintenance. We have developed a functiona
Publikováno v:
Biochemical and Biophysical Research Communications. 281:804-809
Iron is required in all organisms for crucial functions, as a number of proteins need iron for activity. Mutations of the genes encoding proteins involved in iron uptake, transport, and utilization result in various human disorders or animal models w
Publikováno v:
DMW - Deutsche Medizinische Wochenschrift. 125:293-295
Autor:
Gaëlle Fromont, Philippe Berthon, Jyotirmoy Dey, Michael L. Cher, Rahmene Azzouzi, Alain Latil, Olivier Cussenot, Antoine Valeri, Karine Chantrel-Groussard, J. Edson Pontes, Wael Sakr
Publikováno v:
Urologic oncology. 23(2)
Loss of heterozygosity (LOH) is the most consistent genetic change in prostate cancer (CaP). We aimed, to correlate specific LOH and the overall LOH frequency, to disease progression after radical prostatectomy (RP) in high-grade CaP. Between January
Autor:
Michel Koenig, Karine Chantrel-Groussard, Agnès Rötig, Vanna Geromel, Hélène Puccio, Arnold Munnich, Pierre Rustin
Publikováno v:
ResearcherID
Friedreich's ataxia (FRDA) results from a generalized deficiency of mitochondrial iron-sulfur protein activity ascribed to mitochondrial iron overload. However, iron overload appears to be a late event in the disease. Here we show that neither supero
Publikováno v:
Comptes rendus de l’Académie des sciences. Série III, Sciences de la vie
Comptes rendus de l’Académie des sciences. Série III, Sciences de la vie, Elsevier, 2001, 324 (12), pp.1117-23
Comptes rendus de l’Académie des sciences. Série III, Sciences de la vie, Elsevier, 2001, 324 (12), pp.1117-23
International audience; Mammalian cytochrome c oxidase consists of thirteen subunits, ten encoded by the nuclear genome and three by the mitochondrial DNA. In several species, two isoforms have been isolated for nuclear-encoded subunits VIa, VIIa and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a7cdf9c9420d24a386f6b66090be8ab
https://hal.archives-ouvertes.fr/hal-00458870
https://hal.archives-ouvertes.fr/hal-00458870