Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Charles Belon"'
Autor:
Virginie Georget, Philippe Nirdé, Charles Belon, Béatrice Térouanne, René-Benoit Galifer, Charles Sultan
Publikováno v:
The Journal of Steroid Biochemistry and Molecular Biology. 66:35-43
To gain further information concerning the regulation by androgen of AR mRNA expression in cultured genital skin fibroblasts (GSF), we first developed a quantitative reverse transcription-competitive polymerase chain reaction (RT-PCR). This method us
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fd710d23fa542ec6fcc5140ac1170c17
https://doi.org/10.1016/s0960-0760(98)00006-5
https://doi.org/10.1016/s0960-0760(98)00006-5
Autor:
Jean-Marc A. Lobaccaro, Brigitte Ollagnon, Charles Sultan, Serge Lumbroso, Jean Pouget, Charles Belon, Christophe Vial, Geneviève Sassolas
Publikováno v:
Hormone Research. 47:23-29
We have performed a molecular analysis of the androgen receptor gene in two families with suspected Kennedy’s disease (spinal and bulbar muscular atrophy, SBMA) with the aim of making a firm diagnosis of the disease. The 2 patients studied were spo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5b2a801215e26995a0ed6e5495a06bc7
https://doi.org/10.1159/000185363
https://doi.org/10.1159/000185363
Publikováno v:
Clinical Endocrinology. 43:183-188
UNLABELLED The molecular basis for male pseudohermaphroditism produced by the 5 alpha-reductase deficiency is becoming increasingly understood. OBJECTIVE We have performed biochemical and molecular analyses of the 5 alpha-reductase type 2 gene in a T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcf244e15d6d54b598385bc0dee3dc51
https://doi.org/10.1111/j.1365-2265.1995.tb01913.x
https://doi.org/10.1111/j.1365-2265.1995.tb01913.x
Autor:
Serge Lumbroso, Jean-Louis Chaussain, Jean-Marc A. Lobaccaro, Dominique Martin, Charles Sultan, Charles Belon
Publikováno v:
Fertility and Sterility. 60:814-819
Objective To study the androgen receptor gene in a large kindred with complete androgen insensitivity syndrome and positive receptor-binding activity. Design Enzymatic amplification coupled with single strand conformation polymorphism and DNA sequenc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::32f6e183badfbba38175b56d47d3cc5d
https://doi.org/10.1016/s0015-0282(16)56281-5
https://doi.org/10.1016/s0015-0282(16)56281-5
Autor:
Charles Belon, Nicolas Poujol, Charles Sultan, Christel Boudon, Serge Lumbroso, Jean-Marc A. Lobaccaro
Publikováno v:
The Journal of Steroid Biochemistry and Molecular Biology. 46:519-530
The androgen receptor belongs to the family of steroid-thyroid hormone-retinoid nuclear receptors. It contains 3 major domains: a hormone-binding region, a DNA-binding region and an amino-terminal region. Cloning of the cDNA encoding the androgen rec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ad82915ce79c1cda9fcd1e0ea5853b8
https://doi.org/10.1016/0960-0760(93)90178-y
https://doi.org/10.1016/0960-0760(93)90178-y
Autor:
Catherine Chevalier, Jean-Marc A. Lobaccaro, Charles Sultan, Rita Medlej, Charles Belon, Jean-Paul Guthmann, René-Benoit Galifer, Paul Czernichow, Philippe Berta, Robert Dumas
Publikováno v:
Clinical Endocrinology. 38:197-201
Summary OBJECTIVE We explored the possibility of a genetic anomaly in the sex determining region of the Y chromosome, SRY gene, known to be equated to the testis determining region. PATIENTS Four patients with bilateral congenital anorchia, absence o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ab8b8dcf8db9bb1a8be2978df0a91ec8
https://doi.org/10.1111/j.1365-2265.1993.tb00993.x
https://doi.org/10.1111/j.1365-2265.1993.tb00993.x
Publikováno v:
Andrologie. 2:108-113
L’analyse moleculaire des syndromes d’insensibilite aux androgenes est aujourd’hui facilitee par l’utilisation d’outils de genetique moleculaire de plus en plus performants: polymorphismes de restriction, amplification enzymatique, polymorp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1ba26dccbda382efd61ccec2635eac8d
https://doi.org/10.1007/bf03034686
https://doi.org/10.1007/bf03034686
Autor:
G. Magnin, L. Larget-Piet, Charles Belon, R Moustarih, M. Vanderschueren, S. Bernasconi, J C Job, Jean-Edmond Toublanc, P. Lecomte, A Terraza, H. Chaabouni, D. Schoenberg, J M Lobaccaro, N. Bouccekine, M. Bost, Mongia Hachicha, Margherita Bozzola, P Rochiccioli, Ch. Sultan, Jean-Louis Chaussain, J M Limal, Michael B. Ranke, C. Burési, C. Moraine, J L Nivelon, G Malpuech, J Battin
Publikováno v:
Hormone Research. 37:54-59
In patients with androgen insensitivity syndrome (AIS), RFLP study of the androgen receptor gene made it possible to analyze whether deletions or mutations could be responsible for abnormalities in androgen responsiveness. We studied RFLPs of DNA fro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3ced64182bae60d66f5ee130a3e98883
https://doi.org/10.1159/000182282
https://doi.org/10.1159/000182282
Autor:
Patrick Garandeau, Jean-Marc A. Lobaccaro, Charles Belon, Serge Lumbroso, Serge Amram, Charles Sultan, Bruno Bachelard
Publikováno v:
European journal of endocrinology. 130(4)
Lumbroso S, Lobaccaro J-M, Belon C, Amram S, Bachelard B, Garandeau P, Sultan C. Molecular prenatal exclusion of familial partial androgen insensitivity (Reifenstein syndrome). Eur J Endocrinol 1994;130:327–32. ISSN 0804–4643 In a large family wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6394dd44d33f3a294fa3df5da8a0a07a
https://pubmed.ncbi.nlm.nih.gov/8162159
https://pubmed.ncbi.nlm.nih.gov/8162159
Autor:
Jean-Marc A. Lobaccaro, Georges Olewniczack, Jean-Claude Job, Françoise Carré‐Pigeon, Charles Sultan, Charles Belon, Jean-Louis Chaussain, Jean-Edmond Toublanc, Serge Lumbroso
Publikováno v:
Clinical endocrinology. 40(3)
Summary OBJECTIVE Partial androgen Insensitivity syndromes are the cause of genital ambiguity that is at times quite severe; there is, therefore, a high demand for prenatal diagnosis in families already afflicted with this syndrome. When the mutation
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f65c05192fc6e61715287a09dc71450
https://pubmed.ncbi.nlm.nih.gov/8187291
https://pubmed.ncbi.nlm.nih.gov/8187291