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C1 oxidative coupling via bromine activation and tandem catalytic condensation and neutralization over CaO/zeolite compositesII. Product distribution variation and full bromine confinement

Autor: I LORKOVIC, M NOY, W SCHENCK, C BELON, M WEISS, S SUN, J SHERMAN, E MCFARLAND, G STUCKY, P FORD

Publikováno v: Catalysis Today. 98:589-594

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d6ca2ddb54c64ed46be3653962fde401
https://doi.org/10.1016/s0920-5861(04)00579-6

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Molecular analysis of the androgen receptor gene in Kennedy's disease. Report of two families and review of the literature

Autor: S, Lumbroso, J M, Lobaccaro, C, Vial, G, Sassolas, B, Ollagnon, C, Belon, J, Pouget, C, Sultan

Publikováno v: Hormone research. 47(1)

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 spora

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::21d1829f912c74017fecb80eba2d9ae2
https://pubmed.ncbi.nlm.nih.gov/9010714

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[Genetics and endocrinology of male sex differentiation: application to molecular study of male pseudohermaphroditism]

Autor: C, Sultan, S, Lumbroso, N, Poujol, C, Boudon, V, Georget, B, Térouanne, C, Belon, J M, Lobaccaro

Publikováno v: Comptes rendus des seances de la Societe de biologie et de ses filiales. 189(5)

The various processes involved in sexual differentiation have been considerably clarified over the last few years through advances in biochemistry and molecular genetics. The cloning of the gene responsible for testicular determination SRY, of the an

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::07a8bb47154089d8e27ced1c72199f4d
https://pubmed.ncbi.nlm.nih.gov/8673622

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Molecular genetics of androgen insensitivity syndromes

Autor: J M, Lobaccaro, S, Lumbroso, N, Poujol, C, Belon, C, Sultan

Publikováno v: Cellular and molecular biology (Noisy-le-Grand, France). 40(3)

The androgen receptor belongs to the family of nuclear receptors and contains three functional domains: a carboxy-terminal hormone binding region, a central cystein rich DNA binding region and an amino-terminal region involved in the expression of an

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::f69f2566d5f291ec23e818a670dd7df5
https://pubmed.ncbi.nlm.nih.gov/7920176

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[Genes of the Y chromosome and Turner syndrome]

Autor: J M, Lobaccaro, S, Lumbroso, C, Belon, R, Medlej, P, Berta, C, Sultan

Publikováno v: Annales d'endocrinologie. 54(5)

Turner syndrome is a complex human phenotype most commonly seen in association with a 45,X karyotype and it has been proposed that the phenotype is the result of monosomy for genes common to the X and Y chromosomes. Detection of unrecognized Y derive

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::bea29c632dca63c9b2807fbf3e98f7c1
https://pubmed.ncbi.nlm.nih.gov/8085779

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[Sex ambiguity. Contribution of molecular genetics]

Autor: C, Sultan, J M, Lobaccaro, S, Lumbroso, C, Belon, C, Chevalier, A, Terraza, D, Sampaio, H, Mbazogo, R B, Galifer, R, Dumas

Publikováno v: Archives francaises de pediatrie. 50(1)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::1053ff4cea846aa651b89fa16c8e80a2
https://pubmed.ncbi.nlm.nih.gov/8507144

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[Familial form of partial androgen insensitivity (Reifenstein syndrome): arginine-histidine mutation in position 840 in the androgen receptor]

Autor: S, Lumbroso, J M, Lobaccaro, C, Belon, S, Amram, M, Rodier, J, Bringer, C, Sultan

Publikováno v: Comptes rendus des seances de la Societe de biologie et de ses filiales. 187(4)

In a large kindred with Reifenstein syndrome, we performed the molecular analysis of the androgen receptor gene. Since the biochemical characteristics of the androgen receptor, determined on the cultured genital skin fibroblasts, showed a drastic dec

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::2ffd0ca6a4dcbe22bb1f7660e1acc23f
https://pubmed.ncbi.nlm.nih.gov/8019921

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[Dysregulation of plasma 1,25(OH)2D in calcium restriction in hypercalciuric children]

Autor: C, Belon, R, Dumas, C, Tau, R, Sabatier, A, Bourdeau, M, Garabedian

Publikováno v: Archives francaises de pediatrie. 49(6)

The effect of calcium restriction on the plasma concentration of 1,25(OH)2D in normo- and hypercalciuric children remains unknown.We studied phosphate and calcium metabolism of 8 normocalciuric and 8 hypercalciuric children aged 4 to 16 years, under

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::fef045dcfc8a6131e5258f320f64818f
https://pubmed.ncbi.nlm.nih.gov/1449353

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[Physiopathology of androgen insensitivity syndromes. Contribution of molecular biology]

Autor: C, Sultan, J M, Lobaccaro, R, Defay, R, Medlej, R, Ktari, R, Moustarih, C, Belon, A, Terraza

Publikováno v: Annales d'endocrinologie. 52(6)

Molecular genetic study of androgen insensitivity syndrome is now easier by the development of powerful molecular tools. Complementary DNA of the androgen receptor gene has been recently cloned and sequenced. The development of cDNA probes gave the o

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::06f48f341ad8db22e5ac9fa6ae094c7b
https://pubmed.ncbi.nlm.nih.gov/1824494

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