Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Thierry Haag"'
Autor:
Ambrogio P. Londero, Diego Marchesoni, Lorenza Driul, Tiziana Grassi, Serena Bertozzi, A Calcagno, Thierry Haag, Hubert Manhes
Publikováno v:
Minimally Invasive Therapy & Allied Technologies. 22:97-103
We sought to study the advantages of laparoscopic conservative treatment and pelvic reproductive surgery in patients with ectopic pregnancy and predisposing factors of tuboperitoneal infertility.Patients who had undergone laparoscopic treatment for e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2c629ec0414ad4d2829375ef3562de0
https://doi.org/10.3109/13645706.2012.708346
https://doi.org/10.3109/13645706.2012.708346
Publikováno v:
Gynecologic and obstetric investigation. 37(3)
Thirty-one patients complaining of unexplained infertility for at least 36 months and diagnosed elsewhere were reassessed laparoscopically. After staining their pelvic peritoneum with concentrated methylene blue, they presented with extensive areas o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c044e23df6e7f1b8821cda6af751db45
https://pubmed.ncbi.nlm.nih.gov/8005551
https://pubmed.ncbi.nlm.nih.gov/8005551
Autor:
Anne Marie Moustier, Charles Hetru, Thierry Haag, Christine Kappler, Jules A. Hoffmann, Bang Luu
Publikováno v:
Tetrahedron. 44:1397-1408
We have synthesized a tritiated form of 2,22-dideoxyecdysone ((3H2-22,23)-3β,14α, 25-trihydroxy-5β-cholest-7-en-6-one) of high specific activity (2.2 TBq/mmol). We have examined the capacity of various endocrine (prothoracic glands, follicle cells
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1876a2f5a7acc6cdb0c39f5d523f0a2e
https://doi.org/10.1016/s0040-4020(01)85918-4
https://doi.org/10.1016/s0040-4020(01)85918-4
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 22:547-557
High specific activity tritiated 3β, 14α -dihydroxy-5β-cholest-7-en-6-one, has been prepared using a precursor which permits rapid and easy labelling. This compound is converted to ecdysone under in vitro conditions by insect prothoracic glands, a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::95f730eb04ef58ddbd732f3efa060c26
https://doi.org/10.1002/jlcr.2580220604
https://doi.org/10.1002/jlcr.2580220604
Publikováno v:
J. Chem. Soc., Perkin Trans. 1. :2353-2363
We describe here the first synthesis of 2, 22-dideoxyecdysone (3)(3β, 14α, 25-trihydroxy-5β-cholest-7en-6-one), a putative precursor in the biosynthesis of ecdysone (1). All the intermediates synthesized have a cis junction of the A/B rings (5β-H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c57cd79682cb7587f541e6985021c2ba
https://doi.org/10.1039/p19880002353
https://doi.org/10.1039/p19880002353
Publikováno v:
Helvetica Chimica Acta. 72:1809-1816
Tordanone, a Twice Bent Steroid Structure with Ring A/B β-cis(5β)- and Ring B/C α-cis(8α)-Fused The 3β, 14α, 25-trihydroxy-5β, 8α-cholestan-6-one ( = tordanone; 4) has been prepared by stereospecific hydrogenation of 3β, 14α, 25-trihydroxy-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91d1e0b83353a709c83223324c13f89e
https://doi.org/10.1002/hlca.19890720817
https://doi.org/10.1002/hlca.19890720817
Autor:
Bang Luu, Yoichi Nakatani, Christine Kappler, Thierry Haag, Charles Hetru, Bernard Rousseau, Marie-France Meister, J. P. Beaucourt
Publikováno v:
Insect Biochemistry. 17:291-301
We have synthesized a tritiated form of 2,14,22,25-tetradeoxyecdysone (5β-ketol) of high specific activity (115 Ci/mmol). We have examined the capacity of various tissues of Locusta migratoria to use this 5β-ketol, a putative precursor of ecdysone,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8be2eac669c1ade3237fb1f4e59e730f
https://doi.org/10.1016/0020-1790(87)90071-0
https://doi.org/10.1016/0020-1790(87)90071-0
Publikováno v:
ChemInform. 19
We describe here the first synthesis of 2, 22-dideoxyecdysone (3)(3β, 14α, 25-trihydroxy-5β-cholest-7en-6-one), a putative precursor in the biosynthesis of ecdysone (1). All the intermediates synthesized have a cis junction of the A/B rings (5β-H
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d5a42dc78e03f261470ed0cc36b7737
https://doi.org/10.1002/chin.198850269
https://doi.org/10.1002/chin.198850269