Search Results - (Author, Cooperation:G. Salazar)
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1S. Sunagawa ; L. P. Coelho ; S. Chaffron ; J. R. Kultima ; K. Labadie ; G. Salazar ; B. Djahanschiri ; G. Zeller ; D. R. Mende ; A. Alberti ; F. M. Cornejo-Castillo ; P. I. Costea ; C. Cruaud ; F. d'Ovidio ; S. Engelen ; I. Ferrera ; J. M. Gasol ; L. Guidi ; F. Hildebrand ; F. Kokoszka ; C. Lepoivre ; G. Lima-Mendez ; J. Poulain ; B. T. Poulos ; M. Royo-Llonch ; H. Sarmento ; S. Vieira-Silva ; C. Dimier ; M. Picheral ; S. Searson ; S. Kandels-Lewis ; C. Bowler ; C. de Vargas ; G. Gorsky ; N. Grimsley ; P. Hingamp ; D. Iudicone ; O. Jaillon ; F. Not ; H. Ogata ; S. Pesant ; S. Speich ; L. Stemmann ; M. B. Sullivan ; J. Weissenbach ; P. Wincker ; E. Karsenti ; J. Raes ; S. G. Acinas ; P. Bork
American Association for the Advancement of Science (AAAS)
Published 2015Staff ViewPublication Date: 2015-05-23Publisher: American Association for the Advancement of Science (AAAS)Print ISSN: 0036-8075Electronic ISSN: 1095-9203Topics: BiologyChemistry and PharmacologyComputer ScienceMedicineNatural Sciences in GeneralPhysicsKeywords: Databases, Genetic ; Ecosystem ; Gastrointestinal Tract/microbiology ; Genetic Variation ; Humans ; Metagenome ; Microbiota/*genetics ; Oceans and Seas ; Plankton/*classification/genetics/isolation & purification ; Seawater/*microbiologyPublished by: -
2G. Lima-Mendez ; K. Faust ; N. Henry ; J. Decelle ; S. Colin ; F. Carcillo ; S. Chaffron ; J. C. Ignacio-Espinosa ; S. Roux ; F. Vincent ; L. Bittner ; Y. Darzi ; J. Wang ; S. Audic ; L. Berline ; G. Bontempi ; A. M. Cabello ; L. Coppola ; F. M. Cornejo-Castillo ; F. d'Ovidio ; L. De Meester ; I. Ferrera ; M. J. Garet-Delmas ; L. Guidi ; E. Lara ; S. Pesant ; M. Royo-Llonch ; G. Salazar ; P. Sanchez ; M. Sebastian ; C. Souffreau ; C. Dimier ; M. Picheral ; S. Searson ; S. Kandels-Lewis ; G. Gorsky ; F. Not ; H. Ogata ; S. Speich ; L. Stemmann ; J. Weissenbach ; P. Wincker ; S. G. Acinas ; S. Sunagawa ; P. Bork ; M. B. Sullivan ; E. Karsenti ; C. Bowler ; C. de Vargas ; J. Raes
American Association for the Advancement of Science (AAAS)
Published 2015Staff ViewPublication Date: 2015-05-23Publisher: American Association for the Advancement of Science (AAAS)Print ISSN: 0036-8075Electronic ISSN: 1095-9203Topics: BiologyChemistry and PharmacologyComputer ScienceMedicineNatural Sciences in GeneralPhysicsKeywords: Animals ; *Food Chain ; Host Specificity ; Oceans and Seas ; Phylogeny ; Plankton/*classification/*physiology ; Platyhelminths/classification/physiology ; Sunlight ; *Symbiosis ; Viruses/classificationPublished by: -
3Staff View
Publication Date: 2018-05-04Publisher: BMJ PublishingElectronic ISSN: 2044-6055Topics: MedicineKeywords: Open access, Cardiovascular medicinePublished by: -
4Phelps, R P ; Conterras Salazar, G ; Abe, V ; Argue, B J
Oxford, UK : Blackwell Publishing Ltd
Published 1995Staff ViewISSN: 1365-2109Source: Blackwell Publishing Journal Backfiles 1879-2005Topics: Agriculture, Forestry, Horticulture, Fishery, Domestic Science, NutritionType of Medium: Electronic ResourceURL: -
5Staff View
ISSN: 0022-328XSource: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002Topics: Chemistry and PharmacologyType of Medium: Electronic ResourceURL: -
6Cavalie-Barthez, G. ; Montcourrier, P. ; Chambon, M. ; Rogier, H. ; Capony, F. ; Garcie, M. ; Salazar, G. ; Rochefort, H.
Amsterdam : ElsevierStaff ViewISSN: 0022-4731Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002Topics: BiologyChemistry and PharmacologyType of Medium: Electronic ResourceURL: -
7Virsolvy-Vergine, A. ; Salazar, G. ; Sillard, R. ; Denoroy, L. ; Mutt, V. ; Bataille, D.
Springer
Published 1996Staff ViewISSN: 1432-0428Keywords: Endosulfine ; sulphonylurea ; receptor ; endogenous ligandSource: Springer Online Journal Archives 1860-2000Topics: MedicineNotes: Summary Anti-diabetic sulphonylureas act via high affinity binding sites coupled to K-ATP channels. Endosulfine, an endogenous ligand for these binding sites, was shown to exist in two molecular forms, α and Β, in both the pancreas and the central nervous system. We describe here the isolation, and partial structural characterization of α endosulfine derived from porcine brains by means of a series of chromatography runs and gel electrophoresis. Porcine α endosulfine is a protein with a molecular mass of 13,196 daltons as determined by mass spectrometry and which is N-terminally blocked. Tryptic digestion followed by separation of the fragments by HPLC and automated Edman degradation yielded a total of 72 amino acids in four partial sequences. Comparison of these sequences with that present in the National Biomedical Research Foundation protein data bank indicated a 82% identity with a 112-amino acid protein with a molecular mass of 12,353 daltons called ‘cyclic AMP-regulated phosphoprotein-19’, isolated from the bovine brain as a substrate for protein kinase A.Type of Medium: Electronic ResourceURL: -
8Frías-Espericueta, M. G. ; Osuna-López, J. I. ; Sandoval-Salazar, G. ; López-López, G.
Springer
Published 1999Staff ViewISSN: 1432-0800Source: Springer Online Journal Archives 1860-2000Topics: Energy, Environment Protection, Nuclear Power EngineeringMedicineType of Medium: Electronic ResourceURL: -
9Staff View
ISSN: 1573-7217Keywords: benign breast disease ; cathepsin D ; estrogen receptor ; fibrocystic disease ; fine needle aspirates ; lynestrenol ; progestin treatmentSource: Springer Online Journal Archives 1860-2000Topics: MedicineNotes: Summary We studied the effect of a progestin (lynestrenol) on estrogen receptors (ER) and cathepsin D (cath-D) levels immunochemically in successive fine needle aspirates of benign breast disease. Fibrocystic disease was the main pathology (43 out of 47 patients). Thirty-one patients were treated with 10 mg of lynestrenol daily from the fifth to the twenty-fifth day of the menstrual cycle for 1 to 3 months. Sixteen untreated patients were used as controls. Lynestrenol significantly decreased the percentage of ER stained cells. This is in agreement with the antiestrogenic effect of progestin and, for the first time, indicates thatin vivo progestin may decrease the stimulatory effect of estrogens on mammary cells by decreasing their estrogen receptor content. No effect of progestin on cath-D level was found throughout the whole population. However, this level varied more between aspirates of each patient in the treated group than in the control group, suggesting heterogeneity in patient responses to progestin. Since cath-D may have a role in carcinogenesis, clinical follow-up of these patients and more detailed studies are required to determine whether this progestin-challenge test has has any value for detecting high risk mastopathies and for predicting effectiveness of treatment.Type of Medium: Electronic ResourceURL: