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1.
J Obstet Gynaecol ; 32(4): 387-92, 2012 May.
Artículo en Inglés | MEDLINE | ID: mdl-22519488

RESUMEN

Female genital cutting (FGC) is a harmful cultural practice that is perpetrated against women and children. Little is known about the extent of this custom among university students in northern Nigeria. Using self-administered questionnaires, we studied the prevalence and determinants of FGC among female university students in Kano, Nigeria (n =359). The prevalence of FGC was 12.1% (95% confidence interval =8.8-15.8%). Awareness and disapproval of FGC among the study population was very high (96% and 91%, respectively). In multivariate regression models, ethnicity and geographic origin were significant predictors of female circumcision. A comprehensive legal and educational framework and the support of civil society, governments and development partners is required to address this form of gender discrimination.


Asunto(s)
Circuncisión Femenina/estadística & datos numéricos , Conocimientos, Actitudes y Práctica en Salud , Adolescente , Adulto , Circuncisión Femenina/etnología , Cultura , Escolaridad , Femenino , Humanos , Masculino , Nigeria , Prevalencia , Estudiantes , Encuestas y Cuestionarios , Universidades , Adulto Joven
2.
J Antibiot (Tokyo) ; 46(9): 1414-20, 1993 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-8226319

RESUMEN

Aureobasidin A (AbA) is a novel cyclic depsipeptide antifungal antibiotic. The antifungal activity of AbA was studied in vitro and in vivo in comparison with clinically effective antifungal agents, amphotericin B and fluconazole. AbA was highly active in vitro against many pathogenic fungi, including Candida albicans, Cryptococcus neoformans, Blastomyces dermatitidis and Histoplasma capsulatum. The activity was superior to amphotericin B in most cases. AbA exhibited fungicidal action toward growing cultures of C. albicans. It was highly tolerated by mice and showed good efficacy in the treatment of murine systemic candidiasis when given orally or subcutaneously. AbA's fungicidal action in mice with candidiasis was more effective than fluconazole and amphotericin B.


Asunto(s)
Antifúngicos/farmacología , Depsipéptidos , Secuencia de Aminoácidos , Animales , Antifúngicos/química , Antifúngicos/uso terapéutico , Candidiasis/tratamiento farmacológico , Femenino , Riñón/microbiología , Ratones , Ratones Endogámicos ICR , Pruebas de Sensibilidad Microbiana , Datos de Secuencia Molecular , Péptidos Cíclicos/química , Péptidos Cíclicos/farmacología , Péptidos Cíclicos/uso terapéutico , Conformación Proteica
3.
J Antibiot (Tokyo) ; 44(9): 919-24, 1991 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-1938613

RESUMEN

Aureobasidins A to R were isolated from the fermentation broth of Aureobasidium pullulans R106. Aureobasidins are cyclic depsipeptide antibiotics with MW's ranging from 1.070 to 1,148. Aureobasidins showed high in vitro antifungal activity against Candida albicans.


Asunto(s)
Antifúngicos/aislamiento & purificación , Hongos Mitospóricos/química , Antifúngicos/farmacología , Candida albicans/efectos de los fármacos , Fenómenos Químicos , Química , Fermentación , Pruebas de Sensibilidad Microbiana
4.
Microbiol Immunol ; 33(7): 527-38, 1989.
Artículo en Inglés | MEDLINE | ID: mdl-2505023

RESUMEN

It was proved that three spore coat proteins of 48, 36, and 22 kDa (P48, P36, and P22) were the components of the outermost layer (OL) of Bacillus megaterium ATCC 12872 spore by analysis of the isolated OL. And it was indicated that these proteins were deposited not by disulfide bond, but by ionic and/or hydrophobic bonds on the spore. Among them, P36 and P22 were expected to be located on the very surface of the spore by immunological analysis. In the OL deficient mutant of B. megaterium ATCC 12872, MAE05, whose spore was lacking in these OL proteins and galactosamine-6-phosphate polymer, both P36 and P22 were present in the mother cell cytoplasm and deposited on the forespores, but they disappeared with the lysis of mother cells. An OL protein-releasing factor having proteolytic activity was detected in the culture supernatant at the late sporulating stage of both the wild-type and the mutant strains. But the factor could not act on the proteins of the mature spores and the forespores at t10 (tn indicates n hr after the end of exponential growth) of the wild-type strain. Moreover, P36 and P22 were found in the spores of a revertant of MAE05 which could form galactosamine-6-phosphate polymer, suggesting that this sugar polymer played the role in protecting the OL proteins against the protease-like substance after the deposition.


Asunto(s)
Bacillus megaterium/análisis , Proteínas de la Membrana Bacteriana Externa/análisis , Bacillus megaterium/genética , Proteínas de la Membrana Bacteriana Externa/aislamiento & purificación , Citoplasma/análisis , Electroforesis en Gel de Poliacrilamida , Immunoblotting , Inmunoglobulina G/inmunología , Peso Molecular , Mutación , Solubilidad , Sonicación , Esporas Bacterianas/análisis
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