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dc.contributor.authorHortas, ML
dc.contributor.authorCastilla Alcalá, José Antonio 
dc.contributor.authorGil, MT
dc.contributor.authorMolina, J
dc.contributor.authorGarrido, ML
dc.contributor.authorMorell, M
dc.contributor.authorRedondo, M
dc.date.accessioned2025-01-16T10:58:05Z
dc.date.available2025-01-16T10:58:05Z
dc.date.issued2000
dc.identifier.citationHortas ML, Castilla JA, Gil MT, Molina J, Garrido ML, Morell M, Redondo M. Decreased sperm function of patients with myotonic muscular dystrophy. Hum Reprod. 2000 Feb;15(2):445-8.es_ES
dc.identifier.otherPMID: 10655320
dc.identifier.urihttps://hdl.handle.net/10481/99397
dc.description.abstractMyotonic muscular dystrophy (MMD) is a genetic disease caused by a defective enzyme, myotoninkinase. Male patients with MMD are reported to have reduced fertility. The purpose of this work was to study sperm capacitation and acrosome reaction in the ejaculates of sterile males with MMD and of healthy males (control group). The expression of the specific D-mannose receptors was explored by microscopic examination and by flow cytometry analysis. In addition, the binding patterns of Pisum sativum (PSA) lectin to acrosome content and outer acrosomal membrane in the spermatazoa of each group were analysed. Both the capacitation and the acrosome reaction in the spermatozoa of the MMD group were deficient and these findings strongly suggest that these anomalies may account for the sterility of these patients.es_ES
dc.language.isoenges_ES
dc.publisherOxford University Presses_ES
dc.subjectacrosome reactiones_ES
dc.subjectdystrophyes_ES
dc.subjectd-mannosees_ES
dc.subjectspermatozoa es_ES
dc.titleDecreased sperm function of patients with myotonic muscular dystrophyes_ES
dc.typejournal articlees_ES
dc.rights.accessRightsopen accesses_ES
dc.identifier.doi10.1093/humrep/15.2.445
dc.type.hasVersionAMes_ES


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