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1.
J Evol Biol ; 23(5): 966-76, 2010 May.
Artigo em Inglês | MEDLINE | ID: mdl-20298442

RESUMO

Sperm competition is important in species with reproductive strategies that involve multiple mating and prolonged sperm storage such as the simultaneously hermaphroditic land snail Cornu aspersum. Double mating trials in this species have revealed that mating order and courtship behaviour affect paternity success. We investigated the effect of behavioural and anatomical reproductive traits on paternity success from triple mating trials. Triple mating resulted in triple fertilization in 58% of the cases whereas zero paternity was observed in 16% of sperm donors. Third sperm donors achieved higher paternity followed by first and second sperm donors. Snails with a longer epiphallus, the spermatophore forming organ, sired more offspring regardless of their mating order. Genetic compatibility between sperm donor and recipient did not influence paternity success. The results of the present study identified mating order and epiphallus length, as traits affecting the outcome of sperm competition in this species.


Assuntos
Genitália Masculina/anatomia & histologia , Preferência de Acasalamento Animal/fisiologia , Comportamento Sexual Animal/fisiologia , Caramujos/fisiologia , Espermatozoides/fisiologia , Animais , Pesos e Medidas Corporais , Transtornos do Desenvolvimento Sexual , Fertilização/fisiologia , Grécia , Modelos Lineares , Masculino , Caramujos/anatomia & histologia
2.
J Dent Res ; 84(12): 1117-26, 2005 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-16304440

RESUMO

Dental enamel formation is a remarkable example of a biomineralization process. The exact mechanisms involved in this process remain partly obscure. Some of the genes encoding specific enamel proteins have been indicated as candidate genes for amelogenesis imperfecta. Mutational analyses within studied families have supported this hypothesis. Mutations in the amelogenin gene (AMELX) cause X-linked amelogenesis imperfecta, while mutations in the enamelin gene (ENAM) cause autosomal-inherited forms of amelogenesis imperfecta. Recent reports involve kallikrein-4 (KLK4), MMP-20, and DLX3 genes in the etiologies of some cases. This paper focuses mainly on the candidate genes involved in amelogenesis imperfecta and the proteins derived from them, and reviews current knowledge on their structure, localization within the tissue, and correlation with the various types of this disorder.


Assuntos
Amelogênese Imperfeita/genética , Proteínas do Esmalte Dentário/genética , Amelogenina , Proteínas de Homeodomínio/genética , Humanos , Calicreínas/genética , Metaloproteinase 20 da Matriz , Metaloproteinases da Matriz/genética , Mutação/genética , Fatores de Transcrição/genética
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