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Cerebellum ; 17(2): 173-190, 2018 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-29043563

RESUMEN

C57BL/6 mice exhibit spontaneous cerebellar malformations consisting of heterotopic neurons and glia in the molecular layer of the posterior vermis, indicative of neuronal migration defect during cerebellar development. Recognizing that many genetically engineered (GE) mouse lines are produced from C57BL/6 ES cells or backcrossed to this strain, we performed histological analyses and found that cerebellar heterotopia were a common feature present in the majority of GE lines on this background. Furthermore, we identify GE mouse lines that will be valuable in the study of cerebellar malformations including diverse driver, reporter, and optogenetic lines. Finally, we discuss the implications that these data have on the use of C57BL/6 mice and GE mice on this background in studies of cerebellar development or as models of disease.


Asunto(s)
Vermis Cerebeloso/anomalías , Ratones Transgénicos/fisiología , Malformaciones del Sistema Nervioso/genética , Malformaciones del Sistema Nervioso/patología , Animales , Animales Recién Nacidos , Vermis Cerebeloso/patología , Femenino , Hipoxantina Fosforribosiltransferasa/genética , Hipoxantina Fosforribosiltransferasa/metabolismo , Proteínas Luminiscentes/genética , Proteínas Luminiscentes/metabolismo , Masculino , Ratones , Ratones Endogámicos C57BL , Receptor TIE-2/genética , Receptor TIE-2/metabolismo , Receptores de LDL/genética , Receptores de LDL/metabolismo , Proteína 25 Asociada a Sinaptosomas/genética , Proteína 25 Asociada a Sinaptosomas/metabolismo
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