958 resultados para Morus nigra


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本文报道了一只实验室出生的,成年维性苏拉维西猴的肝细胞癌的病理解剖学和病理组织学变化,同时还讨论了自发性糖尿病和D型逆转录病毒与肝细胞癌的关系。

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2004

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Experiments that demonstrated a role for the substantia nigra in eye movements have played an important role in our understanding of the function of the basal ganglia in behavior more broadly. In this review we explore more recent experiments that extend the role of the substantia nigra pars reticulata from a simple gate for eye movements to include a role in cognitive processes for eye movements. We review recent evidence suggesting that basal ganglia nuclei beyond the substantia nigra may also play a role in eye movements and the cognitive events leading up to the production of eye movements. We close by pointing out some unresolved questions in our understanding of the relationship of basal ganglia nuclei and eye movements.

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Confirmation de la présence do Lonicero-Pinetum thalictretosum, climacique dans les Pyrénées aragonaises sur substrats calcaires. Il s’y développe, á l’étage supraméditerranéen, dans des conditions climatiques méditerranéo-continentales mais relativement xérothermiques.

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Contient : 1 Ordonnance faite par CHARLES [V], « aisné filz du roy de France et son lieutenant », en conformité des conseils donnés par l'assemblée des trois états du royaume, pour la suppression de divers abus et l'établissement de plusieurs réglements. Paris, mars 1356 ; 2 Traité de Brétigny, entre le roi de France et le roi d'Angleterre. 8 mai 1460 ; 3 Traité entre François Ier et Henri VIII, roi d'Angleterre, renouvelant et confirmant ceux qui avaient été conclus entre ledit Henri et Louis XII. Londres, 5 avril 1514 ; 4 Traité pour le mariage de Louis XII avec Marie d'Angleterre, conclu à Londres, le 14 septembre 1514 ; 5 Traité conclu entre les ambassadeurs de François Ier et ceux d'Henri VIII, roi d'Angleterre, au sujet du mariage de la princesse Marie d'Angleterre avec le dauphin. Londres, 4 octobre 1518 ; 6 Traité conclu par les mêmes pour la reddition par Henri VIII à François Ier des villes de Tournay, Saint-Amand, Mortagne, etc. Londres, 4 octobre 1518 ; 7 Traité de paix et d'alliance conclu entre la France et l'Angleterre. Londres, 2 octobre 1518 ; 8 Ratification par la régente LOUISE DE SAVOIE, du traité conclu, le 30 août précédent, par ses ambassadeurs auprès d'Henri VIII, roi d'Angleterre, qui se sont engagés à payer une somme de 2 millions de couronnes d'or. Lyon, 26 septembre 1525 ; 9 Ratification par LOUISE DE SAVOIE d'un autre traité conclu par ses ambassadeurs auprès d'Henri VIII, le 30 août précédent, pour la répression des pirateries et des pillages et la réparation des dommages subis par les sujets anglais et français. Lyon, 26 septembre 1525 ; 10 Traité conclu entre François Ier, roi de France, et Henri VIII, roi d'Angleterre. « Campaigne, ez confins d'Ardres et Guynez ». 7 juin 1546 ; 11 Traité conclu en exécution du traité précédent, pour la détermination des limites des comtés de Boulogne et de Guines. Londres, 11 mars 1547 (n. s.) ; 12 Renouvellement avec Edouard VI du traité de paix et alliance conclu par François Ier avec Henri VIII, le 7 juin 1546. Londres, 11 mars 1547 (n. s.) ; 13 « Sommaire instruction pour le faict d'Angleterre. Il est deu au roy d'Angleterre, à cause du traicté de l'an VC. XXV... » ; 14 Varia ; Notes sur les traités de 1518 et 1532, par lesquels « est faicte ligue deffensive entre le roy « de France » et le roy d'Angleterre » ; « Estat abbregé du faict d'Angleterre. Et premièrement pour les deux millions de coronnes. Par le traicté de la paix... faicte à More, en aoust mil cinq cens vingtcinq... » ; Commission donnée par FRANÇOIS Ier au cardinal Du Bellay, à Pierre Remon, seigneur de Courcelles, et à Claude de Laubespine, pour traiter de la paix avec les ambassadeurs du roi d'Angleterre. « Courtignon », 30 août 1544 ; 15 Historia Eduardi IV et Richardi III, regum Angliae, « Thoma Moro authore ». Premiers mots : « Eduardus rex, ejus nominis quartus, actis vite annis quinquaginta tribus, mensibus septem, diebus sex... » ; derniers mots : « ... Qui nepoti ejus coronando fuerat destinatus »

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Many connections in the basal ganglia are made around birth when animals are exposed to a host of new affective, cognitive, and sensori-motor stimuli. It is thought that dopamine modulates cortico-striatal synapses that result in the strengthening of those connections that lead to desired outcomes. We propose that there must be a time before which stimuli cannot be processed into functional connections, otherwise it would imply an effective link between stimulus, response, and reward in uterus. Consistent with these ideas, we present evidence that early in development dopamine neurons are electrically immature and do not produce high-frequency firing in response to salient stimuli. We ask first, what makes dopamine neurons immature? and second, what are the implications of this immaturity for the basal ganglia? As an answer to the first question, we find that at birth the outward current is small (3nS-V), insensitive to Ca2z, TEA, BK, and SK blockers. Rapidly after birth, the outward current increases to 15nS-V and becomes sensitive to Ca2z, TEA, BK, and SK blockers. We make a detailed analysis of the kinetics of the components of the outward currents and produce a model for BK and SK channels that we use to reproduce the outward current, and to infer the geometrical arrangement of BK and Ca2z channels in clusters. In the first cluster, T-type Ca2z and BK channels are coupled within distances of *20 nm (200 A˚). The second cluster consists of L-type Ca2z and BK channels that are spread over distances of at least 60 nm. As for the second question, we propose that early in development, the mechanism of action selection is in a ‘‘locked-in’’ state that would prevent dopamine neurons from reinforcing cortico-striatal synapses that do not have a functional experiential- based value.

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Many connections in the basal ganglia are made around birth when animals are exposed to a host of new affective, cognitive, and sensori-motor stimuli. It is thought that dopamine modulates cortico-striatal synapses that result in the strengthening of those connections that lead to desired outcomes. We propose that there must be a time before which stimuli cannot be processed into functional connections, otherwise it would imply an effective link between stimulus, response, and reward in uterus. Consistent with these ideas, we present evidence that early in development dopamine neurons are electrically immature and do not produce high-frequency firing in response to salient stimuli. We ask first, what makes dopamine neurons immature? and second, what are the implications of this immaturity for the basal ganglia? As an answer to the first question, we find that at birth the outward current is small (3nS-V), insensitive to Ca2+, TEA, BK, and SK blockers. Rapidly after birth, the outward current increases to 15nS-V and becomes sensitive to Ca2+, TEA, BK, and SK blockers. We make a detailed analysis of the kinetics of the components of the outward currents and produce a model for BK and SK channels that we use to reproduce the outward current, and to infer the geometrical arrangement of BK and Ca2+ channels in clusters. In the first cluster, T-type Ca2+ and BK channels are coupled within distances of similar to 20 nm (200 parallel to). The second cluster consists of L-type Ca2+ and BK channels that are spread over distances of at least 60 nm. As for the second question, we propose that early in development, the mechanism of action selection is in a "locked-in" state that would prevent dopamine neurons from reinforcing cortico-striatal synapses that do not have a functional experiential-based value.

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SEight unidentified Gram-positive, rod-shaped organisms were recovered from the tracheas of apparently healthy black storks (Ciconia nigra) and subjected to a polyphasic taxonomic analysis. Based on cellular morphology and biochemical criteria the isolates were tentatively assigned to the genus Corynebacterium, although three of the organisms did not appear to correspond to any recognized species. Comparative 16S rRNA gene sequencing studies demonstrated that all of the isolates were phylogenetically members of the genus Corynebacterium. Five strains were genotypically identified as representing Corynebacterium falsenii, whereas the remaining three strains represented a hitherto unknown subline, associated with a small subcluster of species that includes Corynebacterium mastitidis and its close relatives. On the basis of phenotypic and phylogenetic evidence, it is proposed that the unknown isolates from black storks represent a novel species within the genus Corynebacterium, for which the Corynebacterium ciconiae sp. nov. is proposed. The type strain is CECT 5779(T) (= BS13(T) =CCILIG 47525(T)).