同位素~(106)Cd金属自支撑靶的制备及废靶的再生利用

用滚压技术制备出同位素１０６Ｃｄ自支撑靶，并成功地利用破靶膜的再生方法。制备出可供使用的靶膜。

Milho variedade BR 106 técnicas de plantio.

2004

Yeast screens identify the RNA polymerase II CTD and SPT5 as relevant targets of BRCA1 interaction.

BRCA1 has been implicated in numerous DNA repair pathways that maintain genome integrity, however the function responsible for its tumor suppressor activity in breast cancer remains obscure. To identify the most highly conserved of the many BRCA1 functions, we screened the evolutionarily distant eukaryote Saccharomyces cerevisiae for mutants that suppressed the G1 checkpoint arrest and lethality induced following heterologous BRCA1 expression. A genome-wide screen in the diploid deletion collection combined with a screen of ionizing radiation sensitive gene deletions identified mutants that permit growth in the presence of BRCA1. These genes delineate a metabolic mRNA pathway that temporally links transcription elongation (SPT4, SPT5, CTK1, DEF1) to nucleopore-mediated mRNA export (ASM4, MLP1, MLP2, NUP2, NUP53, NUP120, NUP133, NUP170, NUP188, POM34) and cytoplasmic mRNA decay at P-bodies (CCR4, DHH1). Strikingly, BRCA1 interacted with the phosphorylated RNA polymerase II (RNAPII) carboxy terminal domain (P-CTD), phosphorylated in the pattern specified by the CTDK-I kinase, to induce DEF1-dependent cleavage and accumulation of a RNAPII fragment containing the P-CTD. Significantly, breast cancer associated BRCT domain defects in BRCA1 that suppressed P-CTD cleavage and lethality in yeast also suppressed the physical interaction of BRCA1 with human SPT5 in breast epithelial cells, thus confirming SPT5 as a relevant target of BRCA1 interaction. Furthermore, enhanced P-CTD cleavage was observed in both yeast and human breast cells following UV-irradiation indicating a conserved eukaryotic damage response. Moreover, P-CTD cleavage in breast epithelial cells was BRCA1-dependent since damage-induced P-CTD cleavage was only observed in the mutant BRCA1 cell line HCC1937 following ectopic expression of wild type BRCA1. Finally, BRCA1, SPT5 and hyperphosphorylated RPB1 form a complex that was rapidly degraded following MMS treatment in wild type but not BRCA1 mutant breast cells. These results extend the mechanistic links between BRCA1 and transcriptional consequences in response to DNA damage and suggest an important role for RNAPII P-CTD cleavage in BRCA1-mediated cancer suppression.

Compte rendu: Romain Colonna (dir.) (2014), Les locuteurs et les langues : pouvoirs, non-pouvoirs et contre-pouvoirs, Limoges, Lambert-Lucas, coll. « Linguistique », 370 p. [ISBN : 978-2-35935-106-4]

Résumé non disponible

Statuts de l'ordre des Hospitaliers de Saint-Jean de Jérusalem, arrêtés sous le grand maître Pierre d'Aubusson. (Fol. 21-106).

Contient : Forme abrégée desdits statuts, précédée (fol. 107 v°) de « la declaracion des rubriques et chapitres des establissemens qui s'ensuivent », et (fol. 108 r°) d'une ordonnance de PIERRE D'AUBUSSON, relative à cette forme de statuts, datée de Rhodes, le 5 août 1493 ; Résumé pour les prieurs et châtelain d'Emposte desdits statuts

Les mystères de Londres : drame en cinq actes et dix tableaux. [suivi de] Un vilain monsieur : vaudeville en un acte. Livr. 106 / par Paul Féval ; par MM. A. Decourcelle et Th. Barrière

Collection : Théâtre contemporain illustré ; 106e et 107e livraisons

Les mystères de Londres : drame en cinq actes et dix tableaux. [suivi de] Un vilain monsieur : vaudeville en un acte. Livr. 106 / par Paul Féval ; par MM. A. Decourcelle et Th. Barrière

Collection : Théâtre contemporain illustré ; 106e et 107e livraisons