LA PAIX FAICTE A || CHAMBRAY en || tre lempereur || [et] le tres crestiẽ || Roy de france auec || leurs aliez. — [A la fin :] ¶ Imprime a paris pour philipot le cocq li- || brayre demourãt a chãbray en la rue taueau. S. d. [1508], in-4 goth. de 10 f., dont la page la plus pleine contient 36 lignes, sign. a par 6, b par 4, mar. v., fil., comp., dos orné, tr. dor. (Petit, successeur de Simier.)

Ladam (Nicaise). La Paix faicte a Chambray (1508)

Hepatitis B Virus e Antigen Physically Associates With Receptor-Interacting Serine/Threonine Protein Kinase 2 and Regulates IL-6 Gene Expression.

We previously reported that hepatitis B virus (HBV) e antigen (HBeAg) inhibits production of interleukin 6 by suppressing NF-κB activation. NF-κB is known to be activated through receptor-interacting serine/threonine protein kinase 2 (RIPK2), and we examined the mechanisms of interleukin 6 regulation by HBeAg. HBeAg inhibits RIPK2 expression and interacts with RIPK2, which may represent 2 mechanisms through which HBeAg blocks nucleotide-binding oligomerization domain-containing protein 1 ligand-induced NF-κB activation in HepG2 cells. Our findings identified novel molecular mechanisms whereby HBeAg modulates intracellular signaling pathways by targeting RIPK2, supporting the concept that HBeAg could impair both innate and adaptive immune responses to promote chronic HBV infection.

1.° Liber inscriptus : Cautelae Bagaroti, juris Professoris. — 2.° Anonymi tractatus de causarum exercitiis. — 3.° Summula de libellis : authore Bernardo Dorna, Provinciali. — 4.° Cavillationes domini Uberti de Bobio. — 5.° Distinctiones a domino Ugone compositae, et a domino Alberico consummatae. — 6.° Summa de arbitris a domino B. promulgata, missa ad A. F. Romanae Ecclesiae Cancellarium. — 7.° Opusculum, cujus titulus est : Arbor actionum. — 8.° Anonymi tractatus de actionibus. — 9.° Formularium procurationum, secundum usum curiae Romanae

Colbertinus

The synthesis of 1,2,3,6,6a,7-hexahydro-7-methyl-5-imino-1H-pyrrolo[1,2-c]imidazolo[5,4-b]indole

N-3-(1-Methylindol-3-yl)propan-N-(2,2,2-trichloroethoxysulfonyl)guanidine was synthesized from 3-formyl-1-methylindole in six steps and subjected to conditions intended to convert the side-chain into a 2-iminotetrahydropyrimidine- containing product, of relevance to a possible synthesis of the aplicyanins. An alternative reaction course was observed, resulting in the formation of a new tetracyclic system.

The synthesis of 1,2,3,6,6a,7-hexahydro-7-methyl-5-imino-1H-pyrrolo[1,2-c]imidazolo[5,4-b]indole

N-3-(1-Methylindol-3-yl)propan-N-(2,2,2-trichloroethoxysulfonyl)guanidine was synthesized from 3-formyl-1-methylindole in six steps and subjected to conditions intended to convert the side-chain into a 2-iminotetrahydropyrimidine- containing product, of relevance to a possible synthesis of the aplicyanins. An alternative reaction course was observed, resulting in the formation of a new tetracyclic system.

Luettelo kananmunien säännöstelystä 9 päivänä heinäkuuta 1942 annetun valtioneuvoston päätöksen 6 §:n edellyttämistä keskusliikkeistä (A) ja 7 §:n edellyttämistä hankintaliikkeistä (B)

14 x 20 cm

Luettelo kananmunien säännöstelystä 9 päivänä heinäkuuta 1942 annetun valtioneuvoston päätöksen 6 §:n edellyttämistä keskusliikkeistä (A) ja 7 §:n edellyttämistä hankintaliikkeistä (B)

14 x 20 cm