Per d. Gennaro Celentani, già colonnello del reggimento cavalleria regina : nella Corte suprema di giustizia, a relazione del degnissimo signor presidente consultore Marrano.

Mode of access: Internet.

[Voyage en Italie : 1824-1830]. , S. Gennaro de Poveri à Naples, sur une échelle de 0,001 1/2 PM : [plan d'ensemble, coupe longitdinale et élévation principale] : [dessin] / h. L. [Henri Labrouste]

Référence bibliographique : Weigert, 225

Indirizzo della deputazione israelitica di Roma a nostro signore Papa Pio IX., nell'udienza sovrana accordatale il giorno 10 gennaro 1848

Aus: La Speranza ; N. 10

Dell'argenteo imbusto al primo patrono S. Gennaro da re Carlo Secondo di Angiò decretato : con una disquisizione intorno al Libro delle spese della casa dello stesso re, dove s'indagano gli anni ai quali va assegnato se ne classificato le notizie più interessanti, e si fa accurata rassegna dei pesi e delle misure state in uso nel reame di Napoli /

Last leaf blank.

Aneddoti sulla basilica ostiense di S. Paolo riuniti nel 1823, dopo l'incendio, e recitati nell'Accademia Archeologica il dì 27. gennaro 1825.

Mode of access: Internet.

Elogio funebre alla gloriosa memoria di Ferdinando I, re del regno delle due Sicilie, ne'funerali a proprie spese celebrati nel di 16 gennaro dell'anno 1825 ... /

Mode of access: Internet.

Ne'funerali solenni per sua S.R.M. Ferdinando I, re del regno delle due Sicilie, celebrati nella cappella del Tesoro di S. Gennaro dalla Real Deputazione della medesima a'24 gennajo 1825 : orazione /

Mode of access: Internet.

Novelle del Tevere : discorso, particolarmente in difesa di S. Gregorio Magno, recitato in Academia archeologica il dì 7. gennaro 1819 t/

On t.p., publication date appears before publisher name.

Notizie sulle cripte mortuarie dette catacombe di S. Gennaro de'Poveri.

[Gift of John Harvey Treat, July 15, 1904].

Notizie intorno la colonna sbarcata il giorno 4 di gennaro del corrente anno 1828 : per servire alla riedificazione della basilica di S. Paolo sulla via Ostiense : redatte /

University of Illinois bookplate: "From the library of Conte Antonio Cavagna Sangiuliani di Gualdana Lazelada di Bereguardo, purchased 1921".

B-1 cells modulate oral tolerance in mice

Although the origin and functions of B-1 cells are controversial, they are considered as a cellular element of innate immunity due to their ability to produce natural autoantibodies of the IgM type. These antibodies are encoded by a relatively limited repertoire of V genes, and their resulting diversity is smaller than that produced by conventional B cells. B-1 cells constitute the larger fraction of B cells in the peritoneal cavity and migrate to non-specific inflammation sites. In addition, they contribute to the production of IgA antibodies in the intestinal lamina propria. It has been demonstrated that they participate in the induction and maintenance of peripheral tolerance. Herein, the participation of B-1 cells in inducing oral tolerance is evaluated. Unexpectedly, BALB/Xid mice, the animals deficient in B-1 cells, are not tolerized to OVA but instead are responsive to oral immunization. Conversely, BALB/c mice respond to oral tolerance to this antigen. We used these biological characteristics of these animals to investigate whether BA cells are involved in the induction of oral tolerance to OVA. Results show that B-1 cells from BALB/c mice, treated orally with OVA and adoptively transferred to BALB/Xid mice were able to suppress local hypersensitivity reaction and lymphoproliferative cellular response observed in BALB/.Xid mice. These data demonstrate that B-1 cells have regulatory properties and are involved in the induction of oral tolerance. (C) 2009 Elsevier B.V. All rights reserved.

A fluorescente bicyclic Calix[4] Arene-Oxacyclophane with planar chirality: Resolution, chiroptical, properties, and absolute configuration.

A new inherently chiral calix[4]arene ICC 1 has been disclosed. The dissymmetry of 1 is generated from a chirality plane in the quinol moiety of a 1,3-bridged bicyclic calix[4]arene. ICC 1 has been resolved by enantioselective HPLC, and the chiroptical properties of both isolated antipodes (pS)-1 and (pR)-1 confirm their enantiomeric nature. The absolute configuration of the (pS)-1/(pR)-1 enantiomeric pair was established through time-dependent density functional theory (TDDFT) calculations of electronic circular dichroism (CD) spectra. (C) 2014 Elsevier Ltd. All rights reserved.

Chiroptical and emissive properties of a calix[4]arene-containing chiral poly (P-phenylene ethynylene) with enantioselective recognition ability

Supramolecular chirality was achieved in solutions and thin films of a calixarene-containing chiral aryleneethynylene copolymer. The observed chiroptical activity, which is primarily allied with the formation of aggregates of high molecular weight polymer chains, is the result of a combination of intrachain and interchain effects. The former arises by the adoption of an induced helix-sense by the polymer main-chain while the latter comes from the exciton coupling of aromatic backbone transitions. The co-existence of bulky bis-calixKlarene units and chiral side-chains on the polymer skeleton prevents efficient pi-stacking of neighbouring chains, keeping the chiral assembly highly emissive. In contrast, for a model polymer lacking calixarene moieties, the chiroptical activity is dominated by strong interchain exciton couplings as a result of more favourable packing of polymer chains, leading to a marked decrease of photoluminescence in the aggregate state. The enantiomeric recognition abilities of both polymers towards (R)- and (S)-alpha-methylbenzylamine were examined. It was found that a significant enantiodiscrimination is exhibited by the calixarene-based polymer in the aggregate state.

Inherently chiral calix[4]arenes with planar chirality: two new entries to the family

The synthesis of two new inherently chiral calix[4]arenes (ICCs, 1 and 2), endowed with electron-rich concave surfaces, has been achieved through the desymmetrization of a lower rim distal-bridged oxacyclophane (OCP) macrocycle. The new highly emissive ICCs were resolved by chiral HPLC, and the enantiomeric nature of the isolated antipodes proved by electronic circular dichroism (CD). Using time-dependent density functional calculations of CD spectra, their absolute configurations were established. NMR studies with (S)-Pirkle's alcohol unequivocally showed that the host-guest interactions occur in the chiral pocket comprehending the calix-OCP exo cavities and the carbazole moieties.