Het Beclach van Jencheer Jan van Hembyse : dichtstuk der XVI. eeuw /

"Ph. Blommaert" (p. 52).

Hembyse : histoire gantoise de la fin du XVIe siècle.

Mode of access: Internet.

Der Weg des Landes Appenzell in die Eidgenossenschaft: Das Bündnis von 1513 und seine Vorgeschichte. CD-ROM mit interaktiven Leseübungen und Kommentaren zu Schriftdokumenten im Zusammenhang mit der Aufnahme des Landes Appenzell in die Eidgenossenschaft vor 500 Jahren

Die CD bietet als erste Publikation überhaupt die Möglichkeit, anhand wichtiger Quellen den Weg des Landes Appenzell in die Eidgenossenschaft nachzuvollziehen. Die Dokumente zeigen die Vorgeschichte des Bündnisses vom 17. Dezember 1513, mit welchem Appenzell als 13. Ort in die Eidgenossenschaft aufgenommen wurde. Zudem kann mit der CD ROM das Lesen alter Handschriften erlernt werden. Das bietet die CD ROM nicht nur das Bild und den gesamten Wortlaut der Urkunde von 1513, sondern auch eine Audio-Datei des Dokuments und erstmals auch eine Übertragung des Urkundentexts in modernes Deutsch.

Das Kloster Disentis vom Ausgang des Mittelalters bis zum Tode des Abtes Christian von Castelberg 1584.

Thesis (doctoral)--Universitat Freiburg in der Schweiz.

Increased expression of the auxiliary beta2-subunit of ventricular L-type Ca2+ channels leads to single-channel activity characteristic of heart failure

BACKGROUND: Increased activity of single ventricular L-type Ca(2+)-channels (L-VDCC) is a hallmark in human heart failure. Recent findings suggest differential modulation by several auxiliary beta-subunits as a possible explanation. METHODS AND RESULTS: By molecular and functional analyses of human and murine ventricles, we find that enhanced L-VDCC activity is accompanied by altered expression pattern of auxiliary L-VDCC beta-subunit gene products. In HEK293-cells we show differential modulation of single L-VDCC activity by coexpression of several human cardiac beta-subunits: Unlike beta(1) or beta(3) isoforms, beta(2a) and beta(2b) induce a high-activity channel behavior typical of failing myocytes. In accordance, beta(2)-subunit mRNA and protein are up-regulated in failing human myocardium. In a model of heart failure we find that mice overexpressing the human cardiac Ca(V)1.2 also reveal increased single-channel activity and sarcolemmal beta(2) expression when entering into the maladaptive stage of heart failure. Interestingly, these animals, when still young and non-failing ("Adaptive Phase"), reveal the opposite phenotype, viz: reduced single-channel activity accompanied by lowered beta(2) expression. Additional evidence for the cause-effect relationship between beta(2)-subunit expression and single L-VDCC activity is provided by newly engineered, double-transgenic mice bearing both constitutive Ca(V)1.2 and inducible beta(2) cardiac overexpression. Here in non-failing hearts induction of beta(2)-subunit overexpression mimicked the increase of single L-VDCC activity observed in murine and human chronic heart failure. CONCLUSIONS: Our study presents evidence of the pathobiochemical relevance of beta(2)-subunits for the electrophysiological phenotype of cardiac L-VDCC and thus provides an explanation for the single L-VDCC gating observed in human and murine heart failure.

Xenotransplantation of cryopreserved human ovarian tissue--a systematic review of MII oocyte maturation and discussion of it as a realistic option for restoring fertility after cancer treatment.

OBJECTIVE To systematically review the reporting of MII (MII) oocyte development after xenotransplantation of human ovarian tissue. DESIGN Systematic review in accordance with the guidelines of the Preferred Reporting Items for Systematic Reviews and Meta-analyses (PRISMA). SETTING Not applicable. PATIENT(S) Not applicable. INTERVENTION(S) Formation of MII oocytes after xenotransplantation of human ovarian tissue. MAIN OUTCOME MEASURE(S) Any outcome reported in Pubmed. RESULT(S) Six publications were identified that report on formation of MII oocytes after xenotransplantation of human ovarian tissue. CONCLUSION(S) Xenografting of human ovarian tissue has proved to be a useful model for examining ovarian function and follicle development in vivo. With human follicles that have matured through xenografting, the possibility of cancer transmission and relapse can also be eliminated, because cancer cells are not able to penetrate the zona pellucida. The reported studies have demonstrated that xenografted ovarian tissue from a range of species, including humans, can produce antral follicles that contain mature (MII) oocytes, and it has been shown that mice oocytes have the potential to give rise to live young. Although some ethical questions remain unresolved, xenotransplantation may be a promising method for restoring fertility. This review furthermore describes the value of xenotransplantation as a tool in reproductive biology and discusses the ethical and potential safety issues regarding ovarian tissue xenotransplantation as a means of recovering fertility.