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Each participating partner university is planning for each academic year on 3 outgoing and 3 incoming InMAS students. The InMAS committee will make every effort to achieve an evenly balanced exchange from year to year. Only students enrolled in one of the participating Master programs will be considered. The local coordinator of InMAS will serve as a contact for the student, will assist the student in the application process and help in the compilation of the study program. Andrea Flossmann. Stephan Borrmann.

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Each participating partner university is planning for each academic year on 3 outgoing and 3 incoming InMAS students. The InMAS committee will make every effort to achieve an evenly balanced exchange from year to year.

Only students enrolled in one of the participating Master programs will be considered. The local coordinator of InMAS will serve as a contact for the student, will assist the student in the application process and help in the compilation of the study program.

Andrea Flossmann. Stephan Borrmann. Maya Todua. Bart Geerts. All applications will be examined by the InMAS committee and ranked taking into account:. The InMAS committee will offer places to applicants who appear to have the highest potential for graduate study and who, with the benefit of a graduate education, are the most likely to contribute substantially to their academic or professional fields through teaching, research, or professional practice. Once accepted by the InMAS committee, the student will be eligible to apply for registration at the host university under the terms of this dual program.

The host university, however, has final authority on the administrative admission decisions. Radar X. Procedure of application Only students enrolled in one of the participating Master programs will be considered.

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Race fg and Adam W. E-mail: chawp bristol. We present a new cell membrane modification methodology where the inherent heart tissue homing properties of the infectious bacteria Streptococcus gordonii are transferred to human stem cells. This is achieved via the rational design of a chimeric protein—polymer surfactant cell membrane binding construct, comprising the cardiac fibronectin Fn binding domain of the bacterial adhesin protein CshA fused to a supercharged protein.

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