Franko, Andras; Huypens, Peter; Neschen, Susanne; Irmler, Martin; Rozman, Jan; Rathkolb, Birgit; Neff, Frauke; Prehn, Cornelia; Dubois, Guillaume; Baumann, Martina; Massinger, Rebecca; Gradinger, Daniel; Przemeck, Gerhard K. H.; Repp, Birgit; Aichler, Michaela; Feuchtinger, Annette; Schommers, Philipp; Stoehr, Oliver; Sanchez-Lasheras, Carmen; Adamski, Jerzy; Peter, Andreas; Prokisch, Holger; Beckers, Johannes; Walch, Axel K.; Fuchs, Helmut; Wolf, Eckhard; Schubert, Markus; Wiesner, Rudolf J.; de Angelis, Martin Hrabe

Cardiopulmonary dysfunction in the Osteogenesis imperfecta mouse model Aga2 and human patients are caused by bone-independent mechanisms

HUMAN MOLECULAR GENETICS

IF3.2

2012-05-1561

OAAI

Molecular and functional characterization of Aga2-A mouse model for osteogenesis imperfecta

BONE

IF3.6

2009-06-010

PREAI

The CALM and CALM/AF10 interactor CATS is a marker for proliferation

MOLECULAR ONCOLOGY

IF4.5

2008-09-0439

ER stress-mediated apoptosis in a new mouse model of osteogenesis imperfecta

PLOS GENETICS

IF3.7

2008-02-01139

OAAI

A genetic screen for modifiers of the delta1-dependent notch signaling function in the mouse

GENETICS

IF5.1

2007-03-0124

OAAI

Introducing the German Mouse Clinic:: open access platform for standardized phenotyping

NATURE METHODS

IF32.1

2005-06-01163

PREAI

Gailus-Durner, V; Fuchs, H; Becker, L; Bolle, I; Brielmeier, M; Calzada-Wack, J; Evert, R; Ehrhardt, N; Dalkel, C; Franz, TJ; Grundner-Culemann, E; Hammelbacher, S; Hölter, SM; Hötzlwimmer, G; Horsch, M; Javaheri, A; Kataydjiev, SV; Klempt, M; Kling, E; Kunder, S; Lengger, C; Lisse, T; Mijalski, T; Naton, B; Pedersen, V; Prehn, C; Przemeck, G; Racz, I; Reinhard, C; Reitmeir, P; Schneider, I; Schrewe, A; Steinkamp, R; Zybill, C; Adamski, J; Beckers, J; Behrendt, H; Favor, J; Graw, J; Heldmaier, G; Höfer, H; Ivandic, B; Katus, H; Kirchhof, P; Kiingenspor, M; Kopstock, T; Lengeling, A; Mfitier, W; Ohl, F; Ollert, M; Quintanilla-Martinez, L; Schmidt, J; Schulz, H; Wolf, E; Wurst, W; Zimmer, A; Busch, DH; de Angelis, MH

Targeted disruption of the Walker-Warburg syndrome gene Pomt1 in mouse results in embryonic lethality

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

IF9.1

2004-09-21140

OAAI

Node and midline defects are associated with left-right development in Delta1 mutant embryos

DEVELOPMENT

IF3.6

2003-01-01108

OAAI

Genetic complexity of cellulose synthase A gene function in Arabidopsis embryogenesis

PLANT PHYSIOLOGY