Browse by Journal Title

2023

Neurofibromin 1 mutations impair the function of human induced pluripotent stem cell-derived microglia.
Kuhrt, L.D. and Motta, E. and Elmadany, N. and Weidling, H. and Fritsche-Guenther, R. and Efe, I.E. and Cobb, O. and Chatterjee, J. and Boggs, L.G. and Schnauß, M. and Diecke, S. and Semtner, M. and Anastasaki, C. and Gutmann, D.H. and Kettenmann, H.
Disease Models & Mechanisms 16 (12): dmm049861. December 2023

2022

Autophagy takes it all - autophagy inducers target immune aging.
Zinecker, H. and Simon, A.K.
Disease Models & Mechanisms 15 (1): dmm049345. 31 January 2022

2020

Identification of MYOM2 as a candidate gene in hypertrophic cardiomyopathy and tetralogy of fallot and its functional evaluation in the Drosophila heart.
Auxerre-Plantié, E. and Nielsen, T. and Grunert, M. and Olejniczak, O. and Perrot, A. and Özcelik, C. and Harries, D. and Matinmehr, F. and Dos Remedios, C. and Mühlfeld, C. and Kraft, T. and Bodmer, R. and Vogler, G. and Sperling, S.R.
Disease Models & Mechanisms 13 (12): dmm045377. 18 December 2020

2018

The IgCAM CLMP regulates expression of Connexin43 and Connexin45 in intestinal and ureteral smooth muscle contraction in mice.
Langhorst, H. and Jüttner, R. and Groneberg, D. and Mohtashamdolatshahi, A. and Pelz, L. and Purfürst, B. and Schmidt-Ott, K.M. and Friebe, A. and Rathjen, F.G.
Disease Models & Mechanisms 11 (2): dmm032128. 22 February 2018

2017

Genetic, physiological and comparative genomic studies of hypertension and insulin resistance in the spontaneously hypertensive rat.
Coan, P.M. and Hummel, O. and Diaz, A.I.G. and Barrier, M. and Alfazema, N. and Norsworthy, P.J. and Pravenec, M. and Petretto, E. and Hübner, N. and Aitman, T.J.
Disease Models & Mechanisms 10 (3): 297-306. 1 March 2017

2016

Angiotensin-(1-7) attenuates disuse skeletal muscle atrophy in mice via its receptor, Mas.
Morales, M.G. and Abrigo, J. and Acuna, M.J. and Santos, R.A. and Bader, M. and Brandan, E. and Simonetta, F. and Olguin, H. and Cabrera, D. and Cabello-Verrugio, C.
Disease Models & Mechanisms 9 (4): 441-449. 1 April 2016

2014

A missense mutation accelerating the gating of the lysosomal Cl(-)/H(+)-exchanger ClC-7/Ostm1 causes osteopetrosis with gingival hamartomas in cattle.
Sartelet, A. and Stauber, T. and Coppieters, W. and Ludwig, C.F. and Fasquelle, C. and Druet, T. and Zhang, Z. and Ahariz, N. and Cambisano, N. and Jentsch, T.J. and Charlier, C.
Disease Models & Mechanisms 7 (1): 119-128. January 2014

2011

Human cardiomyopathy mutations induce myocyte hyperplasia and activate hypertrophic pathways during cardiogenesis in zebrafish.
Becker, J.R. and Deo, R.C. and Werdich, A.A. and Panakova, D. and Coy, S. and MacRae, C.A.
Disease Models & Mechanisms 4 (3): 400-410. May 2011