Publications



Patient-Specific Induced Pluripotent Stem-Cell Models for Long-QT Syndrome.


Moretti A, Bellin M, Welling A, Jung CB, Lam JT, Bott-Flügel L, Dorn T, Goedel A, Höhnke C, Hofmann F, Seyfarth M, Sinnecker D, Schömig A, and Laugwitz KL

Early life environment determines the development of adult phobic-like fear responses in BALB/cAnN mice.


Thoeringer CK, Pfeiffer UJ, Rammes G, Pamplona FA, Moosmang S, Wotjak CT

Electrical Activity Suppresses Axon Growth through Cav1.2 Channels in Adult Primary Sensory Neurons.


Enes J, Langwieser N, Ruschel J, Carballosa-Gonzalez MM, Klug A, Traut MH, Ylera B, Tahirovic S, Hofmann F, Stein V, Moosmang S, Hentall ID, Bradke F

Homeostatic Switch in Hebbian Plasticity and Fear Learning after Sustained Loss of Cav1.2 Calcium Channels.


Langwieser N, Christel CJ, Kleppisch T, Hofmann F, Wotjak CT, and Moosmang S

Reply to Kass and Takimoto: Cardiac hypertrophy without cGKI and PDE5 in cardiac myocytes.


Lukowski R, Rybalkin SD, Beavo JA, Hofmann F

Facilitation of murine cardiac L-type Cav1.2 channel is modulated by Calmodulin kinase II–dependent phosphorylation of S1512 and S1570.


Blaich A, Welling A, Fischer S, Wegener JW, Köstner K, Hofmann F, Moosmang S

L-Type Calcium Channel CaV 1.2 in Transgenic Mice Overexpressing Human AbetaPP751 with the London (V717I) and Swedish (K670M/N671L) Mutations.


Willis M, Kaufmann WA, Wietzorrek G, Hutter-Paier B, Moosmang S, Humpel C, Hofmann F, Windisch M, -Günther Knaus H, Marksteiner J

A complex of CaV1.2/PKC is involved in muscarinic signaling in smooth muscle.


Huster M, Frei E, Hofmann F, Wegener JW

Genetic Ablation of L-Type Ca2+ Channels Abolishes Depolarization-Induced Ca2+ Release in Arterial Smooth Muscle.


Fernández-Tenorio M, González-Rodríguez P, Porras C, Castellano A, Moosmang S, Hofmann F, Ureña J, López-Barneo J

Cardiac hypertrophy is not amplified by deletion of cGMP-dependent protein kinase I in cardiomyocytes.


Lukowski R, Rybalkin SD, Loga F, Leiss V, Beavo JA, Hofmann F