F
Franz Hofmann
Researcher at Technische Universität München
Publications - 477
Citations - 51857
Franz Hofmann is an academic researcher from Technische Universität München. The author has contributed to research in topics: Protein kinase A & Voltage-dependent calcium channel. The author has an hindex of 113, co-authored 471 publications receiving 49938 citations. Previous affiliations of Franz Hofmann include Ludwig Maximilian University of Munich & Heidelberg University.
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Journal ArticleDOI
Na+ current properties in islet α‐ and β‐cells reflect cell‐specific Scn3a and Scn9a expression
Quan Zhang,Margarita V. Chibalina,Martin Bengtsson,Lukas N. Groschner,Reshma Ramracheya,Nils J.G. Rorsman,Veronika Leiss,Veronika Leiss,Mohammed A. Nassar,Mohammed A. Nassar,Andrea Welling,Fiona M. Gribble,Frank Reimann,Franz Hofmann,John N. Wood,Frances M. Ashcroft,Patrik Rorsman +16 more
TL;DR: The differential expression explains the different properties of Na+ currents in α‐ and β‐cells and islet Nav1.7 channels are locked in an inactive state due to an islet cell‐specific factor.
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Tissue‐specific expression of splice variants of the mouse voltage‐gated calcium channel α2/δ subunit
Timothy Angelotti,Franz Hofmann +1 more
TL;DR: Five different splice variants of mouse α2/δ subunit isoforms (α2/a‐e) were cloned with a combination of cDNA library screening and RT‐PCR to suggest an important functional role for the differentially spliced variants.
Journal ArticleDOI
International Union of Pharmacology. LI. Nomenclature and Structure-Function Relationships of Cyclic Nucleotide-Regulated Channels
TL;DR: The family of cyclic nucleotide-regulated channels comprises two groups: the cyclicucleotide-gated (CNG[1][1]) channels and the hyperpolarization-activated, cyclic nucleusotide- gated (HCN) channels.
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Enhanced expression of L-type Cav1.3 calcium channels in murine embryonic hearts from Cav1.2 deficient mice
TL;DR: The results imply that calcium channel expression is dynamically regulated during heart development and that the Cav1.3 channel may substitute for Cav.1.2 during early embryogenesis.
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Distribution of cGMP-dependent protein kinase type I and its isoforms in the mouse brain and retina.
TL;DR: It appears that distinct brain regions express distinct cGKI isoforms that signal via distinct pathways, which indicates that the distribution and functional relevance of this pathway in the mammalian brain is broader than previously thought.