Gerhard H. Przemeck
Neuherberg, BY, Germany
Last Updated: 09/26/2026
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Found 18 publications
MODY PDX1P33T: a mouse model reveals phenotypic divergence from human disease.
Journal: Frontiers in endocrinology
Published: August 06, 2025
Mutations within the cGMP-binding domain of CNGA1 causing autosomal recessive retinitis pigmentosa in human and animal model.
Journal: Cell death discovery
Published: July 28, 2022
A point mutation in the Pdia6 gene results in loss of pancreatic β-cell identity causing overt diabetes.
Journal: Molecular metabolism
Published: May 05, 2021
PAX6 mutation alters circadian rhythm and β cell function in mice without affecting glucose tolerance.
Journal: Communications biology
Published: March 04, 2020
Mutation in Bmpr1b Leads to Optic Disc Coloboma and Ventral Retinal Gliosis in Mice.
Journal: Investigative ophthalmology & visual science
Published: February 28, 2020
DLL1- and DLL4-Mediated Notch Signaling Is Essential for Adult Pancreatic Islet Homeostasis.
Journal: Diabetes
Published: August 21, 2019
Correction: From Dynamic Expression Patterns to Boundary Formation in the Presomitic Mesoderm.
Journal: PLoS computational biology
Published: July 03, 2019
Modeling coexistence of oscillation and Delta/Notch-mediated lateral inhibition in pancreas development and neurogenesis.
Journal: Journal of theoretical biology
Published: November 18, 2016
Point mutation of Ffar1 abrogates fatty acid-dependent insulin secretion, but protects against HFD-induced glucose intolerance.
Journal: Molecular metabolism
Published: November 16, 2016
The First Scube3 Mutant Mouse Line with Pleiotropic Phenotypic Alterations.
Journal: G3 (Bethesda, Md.)
Published: November 06, 2016
Viable Ednra Y129F mice feature human mandibulofacial dysostosis with alopecia (MFDA) syndrome due to the homologue mutation.
Journal: Mammalian genome : official journal of the International Mammalian Genome Society
Published: June 27, 2016
Last Updated: 09/26/2026