Search filters

List of works by Gerhard Przemeck

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

scientific article

Cell-based simulation of dynamic expression patterns in the presomitic mesoderm

scientific article

Combination of in silico and in situ hybridisation approaches to identify potential Dll1 associated miRNAs during mouse embryogenesis

scientific article

Cytoplasmic thioredoxin reductase is essential for embryogenesis but dispensable for cardiac development

scientific journal article

DLL1- and DLL4-Mediated Notch Signaling is Essential for Adult Pancreatic Islet Homeostasis

scientific article published on 06 February 2020

Dll1 haploinsufficiency in adult mice leads to a complex phenotype affecting metabolic and immunological processes

scientific journal article

Exome sequencing identifies a nonsense mutation in Fam46a associated with bone abnormalities in a new mouse model for skeletal dysplasia.

scientific article published on 23 January 2016

Fast synchronization of ultradian oscillators controlled by delta-notch signaling with cis-inhibition

scientific article

Genetic complexity of cellulose synthase a gene function in Arabidopsis embryogenesis.

scientific article published in December 2002

In vitro analysis of bone phenotypes in Col1a1 and Jagged1 mutant mice using a standardized osteoblast cell culture system

article

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

scientific article

Isolation and characterization of a novel gene from the DiGeorge chromosomal region that encodes for a mediator subunit

scientific article (publication date: 15 June 2001)

Modeling coexistence of oscillation and Delta/Notch-mediated lateral inhibition in pancreas development and neurogenesis

scientific article published on 23 June 2017

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

scientific article published in January 2003

PAX6 mutation alters circadian rhythm and β cell function in mice without affecting glucose tolerance

scientific article published on 30 October 2020

The First Scube3 Mutant Mouse Line with Pleiotropic Phenotypic Alterations.

scientific article

The German Mouse Clinic: a platform for systemic phenotype analysis of mouse models.

scientific article

Viable Ednra Y129F mice feature human mandibulofacial dysostosis with alopecia (MFDA) syndrome due to the homologue mutation

scientific article

Paulina is supported by:

About Paulina

Help