Tina Märker

Mutations in the gene encoding the basal body protein RPGRIP1L, a nephrocystin-4 interactor, cause Joubert syndrome

Heleen H. Arts, Dan Doherty, Sylvia E. C. van Beersum et al. · Nature Genetics · 2007 · 321 citations

Developmental Biology, Mendelian Disorder, Genetic Disorder +8

The DFNB31 gene product whirlin connects to the Usher protein network in the cochlea and retina by direct association with USH2A and VLGR1

Erwin van Wijk, Bert van der Zwaag, Theo Peters et al. · Human Molecular Genetics · 2006 · 185 citations

Signal Transduction, Developmental Biology, Signaling Pathway +14

Scaffold protein harmonin (USH1C) provides molecular links between Usher syndrome type 1 and type 2

Jan Reiners, Erwin van Wijk, Tina Märker et al. · Human Molecular Genetics · 2005 · 172 citations · Full text

Photoreceptor expression of the Usher syndrome type 1 protein protocadherin 15 (USH1F) and its interaction with the scaffold protein harmonin (USH1C).

Jan Reiners, Tina Märker, Karin Jürgens et al. · PubMed · 2005 · 92 citations

Heat Shock Protein 60 as a Mediator of Adipose Tissue Inflammation and Insulin Resistance

Tina Märker, Henrike Sell, Pia Zilleßen et al. · Diabetes · 2012 · 76 citations · Full text

Immunology, Immune Regulation, Insulin Signaling +24