Tina Märker - Concepedia

Author

Tina Märker

Johannes Gutenberg University Mainz

Also Known As

T Märker, T. Marker, Tina Märker

Publications

1.7K

Citations

H-Index

Concepts

All Affiliations

Johannes Gutenberg University Mainz Radboud University Medical Center Radboud University Nijmegen University Medical Center Utrecht Radboud Institute for Molecular Life Sciences

About

Tina Märker is an author at Johannes Gutenberg University Mainz specializing in medicine, signal transduction, and cell biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	703
2	Cell Biology	5	5	382
3	Health Sciences	1	1	76
4	Biochemistry	1	1	76
5	Cellular Physiology	1	1	33

Tina Märker

Publications

1.1K

Citations

H-Index

Page 1

	Year	Citations
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, Nature Genetics Developmental BiologyMendelian DisorderGenetic DisorderGeneticsInherited Metabolic Disease	2007	321
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, Human Molecular Genetics Signal TransductionDevelopmental BiologySignaling PathwayDevelopmental GeneticsDirect Association	2006	185
Scaffold protein harmonin (USH1C) provides molecular links between Usher syndrome type 1 and type 2 Jan Reiners, Erwin van Wijk, Tina Märker, Human Molecular Genetics	2005	172
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, PubMed	2005	92
Heat Shock Protein 60 as a Mediator of Adipose Tissue Inflammation and Insulin Resistance Tina Märker, Henrike Sell, Pia Zilleßen, Diabetes ImmunologyImmune RegulationInsulin SignalingInflammationMetabolic Syndrome	2012	76
Association of Whirlin with Ca<sub>v</sub>1.3 (α<sub>1D</sub>) Channels in Photoreceptors, Defining a Novel Member of the Usher Protein Network Ferry F.J. Kersten, Erwin van Wijk, Jeroen van Reeuwijk, Investigative Ophthalmology & Visual Science	2010	56
Homozygous disruption of PDZD7 by reciprocal translocation in a consanguineous family: a new member of the Usher syndrome protein interactome causing congenital hearing impairment E. Schneider, Tina Märker, Angelika Daser, Human Molecular Genetics	2008	55
Usher syndrome and Leber congenital amaurosis are molecularly linked via a novel isoform of the centrosomal ninein-like protein Erwin van Wijk, Ferry F.J. Kersten, Aileen Kartono, Human Molecular Genetics	2008	48
Direct interaction of the Usher syndrome 1G protein SANS and myomegalin in the retina Nora Overlack, Dilek Kilic, Katharina Bauß, Biochimica et Biophysica Acta (BBA) - Molecular Cell Research Ganglion CellPhotoreceptor CellSignal TransductionRetinaOphthalmology	2011	47
MPP1 links the Usher protein network and the Crumbs protein complex in the retina Ilse Gosens, Erwin van Wijk, Ferry F.J. Kersten, Human Molecular Genetics Mpp1 ExpressionMolecular BiologyCytoskeletonOrdered DistributionRetina	2007	41

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