Gerd-Jörg Rauch

HBEGF, SRA1, and IK: Three cosegregating genes as determinants of cardiomyopathy (2009)

Friedrichs, Frauke, Zugck, Christian, Rauch, Gerd-Jörg, Ivandic, Boris, Weichenhan, Dieter, Müller-Bardorff, Margit, ...

Human dilated cardiomyopathy (DCM), a disorder of the cardiac muscle, causes considerable morbidity and mortality and is one of the major causes of sudden cardiac death. Genetic factors play a role...

Large-scale mapping of mutations affecting zebrafish development (2007)

Geisler, Robert, Rauch, Gerd-Jörg, Geiger-Rudolph, Silke, Albrecht, Andrea, Van Bebber, Frauke, Berger, Andrea, ...

Abstract Background Large-scale mutagenesis screens in the zebrafish employing the mutagen ENU have isolated several hundred mutant loci that represent putative developmental control genes. In order...

Mariner is defective in myosin VIIA: a zebrafish model for human hereditary deafness (2000)

Ernest, Sylvain, Rauch, Gerd-Jörg, Haffter, Pascal, Geisler, Robert, Petit, Christine, Nicolson, Teresa

The zebrafish (Danio rerio) possesses two mechanosensory organs believed to be homologous to each other: the inner ear, which is responsible for the senses of audition and equilibrium, and the...

A mutation in the Gsk3–binding domain of zebrafish Masterblind/Axin1 leads to a fate transformation of telencephalon and eyes to diencephalon

Heisenberg, Carl-Philipp, Houart, Corinne, Takeuchi, Masaya, Rauch, Gerd-Jörg, Young, Neville, Coutinho, Pedro, ...

Zebrafish embryos homozygous for the masterblind (mbl) mutation exhibit a striking phenotype in which the eyes and telencephalon are reduced or absent and diencephalic fates expand to the front of...

A mutation in the Gsk3–binding domain of zebrafish Masterblind/Axin1 leads to a fate transformation of telencephalon and eyes to diencephalon

Heisenberg, Carl-Philipp, Houart, Corinne, Take-uchi, Masaya, Rauch, Gerd-Jörg, Young, Neville, Coutinho, Pedro, ...

Zebrafish embryos homozygous for the masterblind (mbl) mutation exhibit a striking phenotype in which the eyes and telencephalon are reduced or absent and diencephalic fates expand to the front of...

Leukocyte Tyrosine Kinase Functions in Pigment Cell Development

Lopes, Susana S., Yang, Xueyan, Müller, Jeanette, Carney, Thomas J., McAdow, Anthony R., Rauch, Gerd-Jörg, ...

A fundamental problem in developmental biology concerns how multipotent precursors choose specific fates. Neural crest cells (NCCs) are multipotent, yet the mechanisms driving specific fate choices...

HBEGF, SRA1, and IK: Three cosegregating genes as determinants of cardiomyopathy

Friedrichs, Frauke, Zugck, Christian, Rauch, Gerd-Jörg, Ivandic, Boris, Weichenhan, Dieter, Müller-Bardorff, Margit, ...

Human dilated cardiomyopathy (DCM), a disorder of the cardiac muscle, causes considerable morbidity and mortality and is one of the major causes of sudden cardiac death. Genetic factors play a role...