
Publikationen von G-J Rauch
Alle Typen
Zeitschriftenartikel (21)
1.
Zeitschriftenartikel
4 (3), e1000026 (2008)
Leukocyte tyrosine kinase functions in pigment cell development. PLoS Genetics 2.
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8, 11 (2007)
Large-scale mapping of mutations affecting zebrafish development. BMC Genomics 3.
Zeitschriftenartikel
132 (4), S. 645 - 658 (2005)
Monorail/Foxa2 regulates floorplate differentiation and specification of oligodendrocytes, serotonergic raphé neurones and cranial motoneurones. Development 4.
Zeitschriftenartikel
18 (13), S. 1565 - 1576 (2004)
iguana encodes a novel zinc-finger protein with coiled-coil domains essential for Hedgehog signal transduction in the zebrafish embryo. Genes and Development 5.
Zeitschriftenartikel
428 (6986), S. 955 - 959 (2004)
Mutations in cadherin 23 affect tip links in zebrafish sensory hair cells. Nature 6.
Zeitschriftenartikel
130 (23), S. 5755 - 5768 (2003)
lockjaw encodes a zebrafish tfap2a required for early neural crest development. Development 7.
Zeitschriftenartikel
130 (20), S. 5043 - 5052 (2003)
The zebrafish van gogh mutation disrupts tbx1, which is involved in the DiGeorge deletion syndrome in humans. Development 8.
Zeitschriftenartikel
278 (33), S. 31118 - 31127 (2003)
Heparan sulfate 6-o-sulfotransferase is essential for muscle development in zebrafish. The Journal of Biological Chemistry 9.
Zeitschriftenartikel
129 (14), S. 3281 - 3294 (2002)
parachute/n-cadherin is required for morphogenesis and maintained integrity of the zebrafish neural tube. Development 10.
Zeitschriftenartikel
129 (12), S. 2851 - 2865 (2002)
Retinoic acid signalling in the zebrafish embryo is necessary during pre-segmentation stages to pattern the anterior- posterior axis of the CNS and to induce a pectoral fin bud. Development 11.
Zeitschriftenartikel
129 (5), S. 1175 - 1183 (2002)
her1 and the notch pathway function within the oscillator mechanism that regulates zebrafish somitogenesis. Development 12.
Zeitschriftenartikel
128 (21), S. 4113 - 4125 (2001)
Zebrafish colourless encodes sox10 and specifies non-ectomesenchymal neural crest fates. Development 13.
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128 (16), S. 3081 - 3094 (2001)
The zebrafish neckless mutation reveals a requirement for raldh2 in mesodermal signals that pattern the hindbrain. Development 14.
Zeitschriftenartikel
15 (11), S. 1427 - 1434 (2001)
A mutation in the Gsk3-binding domain of zebrafish Masterblind/Axin1 leads to a fate transformation of telencephalon and eyes to diencephalon. Genes and Development 15.
Zeitschriftenartikel
128 (6), S. 849 - 858 (2001)
The type I serine/threonine kinase receptor Alk8/Lost-a-fin is required for Bmp2b/7 signal transduction during dorsoventral patterning of the zebrafish embryo. Development 16.
Zeitschriftenartikel
165 (12), S. 6984 - 6993 (2000)
Conservation of Mhc class III region synteny between zebrafish and human as determined by radiation hybrid mapping. The Journal of Immunology 17.
Zeitschriftenartikel
9 (14), S. 2189 - 2196 (2000)
Mariner is defective in myosin VIIA: a zebrafish model for human hereditary deafness. Human Molecular Genetics 18.
Zeitschriftenartikel
405 (6782), S. 76 - 81 (2000)
Silberblick/Wnt11 mediates convergent extension movements during zebrafish gastrulation. Nature 19.
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23 (1), S. 86 - 89 (1999)
A radiation hybrid map of the zebrafish genome. Nature Genetics 20.
Zeitschriftenartikel
126 (10), S. 2149 - 2159 (1999)
The smad5 mutation somitabun blocks Bmp2b signaling during early dorsoventral patterning of the zebrafish embryo. Development