Accès ouvert
2008
article
OpenAlex
Susana S. Lopes, Xueyan Yang, Jeanette Müller, Thomas J. Carney et autres
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 remain incompletely understood. Sox10 is required for specification of neural cells and melanocytes from NCCs. Like …
gb, us, de
(code pays fourni par la source)
Accès ouvert
2004
preprint
OpenAlex
Christian M. Wolff, Sudipto Roy, Katharine E. Lewis, Heike E. Schauerte et autres
Signaling by lipid-modified secreted glycoproteins of the Hedgehog family play fundamental roles during pattern formation in animal development and in humans; dysfunction of Hedgehog pathway components is frequently associated with a variety of congenital abnormalities and cancer. Transcriptional regulation of Hedgehog target …
de, sg, gb
(code pays fourni par la source)
Accès ouvert
2003
article
OpenAlex
Tatjana Piotrowski, Dae-gwon Ahn, Thomas Friedrich Schilling, Sreelaja Nair et autres
The van gogh (vgo) mutant in zebrafish is characterized by defects in the ear, pharyngeal arches and associated structures such as the thymus. We show that vgo is caused by a mutation in tbx1, a member of the large family of T-box …
us, de
(code pays fourni par la source)
2002
erratum
OpenAlex
Y. L. Yan, Craig T. Miller, Robert M. Nissen, Amy Singer et autres
2002
article
OpenAlex
Yi‐Lin Yan, Craig T. Miller, Robert M. Nissen, Amy Singer et autres
The molecular genetic mechanisms of cartilage construction are incompletely understood. Zebrafish embryos homozygous for jellyfish (jef) mutations show craniofacial defects and lack cartilage elements of the neurocranium, pharyngeal arches, and pectoral girdle similar to humans with campomelic dysplasia. We show that two …
us, de, tw
(code pays fourni par la source)
2002
article
OpenAlex
Susana S. Lopes, Gerd-Jörg Rauch, Robert Geisler, Pascal Haffter et autres
2001
article
OpenAlex
Kirsten A. Dutton, Angela Pauliny, Susana S. Lopes, Stone Elworthy et autres
Waardenburg-Shah syndrome combines the reduced enteric nervous system characteristic of Hirschsprung's disease with reduced pigment cell number, although the cell biological basis of the disease is unclear. We have analysed a zebrafish Waardenburg-Shah syndrome model. We show that the colourless gene encodes …
gb, de
(code pays fourni par la source)
Accès ouvert
2001
article
OpenAlex
Jau‐Nian Chen, Frauke van Bebber, Allan M. Goldstein, Fabrizio C. Serluca et autres
All internal organs are asymmetric along the left-right axis. Here we report a genetic screen to discover mutations which perturb organ laterality. Our particular focus is upon whether, and how, organs are linked to each other as they achieve their laterally asymmetric …
us, de
(code pays fourni par la source)
Accès ouvert
2000
article
OpenAlex
Barbara Boggetti, Francesco Argenton, Pascal Haffter, Marco Emilio Bianchi et autres
it, de
(code pays fourni par la source)
Accès ouvert
2000
article
OpenAlex
Heike Pöpperl, Holly A. Rikhof, Heather H. Cheng, Pascal Haffter et autres
us, de
(code pays fourni par la source)
Accès ouvert
2000
article
OpenAlex
Aiping Liu, Årindam Majumdar, Heike E. Schauerte, Pascal Haffter et autres
de
(code pays fourni par la source)
Accès ouvert
2000
article
OpenAlex
Jörg Odenthal, Fredericus J. M. van Eeden, Pascal Haffter, Philip William Ingham et autres
de, gb
(code pays fourni par la source)