Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Lorenz Neidhardt"'
Publikováno v:
Development genes and evolution. 207(5)
During vertebrate embryonic development, pairs of metameric units, the somites, bud off at the cranial end of the paraxial mesoderm. The somites soon obtain cranio-caudal and dorso-ventral polarity. Establishment of dorso-ventral and medio-lateral po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a24b24cbeb90c91525eabfc17b542d6
https://pubmed.ncbi.nlm.nih.gov/27747430
https://pubmed.ncbi.nlm.nih.gov/27747430
Publikováno v:
Development. 128:3987-3994
The transcription factor Pax6 is required for eye morphogenesis in humans, mice and insects, and can induce ectopic eye formation in vertebrate and invertebrate organisms. Although the role of Pax6 has intensively been studied, only a limited number
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a8f5899a9caf35cb6f707db80c6b5c31
https://doi.org/10.1242/dev.128.20.3987
https://doi.org/10.1242/dev.128.20.3987
Autor:
Hans Lehrach, Susanne Worpenberg, Franz Obermayr, Stéphan Gasca, Bernhard G. Herrmann, Lorenz Neidhardt, Karin Wertz
Publikováno v:
Mechanisms of Development. 98(1-2):77-93
We have adapted the whole-mount in situ hybridization technique to perform high-throughput gene expression analysis in mouse embryos. A large-scale screen for genes showing specific expression patterns in the mid-gestation embryo was carried out, and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::217b15cac8c8185d774facfc35d76460
Publikováno v:
Web of Science
The axial skeleton develops from the sclerotome, a mesenchymal cell mass derived from the ventral halves of the somites, segmentally repeated units located on either side of the neural tube. Cells from the medial part of the sclerotome form the axial
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2acbe68c269a4d9059fb70ea177aff38
https://doi.org/10.1242/dev.127.11.2259
https://doi.org/10.1242/dev.127.11.2259
Autor:
Sabine Schrinner, Ralf Herwig, Bernhard G. Herrmann, Reha Yildirimman, Yorick Gitton, Manuela Scholze, Ariel Ruiz i Altaba, Lorenz Neidhardt, Hans Lehrach, Alia Benkahla, Sonya Baik, Pascal Kahlem, Nadia Dahmane, Marie-Laure Yaspo
Publikováno v:
Nature
Nature, Nature Publishing Group, 2002, 420 (6915), pp.586-590. ⟨10.1038/nature01270⟩
Nature, 2002, 420 (6915), pp.586-590. ⟨10.1038/nature01270⟩
Nature, Vol. 420, No 6915 (2002) pp. 586-590
Nature, Nature Publishing Group, 2002, 420 (6915), pp.586-590. ⟨10.1038/nature01270⟩
Nature, 2002, 420 (6915), pp.586-590. ⟨10.1038/nature01270⟩
Nature, Vol. 420, No 6915 (2002) pp. 586-590
The DNA sequence of human chromosome 21 (HSA21) has opened the route for a systematic molecular characterization of all of its genes. Trisomy 21 is associated with Down's syndrome, the most common genetic cause of mental retardation in humans. The ph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3e6e83a67b924820b3ade0dab959ca50
https://hal.archives-ouvertes.fr/hal-03092559
https://hal.archives-ouvertes.fr/hal-03092559
