Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Nadja Muncke"'
Autor:
Elizabeth Goldmuntz, Judith A. Goodship, Gudrun A. Rappold, Ralph Roeth, Nadja Muncke, Beate Niesler, Heinz-Juergen Rüdiger, Karin Schön
Publikováno v:
BMC Medical Genetics
BMC Medical Genetics, Vol 6, Iss 1, p 20 (2005)
BMC Medical Genetics, Vol 6, Iss 1, p 20 (2005)
Background PITX2 is a bicoid-related homeodomain transcription factor that plays an important role in asymmetric cardiogenesis. Loss of function experiments in mice cause severe heart malformations, including transposition of the great arteries (TGA)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ee0aa1ff20e7ce83055c0d8d9ab032c
https://pubmed.ncbi.nlm.nih.gov/15890066
https://pubmed.ncbi.nlm.nih.gov/15890066
Autor:
Christof Niehrs, Hajo Delius, Barbara Verbeek, Nadja Muncke, Yan Li, Ursula Fenger, Nicolas Pollet
Publikováno v:
Mechanisms of development. 122(3)
We have carried out a large-scale, semi-automated whole-mount in situ hybridization screen of 8369 cDNA clones in Xenopus laevis embryos. We confirm that differential gene expression is prevalent during embryogenesis since 24% of the clones are expre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::524066c1f9da89d2ae484ffc537d0219
https://pubmed.ncbi.nlm.nih.gov/15763213
https://pubmed.ncbi.nlm.nih.gov/15763213
Autor:
Martijn H. Breuning, Gudrun A. Rappold, V. Endris, Mark T. Ross, David Vetrie, Nadja Muncke, B.S. Wogatzky, Erik A. Sistermans, Coriene E. Catsman-Berrevoets
Publikováno v:
Muncke, N, Wogatzky, B S, Breuning, M, Sistermans, E A, Endris, V, Ross, M, Vetrie, D, Catsman-Berrevoets, C E & Rappold, G 2004, ' Position effect on PLP1 may cause a subset of Pelizaeus-Merzbacher disease symptoms. ', Journal of Medical Genetics, vol. 41, no. 12, pp. e121 . https://doi.org/10.1136/jmg.2004.019141
Journal of Medical Genetics, 41(12). BMJ Publishing Group
Journal of Medical Genetics, 41, e121-e121
Journal of Medical Genetics, 41, 12, pp. e121-e121
Journal of Medical Genetics, 41(12). BMJ Publishing Group
Journal of Medical Genetics, 41, e121-e121
Journal of Medical Genetics, 41, 12, pp. e121-e121
3 ). Two main forms of the disease, a connatal and a classical type, are recognised. The connatal type has a severe course with feeding problems, progressive pyramidal and extrapyramidal symptoms, laryngeal stridor, microce- phaly, very little develo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e0f3f80a33d5152f1ca6907de7ab29e
https://hdl.handle.net/2066/57188
https://hdl.handle.net/2066/57188
Autor:
Nitin Sabherwal, Ralph Röth, Katja U. Schneider, Nadja Muncke, Karin Jantz, Werner F. Blum, Gordon B. Cutler, Gudrun A. Rappold
Publikováno v:
The American Journal of Human Genetics. (1):89-96
Human growth is influenced not only by environmental and internal factors but also by a large number of different genes. One of these genes, SHOX, is believed to play a major role in growth, since defects in this homeobox-containing gene on the sex c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8fb16745f1710e958b5b40442c965f59