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of 876
pro vyhledávání: '"Altmüller, J."'
Autor:
Thomalla, D., Beckmann, L. ∗, Grimm, C., Oliverio, M., Meder, L., Herling, C.D., Nieper, P., Feldmann, T., Merkel, O., Lorsy, E., da Palma Guerreiro, A., von Jan, J., Kisis, I., Wasserburger, E., Claasen, J., Faitschuk-Meyer, E., Altmüller, J., Nürnberg, P., Yang, T.-P., Lienhard, M., Herwig, R., Kreuzer, K.-A., Pallasch, C.P., Büttner, R., Schäfer, S.C., Hartley, J., Abken, H., Peifer, M., Kashkar, H., Knittel, G., Eichhorst, B., Ullrich, R.T., Herling, M., Reinhardt, H.C., Hallek, M., Schweiger, M.R., Frenzel, L.P. ∗∗
Publikováno v:
In Blood 17 November 2022 140(20):2113-2126
Autor:
Oberbeck, S. *, Schrader, A. *, Warner, K. *, Jungherz, D., Crispatzu, G., von Jan, J., Chmielewski, M., Ianevski, A., Diebner, H.H., Mayer, P., Kondo Ados, A., Wahnschaffe, L., Braun, T., Müller, T.A., Wagle, P., Bouska, A., Neumann, T., Pützer, S., Varghese, L., Pflug, N., Thelen, M., Makalowski, J., Riet, N., Göx, H.J.M., Rappl, G., Altmüller, J., Kotrová, M., Persigehl, T., Hopfinger, G., Hansmann, M.L., Schlößer, H., Stilgenbauer, S., Dürig, J., Mougiakakos, D., von Bergwelt-Baildon, M., Roeder, I., Hartmann, S., Hallek, M., Moriggl, R., Brüggemann, M., Aittokallio, T., Iqbal, J., Newrzela, S., Abken, H., Herling, M. *
Publikováno v:
In Blood 10 December 2020 136(24):2786-2802
Autor:
Siede, D., Rapti, K., Gorska, A.A., Katus, H.A., Altmüller, J., Boeckel, J.N., Meder, B., Maack, C., Völkers, M., Müller, O.J., Backs, J., Dieterich, C.
Publikováno v:
In Journal of Molecular and Cellular Cardiology August 2017 109:48-56
Autor:
Zhu, M., Metzen, F., Hopkinson, M., Betz, J., Heilig, J., Sodhi, J., Imhof, T., Niehoff, A., Birk, D.E., Izu, Y., Krüger, M., Pitsillides, A. A., Altmüller, J., van Osch, G.J.V.M., Straub, V., Schreiber, G., Paulsson, M., Koch, M., Brachvogel, B.
Collagen XII, belonging to the fibril-associated collagens, is a homotrimeric secreted extracellular matrix (ECM) protein encoded by the COL12A1 gene. Mutations in the human COL12A1 gene cause an Ehlers-Danlos/myopathy overlap syndrome leading to ske
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=mdc______med::42cfca9c27b74c21064fe137b7cc1f2d
http://edoc.mdc-berlin.de/23567/2/23567suppl.pdf
http://edoc.mdc-berlin.de/23567/2/23567suppl.pdf
Publikováno v:
Breast Cancer: Targets and Therapy, Vol Volume 8, Pp 243-252 (2016)
Lea V Weber,1 Klaudia Al-Refae,1 Gerhard Wölk,2 Gabriele Bonatz,3 Janine Altmüller,4 Christian Becker,4 Günter Gisselmann,1 Hanns Hatt1 1Department of Cell Physiology, Ruhr‑University Bochum, Bochum, 2Herz-Jesu-Krankenhaus, Dernbach, 3Augusta Kl
Externí odkaz:
https://doaj.org/article/801fdf79cbe24d2c878d5db3fa0e6fba
Autor:
Averdunk, L., Al-Thihli, K., Surowy, H., Lüdecke, H.J., Drechsler, M., Yigit, G., Smorag, L., Hallak, B.A., Li, Y., Altmüller, J., Guthoff, T., Wallot, M., Nürnberg, P., Wollnik, B., Abou Jamra, R., Al-Maawali, A., Wieczorek, D.
Protein translation is an essential cellular process and dysfunctional protein translation causes various neurodevelopmental disorders. The eukaryotic translation elongation factor 1A (eEF1A) delivers aminoacyl-tRNA to the ribosome, while the eEF1B c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=mdc______med::fb7cb17a86c78edb2e7c071336847640
http://edoc.mdc-berlin.de/23007/1/23007oa.pdf
http://edoc.mdc-berlin.de/23007/1/23007oa.pdf
Akademický článek
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Autor:
Baur, F., Weiss, K., Osman, K., Saunders, C., Cadieux-Dion, M., So, J., Biswas, S., Altmüller, J., Jungbluth, H., Antebi, A., Dafsari, H. S.
Publikováno v:
Neuropediatrics; 2023 Supplement 1, Vol. 54, pS1-S32, 32p
Autor:
Schmidt, J., Dreha-Kulaczewski, S., Zafeiriou, M.P., Schreiber, M.K., Wilken, B., Funke, R., Neuhofer, C., Altmüller, J., Thiele, H., Nürnberg, P., Biskup, S., Li, Y., Zimmermann, W.H., Kaulfuß, S., Yigit, G., Wollnik, B.
Publikováno v:
Front. Cell Dev. Biol. 10:1025332 (2022)
STAG2 is a component of the large, evolutionarily highly conserved cohesin complex, which has been linked to various cellular processes like genome organization, DNA replication, gene expression, heterochromatin formation, sister chromatid cohesion,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2b32f16f2200a9a871e521858a305b0c
https://doi.org/10.3389/fcell.2022.1025332
https://doi.org/10.3389/fcell.2022.1025332
Autor:
Andreotti, S., Altmüller, J., Quedenau, C., Borodina, T., Nouailles, G., Teixeira Alves, L.G., Landthaler, M., Bieniara, M., Trimpert, J., Wyler, E.
The Roborovski dwarf hamster Phodopus roborovskii belongs to the Phodopus genus, one of seven within Cricetinae subfamily. Like other rodents such as mice, rats or ferrets, hamsters can be important animal models for a range of diseases. Whereas the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=mdc______med::39e7d835ef9488b3dbe8b4ca805b2cc9
http://edoc.mdc-berlin.de/21753/1/21753oa.pdf
http://edoc.mdc-berlin.de/21753/1/21753oa.pdf