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Number of items: 3.

Filatova, Alina and Rey, Linda K. and Lechler, Marion B. and Schaper, Jörg and Hempel, Maja and Posmyk, Renata and Szczaluba, Krzysztof and Santen, Gijs W. E. and Wieczorek, Dagmar and Nuber, Ulrike A. (2019):
Mutations in SMARCB1 and in other Coffin-Siris syndrome genes lead to various brain midline defects.
In: Nature communications, 10 (1), p. 2966, ISSN 2041-1723,
DOI: 10.1038/s41467-019-10849-y,

Wolf, Christine and Rapp, Alexander and Berndt, Nicole and Staroske, Wolfgang and Schuster, Max and Dobrick-Mattheuer, Manuela and Kretschmer, Stefanie and König, Nadja and Kurth, Thomas and Wieczorek, Dagmar and Kast, Karin and Cardoso, M. Cristina and Günther, Claudia and Lee-Kirsch, Min Ae (2016):
RPA and Rad51 constitute a cell intrinsic mechanism to protect the cytosol from self DNA.
In: Nature communications, 7p. 11752, ISSN 2041-1723,

Endele, Sabine and Rosenberger, Georg and Geider, Kirsten and Popp, Bernt and Tamer, Ceyhun and Stefanova, Irina and Milh, Mathieu and Kortüm, Fanny and Fritsch, Angela and Pientka, Friederike K. and Hellenbroich, Yorck and Kalscheuer, Vera M. and Kohlhase, Jürgen and Moog, Ute and Rappold, Gudrun and Rauch, Anita and Ropers, Hans-Hilger and von Spiczak, Sarah and Tönnies, Holger and Villeneuve, Nathalie and Villard, Laurent and Zabel, Bernhard and Zenker, Martin and Laube, Bodo and Reis, André and Wieczorek, Dagmar and Van Maldergem, Lionel and Kutsche, Kerstin (2010):
Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes.
In: Nature genetics, (11), 42. pp. 1021-6, ISSN 1546-1718,

This list was generated on Tue Sep 29 02:33:27 2020 CEST.