Publication Overview

Journal Article (8)

1.
Journal Article
Althoff, G. E. M.; Wolfer, D. P.; Timmesfeld, N.; Kanzler, B.; Schrewe, H.; Axel, P.: Long-Term Expression of Tissue-Inhibitor of Matrix Metalloproteinase-1 in the Murine Central Nervous System Does Not Alter the Morphological and Behavioral Phenotype but Alleviates the Course of Experimental Allergic Encephalomyelitis. The American Journal of Pathology 177 (2), pp. 840 - 853 (2010)
2.
Journal Article
Rocha, P. P.; Scholze, M.; Bleiß, W.; Schrewe, H.: Med12 is essential for early mouse development and for canonical Wnt and Wnt/PCP signaling. Development 137, pp. 2723 - 2731 (2010)
3.
Journal Article
Herrmann, B. G.: Embryology meets cancer research. Public Service Review: Science and Technology 7, pp. 242 - 243 (2010)
4.
Journal Article
Zi, Z.; Liebermeister, W.; Klipp, E.: A quantitative study of the Hog1 MAPK response to fluctuating osmotic stress in Saccharomyces cerevisiae. A Quantitative Study of the Hog1 MAPK Response to Fluctuating Osmotic Stress in Saccharomyces cerevisiae 5 (3), e9522 (2010)
5.
Journal Article
Endele, S.; Rosenberger, G.; Geider, K.; Popp, B.; Tamer, C.; Stefanova, I.; Milh, M.; Kortum, F.; Fritsch, A.; Pientka, F. K. et al.; Hellenbroich, Y.; Kalscheuer, V. M.; Kohlhase, J.; Moog, U.; Rappold, G.; Rauch, A.; Ropers, H. H.; von Spiczak, S.; Tonnies, H.; Villeneuve, N.; Villard, L.; Zabel, B.; Zenker, M.; Laube, B.; Reis, A.; Wieczorek, D.; Van Maldergem, L.; Kutsche, K.: Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes. Nat Genet 42 (11), pp. 1021 - 6 (2010)
6.
Journal Article
Rocha, P. P.; Bleiss, W.; Schrewe, H.: Mosaic Expression of Med12 in Female Mice Leads to Exencephaly, Spina Bifida, and Craniorachischisis. Birth Defects Research Part A: Clinical and Molecular Teratology 88 (8), pp. 626 - 632 (2010)
7.
Journal Article
Slezak, R.; Luczak, K.; Kalscheuer, V.; Neumann, T. E.; Sasiadek, M. M.: Noonan-like/multiple giant cell lesion syndrome in two adult patients with SOS1 gene mutations. Clin Dysmorphol 19 (3), pp. 157 - 60 (2010)
8.
Journal Article
Tzschach, A.; Bisgaard, A. M.; Kirchhoff, M.; Graul-Neumann, L. M.; Neitzel, H.; Page, S.; Ahmed, A.; Muller, I.; Erdogan, F.; Ropers, H. H. et al.; Kalscheuer, V. M.; Ullmann, R.: Chromosome aberrations involving 10q22: report of three overlapping interstitial deletions and a balanced translocation disrupting C10orf11. Eur J Hum Genet 18 (3), pp. 291 - 5 (2010)
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