Publikationen von Stefan Mundlos

Zeitschriftenartikel (266)

201.
Zeitschriftenartikel
Seitz, V.; Stiege, A. C.; Mundlos, S.; Lenze, D.; Lammert, H.; Clermont, A.; Hirsch, B.; Von Der Wall, E.; Müller, H.; Kirsch, A. et al.; Diaz-Espada, F.; Uharek, L.; Anagnostopoulos, I.; Stein, H.; Hummel, M.: Immunoglobulin receptor evolution in follicular lymphoma and a review of literature. Leukemia & Lymphoma 48 (10), S. 2063 - 2067 (2007)
202.
Zeitschriftenartikel
Uhrig, S.; Schlembach, D.; Waldispuehl-Geigl, J.; Schaffer, W.; Geigl, J.; Klopcki, E.; Mundlos, S.; Speicher, M. R.: Impact of array comparative genomic hybridization-derived information on genetic counseling demonstrated by prenatal diagnosis of the TAR (thrombocytopenia-absent-radius) syndrome-associated microdeletion 1q21.1. American Journal of Human Genetics: AJHG 81 (4), S. 866 - 868 (2007)
203.
Zeitschriftenartikel
Lehmann, K.; Seemann, P.; Silan, F.; Goecke, T. O.; Irgang, M.; Kjaer, K. W.; Kjaergaard, S.; Mahoney, M. J.; Morlot, S.; Reissner, C. et al.; Kerr, B.; Wilkie, A. O. M.; Mundlos, S.: A new subtype of brachydactyly type B caused by point mutations in the bone morphogenetic protein antagonist NOGGIN. The American Journal of Human Genetics: AJHG 81 (12), S. 388 - 396 (2007)
204.
Zeitschriftenartikel
Trepczi, B.; Lienau, J.; Schell, H.; Epari, D. R.; Thompson, M. S.; Hoffmann, J.-E.; Kadow-Romacker, A.; Mundlos, S.; Duda, G. N.: Endochondral ossification in vitro is influenced by mechanical bending. Bone 40 (3), S. 597 - 603 (2007)
205.
Zeitschriftenartikel
Kolanczyk, M.; Kossler, N.; Kühnisch, J.; Lavitas, L.; Stricker, S.; Wilkening, U.; Manjubala, I.; Fratzl, P.; Spörle, R.; Herrmann, B. G. et al.; Parada, L. F.; Kornak, U.; Mundlos, S.: Multiple roles for neurofibromin in skeletal development and growth. Human Molecular Genetics 16 (8), S. 232 - 240 (2007)
206.
Zeitschriftenartikel
Castori, M.; Brancati, F.; Mingarelli, R.; Mundlos, S.; Dallapiccola, B.: A novel patient with Cooks syndrome supports splitting from "classic" brachydactyly type B. American Journal of Medical Genetics/ Part A 143 (2), S. 195 - 199 (2007)
207.
Zeitschriftenartikel
Klopocki, E.; Schulze, H.; Strauß, G.; Ott, C.-E.; Hall, J.; Trotier, F.; Fleischhauer, S.; Greenhalgh, L.; Newbury-Ecob, R. A.; Neumann, L. M. et al.; Habenicht, R.; König, R.; Seemanova, E.; Megarbane, A.; Ropers, H.-H.; Ullmann, R.; Mundlos, S.: Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius. American Journal of Human Genetics: AJHG / American Society of Human Genetics 80 (2), S. 232 - 240 (2007)
208.
Zeitschriftenartikel
Klopocki, E.; Schulze, H.; Strauß, G.; Ott, C.-E.; Hall, J.; Trotier, F.; Fleischhauer, S.; Greenhalgh, L.; Newbury-Ecob, R. A.; Neumann, L. M. et al.; Habenicht, R.; König, R.; Seemanova, E.; Megarbane, A.; Ropers, H.-H.; Ullmann, R.; Mundlos, S.: Complex inheritance pattern resembling autosomal recessive inheritance involving a microdeletion in thrombocytopenia-absent radius. American Journal of Human Genetics: AJHG / American Society of Human Genetics 80 (2), S. 232 - 240 (2007)
209.
Zeitschriftenartikel
Zenker, M.; Lehmann, K.; Schulz, A. L.; Barth, H.; Hansmann, D.; Koenig, R.; Korinthenberg, R.; Kreiss-Nachtsheim, M.; Meinecke, P.; Morlot, S. et al.; Mundlos, S.; Quante, A. S.; Raskin, S.; Schnabel, D.; Wehner, L.-E.; Kratz, C. P.; Horn, D.; Kutsche, K.: Expansion of the genotypic and phenotypic spectrum in patients with KRAS germline mutations. Journal of Medical Genetics 44 (2), S. 131 - 135 (2007)
210.
Zeitschriftenartikel
Hecht, J.; Seitz, V.; Urban, M.; Wagner, F.; Robinson, P. N.; Stiege, A.; Dieterich, C.; Kornak, U.; Wilkening, U.; Brieske, N. et al.; Zwingman, C.; Kidess, A.; Stricker, S.; Mundlos, S.: Detection of novel skeletogenesis target genes by comprehensive analysis of a Runx2−/− mouse model. Gene Expression Patterns: A Section of Brain Research Devoted to Patterns of Expression of Genes during the Development, Maturity and Aging of the Central Nervous System 7 (1 - 2), S. 102 - 112 (2007)
211.
Zeitschriftenartikel
Klopocki, E.; Neumann, L. M.; Tönnies, H.; Ropers, H.-H.; Mundlos, S.; Ullmann, R.: Ulnar-mammary syndrome with dysmorphic facies and mental retardation caused by a novel 1.28 Mb deletion encompassing the TBX3 gene. European Journal of Human Genetics: the Official Journal of the European Society of Human Genetics. 14 (121), S. 1274 - 1279 (2006)
212.
Zeitschriftenartikel
Klopocki, E.; Neumann, L. M.; Tönnies, H.; Ropers, H.-H.; Mundlos, S.; Ullmann, R.: Ulnar-mammary syndrome with dysmorphic facies and mental retardation caused by a novel 1.28 Mb deletion encompassing the TBX3 gene. European Journal of Human Genetics: the Official Journal of the European Society of Human Genetics. 14 (121), S. 1274 - 1279 (2006)
213.
Zeitschriftenartikel
Lehmann, K.; Seemann, P.; Boergermann, J.; Morin, G.; Reif, S.; Knaus, P.; Mundlos, S.: A novel R486Q mutation in BMPR1B resulting in either a brachydactyly type C/symphalangism-like phenotype or brachydactyly type A2. European Journal of Human Genetics 14 (12), S. 1248 - 1254 (2006)
214.
Zeitschriftenartikel
Stricker, S.; Van Wijk, N. V.; Witte, F.; Brieske, N.; Seidel, K.; Mundlos, S.: Cloning and expression pattern of chicken Ror2 and functional characterization of truncating mutations in Brachydactyly type B and Robinow syndrome. Developmental Dynamics 235 (12), S. 3456 - 3465 (2006)
215.
Zeitschriftenartikel
Müller, D.; Klopocki, E.; Neumann, L. E.; Mundlos, S.; Taupitz, M.; Schulze, I.; Ropers, H.-H.; Querfeld, U.; Ullmann, R.: A complex phenotype with cystic renal disease. Kidney International: Official Journal of the International Society of Nephrology 70 (9), S. 1656 - 1660 (2006)
216.
Zeitschriftenartikel
Müller, D.; Klopocki, E.; Neumann, L. E.; Mundlos, S.; Taupitz, M.; Schulze, I.; Ropers, H.-H.; Querfeld, U.; Ullmann, R.: A complex phenotype with cystic renal disease. Kidney International: Official Journal of the International Society of Nephrology 70 (9), S. 1656 - 1660 (2006)
217.
Zeitschriftenartikel
Zemojtel, T.; Fröhlich, A.; Palmieri, M. C.; Kolanczyk, M.; Mikula, I.; Wyrwicz, L. S.; Wanker, E. E.; Mundlos, S.; Vingron, M.; Martasek, P. et al.; Durner, J.: Plant nitric oxide synthase: a never-ending story? Trends in Plant Science 11 (11), S. 524 - 525 (2006)
218.
Zeitschriftenartikel
Guo, G.; Booms, P.; Halushka, M.; Dietz, H. C.; Ney, A.; Stricker, S.; Hecht, J.; Mundlos, S.; Robinson, P. N.: Induction of Macrophage Chemotaxis by Aortic Extracts of the mgR Marfan Mouse Model and a GxxPG-Containing Fibrillin-1 Fragment. Circulation 17, S. 1855 - 1862 (2006)
219.
Zeitschriftenartikel
Alt, B.; Elsalini, O. A.; Schrumpf, P.; Haufs, N.; Lawson, N. D.; Schwabe, G. C.; Mundlos, S.; Grüters, A.; Krude, H.; Rohr, K. B.: Arteries define the position of the thyroid gland during its developmental relocalisation. Development 133 (19), S. 3797 - 3804 (2006)
220.
Zeitschriftenartikel
Stricker, S.; Brieske, N.; Haupt, J.; Mundlos, S.: Comparative expression pattern of Odd-skipped related genes Osr1 and Osr2 in chick embryonic development. Gene Expression Patterns 6 (8), S. 826 - 834 (2006)
Zur Redakteursansicht