Zeitschriftenartikel (3038)

3021.
Zeitschriftenartikel
Brunner, B.; Todt, T.; Lenzner, S.; Stout, K.; Schulz, U.; Ropers, H. H.; Kalscheuer, V. M.: Genomic structure and comparative analysis of nine Fugu genes: conservation of synteny with human chromosome Xp22.2-p22.1. Genome Res 9 (5), S. 437 - 48 (1999)
3022.
Zeitschriftenartikel
Krause, R.; Hemberger, M.; Himmelbauer, H.; Kalscheuer, V.; Fundele, R. H.: Identification and characterization of G90, a novel mouse RNA that lacks an extensive open reading frame. Gene 232 (1), S. 35 - 42 (1999)
3023.
Zeitschriftenartikel
van de Wetering, R. A.; Gabreels-Festen, A. A.; Kremer, H.; Kalscheuer, V. M.; Gabreels, F. J.; Mariman, E. C.: Regulation and expression of the murine PMP22 gene. Mamm Genome 10 (4), S. 419 - 22 (1999)
3024.
Zeitschriftenartikel
Neitzel, H.; Kalscheuer, V.; Henschel, S.; Digweed, M.; Sperling, K.: Beta-heterochromatin in mammals: evidence from studies in Microtus agrestis based on the extensive accumulation of L1 and non-L1 retroposons in the heterochromatin. Cytogenet Cell Genet 80 (1-4), S. 165 - 72 (1998)
3025.
Zeitschriftenartikel
Riesewijk, A. M.; Blagitko, N.; Schinzel, A. A.; Hu, L.; Schulz, U.; Hamel, B. C.; Ropers, H. H.; Kalscheuer, V. M.: Evidence against a major role of PEG1/MEST in Silver-Russell syndrome. Eur J Hum Genet 6 (2), S. 114 - 20 (1998)
3026.
Zeitschriftenartikel
Riesewijk, A. M.; Xu, Y. Q.; Schepens, M. T.; Mariman, E. M.; Polychronakos, C.; Ropers, H. H.; Kalscheuer, V. M.: Absence of an obvious molecular imprinting mechanism in a human fetus with monoallelic IGF2R expression. Biochem Biophys Res Commun 245 (1), S. 272 - 7 (1998)
3027.
Zeitschriftenartikel
Riesewijk, A. M.; Hu, L.; Schulz, U.; Tariverdian, G.; Hoglund, P.; Kere, J.; Ropers, H. H.; Kalscheuer, V. M.: Monoallelic expression of human PEG1/MEST is paralleled by parent-specific methylation in fetuses. Genomics 42 (2), S. 236 - 44 (1997)
3028.
Zeitschriftenartikel
Kalscheuer, V.; Singh, A. P.; Nanda, I.; Sperling, K.; Neitzel, H.: Evolution of the gonosomal heterochromatin of Microtus agrestis: rapid amplification of a large, multimeric, repeat unit containing a 3.0-kb (GATA)11-positive, middle repetitive element. Cytogenet Cell Genet 73 (3), S. 171 - 8 (1996)
3029.
Zeitschriftenartikel
Riesewijk, A. M.; Schepens, M. T.; Mariman, E. M.; Ropers, H. H.; Kalscheuer, V. M.: The MAS proto-oncogene is not imprinted in humans. Genomics 35 (2), S. 380 - 2 (1996)
3030.
Zeitschriftenartikel
Riesewijk, A. M.; Schepens, M. T.; Welch, T. R.; van den Berg-Loonen, E. M.; Mariman, E. M.; Ropers, H. H.; Kalscheuer, V. M.: Maternal-specific methylation of the human IGF2R gene is not accompanied by allele-specific transcription. Genomics 31 (2), S. 158 - 66 (1996)
3031.
Zeitschriftenartikel
Adelfalk, C.; Scherthan, H.; Hirsch-Kauffmann, M.; Schweiger, M.: Nuclear deformation characterizes Werner syndrome cells.
3032.
Zeitschriftenartikel
Fritzmann, J.; Morkel, M.; Besser, D.; Budczies, J.; Frauke, K.; Brembeck, F. H.; Stein, U.; Fichtner, I.; Schlag, P. M.; Birchmeier, W.: A colorectal cancer expression profile that includes transforming growth factor ß inhibitor BAMBI predicts metastatic potential.
3033.
Zeitschriftenartikel
Meinel, T.; Krause, A.; Luz, H.; Vingron, M.; Staub, E.: The SYSTERS Protein Family Database in 2005.
3034.
Zeitschriftenartikel
Schlesinger, J.; Schüler, M.: The Cardiac Transcription Network Modulated by Gata4, Mef2a, Nkx2.5, Srf, Histone Modifications, and MircoRNAs.
3035.
Zeitschriftenartikel
Schmid, M.; Davison, T. S.; Henz, S. R.; Pape, U. J.; Demar, M.; Vingron, M.; Schoelkopf, B.; Weigel, D.; Lohmann, J. U.: A gene expression map of Arabidopsis development.
3036.
Zeitschriftenartikel
Steinhoff, C.; Schulz, W. A.: Genome-wide distribution and localization of putative functional human LINE-1 retrotransposons.
3037.
Zeitschriftenartikel
Zanni, G.; van Esch, H.; Bensalem, A.; Saillour, Y.; Poirier, K.; Castelnau, L.; Ropers, H.-H.; . de Brouwer, A. P. M.; Laumonnier, F.; Fryns, J.-P. et al.; Chelly, J.: A novel mutation in the DLG3 gene encoding the synapse-associated protein 102 (SAP102) causes non-syndromic mental retardation.
3038.
Zeitschriftenartikel
Ziegler, G.; Freyer, D.; Harhausen, D.; Khojasteh, U.; Nietfeld, W.; Trendelenburg, G.: Blocking TLR2 in vivo protects against accumulation of inflammatory cells and neuronal injury in experimental stroke.

Buch (9)

3039.
Buch
Mundlos, S.; Horn, D.: Limb Malformations – An Atlas of Genetic Disorders of Limb Development. Springer-Verlag, Berlin, Heidelberg (2014), 767 S.
3040.
Buch
Daskalaki, A.: Medical Advancements in Aging and Regenerative Technologies: Clinical Tools and Applications. IGI Global (2012)
Zur Redakteursansicht