Zeitschriftenartikel (2784)

2761.
Zeitschriftenartikel
Volleth, M.; Stumm, M.; Mohnike, K.; Kalscheuer, V. M.; Jakubiczka, S.; Wieacker, P.: Preferential inactivation of a dupX(q23 --> q27-28) chromosome in a girl with mental retardation and dysmorphy. Hum Hered 52 (3), S. 177 - 82 (2001)
2762.
Zeitschriftenartikel
Blagitko, N.; Mergenthaler, S.; Schulz, U.; Wollmann, H. A.; Craigen, W.; Eggermann, T.; Ropers, H. H.; Kalscheuer, V. M.: Human GRB10 is imprinted and expressed from the paternal and maternal allele in a highly tissue- and isoform-specific fashion. Hum Mol Genet 9 (11), S. 1587 - 95 (2000)
2763.
Zeitschriftenartikel
Brunner, B.; Grutzner, F.; Yaspo, M. L.; Ropers, H. H.; Haaf, T.; Kalscheuer, V. M.: Molecular cloning and characterization of the Fugu rubripes MEST/COPG2 imprinting cluster and chromosomal localization in Fugu and Tetraodon nigroviridis. Chromosome Res 8 (6), S. 465 - 76 (2000)
2764.
Zeitschriftenartikel
Mergenthaler, S.; Blagitko-Dorfs, N.; Wollmann, H. A.; Ranke, M. B.; Ropers, H. H.; Kalscheuer, V. M.; Eggermann, T.: Identification of two new polymorphisms (c2447-125A>G; c2532G>A) in the gamma 2-COP (COPG2) gene by screening of Silver-Russell syndrome patients. Hum Mutat 16 (1), S. 96 (2000)
2765.
Zeitschriftenartikel
Singh, A.; Henschel, S.; Sperling, K.; Kalscheuer, V.; Neitzel, H.: Differences in the meiotic pairing behavior of gonosomal heterochromatin between female and male Microtus agrestis: implications for the mechanism of heterochromatin amplification on the X and Y. Cytogenet Cell Genet 91 (1-4), S. 253 - 60 (2000)
2766.
Zeitschriftenartikel
Blagitko, N.; Schulz, U.; Schinzel, A. A.; Ropers, H. H.; Kalscheuer, V. M.: gamma2-COP, a novel imprinted gene on chromosome 7q32, defines a new imprinting cluster in the human genome. Hum Mol Genet 8 (13), S. 2387 - 96 (1999)
2767.
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)
2768.
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)
2769.
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)
2770.
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)
2771.
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)
2772.
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)
2773.
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)
2774.
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)
2775.
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)
2776.
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)
2777.
Zeitschriftenartikel
Adelfalk, C.; Scherthan, H.; Hirsch-Kauffmann, M.; Schweiger, M.: Nuclear deformation characterizes Werner syndrome cells.
2778.
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.
2779.
Zeitschriftenartikel
Meinel, T.; Krause, A.; Luz, H.; Vingron, M.; Staub, E.: The SYSTERS Protein Family Database in 2005.
2780.
Zeitschriftenartikel
Schlesinger, J.; Schüler, M.: The Cardiac Transcription Network Modulated by Gata4, Mef2a, Nkx2.5, Srf, Histone Modifications, and MircoRNAs.
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