Zeitschriftenartikel (3043)
3021.
Zeitschriftenartikel
9 (11), S. 1587 - 95 (2000)
Human GRB10 is imprinted and expressed from the paternal and maternal allele in a highly tissue- and isoform-specific fashion. Hum Mol Genet 3022.
Zeitschriftenartikel
8 (6), S. 465 - 76 (2000)
Molecular cloning and characterization of the Fugu rubripes MEST/COPG2 imprinting cluster and chromosomal localization in Fugu and Tetraodon nigroviridis. Chromosome Res 3023.
Zeitschriftenartikel
16 (1), S. 96 (2000)
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 3024.
Zeitschriftenartikel
91 (1-4), S. 253 - 60 (2000)
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 3025.
Zeitschriftenartikel
8 (13), S. 2387 - 96 (1999)
gamma2-COP, a novel imprinted gene on chromosome 7q32, defines a new imprinting cluster in the human genome. Hum Mol Genet 3026.
Zeitschriftenartikel
9 (5), S. 437 - 48 (1999)
Genomic structure and comparative analysis of nine Fugu genes: conservation of synteny with human chromosome Xp22.2-p22.1. Genome Res 3027.
Zeitschriftenartikel
232 (1), S. 35 - 42 (1999)
Identification and characterization of G90, a novel mouse RNA that lacks an extensive open reading frame. Gene 3028.
Zeitschriftenartikel
10 (4), S. 419 - 22 (1999)
Regulation and expression of the murine PMP22 gene. Mamm Genome 3029.
Zeitschriftenartikel
80 (1-4), S. 165 - 72 (1998)
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 3030.
Zeitschriftenartikel
6 (2), S. 114 - 20 (1998)
Evidence against a major role of PEG1/MEST in Silver-Russell syndrome. Eur J Hum Genet 3031.
Zeitschriftenartikel
245 (1), S. 272 - 7 (1998)
Absence of an obvious molecular imprinting mechanism in a human fetus with monoallelic IGF2R expression. Biochem Biophys Res Commun 3032.
Zeitschriftenartikel
42 (2), S. 236 - 44 (1997)
Monoallelic expression of human PEG1/MEST is paralleled by parent-specific methylation in fetuses. Genomics 3033.
Zeitschriftenartikel
73 (3), S. 171 - 8 (1996)
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 3034.
Zeitschriftenartikel
35 (2), S. 380 - 2 (1996)
The MAS proto-oncogene is not imprinted in humans. Genomics 3035.
Zeitschriftenartikel
31 (2), S. 158 - 66 (1996)
Maternal-specific methylation of the human IGF2R gene is not accompanied by allele-specific transcription. Genomics 3036.
Zeitschriftenartikel
Nuclear deformation characterizes Werner syndrome cells.
3037.
Zeitschriftenartikel
A colorectal cancer expression profile that includes transforming growth factor ß inhibitor BAMBI predicts metastatic potential.
3038.
Zeitschriftenartikel
The SYSTERS Protein Family Database in 2005.
3039.
Zeitschriftenartikel
The Cardiac Transcription Network Modulated by Gata4, Mef2a, Nkx2.5, Srf, Histone Modifications, and MircoRNAs.
3040.
Zeitschriftenartikel
A gene expression map of Arabidopsis development.