Zeitschriftenartikel (223)
1.
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5 (12), S. e15754 - e15754 (2010)
The effect of MNase on nucleosome positioning data. PLoS ONE 2.
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11 (12), S. 11:144 - 11:144 (2010)
Whole-exome sequencing for finding de novo mutations in sporadic mental retardation. Genome Biology 3.
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123 (Pt 24), S. 4340 - 4350 (2010)
Quantitative analysis of TGFBR2 mutations in Marfan-syndrome-related disorders suggests a correlation between phenotypic severity and Smad signaling activity. Journal of Cell Science 4.
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330 (6010), S. 1543 - 1546 (2010)
Genome expansion and gene loss in powdery mildew fungi reveal tradeoffs in extreme parasitism. Science 5.
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5 (12), S. e15661 - e15661 (2010)
Somatic mutation profiles of MSI and MSS colorectal cancer identified by whole exome next generation sequencing and bioinformatics analysis. PLoS ONE 6.
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17 (12), S. 1591 - 1606 (2010)
Studying the evolution of promoter sequences: a waiting time problem. Journal Computational Biology 7.
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330 (6009), S. 1381 - 1385 (2010)
Plasticity of animal genome architecture unmasked by rapid evolution of a pelagic tunicate. Science 8.
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6 (12), S. e1001231 - e1001231 (2010)
Identification of Y-box binding protein 1 as a core regulator of MEK/ERK pathway dependent gene signatures in colorectal cancer cells. PLoS Genetics 9.
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468 (7324), S. 713 - 716 (2010)
Head swivel on the ribosome facilitates translocation by means of intra-subunit tRNA hybrid sites. Nature 10.
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13 (6), S. 582 - 594 (2010)
Monozygotic twins with neurofibromatosis type 1 (NF1) display differences in methylation of NF1 gene promoter elements, 5' untranslated region, exon and intron 1. Twin Research and Human Genetics: the Official Journal of the International Society for Twin Studies. 11.
Zeitschriftenartikel
152A (12), S. 3016 - 3021 (2010)
Brachydactyly type A1 with short humerus and associated skeletal features. American Journal of Medical Genetics Part A 12.
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A Cyclic AMP Analog, 8-Br-cAMP, Enhances the Induction of Pluripotency in Human Fibroblast Cells. (2010)
13.
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10, S. 10:370 - 10:370 (2010)
The globin gene family of the cephalochordate amphioxus: implications for chordate globin evolution. BMC Evolutionary Biology 14.
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24 (2), S. 1 - 11 (2010)
Integrative analysis of genomic, functional and protein interaction data predicts long-range enhancer-target gene interactions. Nucleic Acids Research 15.
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107 (46), S. 19748 - 19753 (2010)
Cryo-EM structure and rRNA model of a translating eukaryotic 80S ribosome at 5.5-A resolution. Preceedings of the National Academy of Sciences USA 16.
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107 (46), S. 19754 - 19759 (2010)
Localization of eukaryote-specific ribosomal proteins in a 5.5-A cryo-EM map of the 80S eukaryotic ribosome. Proceedings of the National Academy of Sciences USA 17.
Zeitschriftenartikel
129 (2), S. 141 - 148 (2010)
Autosomal recessive mental retardation: homozygosity mapping identifies 27 single linkage intervals, at least 14 nvel loci and several mutation hotspots. Human Genetics 18.
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50 (1), S. 8 - 15 (2010)
Expression analysis of proline rich 15 (Prr15) in mouse and human gastrointestinal tumors. Molecular Carcinogenesis 19.
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152A (11), S. 2749 - 2755 (2010)
Marfan syndrome with neonatal progeroid syndrome-like lipodystrophy associated with a novel frameshift mutation at the 3' terminus of the FBN1-gene. American Journal of Medical Genetics Part A 20.
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31 (11), S. E1851 - E1860 (2010)
Identification of FOXP1 deletions in three unrelated patients with mental retardation and significant speech and language deficits. Human Mutation