Zeitschriftenartikel (247)
41.
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11 (3), S. 246 - 53 (2011)
Alzheimer's genetics in the GWAS era: a continuing story of 'replications and refutations'. Current Neurology and Neuroscience Reports 42.
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95 (4), S. 501 - 4 (2011)
The role of genetics for biomarker development in neurodegeneration. Progress in Neurobiology 43.
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9 (1), S. e1000581 (2011)
SecM-stalled ribosomes adopt an altered geometry at the peptidyl transferase center. PLoS Biology 44.
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118 (20), S. 5583 - 92 (2011)
Mesenchymal stromal cells of myelodysplastic syndrome and acute myeloid leukemia patients have distinct genetic abnormalities compared with leukemic blasts. Blood 45.
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2 (5), S. 393 - 400 (2011)
No evidence for a shift in pyruvate kinase PKM1 to PKM2 expression during tumorigenesis. Oncotarget 46.
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6 (6), S. 859 - 69 (2011)
Monitoring protein expression in whole-cell extracts by targeted label- and standard-free LC-MS/MS. Nature Protocols 47.
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124 (Pt 18), S. 3137 - 48 (2011)
SPOC1 (PHF13) is required for spermatogonial stem cell differentiation and sustained spermatogenesis. J Cell Sci 48.
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286 (3-4), S. 279 - 91 (2011)
Methylation-specific ligation detection reaction (msLDR): a new approach for multiplex evaluation of methylation patterns. Molecular Genetics and Genomics: MGG 49.
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500, S. 79 - 98 (2011)
A strand-specific library preparation protocol for RNA sequencing. Methods in Enzymology 50.
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39 (2), S. 675 - 686 (2011)
Human box C/D snoRNAs with miRNA like functions: expanding the range of regulatory RNAs. Nucleic Acids Research 51.
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Isolated NIBPL missense mutations that cause Cornelia de Lange syndrome alter MAU2 interaction. Eur J Hum Genet (2011)
52.
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16 (3), S. 485 - 98 (2011)
P50 sensory gating and smoking in the general population. Addict Biol 53.
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44 (2), S. 214 - 24 (2011)
Structure and dynamics of the mammalian ribosomal pretranslocation complex. Mol Cell 54.
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44 (2), S. 214 - 24 (2011)
Structure and dynamics of the mammalian ribosomal pretranslocation complex. Molecular Cell 55.
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41 (1), S. 125 - 33 (2011)
A cohort of balanced reciprocal translocations associated with dyslexia: identification of two putative candidate genes at DYX1. Behav Genet 56.
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54 (3), S. 256 - 61 (2011)
Microdeletions of chromosome 7p21, including TWIST1, associated with significant microcephaly, facial dysmorphism, and short stature. Eur J Med Genet 57.
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7 (3), S. e1001113 (2011)
Consensus-phenotype integration of transcriptomic and metabolomic data implies a role for metabolism in the chemosensitivity of tumour cells. PLoS Computational Biology 58.
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103 (16), S. 1227 - 35 (2011)
Comprehensive field synopsis and systematic meta-analyses of genetic association studies in cutaneous melanoma. Journal of the National Cancer Institute 59.
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88 (3), S. 372 - 81 (2011)
Genome-wide association study identifies genetic variation in neurocan as a susceptibility factor for bipolar disorder. Am J Hum Genet 60.
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155A (1), S. 203 - 6 (2011)
Interstitial deletion of 14q24.3-q32.2 in a male patient with plagiocephaly, BPES features, developmental delay, and congenital heart defects. Am J Med Genet A