Zeitschriftenartikel (162)
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Zeitschriftenartikel
192 (3), S. 1138 - 1153 (2014)
Unbiased expression mapping identifies a link between the complement and cholinergic systems in the rat central nervous system. The Journal of Immunology 142.
Zeitschriftenartikel
42 (4), S. 2138 - 2146 (2014)
Structural determinants of DNA recognition by plant MADS-domain transcription factors. Nucleic Acids Research (London) 143.
Zeitschriftenartikel
10 (2), S. 356 - 371 (2014)
Characterization of early autophagy signaling by quantitative phosphoproteomics. Autophagy 144.
Zeitschriftenartikel
24 (1), S. 33 - 34 (2014)
Studying post-translational modifications with protein interaction networks. Current Opinion in Structural Biology 145.
Zeitschriftenartikel
505 (7484), S. 546 - 549 (2014)
The genome of the recently domesticated crop plant sugar beet (Beta vulgaris). Nature 146.
Zeitschriftenartikel
9 (1), e86115 (2014)
Multiscale, converging defects of macro-porosity, microstructure and matrix mineralization impact long bone fragility in NF1. PLoS One 147.
Zeitschriftenartikel
30 (2), S. 284 - 286 (2014)
MEDIPS: genome-wide differential coverage analysis of sequencing data derived from DNA enrichment experiments. Bioinformatics 148.
Zeitschriftenartikel
30 (2), S. 284 - 286 (2014)
MEDIPS: genome wide differential coverage analysis of sequencing data derived from DNA enrichment experiments. Bioinformatics 149.
Zeitschriftenartikel
130 (21), S. 2202 - 2205 (2014)
[Exome sequencing revealed Allan-Herndon-Dudley syndrome underlying multiple disabilities]. Duodecim; lääketieteellinen aikakauskirja 150.
Zeitschriftenartikel
2014, pii: bau101 (2014)
A Web-based database of genetic association studies in cutaneous melanoma enhanced with network-driven data exploration tools. Database: The Journal of Biological Databases and Curation 151.
Zeitschriftenartikel
505 (7484), S. 546 - 549 (2014)
The genome of the recently domesticated crop plant sugar beet (Beta vulgaris). Nature 152.
Zeitschriftenartikel
13 (1), S. 51 - 65 (2014)
Application of high-throughput sequencing for studying genomic variations in congenital heart disease. Briefings in Functional Genomics 153.
Zeitschriftenartikel
13, S. 91 - 99 (2014)
A Novel SLC6A8 Mutation in a Large Family with X-Linked Intellectual Disability: Clinical and Proton Magnetic Resonance Spectroscopy Data of Both Hemizygous Males and Heterozygous Females. JIMD Reports 154.
Zeitschriftenartikel
15, S. 15:537 - 15:537 (2014)
Distribution of segmental duplications in the context of higher order chromatin organisation of human chromosome 7. BMC Genomics 155.
Zeitschriftenartikel
88 (2), S. 820 - 828 (2014)
Crystal structure of pb9, the distal tail protein of bacteriophage T5: a conserved structural motif among all siphophages. Journal of Virology 156.
Zeitschriftenartikel
13 (10), S. 1650 - 1651 (2014)
Previously reported new type of autosomal recessive primary microcephaly is caused by compound heterozygous ASPM gene mutations. Cell Cycle 157.
Zeitschriftenartikel
26 (1), S. 195 - 209 (2014)
The histone deacetylase inhibitor trichostatin a promotes totipotency in the male gametophyte. The Plant Cell 158.
Zeitschriftenartikel
30 (2), S. 284 - 286 (2014)
MEDIPS: genome-wide differential coverage analysis of sequencing data derived from DNA enrichment experiments. Bioinformatics 159.
Zeitschriftenartikel
15 (2), S. 129 - 134 (2014)
Assessment of microRNA-related SNP effects in the 3' untranslated region of the IL22RA2 risk locus in multiple sclerosis. Neurogenetics 160.
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30 (1), S. 32 - 39 (2014)
Genetics of recessive cognitive disorders. Trends in Genetics