Zeitschriftenartikel (123)
81.
Zeitschriftenartikel
5 (2), S. 5:11 - 5:11 (2013)
De novo truncating mutations in ASXL3 are associated with a novel clinical phenotype with similarities to Bohring-Opitz syndrome. Genome Medicine 82.
Zeitschriftenartikel
83, S. 39 - 54 (2013)
Evolutionary entropy predicts the outcome of selection: Competition for resources that vary in abundance and diversity. Theoretical Population Biology 83.
Zeitschriftenartikel
41 (3), S. 1496 - 1507 (2013)
Development and application of a DNA microarray-based yeast two-hybrid system. Nucleic Acids Research (London) 84.
Zeitschriftenartikel
31 (2), S. 126 - 34 (2013)
Evaluation of methods for modeling transcription factor sequence specificity. Nature biotechnology 85.
Zeitschriftenartikel
24 (2), S. 206 - 214 (2013)
The tissue-specific IncRNA Fendrr is an essential regulator of heart and body wall development in the mouse. Developmental Cell 86.
Zeitschriftenartikel
2, 212 (2013)
Warburg effect and translocation-induced genomic instability: two yeast models for cancer cells. Frontiers in Oncology 87.
Zeitschriftenartikel
50 (3), S. 140 - 143 (2013)
Genome-wide significant association of ANKRD55 rs6859219 and multiple sclerosis risk. Journal of Medical Genetics (London) 88.
Zeitschriftenartikel
9 (1), S. 32 - 43 (2013)
Human stromal (mesenchymal) stem cells from bone marrow, adipose tissue and skin exhibit differences in molecular phenotype and differentiation potential. Stem Cell Reviews 89.
Zeitschriftenartikel
29 (13), S. 1600 - 1606 (2013)
Janus-a comprehensive tool investigating the two faces of transcription. Bioinformatics 90.
Zeitschriftenartikel
369 (16), S. 1565 - 1565 (2013)
TREM2 and Neurodegenerative Disease. The New England Journal of Medicine: NEJM / Publ. by the Massachusetts Medical Society 91.
Zeitschriftenartikel
28 (2), S. 131 - 138 (2013)
Distinguishing true from false positives in genomic studies: p values. European Journal of Epidemiology 92.
Zeitschriftenartikel
34 (6), S. 1393 - 402 (2013)
Transcriptomic responses generated by hepatocarcinogens in a battery of liver-based in vitro models. Carcinogenesis 93.
Zeitschriftenartikel
4, S. 4:1531 - 4:1531 (2013)
LGALS3BP regulates centriole biogenesis and centrosome hypertrophy in cancer cells. Nature Communications 94.
Zeitschriftenartikel
83 (1), S. 92 - 95 (2013)
Novel WDR35 mutations in patients with cranioectodermal dysplasia (Sensenbrenner syndrome). Clinical Genetics: an international journal of genetics in medicine 95.
Zeitschriftenartikel
155 (3), S. 567 - 81 (2013)
Hypermutation of the inactive X chromosome is a frequent event in cancer. Cell 96.
Zeitschriftenartikel
91 (9), S. 1095 - 107 (2013)
The enzymatic activity of the VEGFR2 receptor for the biosynthesis of dinucleoside polyphosphates. Journal of Molecular Medicine-JMM 97.
Zeitschriftenartikel
45 (8), S. 927 - 32 (2013)
Recurrent somatic alterations of FGFR1 and NTRK2 in pilocytic astrocytoma. Nature Genetics 98.
Zeitschriftenartikel
50 (1), S. 47 - 53 (2013)
Whole exome sequencing identified a novel zinc-finger gene ZNF141 associated with autosomal recessive postaxial polydactyly type A. Journal of Medical Genetics 99.
Zeitschriftenartikel
41 (Database issue), S. D793 - 800 (2013)
The ConsensusPathDB interaction database: 2013 update. Nucleic Acids Research (London) 100.
Zeitschriftenartikel
12 (12), S. 5512 - 5519 (2013)
Generation and Characterization of a Leishmania tarentolae Strain for Site-Directed in Vivo Biotinylation of Recombinant Proteins. Journal of Proteome Research