Our publications listed in the Puplication Repository of the Max Planck Society (PuRe)
Journal Article (147)
81.
Journal Article
25 (4), pp. 390 - 391 (2007)
Systems biology standards—the community speaks. Nature Biotechnology 82.
Journal Article
46 (4), pp. 359 - 372 (2007)
Amplification and translocation of 3q26 with overexpression of EVI1 in Fanconi anemia-derived childhood acute myeloid leukemia with biallelic FANCD1/BRCA2 disruption. Genes, Chromosomes and Cancer 83.
Journal Article
18 (4), pp. 1385 - 1396 (2007)
Ataxin-2 interacts with the DEAD/H-box RNA helicase DDX6 and interferes with P-bodies and stress granules. Molecular Biology of the Cell 84.
Journal Article
15 (6), pp. 711 - 713 (2007)
Disruption of the CNTNAP2 gene in a t(7;15) translocation family without symptoms of Gilles de la Tourette syndrome. European Journal og Human Genetics: EJHG ; the Official Journal of the European Society of Human Genetics 85.
Journal Article
104 (12), pp. 5014 - 5019 (2007)
A bile acid-like steroid modulates Caenorhabditis elegans lifespan through nuclear receptor signaling. Proceedings of the National Academy of Sciences of the United States of America 86.
Journal Article
70 (2), pp. 311 - 318 (2007)
The essence of DNA sample preparation for MALDI mass spectrometry. Journal of Biochemical and Biophysical Methods 87.
Journal Article
25 (5), pp. 751 - 764 (2007)
Structural basis for interaction of the ribosome with the switch regions of GTP-bound elongation factors. Molecular Cell 88.
Journal Article
2 (3), p. e269 - e269 (2007)
Ligand bound beta1 integrins inhibit procaspase-8 for mediating cell adhesion-mediated drug and radiation resistance in human leukemia cells. PLoS One 89.
Journal Article
15 (3), pp. 375 - 378 (2007)
Mutation screening of brain-expressed X-chromosomal miRNA genes in 464 patients with nonsyndromic X-linked mental retardation. European Journal of Human Genetics: EJHG ; the Official Journal of the European Society of Human Genetics 90.
Journal Article
15 (3), pp. 375 - 378 (2007)
Mutation screening of brain-expressed X-chromosomal miRNA genes in 464 patients with nonsyndromic X-linked mental retardation. European Journal of Human Genetics: EJHG ; the Official Journal of the European Society of Human Genetics 91.
Journal Article
121 (1), pp. 43 - 48 (2007)
Homozygosity mapping in consanguineous families reveals extreme heterogeneity of non-syndromic autosomal recessive mental retardation and identifies 8 novel gene loci. Human Genetics 92.
Journal Article
35 (6), p. e43 - e43 (2007)
Vectors for co-expression of an unrestricted number of proteins. Nucleic Acids Research (London) 93.
Journal Article
40 (3), pp. 597 - 603 (2007)
Endochondral ossification in vitro is influenced by mechanical bending. Bone 94.
Journal Article
13 (3), pp. 324 - 331 (2007)
Hdac2 regulates the cardiac hypertrophic response by modulating Gsk3 beta activity. Nature Medicine 95.
Journal Article
13 (3), pp. 324 - 331 (2007)
Hdac2 regulates the cardiac hypertrophic response by modulating Gsk3bold beta activity. Nature Medicine 96.
Journal Article
16 (8), pp. 232 - 240 (2007)
Multiple roles for neurofibromin in skeletal development and growth. Human Molecular Genetics 97.
Journal Article
101 (1), pp. 250 - 262 (2007)
Identification and characterisation of novel tubulin-binding motifs located within the C-terminus of TRPV1. Journal of Neurochemistry: Official Journal of the International Society for Neurochemistry 98.
Journal Article
23 (2), pp. e44 - e49 (2007)
Simultaneous alignment and annotation of cis-regulatory regions. Bioinformatics 99.
Journal Article
143 (2), pp. 195 - 199 (2007)
A novel patient with Cooks syndrome supports splitting from "classic" brachydactyly type B. American Journal of Medical Genetics/ Part A 100.
Journal Article
143 (2), pp. 172 - 178 (2007)
Characterization of a 5.3 Mb deletion in 15q14 by Comparative Genomic Hybridization using a whole genome ”tiling path” BAC array in a girl with heart defect, cleft palate and developmental delay. American Journal of Medical Genetics Part A