The following publications were published exclusively under the affiliation of the Max Planck Society. For publications by the principal investigator outside of the Max Planck Society, see the links on the lower left.
Journal Article (147)
Journal Article
25 (4), pp. 390 - 391 (2007)
Systems biology standards—the community speaks. Nature Biotechnology
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
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
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
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
Journal Article
70 (2), pp. 311 - 318 (2007)
The essence of DNA sample preparation for MALDI mass spectrometry. Journal of Biochemical and Biophysical Methods
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
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
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
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
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
Journal Article
35 (6), p. e43 - e43 (2007)
Vectors for co-expression of an unrestricted number of proteins. Nucleic Acids Research (London)
Journal Article
40 (3), pp. 597 - 603 (2007)
Endochondral ossification in vitro is influenced by mechanical bending. Bone
Journal Article
13 (3), pp. 324 - 331 (2007)
Hdac2 regulates the cardiac hypertrophic response by modulating Gsk3 beta activity. Nature Medicine
Journal Article
13 (3), pp. 324 - 331 (2007)
Hdac2 regulates the cardiac hypertrophic response by modulating Gsk3bold beta activity. Nature Medicine
Journal Article
16 (8), pp. 232 - 240 (2007)
Multiple roles for neurofibromin in skeletal development and growth. Human Molecular Genetics
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
Journal Article
23 (2), pp. e44 - e49 (2007)
Simultaneous alignment and annotation of cis-regulatory regions. Bioinformatics
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
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