Journal Article (82)
41.
Journal Article
15 (5), pp. 1526 - 1538 (2016)
An impaired respiratory electron chain triggers down-regulation of the energy metabolism and de-ubiquitination of solute carrier amino acid transporters. Molecular and Cellular Proteomics 42.
Journal Article
283 (9), pp. 1669 - 1688 (2016)
Transcriptional signature induced by a metastasis-promoting c-Src mutant in a human breast cell line. The FEBS Journal 43.
Journal Article
15 (5), pp. 1728 - 1739 (2016)
Atxn2-Knock-Out mice show branched chain amino acids and fatty acids pathway alterations. Molecular and Cellular Proteomics 44.
Journal Article
170A (5), pp. 1202 - 1207 (2016)
Femoral facial syndrome associated with a de novo complex chromosome 2q37 rearrangement. American Journal of Medical Genetics Part A 45.
Journal Article
17 (5), pii: E632 (2016)
Advantages and Pitfalls of Mass Spectrometry Based Metabolome Profiling in Systems Biology. International Journal of Molecular Sciences 46.
Journal Article
12 (4), e1005954 (2016)
Chromosomal-Level Assembly of the Asian Seabass Genome Using Long Sequence Reads and Multi-layered Scaffolding. PLoS Genetics 47.
Journal Article
2016, baw052 (2016)
ToxDB: pathway-level interpretation of drug-treatment data. Database (Oxford) 48.
Journal Article
46 (6), pp. 2538 - 2553 (2016)
Phosphorylation of the chromatin remodeling factor DPF3a induces cardiac hypertrophy through releasing HEY repressors from DNA. Nucleic Acids Research (London) 49.
Journal Article
7, 7:11212 (2016)
Serial interactome capture of the human cell nucleus. Nature Communications 50.
Journal Article
32 (4), pp. 225 - 237 (2016)
Breaking TADs: How Alterations of Chromatin Domains Result in Disease. Trends in Genetics 51.
Journal Article
170A (4), pp. 1080 - 1085 (2016)
An overlapping phenotype of Osteogenesis imperfecta and Ehlers-Danlos syndrome due to a heterozygous mutation in COL1A1 and biallelic missense variants in TNXB identified by whole exome sequencing. American Journal of Medical Genetics Part A 52.
Journal Article
11 (4), pp. 813 - 433 (2016)
Genome-wide profiling of RNA polymerase transcription at nucleotide resolution in human cells with native elongating transcript sequencing. Nature Protocols 53.
Journal Article
455, pp. 8 - 21 (2016)
Characterization and refinement of growth related quantitative trait loci in European sea bass (Dicentrarchus labrax) using a comparative approach. Aquaculture 54.
Journal Article
2 (3), e1501502 (2016)
Structures of ribosome-bound initiation factor 2 reveal mechanism of subunit association. Science Advances 55.
Journal Article
98, pp. 1 - 17 (2016)
Mutations in Subunits of the Activating Signal Cointegrator 1 Complex Are Associated with Prenatal Spinal Muscular Atrophy and Congenital Bone Fractures. The American Journal of Human Genetics 56.
Journal Article
170 (3), pp. 615 - 621 (2016)
A homozygous HOXD13 missense mutation causes a severe form of synpolydactyly with metacarpal to carpal transformation. American Journal of Medical Genetics Part A 57.
Journal Article
24 (3), pp. 392 - 399 (2016)
Missense variants in AIMP1 gene are implicated in autosomal recessive intellectual disability without neurodegeneration. European journal of human genetics 58.
Journal Article
16 (2), pp. 549 - 561 (2016)
Characterization of the genome and transcriptome of the blue tit Cyanistes caeruleus: polymorphisms, sex-biased expression and selection signals. Molecular Ecology Resources 59.
Journal Article
67 (1), pp. 78 - 83 (2016)
Identification of a molecular defect in a stillborn fetus with perinatal lethal hypophosphatasia using a disease-associated genome sequencing approach. Polish Journal of Pathology 60.
Journal Article
17 (3), pp. 139 - 154 (2016)
Molecular features of cellular reprogramming and development. Nature Reviews Molecular Cell Biology