Zeitschriftenartikel (1124)
681.
Zeitschriftenartikel
18 (6), S. 366 - 371 (2015)
Virtual Clinical Trials, an Essential Step in Increasing the Effectiveness of the Drug Development Process. Public Health Genomics 682.
Zeitschriftenartikel
15 (7), fov073 (2015)
A link between Sas2-mediated H4 K16 acetylation, chromatin assembly in S-phase by CAF-I and Asf1, and nucleosome assembly by Spt6 during transcription. FEMS Yeast Research 683.
Zeitschriftenartikel
2015, 5634 (2015)
Allele frequencies of BRAFV600 mutations in primary melanomas and matched metastases and their relevance for BRAF inhibitor therapy in metastatic melanoma. Oncotarget 684.
Zeitschriftenartikel
24 (20), S. 5697 - 5710 (2015)
Mutations in the histamine N-methyltransferase gene, HNMT, are associated with nonsyndromic autosomal recessive intellectual disability. Human Molecular Genetics 685.
Zeitschriftenartikel
23 (10), S. 1308 - 1317 (2015)
Redefining the MED13L syndrome. European journal of human genetics 686.
Zeitschriftenartikel
135 (10), S. 2368 - 2376 (2015)
GORAB Missense Mutations Disrupt RAB6 and ARF5 Binding and Golgi Targeting. The Journal of Investigative Dermatology: an International Journal for Research in Cutaneous Biology 687.
Zeitschriftenartikel
23 (10), S. 1378 - 1383 (2015)
Intelligence: shared genetic basis between Mendelian disorders and a polygenic trait. European journal of human genetics 688.
Zeitschriftenartikel
60 (1), S. 146 - 162 (2015)
High-Affinity Sites Form an Interaction Network to Facilitate Spreading of the MSL Complex across the X Chromosome in Drosophila. Molecular Cell 689.
Zeitschriftenartikel
36 (10), S. 688 - 704 (2015)
Ligands for the Nuclear Peroxisome Proliferator-Activated Receptor Gamma. Trends in Pharmacological Sciences 690.
Zeitschriftenartikel
526 (7571), S. 75 - 81 (2015)
An integrated map of structural variation in 2,504 human genomes. Nature 691.
Zeitschriftenartikel
526 (7571), S. 68 - 74 (2015)
A global reference for human genetic variation. Nature 692.
Zeitschriftenartikel
4 (12), S. 891 - 901 (2015)
Bioenergetic cues shift FXR splicing towards FXRα2 to modulate hepatic lipolysis and fatty acid metabolism. Molecular Metabolism 693.
Zeitschriftenartikel
97 (3), S. 483 - 492 (2015)
Recurrent De Novo Mutations Affecting Residue Arg138 of Pyrroline-5-Carboxylate Synthase Cause a Progeroid Form of Autosomal-Dominant Cutis Laxa. The American Journal of Human Genetics 694.
Zeitschriftenartikel
33 (9), S. 933 - 940 (2015)
Prediction of human population responses to toxic compounds by a collaborative competition. Nat Biotechnol 695.
Zeitschriftenartikel
47 (9), S. 1020 - 1029 (2015)
Genomics and drug profiling of fatal TCF3-HLF-positive acute lymphoblastic leukemia identifies recurrent mutation patterns and therapeutic options. Nature Genetics 696.
Zeitschriftenartikel
6 (29), S. 26546 - 26547 (2015)
Insight into miRNA biogenesis with RNA sequencing. Oncotarget 697.
Zeitschriftenartikel
15, S. 33 - 40 (2015)
Network and systems biology: essential steps in virtualising drug discovery and development. Drug Discovery Today: Technology 698.
Zeitschriftenartikel
524 (7563), S. 47 - 53 (2015)
Comprehensive genomic profiles of small cell lung cancer. Nature 699.
Zeitschriftenartikel
97 (2), S. 302 - 310 (2015)
THOC2 Mutations Implicate mRNA-Export Pathway in X-Linked Intellectual Disability. The American Journal of Human Genetics 700.
Zeitschriftenartikel
97 (2), S. 343 - 352 (2015)
Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling. The American Journal of Human Genetics