Zeitschriftenartikel (90)
Zeitschriftenartikel
29 (7), S. 1643 - 1651 (2018)
Mutational analysis uncovers monogenic bone disorders in women with pregnancy-associated osteoporosis: three novel mutations in LRP5, COL1A1, and COL1A2. Osteoporosis International
Zeitschriftenartikel
19 (7), S. 453 - 467 (2018)
Structural variation in the 3D genome. Nature Reviews Genetics
Zeitschriftenartikel
6, 70 (2018)
Designing miRNA-Based Synthetic Cell Classifier Circuits Using Answer Set Programming. Frontiers in Bioengineering and Biotechnology
Zeitschriftenartikel
9 , 9:2386 (2018)
HEPATOKIN1 is a biochemistry-based model of liver metabolism for applications in medicine and pharmacology. Nature Communications
Zeitschriftenartikel
23 (12), S. 3429 - 3437 (2018)
Transient N-6-Methyladenosine Transcriptome Sequencing Reveals a Regulatory Role of m6A in Splicing Efficiency. Cell Reports
Zeitschriftenartikel
38 (12), e00599-17 (2018)
Loss of the hematopoietic stem cell factor GATA2 in the osteogenic lineage impairs trabecularization and mechanical strength of bone. Molecular and Cellular Biology (Washington, DC)
Zeitschriftenartikel
70 (5), e3, S. 881 - 893 (2018)
Structural Visualization of the Formation and Activation of the 50S Ribosomal Subunit during In Vitro Reconstitution. Molecular Cell
Zeitschriftenartikel
20 (6), S. 599 - 607 (2018)
Noncoding copy-number variations are associated with congenital limb malformation. GENETICS IN MEDICINE
Zeitschriftenartikel
23 (8), S. 2509 - 2523 (2018)
Combining NGN2 Programming with Developmental Patterning Generates Human Excitatory Neurons with NMDAR-Mediated Synaptic Transmission. Cell Reports
Zeitschriftenartikel
285 (1878), pii: 20180206 (2018)
Evolution of genomic variation in the burrowing owl in response to recent colonization of urban areas. Proceedings of the Royal Society of London. Series B: Biological Sciences (London)
Zeitschriftenartikel
9 (1), 1925 (2018)
Assessment of Established Techniques to Determine Developmental and Malignant Potential of Human Pluripotent Stem Cells. Nature Communications
Zeitschriftenartikel
10 (5), S. 1537 - 1550 (2018)
X Chromosome Dosage Influences DNA Methylation Dynamics during Reprogramming to Mouse iPSCs. Stem Cell Reports
Zeitschriftenartikel
50 (5), S. 662 - 667 (2018)
Polymer physics predicts the effects of structural variants on chromatin architecture. Nature Genetics
Zeitschriftenartikel
8 (5), S. 600 - 615 (2018)
Genomic and Functional Fidelity of Small Cell Lung Cancer Patient-Derived Xenografts. Cancer Discovery
Zeitschriftenartikel
41 (3), S. 533 - 539 (2018)
Advances in computer-assisted syndrome recognition by the example of inborn errors of metabolism. Journal of Inherited Metabolic Disease
Zeitschriftenartikel
10, 10:34 (2018)
Simple paired heavy- and light-chain antibody repertoire sequencing using endoplasmic reticulum microsomes. Genome Medicine
Zeitschriftenartikel
110 (7), S. 587 - 597 (2018)
Exome sequencing in syndromic brain malformations identifies novel mutations in ACTB, and SLC9A6, and suggests BAZ1A as a new candidate gene. Birth Defects Research
Zeitschriftenartikel
173 (3), S. 624 - 633 (2018)
Cancer-Germline Antigen Expression Discriminates Clinical Outcome to CTLA-4 Blockade. Cell
Zeitschriftenartikel
23 (2), S. 349 - 360 (2018)
Transcriptional Dysregulation of MYC Reveals Common Enhancer-Docking Mechanism. Cell Reports
Zeitschriftenartikel
46 (6), S. 2868 - 2882 (2018)
Genomic dissection of enhancers uncovers principles of combinatorial regulation and dynamic wiring of enhancer-promoter contacts. Nucleic Acids Research (London)