Zeitschriftenartikel (1266)
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)
Zeitschriftenartikel
22 (4), S. 575 - 588 (2018)
A CLK3-HMGA2 Alternative Splicing Axis Impacts Human Hematopoietic Stem Cell Molecular Identity throughout Development. Cell Stem Cell
Zeitschriftenartikel
102 (4), S. 557 - 573 (2018)
Mutations in PMPCB Encoding the Catalytic Subunit of the Mitochondrial Presequence Protease Cause Neurodegeneration in Early Childhood. American Journal of Human Genetics
Zeitschriftenartikel
22, S. 1 - 16 (2018)
Dissecting the Functional Consequences of De Novo DNA Methylation Dynamics in Human Motor Neuron Differentiation and Physiology. Cell Stem Cell
Zeitschriftenartikel
25 (4), S. 327 - 332 (2018)
Global delay in nascent strand DNA methylation. Nature Structural and Molecular Biology
Zeitschriftenartikel
25 (4), S. 355 (2018)
Author Correction: Global delay in nascent strand DNA methylation. Nature Structural and Molecular Biology
Zeitschriftenartikel
145 (7), dev161208 (2018)
Genome-wide strategies identify downstream target genes of connective tissue-associated transcription factors. Development
Zeitschriftenartikel
14 (3), e1007254 (2018)
Large scale variation in the rate of germ-line de novo mutation, base composition, divergence and diversity in humans. PLoS Genetics
Zeitschriftenartikel
9 (1), 1048 (2018)
Integrative genomic profiling of large-cell neuroendocrine carcinomas reveals distinct subtypes of high-grade neuroendocrine lung tumors. Nature Communications
Zeitschriftenartikel
MED13L-related intellectual disability: involvement of missense variants and delineation of the phenotype. Neurogenetics, S. 1 - 11 (2018)
Zeitschriftenartikel
22 (3), S. 369 - 383 (2018)
The Transcriptionally Permissive Chromatin State of Embryonic Stem Cells Is Acutely Tuned to Translational Output. Cell Stem Cell
Zeitschriftenartikel
176 (3), S. 668 - 675 (2018)
Cutis Laxa and Excessive Bone Growth due to de novo mutations in PTDSS1. American Journal of Medical Genetics Part A
Zeitschriftenartikel
9 (1), 9:10 (2018)
X chromosome dosage and presence of SRY shape sex-specific differences in DNA methylation at an autosomal region in human cells. Biology of Sex Differences
Zeitschriftenartikel
7 (2), S. 443 - 451 (2018)
Spatiotemporal Control of TGF-β Signaling with Light. ACS Synthetic Biology
Zeitschriftenartikel
27 (4), S. 589 - 600 (2018)
FRMPD4 mutations cause X-linked intellectual disability and disrupt dendritic spine morphogenesis. Human Molecular Genetics
Zeitschriftenartikel
9, 597 (2018)
Genome-wide tracking of dCas9-methyltransferase footprints. Nature Communications