Zeitschriftenartikel (3055)
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25 (10), e7, S. 2676 - 2688 (2018)
tRNA Translocation by the Eukaryotic 80S Ribosome and the Impact of GTP Hydrolysis. Cell Reports 442.
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177 (8), S. 691 - 699 (2018)
CNKSR1 gene defect can cause syndromic autosomal recessive intellectual disability. Am J Med Genet B Neuropsychiatr Genet 443.
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33, S. 20 - 24 (2018)
Generation of an iPSC line of a patient with Angelman syndrome due to an imprinting defect. Stem Cell Research 444.
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210 (4), S. 1527 - 1542 (2018)
Identification of two novel candidate genes for insulin secretion by comparative genomics of multiple backcross populations. Genetics 445.
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33, S. 120 - 124 (2018)
Generation of two human isogenic iPSC lines from fetal dermal fibroblasts. Stem Cell Research 446.
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7, e40757 (2018)
Targets and genomic constraints of ectopic Dnmt3b expression. eLife 447.
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145 (22), pii: dev168617 (2018)
Comparative genomic analysis of embryonic, lineage-converted and stem cell-derived motor neurons. Development 448.
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563 (7731), S. 325 (2018)
Paying PIs from grants blocks talent and diversity. Nature 449.
Zeitschriftenartikel
16 (1), 138 (2018)
Classifying human promoters by occupancy patterns identifies recurring sequence elements, combinatorial binding, and spatial interactions. BMC Biology 450.
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14 (11), e1007793 (2018)
Synthetic STARR-seq reveals how DNA shape and sequence modulate transcriptional output and noise. PLoS Genetics 451.
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10 (466), eaau7137 (2018)
Wnt1 is an Lrp5-independent bone-anabolic Wnt ligand. Science Translational Medicine 452.
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20, S. 1481 - 1482 (2018)
Response to Peron et al. GENETICS IN MEDICINE 453.
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103 (5), S. 512 - 521 (2018)
Comparison of Bone Microarchitecture Between Adult Osteogenesis Imperfecta and Early-Onset Osteoporosis. Calcified Tissue International 454.
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9, 9:484 (2018)
Network and Pathway Analysis of Toxicogenomics Data. Frontiers in Genetics 455.
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8 (1), 14611 (2018)
Multisite de novo mutations in human offspring after paternal exposure to ionizing radiation. Scientific Reports 456.
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50 (10), S. 1442 - 1451 (2018)
De novo mutations in MSL3 cause an X-linked syndrome marked by impaired histone H4 lysine 16 acetylation. Nature Genetics 457.
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50 (10), S. 1463 - 1473 (2018)
Dynamic 3D chromatin architecture determines enhancer specificity and morphogenetic identity in limb development. Nature Genetics 458.
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2018, 295:S215 (2018)
DMSO-induced drastic changes in cellular processes and epigenetic landscape in vitro. TOXICOLOGY LETTERS 459.
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46 (17), S. 9044 - 9056 (2018)
Chromatin-dependent allosteric regulation of DNMT3A activity by MeCP2. Nucleic Acids Research (London) 460.
Zeitschriftenartikel
7 (3), e3, S. 258 - 268 (2018)
Aligning Single-Cell Developmental and Reprogramming Trajectories Identifies Molecular Determinants of Myogenic Reprogramming Outcome. Cell Systems