Searching journal content for articles similar to Tassy et al. 20 (10): 1459.

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  1. ...MPRAbase A Massively Parallel Reporter Assay database Jingjing Zhao1,2,*, Fotis A. Baltoumas3,*, Maxwell A. Konnaris4,5, Ioannis Mouratidis4, Zhe Liu1,2,6, Jasmine Sims1,2, Vikram Agarwal7, Georgios A. Pavlopoulos3, Ilias Georgakopoulos-Soares4,♱, Nadav Ahituv1,2,♱ 1Department of Bioengineering...
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  2. ...ISWI1 complex proteins facilitate developmental editing in Paramecium Aditi Singh1,5, Lilia Häußermann1,5, Christiane Emmerich1, Emily Nischwitz2, Brandon K.B. Seah1, Falk Butter2,3, Mariusz Nowacki4 and Estienne C. Swart1 1Max Planck Institute for Biology, 72076 Tübingen, Germany; 2Institute...
  3. ...Corresponding author: michael.werner@utah.eduAbstractDevelopmental plasticity enables the production of alternative phenotypes in response to different environmental conditions. Although significant advances in understanding the ecological and evolutionary implications of plasticity have been made...
  4. ...Embryo covers more developmental stages.Next, we compared dbEmbryo with other databases through characteristic tools. The unique aspect of EMAGE is that it contains standardized spatial representations of the sites of gene expression for each gene, denoted against a set of virtual reference embryo models...
  5. ...as the individual nuclei within them. We find myocyte nuclei segregate into two clusters defined by the expression of DUX4 target genes, which is exclusively found in patient/mutant nuclei, whereas MNCs cluster based on developmental states. Patient/mutant myotubes are found in “FSHD-hi” and “FSHD-lo” states...
  6. ...Aberrant homeodomain–DNA cooperative dimerization underlies distinct developmental defects in two dominant CRX retinopathy models Yiqiao Zheng1,2,5, Gary D. Stormo3 and Shiming Chen2,4 1Molecular Genetics and Genomics Graduate Program, Division of Biology & Biomedical Sciences, Washington...
  7. ...studies in discovering thousands of disease-associated genes necessitates developing novel high-throughput functional genomics approaches to elucidate the molecular mechanisms of these genes. Here, we have coupled multiplexed repression of neurodevelopmental disease–associated genes to single...
  8. ...they have exploited distinct cellular niches to propagate, these activities may also be integrated in normal developmental programs. For example, the expression of the murine long interspersed nuclear element-1 family (LINE-1) can be detected shortly after fertilization and peaks at the two-cell stage...
  9. ...for the apparent multitude of translated regions within the same molecules. They also do not take into account the stochasticity of the process that allows alternative translations of the same RNA molecules by different ribosomes. There is a need for formal representations of mRNA complexity that would enable...
  10. ..., proliferated significantly after the late embryonic stage (E3) in sheep and the middle embryonic stage (E2) in goats (Fig. 1A,B). Similar developmental patterns were also observed in different goat cell types (Fig. 1B). Altogether, we generated a spatial and temporal representation of cellular diversity...
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