Searching journal content for articles similar to Sanderson 18 (4): 517.

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  1. ...protein–protein interaction networks is limited (Gandhi et al. 2006). Therefore it is necessary to explore mammalian genetic interactions in the mammalian setting. An additional problem for mammalian cells is the apparent lack of a simple and cheap method for combining alleles of distinct genes...
  2. ...APOL6 function by interacting at the base of the MAD hinge—a region under strong positive selection (shown in dark gray). By recognizing this critical region, antagonists may be able to manipulate APOL6 in different ways. One possibility is that antagonists promote infections by preventing APOL6...
  3. ...estimates of spatial gene–gene dependencies between gene i and j. (C) A sketch of the more complex scenario of a set of interacting cells. Here, the expression of the cell a is affected by all surrounding cells in a distance-dependent way, as illustrated by thin and bold dotted lines for long- and short...
  4. ..., the pluripotent epiblast depends on miRNA activity, the absence of which results in the loss of pluripotent cells. Through the integration of high-sensitivity small RNA expression profiling of individual embryos and protein expression of miRNA targets with public data of protein–protein interactions, we...
  5. ...of myeloproliferative neoplasms (MPNs), for which HC is the first-line treatment, will provide a better understanding of its molecular effects. To explore the effects of HC -wide, transcriptomic analyses were performed on two clinically relevant cell types at different stages of differentiation treated with HC...
  6. ...performed time-series RNA-sequencing analyses of the wild type and 20 mutants to explore the relationships between transcription and morphogenesis. These strains show developmental arrest at different stages, accelerated development, or atypical morphologies. Considering eight major morphological...
  7. ...cortical regions and the cerebellum. An analysis of the predicted regulatory interactions driving these differences revealed the role of transcription factors in species-specific transcriptome changes, and epigenetic modifications were linked to spatial expression differences conserved across species...
  8. ...motifs, gene expression, and chromatin modification data sets as input features. Applying these methods to Drosophila melanogaster, we predict ∼300,000 regulatory edges in a network of ∼600 TFs and 12,000 target genes. We validate our predictions using known regulatory interactions, gene functional...
  9. ...Diego, La Jolla, California 92093, USA Abstract The chimpanzee genome sequence is a long-awaited milestone, providing opportunities to explore primate evolution and genetic contributions to human physiology and disease. Humans and chimpanzees shared a common ancestor ∼5-7 million years ago...
  10. .... The transmembrane protein XFLRT3 forms a complex with FGF receptors and promotes FGF signalling. Nat. Cell Biol. 6 : 38 -44. ↵ Bronchain, O.J., Hartley, K.O., and Amaya, E. 1999 . A gene trap approach in Xenopus . Curr. Biol. 9 : 1195 -1198. ↵ Brown, P.O. and Botstein, D. 1999 . Exploring the new world...
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