Robert S. Fulton

TL;DR: The data production protocols used for this work are those used by the participating centers to produce 16S rDNA sequence for the Human Microbiome Project, and these results can be informative for interpreting the large body of clinical 16s rDNA data produced for this project.

TL;DR: Differences across all hematopoietic cells from syngeneic mouse tumors during unrestrained tumor growth or effective ICT are defined to support the hypothesis that this macrophage polarization/activation results from effects on circulatory monocytes and early macrophages entering tumors, rather than on pre-polarized mature intratumoral macrophaging.

TL;DR: The complete mouse MSY sequence brings to light dramatic forces in sex chromosome evolution: lineage-specific convergent acquisition and amplification of X-Y gene families, possibly fueled by antagonism between acquired X-y homologs.

TL;DR: The Human Tumor Atlas Network (HTAN), part of the NCI Cancer Moonshot Initiative, will establish a clinical, experimental, computational, and organizational framework to generate informative and accessible three-dimensional atlases of cancer transitions for a diverse set of tumor types.

TL;DR: AML relapse after transplantation was not associated with the acquisition of previously unknown AML‐specific mutations or structural variations in immune‐related genes, but it was associated with dysregulation of pathways that may influence immune function, including down‐regulation of MHC class II genes, which are involved in antigen presentation.