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Jordon K. Wang

Researcher at Stanford University

Publications -  11
Citations -  8525

Jordon K. Wang is an academic researcher from Stanford University. The author has contributed to research in topics: Regulation of gene expression & Hox gene. The author has an hindex of 10, co-authored 11 publications receiving 7810 citations.

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Functional Demarcation of Active and Silent Chromatin Domains in Human HOX Loci by Noncoding RNAs

TL;DR: The transcriptional landscape of the four human HOX loci is characterized at five base pair resolution in 11 anatomic sites and 231 HOX ncRNAs are identified that extend known transcribed regions by more than 30 kilobases, suggesting transcription of ncRNA may demarcate chromosomal domains of gene silencing at a distance.
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Long Noncoding RNA as Modular Scaffold of Histone Modification Complexes

TL;DR: The results suggest that lincRNAs may serve as scaffolds by providing binding surfaces to assemble select histone modification enzymes, thereby specifying the pattern of histone modifications on target genes.
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A histone H3 lysine 27 demethylase regulates animal posterior development.

TL;DR: It is shown that the JmjC-domain-containing related proteins UTX and JMJD3 catalyse demethylation of H3K27me3/2, which identifies a small family of H 3K27 demethylases with important, evolutionarily conserved roles in H3k27 methylation regulation and in animal anterior–posterior development.
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Disruption of PPARγ/β-catenin–mediated regulation of apelin impairs BMP-induced mouse and human pulmonary arterial EC survival

TL;DR: APelin could be effective in treating PAH by rescuing BMPR2 and PAEC dysfunction, and administration of apelin reversed PAH in mice with reduced production of APelin resulting from deletion of PPARγ in ECs.
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A dermal HOX transcriptional program regulates site-specific epidermal fate

TL;DR: Reciprocal epithelial-mesenchymal interactions shape site-specific development of skin, and maintenance of appropriate HOX transcriptional program in adult fibroblasts may serve as a source of positional memory to differentially pattern the epithelia during homeostasis and regeneration.