Nature Search

R-spondin-2 is a Wnt agonist that regulates osteoblast activity and bone mass

M. Noelle Knight
Kannan Karuppaiah
Kurt D. Hankenson
ResearchOpen Access14 Aug 2018
Bone Research

Volume: 6, P: 1-14
CD47 is required for mesenchymal progenitor proliferation and fracture repair

Robert L. Zondervan
Christina A. Capobianco
Kurt D. Hankenson
ResearchOpen Access03 Mar 2025
Bone Research

Volume: 13, P: 1-15
Intraoperative delivery of the Notch ligand Jagged-1 regenerates appendicular and craniofacial bone defects

Daniel W. Youngstrom
Rafael Senos
Kurt D. Hankenson
ResearchOpen Access15 Dec 2017
npj Regenerative Medicine

Volume: 2, P: 1-10
Genome-scale Capture C promoter interactions implicate effector genes at GWAS loci for bone mineral density

GWAS have identified numerous genetic loci for bone mineral density (BMD) and fracture risk. Here, the authors map these variants to putative target genes using ATAC-seq and Capture C of human osteoblasts and confirm ING3 and EPDR1 as BMD genes in in vitro osteoblast differentiation experiments.

Alessandra Chesi
Yadav Wagley
Struan F. A. Grant
ResearchOpen Access19 Mar 2019
Nature Communications

Volume: 10, P: 1-11
Immunometabolic cues recompose and reprogram the microenvironment around implanted biomaterials

Immunometabolic cues surrounding implanted biomaterials govern the trafficking of subsets of neutrophils, monocytes and other immune cells, and determine the relative composition of pro-inflammatory and anti-inflammatory immune cell populations.

Chima V. Maduka
Axel D. Schmitter-Sánchez
Christopher H. Contag
Research04 Oct 2024
Nature Biomedical Engineering

Volume: 8, P: 1308-1321
Use of quantitative polymerase chain reaction analysis to compare quantity and stability of isolated murine DNA

Laura M. Garzel
F. Claire Hankenson
Kurt D. Hankenson
Research01 Sept 2010
Lab Animal

Volume: 39, P: 283-289
An anionic, endosome-escaping polymer to potentiate intracellular delivery of cationic peptides, biomacromolecules, and nanoparticles

Most reagents designed to deliver cargo into cells are cationic and so cannot deliver cationic cargo. Here the authors show that pretreating cells with the anionic polymer poly(propylacrylic acid) facilitates the uptake and endosomal escape of a wide variety of cationic cargo in numerous cell types.

Brian C. Evans
R. Brock Fletcher
Craig L. Duvall
ResearchOpen Access01 Nov 2019
Nature Communications

Volume: 10, P: 1-19
Implicating candidate genes at GWAS signals by leveraging topologically associating domains

Gregory P Way
Daniel W Youngstrom
Struan FA Grant
Research09 Aug 2017
European Journal of Human Genetics

Volume: 25, P: 1286-1289

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