Area of research
General Health Professions · Archeology
Research interest
Research focused on Erythropoietin and Hypoxia (environmental), with related work in Kidney, Stromal cell, Endocrinology. Notable publications include 'Erythropoietin production by PDGFR-β+ cells', 'Different subpopulations of kidney interstitial cells produce erythropoietin and factors supporting tissue oxygenation in response to hypoxia in vivo', and 'Inhibition of transforming growth factor β1 signaling in resident interstitial cells attenuates profibrotic gene expression and preserves erythropoietin production during...'.
Fibroblast growth factor 23 and fibroblast growth factor receptor 4 promote cardiac metabolic remodeling in chronic kidney disease
Hypoxia‐inducible factor‐2 stabilization is not sufficient to induce erythropoietin production in deeper medullary fibroblasts
Intestinal Cyp24a1 regulates vitamin D locally independent of systemic regulation by renal Cyp24a1 in mice
Flexible and multifaceted: the plasticity of renin-expressing cells
Intact prostaglandin signaling through EP2 and EP4 receptors in stromal progenitor cells is required for normal development of the renal cortex in mice
Localization and characterization of proenkephalin-A as a potential biomarker for kidney disease in murine and human kidneys
The fate of erythropoietin-producing cells: another piece of the puzzle
Inhibition of transforming growth factor β1 signaling in resident interstitial cells attenuates profibrotic gene expression and preserves erythropoietin production during experimental kidney fibrosis in mice
Localization of angiotensin II type 1 receptor gene expression in rodent and human kidneys
Prolyl‐4‐hydroxylases 2 and 3 control erythropoietin production in renin‐expressing cells of mouse kidneys
Endothelin receptors in renal interstitial cells do not contribute to the development of fibrosis during experimental kidney disease
Different subpopulations of kidney interstitial cells produce erythropoietin and factors supporting tissue oxygenation in response to hypoxia in vivo
Apparently normal kidney development in mice with conditional disruption of ANG II-AT<sub>1</sub>receptor genes in FoxD1-positive stroma cell precursors
Activation of Hypoxia Signaling in Stromal Progenitors Impairs Kidney Development
Erythropoietin production by PDGFR-β+ cells