Area of research
Molecular Biology · Hematology
Research interest
Research interests include RNA Research and Splicing, Acute Myeloid Leukemia Research, Spaceflight effects on biology, and Hematopoietic Stem Cell Transplantation.
Nanobioreactor detection of space-associated hematopoietic stem and progenitor cell aging
Accelerated Hematopoietic Stem Cell Aging in Space
Reversal of malignant ADAR1 splice isoform switching with Rebecsinib
3171 – MOUSE MULTIPOTENT PROGENITOR 5 CELLS ARE LOCATED AT THE INTERPHASE BETWEEN HEMATOPOIETIC STEM AND PROGENITOR CELLS
Niche derived netrin-1 regulates hematopoietic stem cell dormancy via its receptor neogenin-1
Mouse multipotent progenitor 5 cells are located at the interphase between hematopoietic stem and progenitor cells
Selective antisense oligonucleotide inhibition of human IRF4 prevents malignant myeloma regeneration via cell cycle disruption
Inflammation-driven deaminase deregulation fuels human pre-leukemia stem cell evolution
Differential Alternative Polyadenylation Landscapes Mediate Hematopoietic Stem Cell Activation and Regulate Glutamine Metabolism
2007 – DIFFERENTIAL ALTERNATIVE POLYADENYLATION LANDSCAPES MEDIATE HEMATOPOIETIC STEM CELL ACTIVATION AND REGULATE GLUTAMINE METABOLISM
The long non-coding RNA Meg3 is dispensable for hematopoietic stem cells
ALTERNATIVE POLYADENYLATION REGULATES HEMATOPOIETIC STEM CELL METABOLISM
The Netrin-1 - Neogenin Axis Regulates Hematopoietic Stem Cell Dormancy and Function with Implications for Stem Cell Ageing
Hematopoietic Stem Cells are Regulated by Alternative Polyadenylation
Vitamin A-Retinoic Acid Signaling Regulates Hematopoietic Stem Cell Dormancy
Vitamin A/ retinoic acid signaling regulates hematopoietic stem cell dormancy
Inherent engraftment differences between CD45.1 and CD45.2 HSCs are caused by differential expression of Cxcr4
The role of the lncRNA Meg3 in the adult hematopoietic compartment
Neogenin regulates hematopoietic stem cell quiescence and maintenance
Transition out of HSC Dormancy By a Continuous Upregulation of Metabolism Is Controlled Via Dietary Vitamin A/ Retinoic Acid Signaling