Her scientific interests lie mostly in Cell biology, Stem cell, Bone marrow, Adult stem cell and Immunology. Her research links Chemokine binding with Cell biology. Her Stem cell research integrates issues from Endothelial stem cell, Embryonic stem cell, Induced pluripotent stem cell, Stem cell transplantation for articular cartilage repair and Pathology.
As part of one scientific family, Janina Ratajczak deals mainly with the area of Immunology, narrowing it down to issues related to the Haematopoiesis, and often CXCR4, Myeloid, Granulocyte and Granulocyte colony-stimulating factor. Her study in Progenitor cell is interdisciplinary in nature, drawing from both Biochemistry and Cellular differentiation. Her research in Hepatocyte growth factor tackles topics such as Metastasis which are related to areas like Cancer research.
Her main research concerns Stem cell, Cell biology, Haematopoiesis, Bone marrow and Progenitor cell. Her Stem cell research incorporates themes from Embryonic stem cell, Adult stem cell, Oct-4, Induced pluripotent stem cell and Homeobox protein NANOG. Her Cell biology research includes themes of Endothelial stem cell, Clinical uses of mesenchymal stem cells, Stromal cell and Cellular differentiation.
Her Haematopoiesis study integrates concerns from other disciplines, such as Homing, CXCR4, Immunology, Molecular biology and Transplantation. She combines subjects such as CD34, Endocrinology and Cancer research with her study of Bone marrow. Her Hematopoietic Stem Cell Mobilization study in the realm of Progenitor cell connects with subjects such as Proteolytic enzymes.
Her primary areas of study are Cell biology, Stem cell, Progenitor cell, Haematopoiesis and Bone marrow. Janina Ratajczak has researched Cell biology in several fields, including Receptor and Innate immune system. The various areas that Janina Ratajczak examines in her Stem cell study include Embryonic stem cell, Cancer research, Stromal cell, Cell migration and Immunology.
Her Progenitor cell research incorporates elements of Complement system, Plerixafor, Mesenchymal stem cell and Granulocyte colony-stimulating factor. Her studies deal with areas such as Inflammasome, Endocrinology, Homing and Internal medicine, Transplantation as well as Haematopoiesis. Her studies in Bone marrow integrate themes in fields like Umbilical cord and In vivo.
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Embryonic stem cell-derived microvesicles reprogram hematopoietic progenitors: evidence for horizontal transfer of mRNA and protein delivery.
J Ratajczak;K Miekus;M Kucia;J Zhang.
Leukemia (2006)
Membrane-derived microvesicles: important and underappreciated mediators of cell-to-cell communication.
J Ratajczak;M Wysoczynski;F Hayek;A Janowska-Wieczorek.
Leukemia (2006)
Haploinsufficiency of CBFA2 causes familial thrombocytopenia with propensity to develop acute myelogenous leukaemia
W.-J. Song;M. G. Sullivan;R. D. Legare;S. Hutchings.
Nature Genetics (1999)
A population of very small embryonic-like (VSEL) CXCR4 + SSEA-1 + Oct-4 + stem cells identified in adult bone marrow
M Kucia;R Reca;F R Campbell;E Zuba-Surma.
Leukemia (2006)
Trafficking of Normal Stem Cells and Metastasis of Cancer Stem Cells Involve Similar Mechanisms: Pivotal Role of the SDF-1–CXCR4 Axis
Magda Kucia;Ryan Reca;Katarzyna Miekus;Jens Wanzeck.
Stem Cells (2005)
CXCR4-SDF-1 signalling, locomotion, chemotaxis and adhesion.
Magda Kucia;Kacper Jankowski;Ryan Reca;Marcin Wysoczynski.
Journal of Molecular Histology (2003)
Migration of Bone Marrow and Cord Blood Mesenchymal Stem Cells In Vitro Is Regulated by Stromal-Derived Factor-1-CXCR4 and Hepatocyte Growth Factor-c-met Axes and Involves Matrix Metalloproteinases
Bo‐Ra Son;Leah A. Marquez‐Curtis;Magda Kucia;Marcin Wysoczynski.
Stem Cells (2006)
Microvesicles derived from activated platelets induce metastasis and angiogenesis in lung cancer.
Anna Janowska-Wieczorek;Marcin Wysoczynski;Marcin Wysoczynski;Jacek Kijowski;Jacek Kijowski;Leah Marquez-Curtis;Leah Marquez-Curtis.
International Journal of Cancer (2005)
Numerous growth factors, cytokines, and chemokines are secreted by human CD34(+) cells, myeloblasts, erythroblasts, and megakaryoblasts and regulate normal hematopoiesis in an autocrine/paracrine manner.
Marcin Majka;Marcin Majka;Anna Janowska-Wieczorek;Anna Janowska-Wieczorek;Janina Ratajczak;Janina Ratajczak;Karen Ehrenman;Karen Ehrenman.
Blood (2001)
The pleiotropic effects of the SDF-1-CXCR4 axis in organogenesis, regeneration and tumorigenesis.
M Z Ratajczak;E Zuba-Surma;M Kucia;R Reca.
Leukemia (2006)
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