Allen C. Eaves mainly investigates Stem cell, Immunology, Progenitor cell, Haematopoiesis and Myeloid leukemia. In his study, Cell cycle is strongly linked to Cell culture, which falls under the umbrella field of Stem cell. Allen C. Eaves works in the field of Immunology, namely Bone marrow.
The various areas that Allen C. Eaves examines in his Progenitor cell study include Molecular biology, In vitro, Cell type and Induced pluripotent stem cell. His Haematopoiesis research includes themes of Cell division, Progenitor and Cellular differentiation. His Myeloid leukemia study necessitates a more in-depth grasp of Cancer research.
Allen C. Eaves mostly deals with Immunology, Progenitor cell, Haematopoiesis, Stem cell and Myeloid leukemia. His Immunology research incorporates themes from CD34, Nod, In vivo and Transplantation. His research investigates the connection between Progenitor cell and topics such as In vitro that intersect with issues in Erythropoietin.
His Haematopoiesis research includes elements of Stromal cell, Cord blood, Molecular biology, Growth factor and Bone marrow. His Stem cell study is concerned with Cell biology in general. His work on Imatinib mesylate as part of general Cancer research study is frequently linked to Philadelphia chromosome, therefore connecting diverse disciplines of science.
His primary scientific interests are in Cell biology, Mesenchymal stem cell, Molecular biology, Haematopoiesis and Progenitor cell. His work on Stem cell as part of general Cell biology study is frequently connected to Component, therefore bridging the gap between diverse disciplines of science and establishing a new relationship between them. His research in Stem cell intersects with topics in Endothelial stem cell and Cell culture.
His Haematopoiesis study integrates concerns from other disciplines, such as Immunology, Cord blood, Bone marrow and CD34. CD34 is closely attributed to Myeloid leukemia in his research. His research integrates issues of In vitro and Serum free in his study of Progenitor cell.
Allen C. Eaves focuses on Cell biology, Haematopoiesis, CD34, Bone marrow and Andrology. His Cell biology study incorporates themes from Cell culture, Cytokine, Induced pluripotent stem cell and Mesoderm. His work deals with themes such as Immunology and Cord blood, which intersect with Haematopoiesis.
The various areas that he examines in his CD34 study include Cytotoxic T cell, In vitro, Progenitor cell, Myeloid leukemia and Drug resistance. In Bone marrow, he works on issues like Cancer research, which are connected to Stem cell. His work in Andrology addresses subjects such as Fetal bovine serum, which are connected to disciplines such as Umbilical cord and Mesenchymal stem cell.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Mechanisms that regulate the cell cycle status of very primitive hematopoietic cells in long-term human marrow cultures. II. Analysis of positive and negative regulators produced by stromal cells within the adherent layer.
CJ Eaves;JD Cashman;RJ Kay;GJ Dougherty.
Blood (1991)
Chronic myeloid leukemia stem cells possess multiple unique features of resistance to BCR-ABL targeted therapies.
X Jiang;X Jiang;Y Zhao;C Smith;C Smith;M Gasparetto.
Leukemia (2007)
Enzymatic treatment of long-term human marrow cultures reveals the preferential location of primitive hemopoietic progenitors in the adherent layer
L Coulombel;AC Eaves;CJ Eaves.
Blood (1983)
Human marrow cells capable of erythropoietic differentiation in vitro: definition of three erythroid colony responses.
Connie J. Gregory;Allen C. Eaves.
Blood (1977)
Erythropoietin (Ep) dose-response curves for three classes of erythroid progenitors in normal human marrow and in patients with polycythemia vera
Connie J. Eaves;Allen C. Eaves.
Blood (1978)
Three stages of erythropoietic progenitor cell differentiation distinguished by a number of physical and biologic properties.
Connie J. Gregory;Allen C. Eaves.
Blood (1978)
Normal and leukemic SCID-repopulating cells (SRC) coexist in the bone marrow and peripheral blood from CML patients in chronic phase, whereas leukemic SRC are detected in blast crisis.
Christian Sirard;Tsvee Lapidot;Josef Vormoor;Jody D. Cashman.
Blood (1996)
Enumeration of neural stem and progenitor cells in the neural colony-forming cell assay.
Sharon A. Louis;Rodney L. Rietze;Loic Deleyrolle;Ravenska E. Wagey.
Stem Cells (2008)
High level engraftment of NOD/SCID mice by primitive normal and leukemic hematopoietic cells from patients with chronic myeloid leukemia in chronic phase
J.C.Y. Wang;T. Lapidot;J.D. Cashman;M. Doedens.
Blood (1998)
Prognostic implications of differences in telomere length between normal and malignant cells from patients with chronic myeloid leukemia measured by flow cytometry
Tim H. Brümmendorf;Tessa L. Holyoake;Nathalie Rufer;Michael J. Barnett.
Blood (2000)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:
University of British Columbia
University of British Columbia
University of British Columbia
BC Cancer Agency
University of Glasgow
University of British Columbia
Simon Fraser University
University of British Columbia
The University of Texas Health Science Center at Houston
University of Toronto
Singapore University of Technology and Design
Athens University of Economics and Business
University of Sharjah
Tencent (China)
National Taiwan University
Swansea University
King Juan Carlos University
Osaka University
University of Alberta
Université Laval
United States Department of Agriculture
Florey Institute of Neuroscience and Mental Health
Stanford University
Johns Hopkins University School of Medicine
Wellesley College
University of Minnesota