D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Biology and Biochemistry D-index 56 Citations 9,320 156 World Ranking 10082 National Ranking 346

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Immune system
  • Internal medicine

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.

His most cited work include:

  • Chronic myeloid leukemia stem cells possess multiple unique features of resistance to BCR-ABL targeted therapies. (317 citations)
  • Chronic myeloid leukemia stem cells possess multiple unique features of resistance to BCR-ABL targeted therapies. (317 citations)
  • 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. (279 citations)

What are the main themes of his work throughout his whole career to date?

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.

He most often published in these fields:

  • Immunology (47.09%)
  • Progenitor cell (51.32%)
  • Haematopoiesis (45.50%)

What were the highlights of his more recent work (between 2011-2021)?

  • Cell biology (31.75%)
  • Mesenchymal stem cell (14.81%)
  • Molecular biology (25.93%)

In recent papers he was focusing on the following fields of study:

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.

Between 2011 and 2021, his most popular works were:

  • Targeting primitive chronic myeloid leukemia cells by effective inhibition of a new AHI-1-BCR-ABL-JAK2 complex. (58 citations)
  • Long-term deregulated human hematopoiesis in goats transplanted in utero with BCR-ABL-transduced lin(-)CD34(+) cord blood cells. (3 citations)
  • Long-term deregulated human hematopoiesis in goats transplanted in utero with BCR-ABL-transduced lin(-)CD34(+) cord blood cells. (3 citations)

In his most recent research, the most cited papers focused on:

  • Gene
  • Immune system
  • Internal medicine

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.

Best Publications

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)

427 Citations

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)

427 Citations

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)

425 Citations

Human marrow cells capable of erythropoietic differentiation in vitro: definition of three erythroid colony responses.

Connie J. Gregory;Allen C. Eaves.
Blood (1977)

370 Citations

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)

362 Citations

Three stages of erythropoietic progenitor cell differentiation distinguished by a number of physical and biologic properties.

Connie J. Gregory;Allen C. Eaves.
Blood (1978)

360 Citations

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)

259 Citations

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)

246 Citations

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)

244 Citations

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)

244 Citations

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