Utvidet returrett til 31. januar 2025

Signaling Modulators in Bone Marrow Microenvironment and HSC Fate

Om Signaling Modulators in Bone Marrow Microenvironment and HSC Fate

In the article "Signaling Modulators in Bone Marrow Microenvironment and HSC Fate," V. P. Kale delves into the intricate signaling mechanisms in the bone marrow microenvironment that regulate the fate of hematopoietic stem cells (HSCs). The author highlights the critical role of various signaling modulators, including cytokines, chemokines, growth factors, and extracellular matrix proteins, in HSC maintenance, proliferation, and differentiation. He also discusses the potential implications of abnormal signaling pathways in HSC fate and the development of hematological disorders such as leukemia. This article is a valuable resource for researchers and clinicians interested in the molecular mechanisms underlying HSC function and the potential therapeutic targets for hematological diseases.

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  • Språk:
  • Engelsk
  • ISBN:
  • 9782353691678
  • Bindende:
  • Paperback
  • Sider:
  • 126
  • Utgitt:
  • 5. april 2023
  • Dimensjoner:
  • 152x8x229 mm.
  • Vekt:
  • 195 g.
  • BLACK NOVEMBER
  Gratis frakt
Leveringstid: 2-4 uker
Forventet levering: 20. desember 2024
Utvidet returrett til 31. januar 2025

Beskrivelse av Signaling Modulators in Bone Marrow Microenvironment and HSC Fate

In the article "Signaling Modulators in Bone Marrow Microenvironment and HSC Fate," V. P. Kale delves into the intricate signaling mechanisms in the bone marrow microenvironment that regulate the fate of hematopoietic stem cells (HSCs).
The author highlights the critical role of various signaling modulators, including cytokines, chemokines, growth factors, and extracellular matrix proteins, in HSC maintenance, proliferation, and differentiation. He also discusses the potential implications of abnormal signaling pathways in HSC fate and the development of hematological disorders such as leukemia.
This article is a valuable resource for researchers and clinicians interested in the molecular mechanisms underlying HSC function and the potential therapeutic targets for hematological diseases.

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