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Related Concept Videos

Stem Cell Culture01:17

Stem Cell Culture

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Stem cell research aims to find ways to use stem cells to regenerate and repair cellular damage. Over time, most adult cells undergo the wear and tear of aging and lose their ability to divide and repair themselves. Stem cells do not display a particular morphology or function. Adult stem cells, which exist as a small subset of cells in most tissues, keep dividing and can differentiate into a number of specialized cells generally formed by that tissue. These cells enable the body to renew and...
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Stem Cell Therapy for Tissue Regeneration01:21

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Stem cell therapy is a method used in regenerative medicine to repair and restore function to damaged tissues and organs. Stem cells have the potential to proliferate and differentiate into various tissue types, making them ideal candidates for tissue regeneration. For example, hematopoietic stem cell transplants are commonly used in blood cancer treatment to replenish damaged bone marrow and restore healthy blood cells.
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Embryonic Stem Cells00:57

Embryonic Stem Cells

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Embryonic stem (ES) cells were first discovered in mice in 1981 by Martin Evans. In 1998, James Thomson identified a method to isolate embryonic stem cells from humans. Human embryonic stem cells (hESCs) are obtained from 3-5 day old embryos that remain unused after an in vitro fertilization procedure.
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Embryonic Stem Cells00:58

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Embryonic stem (ES) cells are undifferentiated pluripotent cells, meaning they can produce any cell type in the body. This gives them tremendous potential in science and medicine since they can generate specific cell types for use in research or to replace body cells lost due to damage or disease.
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iPS Cell Differentiation01:22

iPS Cell Differentiation

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The ability of induced pluripotent stem cells or iPSCs to differentiate into most body cell types has stimulated repair and regenerative medicine research over the past few decades. iPSC-derived blood cells, hepatocytes, beta islet cells, cardiomyocytes, neurons, and other cell types can repair injuries or regenerate damaged tissue in diseases such as diabetes and neurodegenerative disorders.
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Induced Pluripotent Stem Cells01:13

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Stem cells are undifferentiated cells that divide and produce different types of cells. Ordinarily, cells that have differentiated into a specific cell type are post-mitotic—that is, they no longer divide. However, scientists have found a way to reprogram these mature cells so that they “de-differentiate” and return to an unspecialized, proliferative state. These cells are also pluripotent like embryonic stem cells—able to produce all cell types—and are therefore...
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CRISPR/Cas9 Gene Editing of Hematopoietic Stem and Progenitor Cells for Gene Therapy Applications
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Human embryonic stem cell therapy for aplastic anemia.

Geeta Shroff1, Rakesh Gupta2, Lalduhawmi Zadeng1

  • 1Nutech Mediworld New Delhi India.

Clinical Case Reports
|June 8, 2017
PubMed
Summary

Human embryonic stem cell (hESC) therapy offers a safe and effective treatment for aplastic anemia (AA). This groundbreaking approach demonstrated significant patient improvement with no adverse events, highlighting its therapeutic potential.

Keywords:
Aplastic anemiahuman embryonic stem cellsstem cellstransplantation

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Area of Science:

  • Regenerative Medicine
  • Hematology

Background:

  • Aplastic anemia (AA) is a rare but serious condition where the bone marrow doesn't produce enough blood cells.
  • Current treatments for AA have limitations and potential side effects.

Observation:

  • A single patient with aplastic anemia received human embryonic stem cell (hESC) therapy.
  • The patient was monitored for therapeutic efficacy and safety.

Findings:

  • The patient exhibited remarkable clinical improvement following hESC administration.
  • No adverse events were recorded during the treatment period, indicating a favorable safety profile.

Implications:

  • hESC therapy presents a promising and safe therapeutic option for aplastic anemia patients.
  • Further research into hESC therapy could revolutionize the treatment of bone marrow failure syndromes.