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Related Concept Videos

Lethal Alleles02:41

Lethal Alleles

Agouti: A Lethal Allele
Lucien Cuénot discovered lethal alleles in 1905 while studying the inheritance of coat color in mice. The agouti gene is responsible for the color of the coat in mice. This gene codes for an agouti-signaling protein, which is responsible for melanin distribution in mammals. The wild-type allele gives rise to gray-brown coat color in mice, while the mutant allele gives rise to yellow coat color. In addition to coat color, the agouti gene is associated with the yellow...
Differentiation of Common Myeloid Progenitor Cells01:15

Differentiation of Common Myeloid Progenitor Cells

Common myeloid progenitors (CMPs) are oligopotent cells that can differentiate into granulocytes and macrophages. Granulocytes and macrophages are essential for protecting the body against bacterial, viral, or fungal infections. They migrate from the bone marrow into the circulating blood to reach specific tissue sites where they differentiate and help in immune surveillance. However, they survive only for a few days and must be continuously made available to the organism to maintain a robust...
Combination Therapies and Personalized Medicine02:50

Combination Therapies and Personalized Medicine

Combining two or more treatment methods increases the life span of cancer patients while reducing damage to vital organs or tissue from the overuse of a single treatment. Combination therapy also targets different cancer-inducing pathways, thus reducing the chances of developing resistance to treatment.
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Bone Marrow Sampling and Transplants01:22

Bone Marrow Sampling and Transplants

Bone marrow transplant is a potential cure for several diseases, including cancer and specific genetic disorders. Notably, this procedure is applicable for patients suffering from aplastic anemia, certain types of leukemia, severe combined immunodeficiency disease (SCID), Hodgkin's disease, non-Hodgkin's lymphoma, multiple myeloma, thalassemia, sickle-cell disease, and certain cancers.
The transplant begins with high doses of chemotherapy and radiation treatment, which aim to destroy the...
Translation01:31

Translation

Lesson: Translation
Translation is the process of synthesizing proteins from the genetic information carried by messenger RNA (mRNA). Following transcription, it constitutes the final step in the expression of genes. This process is carried out by ribosomes, complexes of protein and specialized RNA molecules. Ribosomes, transfer RNA (tRNA), and other proteins produce a chain of amino acids—the polypeptide—as the end product of translation.
Translation Produces the Building Blocks of Life
Translation01:31

Translation

Lesson: Translation
Translation is the process of synthesizing proteins from the genetic information carried by messenger RNA (mRNA). Following transcription, it constitutes the final step in the expression of genes. This process is carried out by ribosomes, complexes of protein and specialized RNA molecules. Ribosomes, transfer RNA (tRNA), and other proteins produce a chain of amino acids—the polypeptide—as the end product of translation.
Translation Produces the Building Blocks of Life

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Updated: Jun 16, 2026

Simplified Intrafemoral Injections Using Live Mice Allow for Continuous Bone Marrow Analysis
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Acute myeloid leukemia as a genetic disease. Review article.

S Al-Bahar1, Z Adriana, R Pandita

  • 1Department of Hematology, Hussein Makki Al-Juma Centre for Specialised Surgery, State of Kuwait.

The Gulf Journal of Oncology
|January 21, 2010
PubMed
Summary

Genetic abnormalities in acute myeloid leukemia (AML) are increasingly identified, offering insights into cancer biology. Understanding these genetic changes aids in developing targeted therapies for leukemia.

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Area of Science:

  • Hematology
  • Oncology
  • Molecular Biology
  • Genetics

Background:

  • Acute myeloid leukemia (AML) is extensively studied, with numerous recurring genetic abnormalities identified.
  • Clonal chromosome abnormalities are prevalent in AML patients and linked to specific leukemia subsets.
  • Chromosome rearrangements often lead to gene fusions, producing oncogenic proteins.

Purpose of the Study:

  • To review the current understanding of genetic abnormalities in AML.
  • To highlight the association between specific genetic changes and AML subtypes.
  • To emphasize the role of genetic discoveries in advancing AML therapy.

Main Methods:

  • Combined cytogenetic and molecular genetic analyses.
  • Detailed characterization of chromosomal rearrangements in AML.
  • Identification and functional analysis of genes implicated in leukemogenesis.

Main Results:

  • A growing number of recurrent genetic abnormalities are recognized in AML.
  • Specific chromosomal abnormalities are closely associated with distinct AML subsets.
  • Gene fusions resulting from rearrangements create abnormal proteins with oncogenic potential.

Conclusions:

  • Continued genetic research deepens the understanding of AML's molecular basis.
  • Identification of leukemia-associated genes is crucial for developing targeted therapies.
  • Advances in molecular genetics are transforming the approach to biologically based cancer treatments.