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Blurring the Lines: NPM1 Mutation in Blast Phase CML Challenges Traditional Paradigms

Smeeta Gajendra1, Leena Gupta1, Deepshi Thakral1

  • 1Department of Laboratory Oncology, Dr. B.R.A.I.R.C.H, All India Institute of Medical Sciences, Room No. 239, Second Floor, New Delhi, 110029 India.

Indian Journal of Hematology & Blood Transfusion : an Official Journal of Indian Society of Hematology and Blood Transfusion
|June 23, 2026
PubMed
Summary

No abstract available in PubMed .

Keywords:
Acute myeloid leukemiaBCR::ABL1 fusion geneBlast crisisChronic myeloid leukemiaNPM1 mutation

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Organisms are capable of detecting and fixing nucleotide mismatches that occur during DNA replication. This sophisticated process requires identifying the new strand and replacing the erroneous bases with correct nucleotides. Mismatch repair is coordinated by many proteins in both prokaryotes and eukaryotes.
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The human genome has more than 3 billion base pairs of DNA per cell. Prior to cell division, that vast amount of genetic...
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Point mutations are genetic alterations involving the change of a single nucleotide base pair in DNA. Depending on how the alteration affects protein synthesis, they can lead to various consequences.Point mutations fall into the following types:Silent mutations occur when a nucleotide change does not alter the amino acid sequence due to the redundancy of the genetic code. For instance, changing ACC to ACA still encodes threonine, leaving the protein function unaffected. This occurs because...

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