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Rare point mutation at codon 301 and 969 of FMS/M-CSF receptor in acute myelomonocytic and monocytic leukemia

  • Toshiki Natazuka
  • , Toshimitsu Matsui
  • , Mitsuhiro Ito
  • , Hirohisa Nakata
  • , Toshitaro Nakagawa
  • , Hiroyuki Nakamura
  • , Toru Masaoka
  • , Takashi Isobe
  • , Yoshinobu Nakao

Research output: Contribution to journalArticlepeer-review

4 Scopus citations

Abstract

We have investigated whether point mutations occurred at codon 301 or 969 of FMS (M-CSF receptor) in 19 patients with acute myelomonocytic (M4) and monocytic leukemia (M5). Nineteen peripheral blood and bone marrow blood samples collected from M4 and M5 patients were examined by using polymerase chain reaction and hybridization to allele specific oligonucleotide probes. Mutations at codon 301 and 969 of FMS were not detected in any samples. FMS gene mutations at codon 301 and 969 were rarely involved in M4 and M5 patients in Japan.

Original languageEnglish
Pages (from-to)541-543
Number of pages3
JournalLeukemia Research
Volume16
Issue number5
DOIs
StatePublished - May 1992
Externally publishedYes

Keywords

  • AML
  • AMoL
  • M-CSF
  • PCR
  • c-fms
  • point mutation

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