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Megaloblastosis: From Morphos to Molecules
Author(s) -
K. C. Das,
Monisha Das,
D. Mohanty,
M.M. Jadaon,
Amar Nath Gupta,
Rajaa Marouf,
S.K. Easow
Publication year - 2005
Publication title -
medical principles and practice
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.426
H-Index - 45
eISSN - 1423-0151
pISSN - 1011-7571
DOI - 10.1159/000086179
Subject(s) - bone marrow , megaloblastic anemia , pathology , biology , vitamin b12 , medicine , biochemistry
Megaloblastosis (i.e., megaloblastic transformation of erythroid precursor cells in the bone marrow) is the cytomorphological hallmark of megaloblastic anemia resulting from vitamin B12 and folate deficiency. It is characterized by a finely stippled lacy pattern of nuclear chromatin, which is believed to be an expression of deranged cellular DNA synthesis. However, the molecular basis of these cytomorphological aberrations still remains obscure. The current presentation describes the results of our studies on some molecular events associated with the development of megaloblastosis.

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