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1 mutant, frascati (frs), that shows profound hypochromic anaemia and erythroid maturation arrest owin
4 ing to identify the gene responsible for the hypochromic anaemia of the zebrafish mutant weissherbst.
5 ish mutant sauternes (sau) has a microcytic, hypochromic anaemia, suggesting that haemoglobin product
10 continued, weh(Tp85c-/-) zebrafish developed hypochromic anemia and impaired erythroid maturation des
12 use mutant, which suffers from a microcytic, hypochromic anemia apparently due to defective iron tran
13 autosomal recessively inherited, microcytic, hypochromic anemia associated with abnormal reticulocyte
15 cation and characterization of the zebrafish hypochromic anemia mutant, gavi, which exhibits transfer
16 afish have resulted in the identification of hypochromic anemia mutants with a range of mutations aff
17 ron deficiency and eventually the microcytic hypochromic anemia or iron deficiency anemia that is the
20 n iron/heme deficiency results in microcytic hypochromic anemia, the most prevalent anemia globally.
22 distribution width (RDW), the percentage of hypochromic cells (which is an indicator of insufficient
24 ast, Fe(III)Blm and HO(2)-Co(III)Blm induced hypochromic effects in the CD spectrum of I and altered
25 DNA base stacking in Pf3, as judged by Raman hypochromic effects, differs significantly from that occ
31 a low hemoglobin level, i.e. 10.9 g/dL with hypochromic microcytic anemia pattern seen in complete b
33 e zebrafish chianti (cia) mutant manifests a hypochromic, microcytic anemia after the onset of embryo
35 antation analyses reveal a mild, congenital, hypochromic, microcytic anemia intrinsic to the hematopo
36 ristics and pathogenesis of a new recessive, hypochromic, microcytic anemia mouse mutant, nm1054.
38 of chardonnay (cdy), a zebrafish mutant with hypochromic, microcytic anemia, and positioned the mutan
39 sis reveals a moderately severe, congenital, hypochromic, microcytic anemia, with an elevated red cel
43 ysplastic syndrome [ATMDS]) characterized by hypochromic, microcytic, anisopoikilocytic red blood cel
45 /-) adults have mild anemia characterized by hypochromic red blood cells (RBCs), reticulocytosis, and
48 2 and G2A2G5A2G2 are very shallow with small hypochromic shifts denoting negligible binding at physio
49 lectual disability, intractable seizures and hypochromic skin patches, we identified the ribosomal pr