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1 wild-type sperm whale myoglobin and soybean leghemoglobin.
2 d for the carbon monoxide complex of soybean leghemoglobin.
3 ongly decreased expression of the associated leghemoglobin.
4 n-regulated, in particular all the genes for leghemoglobins.
6 r of cyanoglobin was more similar to that of leghemoglobin a than to that of sperm whale myoglobin.
8 in sperm whale myoglobin, Tyr133 in soybean leghemoglobin, and either alphaTyr42, betaTyr35, or beta
16 its highest expression level occurred after leghemoglobin (lb) gene induction, a molecular marker fo
17 our systems for restoring functional ferrous leghemoglobin (LB2+) from its inactive, ferric form.
19 ea (Vigna unguiculata) nodules contain three leghemoglobins (LbI, LbII, and LbIII) that are encoded b
20 have two types of hemoglobins: symbiotic or leghemoglobins (Lbs) and nonsymbiotic or phytoglobins (G
21 nts, the most abundant Hbs are the symbiotic leghemoglobins (Lbs) that scavenge O(2) and facilitate i
22 indings indicate that the origins of the NLP-leghemoglobin module for O(2) buffering in nodules can b
24 ns, such as the production of oxygen-binding leghemoglobin proteins and the formation of an oxygen di
25 onstrated that, as in vertebrate globins and leghemoglobin, proximal influences operate to determine
27 the activity of bacterial nitrogenase, plant leghemoglobin, respiratory oxidases, and other Fe protei
29 and NIN directly activate the expression of leghemoglobins through a promoter motif, resembling a "d
30 expression analysis demonstrates that nodule leghemoglobin transcripts were significantly more abunda
31 oglobin, the resultant ultrahigh affinity of leghemoglobin would prevent oxygen transport in root nod