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1 here are 25,000 copies of ID elements in the deer mouse, 1,500 copies in the gerbil (both cricetid ro
3 tion into the functional significance of the deer mouse beta-globin polymorphism was motivated by the
4 ence of individual ID elements in gerbil and deer mouse further confirms BC1 as a master gene in ID a
8 um revealed that high-altitude adaptation of deer mouse hemoglobin involves parallel functional diffe
10 rred outside the range of its reservoir (the deer mouse Peromyscus maniculatus), an investigation sou
11 f the Norway rat (Rattus norvegicus) and the deer mouse (Peromyscus maniculatus) are attributable to
13 tent infection in its natural reservoir, the deer mouse (Peromyscus maniculatus), despite a strong ho
14 cell responses from one such reservoir, the deer mouse (Peromyscus maniculatus), infected with Sin N
15 (Mus musculus), rat (Rattus norvegicus), and deer mouse (Peromyscus maniculatus), to identify rapidly
16 ence of rat and mouse but also following the deer mouse (Peromyscus) and hamster split, with no evide
17 na and S. xerampelinus ("singing mice"), the deer mouse, Peromyscus maniculatus, and the lab mouse, M
25 We have determined that infection of the deer mouse with its homologous hantavirus, Sin Nombre vi
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