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1 RBCs) obtained from subjects with homozygous hereditary elliptocytosis.
2      We studied this developmental switch in hereditary elliptocytosis 4.1Alg, in which a DNA rearran
3                  Mutations in 4.1R can cause hereditary elliptocytosis, a disease characterized by a
4 n clinically about the resulting conditions (hereditary elliptocytosis and pyropoikilocytosis), the d
5  membrane, such as hereditary spherocytosis, hereditary elliptocytosis, and hereditary pyropoikilocyt
6                                              Hereditary elliptocytosis (HE) and hereditary pyropoikil
7                                              Hereditary elliptocytosis (HE) and hereditary pyropoikil
8                              The most common hereditary elliptocytosis (HE) and hereditary pyropoikil
9 t in severe hereditary spherocytosis (HS) or hereditary elliptocytosis (HE) in mice and humans.
10         In hereditary spherocytosis (HS) and hereditary elliptocytosis (HE), deficiencies of membrane
11  result in a variety of syndromes, including hereditary elliptocytosis (HE), hereditary pyropoikilocy
12 on of spectrin dimers to tetramers result in hereditary elliptocytosis (HE), whereas a deficiency of
13  cell pathologies (hereditary spherocytosis, hereditary elliptocytosis, hereditary hydrocytosis, Sout
14 the tetramer formation site, modeled after a hereditary elliptocytosis mutation in human erythrocyte
15 ss spectrometry characterization of a common hereditary elliptocytosis-related mutation of alpha-spec

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