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1  appeared mature, but the mice were severely hypohidrotic.
2                                              Hypohidrotic (anhidrotic) ectodermal dysplasia (HED), a
3                           Autosomal dominant hypohidrotic ectodermal dysplasia (ADHED) is a disorder
4 T and Ta mice identified critical anhidrotic/hypohidrotic ectodermal dysplasia (EDA) effectors in fou
5                          X-linked anhidrotic/hypohidrotic ectodermal dysplasia (EDA) is caused by mut
6                                Patients with hypohidrotic ectodermal dysplasia (HED) and Tabby (Ta) m
7                                              Hypohidrotic ectodermal dysplasia (HED) results from mut
8  Inactivating mutations in Eda or Edar cause hypohidrotic ectodermal dysplasia (HED), a condition cha
9                                              Hypohidrotic ectodermal dysplasia (HED), a congenital di
10                                     X-linked hypohidrotic ectodermal dysplasia (XLHED) is a heritable
11                                     X-Linked hypohidrotic ectodermal dysplasia (XLHED) is a human con
12 todysplasin A (EDA) are affected by X-linked hypohidrotic ectodermal dysplasia (XLHED), a condition c
13                                 The X-linked hypohidrotic ectodermal dysplasia (XLHED), resulting fro
14                                     X-linked hypohidrotic ectodermal dysplasia (XLHED), the most comm
15 s is the cause of incontinentia pigmenti and hypohidrotic ectodermal dysplasia and immunodeficiency (
16 to identify a LRP6 mutation in patients with hypohidrotic ectodermal dysplasia and reveal the dynamic
17 forms, EDA-A1 and EDA-A2, result in X-linked hypohidrotic ectodermal dysplasia characterized by defec
18   Of the remaining 25 males, one infant with hypohidrotic ectodermal dysplasia had a mutation of NEMO
19   Mutations in Edar-or its ligand, Eda-cause hypohidrotic ectodermal dysplasia in humans and mice.
20                   The crinkled mutant has an hypohidrotic ectodermal dysplasia phenotype identical to
21 P6 mutation (c.2292G>A; p.W764*) presented a hypohidrotic ectodermal dysplasia phenotype.
22                                     X-linked hypohidrotic ectodermal dysplasia results in abnormal mo
23 n have an X-linked syndrome characterized by hypohidrotic ectodermal dysplasia with immune deficiency
24 f the zinc finger are found in patients with hypohidrotic ectodermal dysplasia with immunodeficiency
25 c disorders, incontinentia pigmenti (IP) and hypohidrotic ectodermal dysplasia with severe immunodefi
26   Mutations in the EDA gene cause anhidrotic/hypohidrotic ectodermal dysplasia, a disorder characteri
27 DAR, or the downstream adaptor EDARADD cause hypohidrotic ectodermal dysplasia.
28 D, that is present in a family affected with hypohidrotic ectodermal dysplasia.
29  murine Eda (Tabby) phenocopy human X-linked hypohidrotic ectodermal dysplasia.
30 e development, leading to the human disorder hypohidrotic ectodermal dysplasia.
31 ppaB signaling during development results in hypohidrotic ectodermal dysplasia.
32 asias and 2.8 (95% CI, 1.8-3.8) for X-linked hypohidrotic ectodermal dysplasias.