ライフサイエンスコーパス: hypohidrotic

コーパス検索結果 (１語後でソート)

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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 Of the remaining 25 males, one infant with hypohidrotic ectodermal dysplasia had a mutation of NEMO

17 Mutations in Edar-or its ligand, Eda-cause hypohidrotic ectodermal dysplasia in humans and mice.

18 The crinkled mutant has an hypohidrotic ectodermal dysplasia phenotype identical to

19 X-linked hypohidrotic ectodermal dysplasia results in abnormal mo

20 n have an X-linked syndrome characterized by hypohidrotic ectodermal dysplasia with immune deficiency

21 f the zinc finger are found in patients with hypohidrotic ectodermal dysplasia with immunodeficiency

22 c disorders, incontinentia pigmenti (IP) and hypohidrotic ectodermal dysplasia with severe immunodefi

23 Mutations in the EDA gene cause anhidrotic/hypohidrotic ectodermal dysplasia, a disorder characteri

24 DAR, or the downstream adaptor EDARADD cause hypohidrotic ectodermal dysplasia.

25 D, that is present in a family affected with hypohidrotic ectodermal dysplasia.

26 murine Eda (Tabby) phenocopy human X-linked hypohidrotic ectodermal dysplasia.

27 e development, leading to the human disorder hypohidrotic ectodermal dysplasia.

28 ppaB signaling during development results in hypohidrotic ectodermal dysplasia.

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