ライフサイエンスコーパス: nephrogenic diabetes insipidus

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1 and trafficking, the absence of which causes nephrogenic diabetes insipidus.

2 alcitonin has a potential therapeutic use in nephrogenic diabetes insipidus.

3 VP, a vasopressin analog), characteristic of nephrogenic diabetes insipidus.

4 nt selected alleles responsible for X-linked nephrogenic diabetes insipidus.

5 otypes--ranging from congenital cataracts to nephrogenic diabetes insipidus.

6 were compatible with a diagnosis of partial nephrogenic diabetes insipidus.

7 deletion in mice produces distinct forms of nephrogenic diabetes insipidus.

8 ility; mutations or downregulation can cause nephrogenic diabetes insipidus.

9 in renal handling of water in health and in nephrogenic diabetes insipidus.

10 MIP underlie an autosomal recessive form of nephrogenic diabetes insipidus and absence of the Colton

11 -of-function mutations in aquaporins include nephrogenic diabetes insipidus and congenital cataracts.

12 cost of severe renal side effects, including nephrogenic diabetes insipidus and rarely, ESRD.

13 these results identify a novel mechanism of nephrogenic diabetes insipidus and uncover a role of SOC

14 familiar diseases such as Gaucher's disease, nephrogenic diabetes insipidus, and Creutzfeldt-Jakob di

15 e for retinitis pigmentosa, color blindness, nephrogenic diabetes insipidus, familial ACTH resistance

16 hium, a potent inhibitor of GSK3beta, causes nephrogenic diabetes insipidus, GSK3beta may play a cruc

17 vasopressin 2 receptor and aquaporin 2 cause nephrogenic diabetes insipidus; however, expression of t

18 Other features included nephrogenic diabetes insipidus in 87% and hypertension i

19 children, and distal tubular toxicity caused nephrogenic diabetes insipidus in one.

20 ion R137H, which is associated with familial nephrogenic diabetes insipidus, induces constitutive arr

21 The most common cause of hereditary nephrogenic diabetes insipidus is a nonfunctional vasopr

22 This nephrogenic diabetes insipidus leads to dehydration and

23 To reduce lithium-induced nephrogenic diabetes insipidus (lithium-NDI), patients w

24 chronic experimental iron overload leads to nephrogenic diabetes insipidus marked by AVP-resistant u

25 aquaporin-2 (AQP2) point mutants that cause nephrogenic diabetes insipidus (NDI) are retained in the

26 Congenital nephrogenic diabetes insipidus (NDI) is a rare disease c

27 Nephrogenic diabetes insipidus (NDI) is caused by impair

28 Hereditary non-X-linked nephrogenic diabetes insipidus (NDI) is caused by mutati

29 A Mexican family with partial congenital nephrogenic diabetes insipidus (NDI) that resulted from

30 n-2 (AQP2) mutations that cause non-X-linked nephrogenic diabetes insipidus (NDI) were characterized

31 20% of patients treated with lithium develop nephrogenic diabetes insipidus (NDI), a disorder charact

32 fect in urinary concentrating ability, i.e., nephrogenic diabetes insipidus (NDI), but the molecular

33 ep in generating a transgenic mouse model of nephrogenic diabetes insipidus (NDI), we have analyzed t

34 r processing can produce autosomal recessive nephrogenic diabetes insipidus (NDI).

35 pressin and defective trafficking results in nephrogenic diabetes insipidus (NDI).

36 Our findings establish a form of nephrogenic diabetes insipidus produced by impaired wate

37 The nephrogenic diabetes insipidus symptoms and the absence

38 have shown that a molecular determinant for nephrogenic diabetes insipidus, the vasopressin receptor

39 ceptors known to be responsible for X-linked nephrogenic diabetes insipidus were used as model system

40 hat Foxa1(-/-) mice represent a new model of nephrogenic diabetes insipidus with unique molecular eti

41 a nonsense mutation known to cause X-linked nephrogenic diabetes insipidus (XNDI) in humans (Glu242s

42 X-linked nephrogenic diabetes insipidus (XNDI) is a severe kidney

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