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1 and the responses underlying lithium-induced nephrogenic diabetes insipidus.
2  in renal handling of water in health and in nephrogenic diabetes insipidus.
3 and trafficking, the absence of which causes nephrogenic diabetes insipidus.
4 alcitonin has a potential therapeutic use in nephrogenic diabetes insipidus.
5 VP, a vasopressin analog), characteristic of nephrogenic diabetes insipidus.
6 nt selected alleles responsible for X-linked nephrogenic diabetes insipidus.
7 otypes--ranging from congenital cataracts to nephrogenic diabetes insipidus.
8  deletion in mice produces distinct forms of nephrogenic diabetes insipidus.
9 ility; mutations or downregulation can cause nephrogenic diabetes insipidus.
10  were compatible with a diagnosis of partial nephrogenic diabetes insipidus.
11  MIP underlie an autosomal recessive form of nephrogenic diabetes insipidus and absence of the Colton
12 -of-function mutations in aquaporins include nephrogenic diabetes insipidus and congenital cataracts.
13 nstay treatment for bipolar disorder, causes nephrogenic diabetes insipidus and hypercalcemia in abou
14 cost of severe renal side effects, including nephrogenic diabetes insipidus and rarely, ESRD.
15  these results identify a novel mechanism of nephrogenic diabetes insipidus and uncover a role of SOC
16 familiar diseases such as Gaucher's disease, nephrogenic diabetes insipidus, and Creutzfeldt-Jakob di
17    Finally, renal distal tubular acidosis or nephrogenic diabetes insipidus can be caused by autoanti
18 e for retinitis pigmentosa, color blindness, nephrogenic diabetes insipidus, familial ACTH resistance
19 hium, a potent inhibitor of GSK3beta, causes nephrogenic diabetes insipidus, GSK3beta may play a cruc
20 vasopressin 2 receptor and aquaporin 2 cause nephrogenic diabetes insipidus; however, expression of t
21                      Other features included nephrogenic diabetes insipidus in 87% and hypertension i
22 children, and distal tubular toxicity caused nephrogenic diabetes insipidus in one.
23  forms of diabetes insipidus (e.g., X-linked nephrogenic diabetes insipidus) in which the kidney resp
24 ion R137H, which is associated with familial nephrogenic diabetes insipidus, induces constitutive arr
25          The most common cause of hereditary nephrogenic diabetes insipidus is a nonfunctional vasopr
26                                         This nephrogenic diabetes insipidus leads to dehydration and
27  with tolvaptan, a VR2 blocker that causes a nephrogenic diabetes insipidus-like excessive loss of hy
28                    To reduce lithium-induced nephrogenic diabetes insipidus (lithium-NDI), patients w
29  chronic experimental iron overload leads to nephrogenic diabetes insipidus marked by AVP-resistant u
30  aquaporin-2 (AQP2) point mutants that cause nephrogenic diabetes insipidus (NDI) are retained in the
31       Animal models of a variety of acquired nephrogenic diabetes insipidus (NDI) disorders have iden
32                                   Congenital nephrogenic diabetes insipidus (NDI) is a rare disease c
33                                              Nephrogenic diabetes insipidus (NDI) is caused by impair
34                      Hereditary non-X-linked nephrogenic diabetes insipidus (NDI) is caused by mutati
35 wn in a variety of animal models of acquired nephrogenic diabetes insipidus (NDI) that loss of the aq
36     A Mexican family with partial congenital nephrogenic diabetes insipidus (NDI) that resulted from
37 n-2 (AQP2) mutations that cause non-X-linked nephrogenic diabetes insipidus (NDI) were characterized
38 20% of patients treated with lithium develop nephrogenic diabetes insipidus (NDI), a disorder charact
39 fect in urinary concentrating ability, i.e., nephrogenic diabetes insipidus (NDI), but the molecular
40 ep in generating a transgenic mouse model of nephrogenic diabetes insipidus (NDI), we have analyzed t
41 tein expression in mice with lithium-induced nephrogenic diabetes insipidus (NDI).
42 pressin and defective trafficking results in nephrogenic diabetes insipidus (NDI).
43 r processing can produce autosomal recessive nephrogenic diabetes insipidus (NDI).
44                                   Congenital nephrogenic diabetes insipidus (NDI; also known as argin
45             The mice had severe polyuria and nephrogenic diabetes insipidus, potentially due to great
46             Our findings establish a form of nephrogenic diabetes insipidus produced by impaired wate
47                                          The nephrogenic diabetes insipidus symptoms and the absence
48  have shown that a molecular determinant for nephrogenic diabetes insipidus, the vasopressin receptor
49 ceptors known to be responsible for X-linked nephrogenic diabetes insipidus were used as model system
50 hat Foxa1(-/-) mice represent a new model of nephrogenic diabetes insipidus with unique molecular eti
51  a nonsense mutation known to cause X-linked nephrogenic diabetes insipidus (XNDI) in humans (Glu242s
52                                     X-linked nephrogenic diabetes insipidus (XNDI) is a severe kidney