ライフサイエンスコーパス: distal renal tubular acidosis

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1 with early-onset sensorineural deafness and distal renal tubular acidosis.

2 1) causing both hereditary spherocytosis and distal renal tubular acidosis.

3 d cells is prevented and the animals develop distal renal tubular acidosis.

4 kidney was disrupted and the mice exhibited distal renal tubular acidosis.

5 the B1-isoform, cause the clinical condition distal renal tubular acidosis.

6 types of hereditary hemolytic anemias and/or distal renal tubular acidosis.

7 ephropathy, primary hyperparathyroidism, and distal renal tubular acidosis.

8 diating distal nephron acid secretion, cause distal renal tubular acidosis, a condition characterized

9 and its role in hereditary spherocytosis and distal renal tubular acidosis are described.

10 mbination of renal concentration defects and distal renal tubular acidosis as a result of impaired V-

11 netic deletion of Slc26a7 expression develop distal renal tubular acidosis, as manifested by metaboli

12 The distal renal tubular acidosis-associated AE1 901X mutant

13 Autosomal dominant distal renal tubular acidosis (ddRTA) is caused by mutat

14 Autosomal-dominant and -recessive forms of distal renal tubular acidosis (dRTA) are caused by mutat

15 Autosomal recessive distal renal tubular acidosis (dRTA) is a severe disorde

16 Primary distal renal tubular acidosis (dRTA) is characterized by

17 Distal renal tubular acidosis (dRTA) is characterized by

18 Chronically reduced renal acid excretion in distal renal tubular acidosis (dRTA) may lead to nephroc

19 in intercalated cells (ICs) leads to type I distal renal tubular acidosis (dRTA), a disease associat

20 th Sjogren's syndrome and a secretory-defect distal renal tubular acidosis (dRTA), absence of vacuola

21 The primary or hereditary form of distal renal tubular acidosis (dRTA), although rare, has

22 a-intercalated cell cause autosomal dominant distal renal tubular acidosis (dRTA).

23 s and the consequent development of complete distal renal tubular acidosis (dRTA).

24 de challenge showed the child has incomplete distal renal tubular acidosis (dRTA).

25 mutations that lead to inheritable forms of distal renal tubular acidosis (dRTA).

26 B1 and a4 subunit isoforms, cause recessive distal renal tubular acidosis (dRTA).

27 unit gene ATP6V1B1 cause autosomal-recessive distal renal tubular acidosis (dRTA).

28 base homeostasis and, when defective, causes distal renal tubular acidosis (dRTA).

29 Mutations of the human ATP6V1B1 gene cause distal renal tubular acidosis (dRTA; OMIM #267300) often

30 ients with a clinical diagnosis of inherited distal renal tubular acidosis has no identified causativ

31 secretes protons in the distal nephron cause distal renal tubular acidosis in humans, a condition cha

32 tly been shown to cause an inherited form of distal renal tubular acidosis in humans.

33 le discusses a likely mechanism for dominant distal renal tubular acidosis in which associations betw

34 The involvement of band 3 in distal renal tubular acidosis is reviewed.

35 conditions including primary aldosteronism, distal renal tubular acidosis, Liddle's disease, apparen

36 stigated as a potential cause of unexplained distal renal tubular acidosis or decreased gastric acid

37 omatocytosis, south-east Asian ovalocytosis, distal renal tubular acidosis, Rhnull), associated with

38 ion in the proximal tubule in the context of distal renal tubular acidosis will require further clari

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