ライフサイエンスコーパス: autosomal recessive polycystic kidney

1 Standard texts describe human autosomal recessive polycystic kidney disease (ARPKD) as

2 at HNF-1beta regulates the expression of the autosomal recessive polycystic kidney disease (ARPKD) ge

3 o the Chlamydomonas gene IFT88 and the mouse autosomal recessive polycystic kidney disease (ARPKD) ge

4 Autosomal recessive polycystic kidney disease (ARPKD) is

5 Autosomal recessive polycystic kidney disease (ARPKD) is

6 Autosomal recessive polycystic kidney disease (ARPKD) is

7 Autosomal recessive polycystic kidney disease (ARPKD) is

8 Autosomal recessive polycystic kidney disease (ARPKD) is

9 Autosomal recessive polycystic kidney disease (ARPKD) is

10 Autosomal recessive polycystic kidney disease (ARPKD) is

11 Autosomal recessive polycystic kidney disease (ARPKD) is

12 mechanism of cyst formation and expansion in autosomal recessive polycystic kidney disease (ARPKD) is

13 tients and several different mouse models of autosomal recessive polycystic kidney disease (ARPKD) is

14 Autosomal recessive polycystic kidney disease (ARPKD) is

15 cific expression pattern of c-ErbB2 in human autosomal recessive polycystic kidney disease (ARPKD) wa

16 ease 1 (PKHD1) gene have been shown to cause autosomal recessive polycystic kidney disease (ARPKD), b

17 PCK rats, an animal model of autosomal recessive polycystic kidney disease (ARPKD), d

18 hich is derived from the PCK rat, a model of autosomal recessive polycystic kidney disease (ARPKD), d

19 cystogenesis and an in vivo animal model of autosomal recessive polycystic kidney disease (ARPKD), o

20 Autosomal recessive polycystic kidney disease (ARPKD), t

21 BACKGROUND & AIMS: Autosomal recessive polycystic kidney disease (ARPKD), t

22 Autosomal recessive polycystic kidney disease (ARPKD), u

23 us, PKHD1, are responsible for causing human autosomal recessive polycystic kidney disease (ARPKD).

24 tic fibrosis (CHF), Caroli disease (CD), and autosomal recessive polycystic kidney disease (ARPKD).

25 he gene product of PKHD1, is responsible for autosomal recessive polycystic kidney disease (ARPKD).

26 the most extensively characterized model of autosomal recessive polycystic kidney disease (ARPKD).

27 cretion in cyst formation and enlargement in autosomal recessive polycystic kidney disease (ARPKD).

28 PKHD1 gene, which encodes fibrocystin, cause autosomal recessive polycystic kidney disease (ARPKD).

29 Autosomal recessive polycystic kidney disease (ARPKD; MI

30 ct encoded by the PKHD1 gene responsible for autosomal recessive polycystic kidney disease (PKD) in h

31 teins associated with autosomal dominant and autosomal recessive polycystic kidney disease (polycysti

32 ed by the PKHD1 gene that is responsible for autosomal recessive polycystic kidney disease among huma

33 -wide basis of heterozygous mutations in the autosomal recessive polycystic kidney disease gene PKHD1

34 ing sequence (CTS) of fibrocystin, the human autosomal recessive polycystic kidney disease gene produ

35 and hepatic disease 1) gene responsible for autosomal recessive polycystic kidney disease has been m

36 PKHD1, the gene mutated in human autosomal recessive polycystic kidney disease has recent

37 ntiation in vitro, and is expressed in human autosomal recessive polycystic kidney disease in cyst ep

38 c phenotypes including a syndrome similar to autosomal recessive polycystic kidney disease in humans.

39 Autosomal recessive polycystic kidney disease is a hered

40 Autosomal recessive polycystic kidney disease is caused

41 It is proposed that the pathogenesis of autosomal recessive polycystic kidney disease is linked

42 Autosomal recessive polycystic kidney disease is one of

43 ur data suggest that hepatic cystogenesis in autosomal recessive polycystic kidney disease may involv

44 cM critical region defined for another mouse autosomal recessive polycystic kidney disease model, juv

45 ephronophthisis locus on chromosome 2q13 and autosomal recessive polycystic kidney disease on chromos

46 Autosomal recessive polycystic kidney disease results fr

47 kidney (PCK) rats are a spontaneous model of autosomal recessive polycystic kidney disease that exhib

48 itulates phenotypic characteristics of human autosomal recessive polycystic kidney disease was produc

49 0q25 and is excluded as a candidate gene for autosomal recessive polycystic kidney disease, autosomal

50 ges in the kidney, such as nephronophthisis, autosomal recessive polycystic kidney disease, or medull

51 in report the case of a 21-year-old man with autosomal recessive polycystic kidney disease, presentin

52 ed in the Tg737(orpk)and cpk mouse models of autosomal recessive polycystic kidney disease, respectiv

53 D1 gene are responsible for typical forms of autosomal recessive polycystic kidney disease.

54 idney size by half in the BPK mouse model of autosomal recessive polycystic kidney disease.

55 cystic kidney (PCK) rats, the ARPKD model of autosomal recessive polycystic kidney disease.

56 renal-hepatic-pancreatic dysplasia found in autosomal recessive polycystic kidney disease.

57 disease with congenital hepatic fibrosis and autosomal recessive polycystic kidney disease.

58 nt that provides a new mouse model for human autosomal recessive polycystic kidney disease.

59 iver, this causes a phenotype that resembles autosomal recessive polycystic kidney disease.

60 e in Cys1(cpk/cpk) mice, a model that mimics autosomal recessive polycystic kidney disease.

61 disease in Cys1(cpk) mice, a mouse model of autosomal recessive polycystic kidney disease; this gene

62 Autosomal-recessive polycystic kidney disease (ARPKD) is

63 cystic kidney (PCK) rats, an animal model of autosomal-recessive polycystic kidney disease (ARPKD), d

64 ene (inv/inv) develop renal cysts resembling autosomal-recessive polycystic kidney disease.

65 mportant of which are autosomal dominant and autosomal recessive polycystic kidney diseases, are incu