ライフサイエンスコーパス: spinal and bulbar muscular atrophy

1 ress is also involved in the pathogenesis of spinal and bulbar muscular atrophy.

2 peutic potential of arimoclomol in mice with spinal and bulbar muscular atrophy.

3 ndrogen receptor, an Hsp90 client mutated in spinal and bulbar muscular atrophy.

4 ell culture and in a knock-in mouse model of spinal and bulbar muscular atrophy.

5 Spinal and bulbar muscular atrophy, also known as Kenned

6 ve therapeutic potential in the treatment of spinal and bulbar muscular atrophy and may also be a pos

7 ould potentially be a therapeutic target for spinal and bulbar muscular atrophy and related polygluta

8 nclude dentatorubral pallidoluysian atrophy, spinal and bulbar muscular atrophy, and the spinocerebel

9 RA24 to the longer poly-Q AR in the X-linked spinal and bulbar muscular atrophied AR could contribute

10 n the human neurodegenerative disease distal spinal and bulbar muscular atrophy (dSBMA).

11 nd FRAXE loci), myotonic dystrophy, X-linked spinal and bulbar muscular atrophy, Huntington's disease

12 n in the androgen receptor, causing X-linked spinal and bulbar muscular atrophy, impairs its function

13 X-linked spinal and bulbar muscular atrophy is a degenerative dis

14 Spinal and bulbar muscular atrophy is an X-linked degene

15 Spinal and bulbar muscular atrophy is an X-linked motor

16 Kennedy disease (KD, or spinal and bulbar muscular atrophy) is caused by a CAG/p

17 Spinal and bulbar muscular atrophy mice that carry 100 p

18 sis in cultured embryonic motor neurons from spinal and bulbar muscular atrophy mice, which was accom

19 The neurodegenerative disorder spinal and bulbar muscular atrophy or Kennedy disease is

20 by redefining the role of AR proteolysis in spinal and bulbar muscular atrophy pathogenesis.

21 have a positive effect on muscle function in spinal and bulbar muscular atrophy patients, in addition

22 , we show that, in the polyglutamine disease spinal and bulbar muscular atrophy, proteolysis of the m

23 polyQ) has been linked to the development of spinal and bulbar muscular atrophy (SBMA or Kennedy dise

24 ion within the androgen receptor (AR) causes spinal and bulbar muscular atrophy (SBMA) and is associa

25 Spinal and bulbar muscular atrophy (SBMA) impairs motor

26 Spinal and bulbar muscular atrophy (SBMA) is a heritable

27 Spinal and bulbar muscular atrophy (SBMA) is a motor neu

28 Spinal and bulbar muscular atrophy (SBMA) is a motor neu

29 Spinal and bulbar muscular atrophy (SBMA) is a neurodege

30 Spinal and bulbar muscular atrophy (SBMA) is a neuromusc

31 Spinal and bulbar muscular atrophy (SBMA) is a progressi

32 Spinal and bulbar muscular atrophy (SBMA) is a progressi

33 X-linked spinal and bulbar muscular atrophy (SBMA) is a rare form

34 Spinal and bulbar muscular atrophy (SBMA) is an inherite

35 X-linked spinal and bulbar muscular atrophy (SBMA) is an inherite

36 Spinal and bulbar muscular atrophy (SBMA) is an X-linked

37 X-linked spinal and bulbar muscular atrophy (SBMA) is caused by a

38 Spinal and bulbar muscular atrophy (SBMA) is caused by p

39 X-linked spinal and bulbar muscular atrophy (SBMA) is characteriz

40 Spinal and bulbar muscular atrophy (SBMA) is characteriz

41 Spinal and bulbar muscular atrophy (SBMA) is one of a gr

42 Spinal and bulbar muscular atrophy (SBMA) is one of eigh

43 the androgen receptor (AR) protein leads to spinal and bulbar muscular atrophy (SBMA), a neurodegene

44 ested in creating a mouse model for X-linked spinal and bulbar muscular atrophy (SBMA), a neuromuscul

45 sterone levels is a therapeutic approach for spinal and bulbar muscular atrophy (SBMA), a polyglutami

46 Here we consider X-linked spinal and bulbar muscular atrophy (SBMA), a repeat diso

47 ransgenic model of the polyglutamine disease spinal and bulbar muscular atrophy (SBMA), an adult-onse

48 Spinal and bulbar muscular atrophy (SBMA), an adult-onse

49 pansion in the androgen receptor (AR) causes spinal and bulbar muscular atrophy (SBMA), an X-linked n

50 gen receptor (AR), a protein associated with spinal and bulbar muscular atrophy (SBMA), and the nucle

51 CAG repeat polyglutamine diseases, including Spinal and Bulbar Muscular Atrophy (SBMA), Huntington's

52 by a CAG/polyglutamine expansion, including spinal and bulbar muscular atrophy (SBMA), Huntington's

53 Spinal and bulbar muscular atrophy (SBMA), or Kennedy's

54 tamine (polyQ)-expanded AR proteotoxicity in spinal and bulbar muscular atrophy (SBMA).

55 e tract in the androgen receptor (AR) causes spinal and bulbar muscular atrophy (SBMA).

56 Spinal and bulbar muscular atrophy (SBMA, also known as

57 X syndrome (FRAX), myotonic dystrophy (DM), spinal and bulbar muscular atrophy (SBMA, also known as

58 Spinal and bulbar muscular atrophy (SBMA, Kennedy's dise

59 X-linked spinal and bulbar muscular atrophy (SBMA; Kennedy's dise

60 Using a mouse model of spinal and bulbar muscular atrophy that exhibits many of

61 receptor (AR) to Kennedy's disease (X-linked spinal and bulbar muscular atrophy) was a major step for