ライフサイエンスコーパス: Machado-Joseph disease

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1 , which causes the neurodegenerative disease Machado-Joseph disease.

2 3, a deubiquitinating enzyme associated with Machado-Joseph disease.

3 I, dentatorubral-pallidoluysian atrophy, and Machado-Joseph disease.

4 epresents a promising therapeutic target for Machado-Joseph disease.

5 signalling is beneficial in animal models of Machado-Joseph disease.

6 Mutant ataxin-3, the genetic cause of Machado-Joseph Disease, also contains an expanded CAG re

7 increased longevity in a Drosophila model of Machado-Joseph disease and effectively reduced aggregate

8 a potentially promising therapeutic drug for Machado-Joseph disease and possibly other neurological p

9 nerative polyglutamine disease known both as Machado-Joseph disease and spinocerebellar ataxia type 3

10 cerebellar ataxia type-3 (SCA3), also called Machado-Joseph disease, and is cleaved in mammalian cell

11 nts, which correlated with preservation from Machado-Joseph disease-associated neuropathology, namely

12 spinocerebellar ataxia type 3, also known as Machado-Joseph disease, causes dendritic and synapse los

13 Patients with Machado-Joseph disease exhibit significant motor impairm

14 -expanded neurotoxic protein (MJDtr78Q; MJD, Machado-Joseph disease) in the major timeless (tim)-expr

15 Machado-Joseph disease is a neurodegenerative disease wi

16 Machado-Joseph disease is caused by an expansion of a tr

17 ter among Jews of North African descent, and Machado-Joseph disease is particularly frequent in Yemen

18 ctive treatment of symptomatic patients with Machado-Joseph disease may require cell replacement, whi

19 transplantation into the cerebellum of adult Machado-Joseph disease mice, cerebellar neural stem cell

20 Huntington's disease (HD) and Machado Joseph Disease (MJD) are severe neurological dis

21 dentatorubral pallidoluysian atrophy (DRPLA) Machado-Joseph disease (MJD or SCA3) and SCA2.

22 These include Machado-Joseph disease (MJD) and Huntington's disease (H

23 Machado-Joseph disease (MJD) is a late-onset, progressiv

24 Machado-Joseph disease (MJD) is a neurodegenerative diso

25 Machado-Joseph disease (MJD) is a neurodegenerative diso

26 Machado-Joseph disease (MJD) is an autosomal dominant ne

27 Machado-Joseph disease (MJD) is an inherited neurodegene

28 Machado-Joseph disease (MJD) is one of at least six neur

29 The neurodegenerative disease Machado-Joseph disease (MJD), also known as spinocerebel

30 e frequency of SCA2 compared with SCA1, SCA3/Machado-Joseph disease (MJD), and dentatorubropallidoluy

31 RPLA), spinocerebellar ataxia type 1 (SCA1), Machado-Joseph disease (MJD), and Friedreich ataxia.

32 rebellar ataxia type 3 (SCA3), also known as Machado-Joseph disease (MJD), is an autosomal-dominant n

33 rformed in patients of Japanese descent with Machado-Joseph disease (MJD), it was reported that disea

34 (ATXN3), a deubiquitylase (DUB) involved in Machado-Joseph Disease (MJD), remains elusive.

35 Machado-Joseph disease (MJD; MIM 109150) is a late-onset

36 T3) results in spinocerebellar ataxia type 3/Machado-Joseph disease, one of the nine polyglutamine ne

37 Machado-Joseph disease or spinocerebellar ataxia 3 (SCA3

38 Spinocerebellar ataxia type 3 (SCA3)/Machado Joseph disease results from expansion of the pol

39 Spinocerebellar ataxia type-3 or Machado-Joseph disease (SCA3/MJD) is a member of the CAG

40 Spinocerebellar ataxia type 3, also known as Machado-Joseph disease (SCA3/MJD), is one of at least ei

41 ase protein in spinocerebellar ataxia type 3/Machado-Joseph disease (SCA3/MJD), or an unrelated green

42 spinocerebellar ataxia type 3, also known as Machado-Joseph disease (SCA3/MJD), we show that the dise

43 Machado-Joseph disease (spinocerebellar ataxia type 3) (

44 dominant ataxias was high, particularly for Machado-Joseph disease (spinocerebellar ataxia type 3).

45 e siRNA that exclusively silenced the mutant Machado-Joseph disease/spinocerebellar ataxia type 3 all

46 replacement and neuroprotective approach for Machado-Joseph disease therapy.

47 ural stem cells into the cerebellum of adult Machado-Joseph disease transgenic mice and assessed the

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