Results 121 to 130 of about 6,741 (226)

Polyglutamine-expanded ataxin3 alter specific gene expressions through changing DNA methylation status in SCA3/MJD

, 2020
Dongxue Ding, Chunrong Wang, Chen Zhao, Kun Xia, Beisha Tang, Rong Qiu, Hong Jiang   +6 more
openalex   +2 more sources

Evidence for Proteasome Involvement in Polyglutamine Disease: Localization to Nuclear Inclusions in SCA3/MJD and Suppression of Polyglutamine Aggregation in vitro [PDF]

, 1999
Y. Chai, Stacia L. Koppenhafer, S. J. Shoesmith, Matthew K. Perez, Henry L. Paulson   +4 more
openalex   +1 more source

The association of expanded CAG repeats in the expanded ATXN3 gene with age at onset (AO) in SCA3/MJD patients.

, 2015
The X-axis indicates the expanded CAG repeat lengths and the Y-axis denotes AO in years. AO of SCA3/MJD is inversely correlated with the length of CAG repeat (r = －0.694, p = 0.000).
Zhao Chen (92571), Qian Pan (77107), Kun Xia (9853), Xuan Hou (692988), Beisha Tang (77106), Wei Ye (105005), Tetsuo Ashizawa (247621), Huirong Peng (692987), Dongxue Ding (692989), Fengzhen Huang (692986), Hong Jiang (79543), Zhe Long (692984), Chunrong Wang (692985), Junling Wang (252266), Jiada Li (692990)   +14 more
core   +1 more source

Freqüência das mutações que causam ataxia espinocerebelar (SCA1, SCA2, MJD/SCA3 e DRPLA) em um grupo numeroso de pacientes Brasileiros

, 2014
Spinocerebellar ataxia type 1 (SCA1), spinocerebellar ataxia type 2 (SCA2) and Machado-Joseph disease or spinocerebellar ataxia type 3 (MJD/SCA3) are three distinctive forms of autosomal dominant spinocerebellar ataxia (SCA) caused by expansions of an ...
Cardoso, Francisco, Santos, André S., Correa Neto, Ylmar, Teive, Hélio G.A., Mello, Luiz R., Radvany, João, Araújo, Abelardo Q.C., Carakushansky, Gerson, Steiner, Carlos E., Jardim, Laura B., Viana, Erika, Maciel, Jaime A., Silveira, Isabel, Lopes-Cendesi, Iscia, Pinto-Júnior, Walter, Werneck, Lineu C., da Costa, Jaderson C., Arruda, Walter O., Trevisol-Bittencourt, Paulo C., Calcagnotto, Maria E, Rosa Neto, Pedro, Rouleau, Guy A.   +21 more
core  

Effects of SCA1, MJD, and DPRLA triplet repeat polymorphisms on cognitive phenotypes in a normal population of adolescent twins [PDF]

, 2006
Michelle Luciano, Emma Hine, Margaret J. Wright, David L. Duffy, J. MacMillan, Nicholas G. Martin   +5 more
openalex   +1 more source

IMAN-cipation – Identity Politics of young Muslim Women within the “Muslim Youth in Germany e.V. (MJD)” between Agency, Submission and Repression. An Analysis of the Transformation of Gender-Roles [PDF]

, 2017
Verena Maske
openalex   +1 more source

Graft-derived neurons and bystander effects are maintained for six months after human iPSC-derived NESC transplantation in mice’s cerebella

Scientific Reports
Machado-Joseph disease (MJD) is a neurodegenerative disorder characterized by widespread neuronal death affecting the cerebellum. Cell therapy can trigger neuronal replacement and neuroprotection through bystander effects providing a therapeutic option ...
Liliana S. Mendonça, Daniel Henriques, Vanessa Fernandes, Ricardo Moreira, João Brás, Sónia Duarte, Jens C. Schwamborn, Luís Pereira de Almeida   +7 more
doaj   +1 more source

Lithium carbonate and coenzyme Q10 reduce cell death in a cell model of Machado-Joseph disease

Brazilian Journal of Medical and Biological Research
Machado-Joseph disease (MJD) or spinocerebellar ataxia type 3 (SCA3) is an autosomal dominant neurodegenerative disorder caused by expansion of the polyglutamine domain of the ataxin-3 (ATX3) protein.
C.M. Lopes-Ramos, T.C. Pereira, D.B. Dogini, R. Gilioli, I. Lopes-Cendes   +4 more
doaj   +1 more source

Avaliar potencial da celulas do estroma mesenquimatosas na promoçao de melhorias na quebra de barreira de MJD

Dissertação de Mestrado em Biotecnologia Farmacêutica apresentada à Faculdade de FarmáciaA Doença de Machado-Joseph (MJD), ou ataxia espinocerebelosa do tipo 3 (SCA3) éuma doença neurodegenerativa hereditária autossómica dominante.
Gonzaga, Daniela Jacinto
core  

Stratigraphic model depicting the relationship between the Oldman-Dinosaur Park discontinuity (ODPD) and the mid-Judith discontinuity (MJD).

The model is based on data and correlations presented here from cross-section A–A’ (Fig 1, Table 1, S1 Fig) and differs from that of Rogers et al. [9] in that the ODPD and MJD are litho- and chronostratigraphically separate in southeastern-most Alberta ...
David A. Eberth (9411406)
core   +1 more source