Keywords: بیماری ماچادو جوزف; Machado-Joseph disease; Sleep disorders; Polysomnography; Excessive fragmentary myoclonus; Spinocerebellar ataxia; Nonmotor symptoms;
مقالات ISI بیماری ماچادو جوزف (ترجمه نشده)
مقالات زیر هنوز به فارسی ترجمه نشده اند.
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در صورتی که به ترجمه آماده هر یک از مقالات زیر نیاز داشته باشید، می توانید سفارش دهید تا مترجمان با تجربه این مجموعه در اسرع وقت آن را برای شما ترجمه نمایند.
Keywords: بیماری ماچادو جوزف; Machado-Joseph disease; Spinocerebellar ataxia; Oxidative stress; Genotoxicity; Antioxidant enzymes;
Experimental and Clinical Strategies for Treating Spinocerebellar Ataxia Type 3
Keywords: بیماری ماچادو جوزف; atx-3,; ataxin-3; BDNF,; brain-derived neurotrophic factor; C. elegans,; Caenorhabditis elegans; CBP,; cAMP response element-binding protein CREB-binding protein; CHIP,; C-terminal Hsp70-interacting protein; CK2,; casein kinase 2; DRPLA,; dentatorubral-pa
Short CommunicationCancer in Machado-Joseph disease patients-low frequency as a cause of death
Keywords: بیماری ماچادو جوزف; Cancer; causes of death; Machado-Joseph disease; polyglutamine diseases; spinocerebellar ataxia type 3;
Cervical and ocular vestibular evoked potentials in Machado-Joseph disease: Functional involvement of otolith pathways
Keywords: بیماری ماچادو جوزف; Spinocerebellar ataxia type 3; SCA3; Machado-Joseph disease; MJD; Otolith pathways; Vestibular evoked myogenic potentials; VEMP;
Spin labeling artery method perfusion MRI study of SPG4 and SCA3/MJD
Keywords: بیماری ماچادو جوزف; Spinocerebellar ataxia type 3; Machado-Joseph disease; Hereditary spastic paraplegia 4; Arterial spin labeling;
Create and preserve: Proteostasis in development and aging is governed by Cdc48/p97/VCP
Keywords: بیماری ماچادو جوزف; AAA; ATPase associated with diverse cellular activities; AD; Alzheimer's disease; ALS; amyotrophic lateral sclerosis; AMPK; adenosine monophosphate activated kinase; Cdc48/CDC-48; cell division cycle protein 48; DUB; de-ubiquitylating enzyme; ERAD; endopl
Ataxin-3 protein modification as a treatment strategy for spinocerebellar ataxia type 3: Removal of the CAG containing exon
Keywords: بیماری ماچادو جوزف; SCA3; spinocerebellar ataxia type 3; MJD; Machado-Joseph disease; PolyQ; polyglutamine; ATXN3; ataxin-3; UIMs; ubiquitin interacting motifs; RNAi; RNA interference; AON; antisense oligonucleotide; SNP; single nucleotide polymorphism; DMD; Duchenne muscu
DRPLA transgenic mouse substrains carrying single copy of full-length mutant human DRPLA gene with variable sizes of expanded CAG repeats exhibit CAG repeat length- and age-dependent changes in behavioral abnormalities and gene expression profiles
Keywords: بیماری ماچادو جوزف; ANOVA; analysis of variance; CDK; cyclin-dependent kinase; CREB; cAMP response element-binding protein; DRPLA; dentatorubral-pallidoluysian atrophy; GO; gene ontology; KO; knock-out; MAPK; mitogen-activated protein kinase; MJD; Machado-Joseph disease; N
Toward understanding Machado-Joseph disease
Keywords: بیماری ماچادو جوزف; ATXN3; ataxin-3; bZIP; basic leucine zipper motif; CBPC; REB binding protein; cDNA; complementary DNA; CHIP; C-terminus of Hsc70 interacting protein; CK2; casein kinase 2; CMV; cytomegalovirus; CNS; central nervous system; CREB; cAMP-response element bind
Thiol-protease oxidation in age-related neuropathology
Keywords: بیماری ماچادو جوزف; AD; Alzheimer disease; Atg; autophagin; IDE; insulysin; MJD; Machado-Joseph disease; MMP; matrix metalloproteinase; NEP; neprilysin; PD; Parkinson disease; SENP; sentrin-specific protease; SUMO; small-ubiquitin modifier; TIMP-1; tissue inhibitor of meta
ATX-3, CDC-48 and UBXN-5: A new trimolecular complex in Caenorhabditis elegans
Keywords: بیماری ماچادو جوزف; Ataxin-3; Polyglutamine; Machado-Joseph disease; Spinocerebellar ataxia type 3; Ubiquitin-proteasome pathway; Deubiquitylating enzyme; Valosin-containing protein;
Cambodian founder effect for spinocerebellar ataxia type 3 (Machado-Joseph disease)
Keywords: بیماری ماچادو جوزف; Ataxia; Spinocerebellar ataxia; Machado-Joseph disease; Neurogenetics; Cambodia; Trinucleotide repeats;
Ectoine alters subcellular localization of inclusions and reduces apoptotic cell death induced by the truncated Machado-Joseph disease gene product with an expanded polyglutamine stretch
Keywords: بیماری ماچادو جوزف; Machado-Joseph disease; Ataxin-3; Polyglutamine; Ectoine; Compatible solute; Inclusion; Apoptotic cell death;