| scholarly article | Q13442814 |
| P819 | ADS bibcode | 2014PLoSO...9k1356Z |
| P356 | DOI | 10.1371/JOURNAL.PONE.0111356 |
| P932 | PMC publication ID | 4219713 |
| P698 | PubMed publication ID | 25369462 |
| P5875 | ResearchGate publication ID | 267813924 |
| P2093 | author name string | Qi Zhou | |
| Ning Wang | |||
| Yi Dong | |||
| Zhi-Ying Wu | |||
| Shi-Rui Gan | |||
| Wang Ni | |||
| P2860 | cites work | Spinocerebellar ataxia 3 and Machado-Joseph disease: clinical, molecular, and neuropathological features. | Q51034618 |
| Interaction of normal and expanded CAG repeat sizes influences age at onset of Huntington disease | Q57628958 | ||
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| The APOE ε2 Allele Increases the Risk of Earlier Age at Onset in Machado-Joseph Disease | Q59199944 | ||
| Human E apoprotein heterogeneity. Cysteine-arginine interchanges in the amino acid sequence of the apo-E isoforms | Q70875567 | ||
| A clinical and pathologic study of a large Japanese family with Machado-Joseph disease tightly linked to the DNA markers on chromosome 14q | Q72071756 | ||
| APOE ε2 allele may decrease the age at onset in patients with spinocerebellar ataxia type 3 or Machado-Joseph disease from the Chinese Han population | Q87710267 | ||
| Genotypes at the GluR6 kainate receptor locus are associated with variation in the age of onset of Huntington disease | Q24685210 | ||
| Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families | Q27860677 | ||
| CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1 | Q28235526 | ||
| High frequency of Machado-Joseph disease identified in southeastern Chinese kindreds with spinocerebellar ataxia | Q33545469 | ||
| Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond | Q33665814 | ||
| APOE epsilon4 and the cognitive genetics of multiple sclerosis | Q33871703 | ||
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| Age of onset in Huntington disease: sex specific influence of apolipoprotein E genotype and normal CAG repeat length. | Q35431655 | ||
| Apolipoprotein E genotypes do not influence the age of onset in Huntington's disease. | Q35478096 | ||
| Correlation between CAG repeat length and clinical features in Machado-Joseph disease | Q35643559 | ||
| A familial factor independent of CAG repeat length influences age at onset of Machado-Joseph disease | Q35882878 | ||
| Replication of twelve association studies for Huntington's disease residual age of onset in large Venezuelan kindreds. | Q37004508 | ||
| Apolipoprotein E in Alzheimer's disease and other neurological disorders | Q37846932 | ||
| Normal ATXN3 Allele but Not CHIP Polymorphisms Modulates Age at Onset in Machado-Joseph Disease. | Q41443029 | ||
| Apolipoprotein E and presenilin-1 genotypes in Huntington's disease | Q45298913 | ||
| Apolipoprotein E gene mapping and expression: localization of the structural gene to human chromosome 19 and expression of ApoE mRNA in lipoprotein- and non-lipoprotein-producing tissues | Q48470999 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 11 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | Machado-Joseph disease | Q3026441 |
| P304 | page(s) | e111356 | |
| P577 | publication date | 2014-11-04 | |
| P1433 | published in | PLOS One | Q564954 |
| P1476 | title | The role of apolipoprotein E as a risk factor for an earlier age at onset for Machado-Joseph disease is doubtful | |
| P478 | volume | 9 |
| Q51369234 | (CAG)n loci as genetic modifiers of age-at-onset in patients with Machado-Joseph disease from mainland China. |
| Q90358107 | Childhood-Onset Spinocerebellar Ataxia 3: Tongue Dystonia as an Early Manifestation |
| Q52149995 | Mitochondrial NADH Dehydrogenase Subunit 3 Polymorphism Associated with an Earlier Age at Onset in Male Machado-Joseph disease Patients. |
| Q52152081 | Replicating studies of genetic modifiers in spinocerebellar ataxia type 3: can homogeneous cohorts aid? |
| Q92684465 | State biomarkers for Machado Joseph disease: Validation, feasibility and responsiveness to change |
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