| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1016925362 |
| P356 | DOI | 10.1186/S13041-015-0160-8 |
| P932 | PMC publication ID | 4625465 |
| P698 | PubMed publication ID | 26515641 |
| P5875 | ResearchGate publication ID | 283967543 |
| P50 | author | Wojciech J Szlachcic | Q60655048 |
| Małgorzata Kurkowiak | Q114453789 | ||
| Maciej Figiel | Q59618025 | ||
| P2093 | author name string | Pawel M Switonski | |
| Kalina Wiatr | |||
| P2860 | cites work | A candidate gene for X-linked spinal muscular atrophy | Q67918173 |
| Inflammatory genes are upregulated in expanded ataxin-3-expressing cell lines and spinocerebellar ataxia type 3 brains | Q74244366 | ||
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| Transgenic animal models for study of the pathogenesis of Huntington's disease and therapy | Q26849677 | ||
| Mouse models of polyglutamine diseases: review and data table. Part I | Q26853025 | ||
| Mouse models of polyglutamine diseases in therapeutic approaches: review and data table. Part II. | Q27005950 | ||
| Autophagy in polyglutamine disease: Imposing order on disorder or contributing to the chaos? | Q27011387 | ||
| A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes. | Q27860836 | ||
| CAG expansions in a novel gene for Machado-Joseph disease at chromosome 14q32.1 | Q28235526 | ||
| Dentatorubral and pallidoluysian atrophy expansion of an unstable CAG trinucleotide on chromosome 12p | Q28250966 | ||
| Unstable expansion of CAG repeat in hereditary dentatorubral-pallidoluysian atrophy (DRPLA) | Q28250990 | ||
| Autosomal dominant cerebellar ataxia (SCA6) associated with small polyglutamine expansions in the alpha 1A-voltage-dependent calcium channel | Q28300848 | ||
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| ZFN, TALEN, and CRISPR/Cas-based methods for genome engineering | Q29615505 | ||
| The International Mouse Phenotyping Consortium Web Portal, a unified point of access for knockout mice and related phenotyping data | Q30441320 | ||
| The NCBI BioSystems database | Q33600694 | ||
| Androgen receptor gene mutations in X-linked spinal and bulbar muscular atrophy | Q34023072 | ||
| Gene Expression Atlas update--a value-added database of microarray and sequencing-based functional genomics experiments | Q34069373 | ||
| SCA17, a novel autosomal dominant cerebellar ataxia caused by an expanded polyglutamine in TATA-binding protein | Q34083719 | ||
| The International Mouse Phenotyping Consortium: past and future perspectives on mouse phenotyping | Q34297070 | ||
| Expansion of an unstable trinucleotide CAG repeat in spinocerebellar ataxia type 1. | Q34353488 | ||
| Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2. | Q34405223 | ||
| The Mouse Genome Database (MGD): facilitating mouse as a model for human biology and disease | Q34445051 | ||
| A knockin mouse model of spinocerebellar ataxia type 3 exhibits prominent aggregate pathology and aberrant splicing of the disease gene transcript. | Q35063135 | ||
| The role of the immune system in triplet repeat expansion diseases | Q35271805 | ||
| Disturbed calcium signaling in spinocerebellar ataxias and Alzheimer's disease | Q38408049 | ||
| Huntington's disease is a four-repeat tauopathy with tau nuclear rods. | Q45300275 | ||
| A new humanized ataxin-3 knock-in mouse model combines the genetic features, pathogenesis of neurons and glia and late disease onset of SCA3/MJD. | Q48491103 | ||
| A neurological disease caused by an expanded CAG trinucleotide repeat in the TATA-binding protein gene: a new polyglutamine disease? | Q55670781 | ||
| An expanded CAG repeat sequence in spinocerebellar ataxia type 7 | Q57970953 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 1 | |
| P921 | main subject | database | Q8513 |
| neurodegeneration | Q1755122 | ||
| P304 | page(s) | 69 | |
| P577 | publication date | 2015-10-29 | |
| P1433 | published in | Molecular Brain | Q6895938 |
| P1476 | title | Mouse polyQ database: a new online resource for research using mouse models of neurodegenerative diseases | |
| P478 | volume | 8 |
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