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SMAFIRA-Case-Studies-24204323
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SMAFIRA-Case-Studies-24204323
Documents
(102)
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# proj.
# Ann.
updated_at
PubMed
27979358
DNA repair in the trinucleotide repeat disorders. BACKGROUND: Inherited diseases caused by unstable
2.35 KB
2020-02-21
6
0
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PubMed
27913616
Genetic Contributors to Intergenerational CAG Repeat Instability in Huntington's Disease Knock-In Mi
1.6 KB
2020-02-21
9
0
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PubMed
27155933
Absence of MutSβ leads to the formation of slipped-DNA for CTG/CAG contractions at primate replicati
1.83 KB
2020-02-21
9
0
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PubMed
27131875
Mismatch repair enhances convergent transcription-induced cell death at trinucleotide repeats by act
1.39 KB
2017-09-04
7
0
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PubMed
27044000
DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseases.
1.83 KB
2017-09-04
8
0
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PubMed
26994442
A polymorphism in the MSH3 mismatch repair gene is associated with the levels of somatic instability
2.1 KB
2020-02-21
8
0
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PubMed
26774442
Disease-associated repeat instability and mismatch repair. Expanded tandem repeat sequences in DNA a
1.82 KB
2020-02-21
7
0
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PubMed
26581643
Differential proteomic and genomic profiling of mouse striatal cell model of Huntington's disease an
3.6 KB
2020-01-28
26
0
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PubMed
26333255
Novel BAC Mouse Model of Huntington's Disease with 225 CAG Repeats Exhibits an Early Widespread and
2.09 KB
2020-01-28
12
0
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PubMed
26295712
HdhQ111 Mice Exhibit Tissue Specific Metabolite Profiles that Include Striatal Lipid Accumulation. T
2.48 KB
2016-01-24
9
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