eQTL mapping in transgenic alpha-synuclein carrying Caenorhabditis elegans recombinant inbred lines.
- Published in:
- Human Molecular Genetics, 2024, v. 33, n. 24, p. 2123, doi. 10.1093/hmg/ddae148
- By:
- Publication type:
- Article
Works matching IS 09646906 AND DT 2024 AND VI 33 AND IP 24
Results: 7
1
2
Increased intrinsic membrane excitability is associated with olivary hypertrophy in spinocerebellar ataxia type 1.
- Published in:
- Human Molecular Genetics, 2024, v. 33, n. 24, p. 2159, doi. 10.1093/hmg/ddae146
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- Publication type:
- Article
3
Delivering large genes using adeno-associated virus and the CRE-lox DNA recombination system.
- Published in:
- Human Molecular Genetics, 2024, v. 33, n. 24, p. 2094, doi. 10.1093/hmg/ddae144
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- Publication type:
- Article
4
Correction to: Reduced levels of MRE11 cause disease phenotypes distinct from ataxia telangiectasia-like disorder.
- Published in:
- Human Molecular Genetics, 2024, v. 33, n. 24, p. 2177, doi. 10.1093/hmg/ddae145
- Publication type:
- Article
5
Identifying X-chromosome variants associated with age-related macular degeneration.
- Published in:
- Human Molecular Genetics, 2024, v. 33, n. 24, p. 2085, doi. 10.1093/hmg/ddae141
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- Publication type:
- Article
6
A novel GFAP frameshift variant identified in a family with optico-retinal dysplasia and vision impairment.
- Published in:
- Human Molecular Genetics, 2024, v. 33, n. 24, p. 2145, doi. 10.1093/hmg/ddae134
- By:
- Publication type:
- Article
7
HDAC1-mediated regulation of KDM1A in pemphigus vulgaris: unlocking mechanisms on ERK pathway activation and cohesion loss.
- Published in:
- Human Molecular Genetics, 2024, v. 33, n. 24, p. 2133, doi. 10.1093/hmg/ddae090
- By:
- Publication type:
- Article