Works matching IS 09646906 AND DT 2018 AND VI 27 AND IP 16
Results: 13
TSPO–PET imaging using [18F]PBR06 is a potential translatable biomarker for treatment response in Huntington’s disease: preclinical evidence with the p75NTR ligand LM11A-31.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 16, p. 2893, doi. 10.1093/hmg/ddy202
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- Article
Temporal and tissue-specific variability of SMN protein levels in mouse models of spinal muscular atrophy.
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- Human Molecular Genetics, 2018, v. 27, n. 16, p. 2851, doi. 10.1093/hmg/ddy195
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- Article
Regulation of the neuropathy-associated Pmp22 gene by a distal super-enhancer.
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- Human Molecular Genetics, 2018, v. 27, n. 16, p. 2830, doi. 10.1093/hmg/ddy191
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- Article
A promotive effect for halofuginone on membrane repair and synaptotagmin-7 levels in muscle cells of dysferlin-null mice.
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- Human Molecular Genetics, 2018, v. 27, n. 16, p. 2817, doi. 10.1093/hmg/ddy185
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- Article
PAK1 regulates ATXN1 levels providing an opportunity to modify its toxicity in spinocerebellar ataxia type 1.
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- Human Molecular Genetics, 2018, v. 27, n. 16, p. 2863, doi. 10.1093/hmg/ddy200
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- Article
Mechanisms of skeletal muscle wasting in a mouse model for myotonic dystrophy type 1.
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- Human Molecular Genetics, 2018, v. 27, n. 16, p. 2789, doi. 10.1093/hmg/ddy192
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- Article
Loss of fragile X protein FMRP impairs homeostatic synaptic downscaling through tumor suppressor p53 and ubiquitin E3 ligase Nedd4-2.
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- Human Molecular Genetics, 2018, v. 27, n. 16, p. 2805, doi. 10.1093/hmg/ddy189
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- Article
The inhibition of CTGF/CCN2 activity improves muscle and locomotor function in a murine ALS model.
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- Human Molecular Genetics, 2018, v. 27, n. 16, p. 2913, doi. 10.1093/hmg/ddy204
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- Article
Genome-wide survey of parent-of-origin effects on DNA methylation identifies candidate imprinted loci in humans.
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- Human Molecular Genetics, 2018, v. 27, n. 16, p. 2927, doi. 10.1093/hmg/ddy206
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- Article
Functional analysis of a hypomorphic allele shows that MMP14 catalytic activity is the prime determinant of the Winchester syndrome phenotype.
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- Human Molecular Genetics, 2018, v. 27, n. 16, p. 2775, doi. 10.1093/hmg/ddy168
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- Article
DNA methylation and inflammation marker profiles associated with a history of depression.
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- Human Molecular Genetics, 2018, v. 27, n. 16, p. 2840, doi. 10.1093/hmg/ddy199
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- Article
Discovery, fine-mapping, and conditional analyses of genetic variants associated with C-reactive protein in multiethnic populations using the Metabochip in the Population Architecture using Genomics and Epidemiology (PAGE) study.
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- Human Molecular Genetics, 2018, v. 27, n. 16, p. 2940, doi. 10.1093/hmg/ddy211
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- Article
Benfotiamine treatment activates the Nrf2/ARE pathway and is neuroprotective in a transgenic mouse model of tauopathy.
- Published in:
- Human Molecular Genetics, 2018, v. 27, n. 16, p. 2874, doi. 10.1093/hmg/ddy201
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- Article