Works matching IS 09646906 AND DT 2021 AND VI 30 AND IP 15
Results: 7
Systemic antisense therapeutics inhibiting DUX4 expression ameliorates FSHD-like pathology in an FSHD mouse model.
- Published in:
- Human Molecular Genetics, 2021, v. 30, n. 15, p. 1398, doi. 10.1093/hmg/ddab136
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- Article
Novel Dent disease 1 cellular models reveal biological processes underlying ClC-5 loss-of-function.
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- Human Molecular Genetics, 2021, v. 30, n. 15, p. 1413, doi. 10.1093/hmg/ddab131
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- Article
Phenotypic recapitulation and correction of desmoglein-2-deficient cardiomyopathy using human-induced pluripotent stem cell-derived cardiomyocytes.
- Published in:
- Human Molecular Genetics, 2021, v. 30, n. 15, p. 1384, doi. 10.1093/hmg/ddab127
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- Article
Comparison of adaptive multiple phenotype association tests using summary statistics in genome-wide association studies.
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- Human Molecular Genetics, 2021, v. 30, n. 15, p. 1371, doi. 10.1093/hmg/ddab126
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- Article
Cross-ancestry genome-wide association studies identified heterogeneous loci associated with differences of allele frequency and regulome tagging between participants of European descent and other ancestry groups from the UK Biobank.
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- Human Molecular Genetics, 2021, v. 30, n. 15, p. 1457, doi. 10.1093/hmg/ddab114
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- Article
Modeling gap junction beta 2 gene-related deafness with human iPSC.
- Published in:
- Human Molecular Genetics, 2021, v. 30, n. 15, p. 1429, doi. 10.1093/hmg/ddab097
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- Article
Allele-specific variation at APOE increases nonalcoholic fatty liver disease and obesity but decreases risk of Alzheimer's disease and myocardial infarction.
- Published in:
- Human Molecular Genetics, 2021, v. 30, n. 15, p. 1443, doi. 10.1093/hmg/ddab096
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- Article