Works matching IS 09646906 AND DT 2022 AND VI 31 AND IP 10
Results: 14
Dysregulated mitochondrial and cytosolic tRNA m1A methylation in Alzheimer's disease.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 10, p. 1673, doi. 10.1093/hmg/ddab357
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- Article
Impaired cooperation between IFT74/BBS22–IFT81 and IFT25–IFT27/BBS19 causes Bardet-Biedl syndrome.
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- Human Molecular Genetics, 2022, v. 31, n. 10, p. 1681, doi. 10.1093/hmg/ddab354
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- Article
Canine DUXC: implications for DUX4 retrotransposition and preclinical models of FSHD.
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- Human Molecular Genetics, 2022, v. 31, n. 10, p. 1694, doi. 10.1093/hmg/ddab352
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- Article
Interaction of huntingtin with PRMTs and its subsequent arginine methylation affects HTT solubility, phase transition behavior and neuronal toxicity.
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- Human Molecular Genetics, 2022, v. 31, n. 10, p. 1651, doi. 10.1093/hmg/ddab351
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- Article
Antisense oligonucleotides targeting the SMN2 promoter region enhance SMN2 expression in spinal muscular atrophy cell lines and mouse model.
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- Human Molecular Genetics, 2022, v. 31, n. 10, p. 1635, doi. 10.1093/hmg/ddab350
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- Article
WNT11, a new gene associated with early onset osteoporosis, is required for osteoblastogenesis.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 10, p. 1622, doi. 10.1093/hmg/ddab349
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- Article
Disease-associated c-MYC downregulation in human disorders of transcriptional regulation.
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- Human Molecular Genetics, 2022, v. 31, n. 10, p. 1599, doi. 10.1093/hmg/ddab348
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- Article
Novel role of prostate cancer risk variant rs7247241 on PPP1R14A isoform transition through allelic TF binding and CpG methylation.
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- Human Molecular Genetics, 2022, v. 31, n. 10, p. 1610, doi. 10.1093/hmg/ddab347
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- Article
Interpreting ciliopathy-associated missense variants of uncertain significance (VUS) in Caenorhabditis elegans.
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- Human Molecular Genetics, 2022, v. 31, n. 10, p. 1574, doi. 10.1093/hmg/ddab344
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- Article
Development and validation of prognostic and diagnostic model for pancreatic ductal adenocarcinoma based on scRNA-seq and bulk-seq datasets.
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- Human Molecular Genetics, 2022, v. 31, n. 10, p. 1705, doi. 10.1093/hmg/ddab343
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- Article
Skin depletion of Kif3a resembles the pediatric atopic dermatitis transcriptome profile.
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- Human Molecular Genetics, 2022, v. 31, n. 10, p. 1588, doi. 10.1093/hmg/ddab342
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- Publication type:
- Article
Metformin induces lactate accumulation and accelerates renal cyst progression in Pkd1-deficient mice.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 10, p. 1560, doi. 10.1093/hmg/ddab340
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- Publication type:
- Article
Mitochondrial genome-wide analysis of nuclear DNA methylation quantitative trait loci.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 10, p. 1720, doi. 10.1093/hmg/ddab339
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- Article
Investigation of the causal relationships between human IgG N-glycosylation and 12 common diseases associated with changes in the IgG N-glycome.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 10, p. 1545, doi. 10.1093/hmg/ddab335
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- Article