Found: 14
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Exosomal transfer of activated neutrophil-derived lncRNA CRNDE promotes proliferation and migration of airway smooth muscle cells in asthma.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 4, p. 638, doi. 10.1093/hmg/ddab283
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- Publication type:
- Article
Strong evidence for genotype–phenotype correlations in Phelan-McDermid syndrome: results from the developmental synaptopathies consortium.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 4, p. 625, doi. 10.1093/hmg/ddab280
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- Publication type:
- Article
Methylome-wide association study of early life stressors and adult mental health.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 4, p. 651, doi. 10.1093/hmg/ddab274
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- Publication type:
- Article
Identification of causal metabolites related to multiple autoimmune diseases.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 4, p. 604, doi. 10.1093/hmg/ddab273
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- Publication type:
- Article
Deep structure of DNA for genomic analysis.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 4, p. 576, doi. 10.1093/hmg/ddab272
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- Publication type:
- Article
Hyperactive HRAS dysregulates energetic metabolism in fibroblasts from patients with Costello syndrome via enhanced production of reactive oxidizing species.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 4, p. 561, doi. 10.1093/hmg/ddab270
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- Publication type:
- Article
Mitochondrial enzyme GPT2 regulates metabolic mechanisms required for neuron growth and motor function in vivo.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 4, p. 587, doi. 10.1093/hmg/ddab269
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- Publication type:
- Article
Deficiency of the neurodevelopmental disorder-associated gene Cyfip2 alters the retinal ganglion cell properties and visual acuity.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 4, p. 535, doi. 10.1093/hmg/ddab268
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- Publication type:
- Article
vitamin A transporter STRA6 adjusts the stoichiometry of chromophore and opsins in visual pigment synthesis and recycling.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 4, p. 548, doi. 10.1093/hmg/ddab267
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- Publication type:
- Article
Genomic editing of metformin efficacy-associated genetic variants in SLC47A1 does not alter SLC47A1 expression.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 4, p. 491, doi. 10.1093/hmg/ddab266
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- Publication type:
- Article
CFTR corrector C17 is effective in muscular dystrophy, in vivo proof of concept in LGMDR3.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 4, p. 499, doi. 10.1093/hmg/ddab260
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- Publication type:
- Article
Elucidating the molecular mechanisms associated with TARS2-related mitochondrial disease.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 4, p. 523, doi. 10.1093/hmg/ddab257
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- Publication type:
- Article
Compound heterozygous variants in SHQ1 are associated with a spectrum of neurological features, including early-onset dystonia.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 4, p. 614, doi. 10.1093/hmg/ddab247
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- Publication type:
- Article
Genetic modeling of GNAO1 disorder delineates mechanisms of Gαo dysfunction.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 4, p. 510, doi. 10.1093/hmg/ddab235
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- Publication type:
- Article