Works matching IS 09646906 AND DT 2019 AND VI 28 AND IP 16
Results: 14
MiR-144 overexpression as a promising therapeutic strategy to overcome glioblastoma cell invasiveness and resistance to chemotherapy.
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- Human Molecular Genetics, 2019, v. 28, n. 16, p. 2738, doi. 10.1093/hmg/ddz099
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- Article
LRRK2 interacts with the vacuolar-type H<sup>+</sup>-ATPase pump a1 subunit to regulate lysosomal function.
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- Human Molecular Genetics, 2019, v. 28, n. 16, p. 2696, doi. 10.1093/hmg/ddz088
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- Article
Human IFT52 mutations uncover a novel role for the protein in microtubule dynamics and centrosome cohesion.
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- Human Molecular Genetics, 2019, v. 28, n. 16, p. 2720, doi. 10.1093/hmg/ddz091
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Laminin-111 protein therapy enhances muscle regeneration and repair in the GRMD dog model of Duchenne muscular dystrophy.
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- Human Molecular Genetics, 2019, v. 28, n. 16, p. 2686, doi. 10.1093/hmg/ddz086
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Functional rescue in a mouse model of congenital muscular dystrophy with megaconial myopathy.
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- Human Molecular Genetics, 2019, v. 28, n. 16, p. 2635, doi. 10.1093/hmg/ddz068
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- Article
Evolutionary and functional analysis of RBMY1 gene copy number variation on the human Y chromosome.
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- Human Molecular Genetics, 2019, v. 28, n. 16, p. 2785, doi. 10.1093/hmg/ddz101
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Cellular stressors may alter islet hormone cell proportions by moderation of alternative splicing patterns.
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- Human Molecular Genetics, 2019, v. 28, n. 16, p. 2763, doi. 10.1093/hmg/ddz094
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- Article
Cdkn2a (Arf) loss drives NF1-associated atypical neurofibroma and malignant transformation.
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- Human Molecular Genetics, 2019, v. 28, n. 16, p. 2752, doi. 10.1093/hmg/ddz095
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- Article
Placental DNA methylation levels at CYP2E1 and IRS2 are associated with child outcome in a prospective autism study.
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- Human Molecular Genetics, 2019, v. 28, n. 16, p. 2659, doi. 10.1093/hmg/ddz084
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Pathogenic effects of agrin V1727F mutation are isoform specific and decrease its expression and affinity for HSPGs and LRP4.
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- Human Molecular Genetics, 2019, v. 28, n. 16, p. 2648, doi. 10.1093/hmg/ddz081
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MRPS25 mutations impair mitochondrial translation and cause encephalomyopathy.
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- Human Molecular Genetics, 2019, v. 28, n. 16, p. 2711, doi. 10.1093/hmg/ddz093
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A null allele of Dnaaf2 displays embryonic lethality and mimics human ciliary dyskinesia.
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- Human Molecular Genetics, 2019, v. 28, n. 16, p. 2775, doi. 10.1093/hmg/ddz106
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- Article
Motor neurons from ALS patients with mutations in C9ORF72 and SOD1 exhibit distinct transcriptional landscapes.
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- Human Molecular Genetics, 2019, v. 28, n. 16, p. 2799, doi. 10.1093/hmg/ddz104
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- Article
Somatic mutation that affects transcription factor binding upstream of CD55 in the temporal cortex of a late-onset Alzheimer disease patient.
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- Human Molecular Genetics, 2019, v. 28, n. 16, p. 2675, doi. 10.1093/hmg/ddz085
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- Article