Works matching IS 09646906 AND DT 2021 AND VI 30 AND IP 19
Results: 8
Placental endocrine insufficiency programs anxiety, deficits in cognition and atypical social behaviour in offspring.
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- Human Molecular Genetics, 2021, v. 30, n. 19, p. 1863, doi. 10.1093/hmg/ddab154
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- Article
Functional and behavioral effects of de novo mutations in calcium-related genes in patients with bipolar disorder.
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- Human Molecular Genetics, 2021, v. 30, n. 19, p. 1851, doi. 10.1093/hmg/ddab152
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- Article
Identification of microRNAs and gene regulatory networks in cleft lip common in humans and mice.
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- Human Molecular Genetics, 2021, v. 30, n. 19, p. 1881, doi. 10.1093/hmg/ddab151
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- Article
Targeted HAI-2 deletion causes excessive proteolysis with prolonged active prostasin and depletion of HAI-1 monomer in intestinal but not epidermal epithelial cells.
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- Human Molecular Genetics, 2021, v. 30, n. 19, p. 1833, doi. 10.1093/hmg/ddab150
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- Article
Cognitive deficits in episodic ataxia type 2 mouse models.
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- Human Molecular Genetics, 2021, v. 30, n. 19, p. 1811, doi. 10.1093/hmg/ddab149
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- Article
Toxicity of pathogenic ataxin-2 in Drosophila shows dependence on a pure CAG repeat sequence.
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- Human Molecular Genetics, 2021, v. 30, n. 19, p. 1797, doi. 10.1093/hmg/ddab148
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- Article
Variants in USP48 encoding ubiquitin hydrolase are associated with autosomal dominant non-syndromic hereditary hearing loss.
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- Human Molecular Genetics, 2021, v. 30, n. 19, p. 1785, doi. 10.1093/hmg/ddab145
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- Article
Genetic meta-analysis of twin birth weight shows high genetic correlation with singleton birth weight.
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- Human Molecular Genetics, 2021, v. 30, n. 19, p. 1894, doi. 10.1093/hmg/ddab121
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- Article