Works matching IS 09646906 AND DT 2021 AND VI 30 AND IP 22
Results: 12
Aberrant lung lipids cause respiratory impairment in a Mecp2-deficient mouse model of Rett syndrome.
- Published in:
- Human Molecular Genetics, 2021, v. 30, n. 22, p. 2161, doi. 10.1093/hmg/ddab182
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- Article
Integrative analysis of genomic and epigenomic data reveal underlying superenhancer-mediated microRNA regulatory network for human bone mineral density.
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- Human Molecular Genetics, 2021, v. 30, n. 22, p. 2177, doi. 10.1093/hmg/ddab181
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- Article
Stress modulates Ahi1-dependent nuclear localization of ten-eleven translocation protein 2.
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- Human Molecular Genetics, 2021, v. 30, n. 22, p. 2149, doi. 10.1093/hmg/ddab179
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- Article
UHRF1 regulates alternative splicing by interacting with splicing factors and U snRNAs in a H3R2me involved manner.
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- Human Molecular Genetics, 2021, v. 30, n. 22, p. 2110, doi. 10.1093/hmg/ddab178
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- Article
Continental-scale genomic analysis suggests shared post-admixture adaptation in the Americas.
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- Human Molecular Genetics, 2021, v. 30, n. 22, p. 2123, doi. 10.1093/hmg/ddab177
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- Article
Redefining the PTEN promoter: identification of novel upstream transcription start regions.
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- Human Molecular Genetics, 2021, v. 30, n. 22, p. 2135, doi. 10.1093/hmg/ddab175
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- Article
GWAS in Africans identifies novel lipids loci and demonstrates heterogenous association within Africa.
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- Human Molecular Genetics, 2021, v. 30, n. 22, p. 2205, doi. 10.1093/hmg/ddab174
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- Article
ZNF224 is a mediator of TGF-β pro-oncogenic function in melanoma.
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- Human Molecular Genetics, 2021, v. 30, n. 22, p. 2100, doi. 10.1093/hmg/ddab173
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- Article
Prenatal inflammation as a link between placental expression signature of tryptophan metabolism and preterm birth.
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- Human Molecular Genetics, 2021, v. 30, n. 22, p. 2053, doi. 10.1093/hmg/ddab169
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- Article
Genome-wide association study of body fat distribution traits in Hispanics/Latinos from the HCHS/SOL.
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- Human Molecular Genetics, 2021, v. 30, n. 22, p. 2190, doi. 10.1093/hmg/ddab166
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- Article
Expanding the phenotype of NUP85 mutations beyond nephrotic syndrome to primary autosomal recessive microcephaly and Seckel syndrome spectrum disorders.
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- Human Molecular Genetics, 2021, v. 30, n. 22, p. 2068, doi. 10.1093/hmg/ddab160
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- Article
Expression of Ripk1 and DAM genes correlates with severity and progression of Krabbe disease.
- Published in:
- Human Molecular Genetics, 2021, v. 30, n. 22, p. 2082, doi. 10.1093/hmg/ddab159
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- Article