Found: 17
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Molecular association of pathogenetic contributors to pre-eclampsia (pre-eclampsia associome).
- Published in:
- BMC Systems Biology, 2015, v. 9, p. 1, doi. 10.1186/1752-0509-9-S2-S4
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- Article
Genome-wide analysis shows association of epigenetic changes in regulators of Rab and Rho GTPases with spinal muscular atrophy severity.
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- European Journal of Human Genetics, 2013, v. 21, n. 9, p. 988, doi. 10.1038/ejhg.2012.293
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- Article
Telomere Length in Chromosomally Normal and Abnormal Miscarriages and Ongoing Pregnancies and Its Association with 5-hydroxymethylcytosine Patterns.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 12, p. 6622, doi. 10.3390/ijms22126622
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- Article
Telomere Length in Metaphase Chromosomes of Human Triploid Zygotes.
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- International Journal of Molecular Sciences, 2021, v. 22, n. 11, p. 5579, doi. 10.3390/ijms22115579
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- Article
Pathogenomics of Uterine Fibroids Development.
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- International Journal of Molecular Sciences, 2019, v. 20, n. 24, p. 6151, doi. 10.3390/ijms20246151
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- Article
Identification of Genetic Risk Factors of Severe COVID-19 Using Extensive Phenotypic Data: A Proof-of-Concept Study in a Cohort of Russian Patients.
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- Genes, 2022, v. 13, n. 3, p. 534, doi. 10.3390/genes13030534
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- Article
Genomic distribution of 5‐formylcytosine and 5‐carboxylcytosine in human preimplantation embryos.
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- Molecular Reproduction & Development, 2018, v. 85, n. 12, p. 893, doi. 10.1002/mrd.23074
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- Article
202. Effect of Modification with Lipophilic Fragments and Inclusion of Endosomolytic Peptide on Transfection Efficiency Mediated by Lysine Dendrimers<sup>*</sup>.
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- Molecular Therapy, 2006, v. 13, p. S78, doi. 10.1016/j.ymthe.2006.08.226
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- Article
Analysis of the Spectrum of ACE2 Variation Suggests a Possible Influence of Rare and Common Variants on Susceptibility to COVID-19 and Severity of Outcome.
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- Frontiers in Genetics, 2020, v. 11, p. N.PAG, doi. 10.3389/fgene.2020.551220
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- Article
Molecular Genetics and Pathogenesis of the Floating Harbor Syndrome: Case Report of Long-Term Growth Hormone Treatment and a Literature Review.
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- Frontiers in Genetics, 2022, v. 13, p. 1, doi. 10.3389/fgene.2022.846101
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- Article
Genetic and expression studies of SMN2 gene in Russian patients with spinal muscular atrophy type II and III.
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- BMC Medical Genetics, 2011, v. 12, n. 1, p. 96, doi. 10.1186/1471-2350-12-96
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- Article
Cytogenomic Profile of Uterine Leiomyoma: In Vivo vs. In Vitro Comparison.
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- Biomedicines, 2021, v. 9, n. 12, p. 1777, doi. 10.3390/biomedicines9121777
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- Article
Uterine Leiomyomas with an Apparently Normal Karyotype Comprise Minor Heteroploid Subpopulations Differently Represented in vivo and in vitro.
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- Cytogenetic & Genome Research, 2021, v. 161, n. 1/2, p. 43, doi. 10.1159/000513173
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- Article
Inter-Cell and Inter-Chromosome Variability of 5-Hydroxymethylcytosine Patterns in Noncultured Human Embryonic and Extraembryonic Cells.
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- Cytogenetic & Genome Research, 2018, v. 156, n. 3, p. 150, doi. 10.1159/000493906
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- Publication type:
- Article
Synergistic Anti-Angiogenic Effects Using Peptide-Based Combinatorial Delivery of siRNAs Targeting VEGFA, VEGFR1, and Endoglin Genes.
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- Pharmaceutics, 2019, v. 11, n. 6, p. 261, doi. 10.3390/pharmaceutics11060261
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- Article
Placental microRNA expression in pregnancies complicated by superimposed pre-eclampsia on chronic hypertension.
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- Molecular Medicine Reports, 2016, v. 14, n. 1, p. 22, doi. 10.3892/mmr.2016.5268
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- Article
Methylation Levels of SLC23A2 and NCOR2 Genes Correlate with Spinal Muscular Atrophy Severity.
- Published in:
- PLoS ONE, 2015, v. 10, n. 3, p. 1, doi. 10.1371/journal.pone.0121964
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- Article