Found: 8
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Genotypic–Phenotypic Correlations of Hereditary Hyperferritinemia-Cataract Syndrome: Case Series of Three Brazilian Families.
- Published in:
- International Journal of Molecular Sciences, 2023, v. 24, n. 15, p. 11876, doi. 10.3390/ijms241511876
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- Publication type:
- Article
Expression of Micrornas Mir‐126, Mir‐133b and Mir‐221 Associated With Apoptosis in Rats Submitted to Focal Cerebral Ischemia and Physical Exercise.
- Published in:
- FASEB Journal, 2022, v. 36, p. N.PAG, doi. 10.1096/fasebj.2022.36.S1.L7874
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- Publication type:
- Article
Chronic Granulomatous Disease and Myelodysplastic Syndrome in a Patient with a Novel Mutation in CYBB.
- Published in:
- Genes, 2021, v. 12, n. 10, p. 1476, doi. 10.3390/genes12101476
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- Publication type:
- Article
Novel Mutation in CRYBB3 Causing Pediatric Cataract and Microphthalmia.
- Published in:
- Genes, 2021, v. 12, n. 7, p. 1069, doi. 10.3390/genes12071069
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- Publication type:
- Article
Whole-exome sequencing reveals insights into genetic susceptibility to Congenital Zika Syndrome.
- Published in:
- PLoS Neglected Tropical Diseases, 2021, v. 15, n. 6, p. 1, doi. 10.1371/journal.pntd.0009507
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- Article
Molecular alterations in the extracellular matrix in the brains of newborns with congenital Zika syndrome.
- Published in:
- Science Signaling, 2020, v. 13, n. 635, p. 1, doi. 10.1126/scisignal.aay6736
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- Article
Zika virus infects human blood mononuclear cells.
- Published in:
- 2019
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- Publication type:
- journal article
MicroRNAs 145 and 148a Are Upregulated During Congenital Zika Virus Infection.
- Published in:
- ASN Neuro (Sage Publications, Ltd.), 2019, v. 11, p. N.PAG, doi. 10.1177/1759091419850983
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- Publication type:
- Article