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Loop profile: 730758

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Employment (1)

Universidad Nacional de Luján: Lujan, AR

(Departamento de Ciencias Básicas)
Employment
Source: Self-asserted source
Fiorella S. Belforte

Education and qualifications (2)

Universidad de Buenos Aires: Buenos Aires, AR

Biochemist (Facultad de Farmacia y Bioquímica)
Education
Source: Self-asserted source
Fiorella S. Belforte

Universidad de Buenos Aires: Buenos Aires, AR

PhD (Facultad de Farmacia y Bioquímica)
Education
Source: Self-asserted source
Fiorella S. Belforte

Works (11)

Comprehensive Phenotyping in Inflammatory Bowel Disease: Search for Biomarker Algorithms in the Transkingdom Interactions Context

Microorganisms
2022-11 | Journal article | Author
DOI: 10.3390/microorganisms10112190
Contributors: Ayelén D. Rosso; Aguilera Pablo; Sofía Quesada; Florencia Mascardi; Sebastian N. Mascuka; María C. Cimolai; Jimena Cerezo; Renata Spiazzi; Carolina Conlon; Claudia Milano et al.
Source: check_circle
Multidisciplinary Digital Publishing Institute

Impact of exposure to arsenic on the bacterial microbiota associated with river biofilms in the Pampas region

Aquatic Toxicology
2022-11 | Journal article
DOI: 10.1016/j.aquatox.2022.106319
Contributors: GA de Diego; A Penas-Steinhardt; JP Ferro; MJ Palacio; NA Ossana; BL Eissa; F Belforte
Source: check_circle
Crossref

[Transient congenital hypothyroidism due to biallelic defects of DUOX2 gene. Two clinical cases].

Archivos argentinos de pediatria
2017-06-01 | Journal article
DOI: 10.5546/aap.2017.e162
PMID: 28504502
Source: Self-asserted source
Fiorella S. Belforte

The NSL Chromatin-Modifying Complex Subunit KANSL2 Regulates Cancer Stem-like Properties in Glioblastoma That Contribute to Tumorigenesis.

Cancer research
2016-07-12 | Journal article
DOI: 10.1158/0008-5472.CAN-15-3159
PMID: 27406830
PMC: PMC5026635
Source: Self-asserted source
Fiorella S. Belforte

Compound heterozygous DUOX2 gene mutations (c.2335-1G>C/c.3264_3267delCAGC) associated with congenital hypothyroidism. Characterization of complex cryptic splice sites by minigene analysis.

Molecular and cellular endocrinology
2015-10-24 | Journal article
DOI: 10.1016/j.mce.2015.10.014
PMID: 26506010
Source: Self-asserted source
Fiorella S. Belforte

Kinetic characterization of human thyroperoxidase. Normal and pathological enzyme expression in Baculovirus system: a molecular model of functional expression.

Molecular and cellular endocrinology
2015-01-07 | Journal article
DOI: 10.1016/j.mce.2014.12.026
PMID: 25576858
Source: Self-asserted source
Fiorella S. Belforte

Toll-like receptor 4 D299G polymorphism in metabolic disorders: a meta-analysis.

Molecular biology reports
2012-12-29 | Journal article
DOI: 10.1007/s11033-012-2374-5
PMID: 23275193
Source: Self-asserted source
Fiorella S. Belforte

Functional characterization of TLR4 +3725 G/C polymorphism and association with protection against overweight.

PloS one
2012-12-11 | Journal article
DOI: 10.1371/journal.pone.0050992
PMID: 23239997
PMC: PMC3519812
Source: Self-asserted source
Fiorella S. Belforte

New insights into thyroglobulin gene: molecular analysis of seven novel mutations associated with goiter and hypothyroidism.

Molecular and cellular endocrinology
2012-11-16 | Journal article
DOI: 10.1016/j.mce.2012.11.002
PMID: 23164529
Source: Self-asserted source
Fiorella S. Belforte

Congenital goitrous hypothyroidism: mutation analysis in the thyroid peroxidase gene.

Clinical endocrinology
2012-04-01 | Journal article
DOI: 10.1111/j.1365-2265.2011.04249.x
PMID: 21981063
Source: Self-asserted source
Fiorella S. Belforte

Genotyping of resistance to thyroid hormone in South American population. Identification of seven novel missense mutations in the human thyroid hormone receptor beta gene.

Molecular and cellular probes
2009-03-04 | Journal article
DOI: 10.1016/j.mcp.2009.02.002
PMID: 19268523
Source: Self-asserted source
Fiorella S. Belforte
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