F. Belforte

发表

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

E. Poskus, F. Coluccio Leskow, A. Penas Steinhardt, 2013, Molecular Biology Reports.

Mutational screening of the TPO and DUOX2 genes in Argentinian children with congenital hypothyroidism due to thyroid dyshormonogenesis

R. González-Sarmiento, H. Targovnik, A. Chiesa, 2022, Endocrine.

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

G. Iraola, M. C. Cimolai, F. Belforte, 2022, Microorganisms.

A Two-Time Point Analysis of Gut Microbiota in the General Population of Buenos Aires and Its Variation Due to Preventive and Compulsory Social Isolation During the COVID-19 Pandemic

P. Aguilera, G. Iraola, Ignacio Llovet, 2022, Frontiers in Microbiology.

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

J. Espinosa, G. Sevlever, M. Rossi, 2016, Cancer research.

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

R. González-Sarmiento, Cintia E. Citterio, H. Targovnik, 2015, Molecular and Cellular Endocrinology.

Congenital goitrous hypothyroidism: mutation analysis in the thyroid peroxidase gene

R. González-Sarmiento, H. Targovnik, L. Gruñeiro-Papendieck, 2012, Clinical endocrinology.

Biallelic Stop Codon Mutations (p.F353Pfs*36/p.Y425X) in DUOX2 Gene Associated with Transient Congenital Hypothyroidism: Report of a Family and Literature Review

H. Targovnik, L. Gruñeiro-Papendieck, A. Chiesa, 2016 .

Getting to Know the Gut Microbial Diversity of Metropolitan Buenos Aires Inhabitants

R. Burcelin, G. Cerrone, M. C. Cimolai, 2019, Front. Microbiol..

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

Cintia E. Citterio, H. Targovnik, M. Miras, 2016, Molecular and Cellular Endocrinology.

Functional Characterization of TLR4 +3725 G/C Polymorphism and Association with Protection against Overweight

J. Vilariño, M. Martínez-Larrad, M. Serrano-Ríos, 2012, PloS one.

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

K. Lachlan, R. González-Sarmiento, Cintia E. Citterio, 2013, Molecular and Cellular Endocrinology.

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

R. González-Sarmiento, F. Cassorla, H. Targovnik, 2009, Molecular and cellular probes.

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

E. Poskus, F. Coluccio Leskow, A. Penas Steinhardt, 2013, Molecular Biology Reports.

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

H. Targovnik, L. Gruñeiro-Papendieck, A. Chiesa, 2017, Archivos argentinos de pediatria.

New insights in Ulcerative Colitis Associated Gut Microbiota in South American Population: Akkermansia and Collinsella, two distinctive genera found in Argentine subjects.

G. Iraola, Rosso Ayelén, Aguilera Pablo, 2020, medRxiv.

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

J. Espinosa, G. Sevlever, M. Rossi, 2016, Cancer research.