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The role of thyroglobulin in thyroid hormonogenesis

Nature reviews. Endocrinology, 2019-06, Vol.15 (6), p.323-338

2019

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Iodide Handling Disorders (NIS, TPO, TG, IYD)

Baillière's best practice & research. Clinical endocrinology & metabolism, 2017-03, Vol.31 (2), p.195-212

2017

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Defects in protein folding in congenital hypothyroidism

Molecular and cellular endocrinology, 2020-02, Vol.501, p.110638-110638, Article 110638

2020

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Structure and genetic variants of thyroglobulin: Pathophysiological implications

Molecular and cellular endocrinology, 2021-05, Vol.528, p.111227-111227, Article 111227

2021

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Genetics and phenomics of hypothyroidism and goiter due to thyroglobulin mutations

Molecular and cellular endocrinology, 2010-06, Vol.322 (1), p.44-55

2010

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Engineering of the baculovirus expression system for optimized protein production

Applied microbiology and biotechnology, 2019, Vol.103 (1), p.113-123

2019

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Solutions against emerging infectious and noninfectious human diseases through the application of baculovirus technologies

Applied microbiology and biotechnology, 2021-11, Vol.105 (21-22), p.8195-8226

2021

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Curating the gnomAD database: Report of novel variants in the thyrogobulin gene using in silico bioinformatics algorithms

Molecular and cellular endocrinology, 2021-08, Vol.534, p.111359-111359, Article 111359

2021

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Curating the gnomAD database: Report of novel variants in the thyroid peroxidase gene using in silico bioinformatics algorithms and a literature review

Molecular and cellular endocrinology, 2022-12, Vol.558, p.111748-111748, Article 111748

2022

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The p.Cys1281Tyr variant in the hinge module/flap region of thyroglobulin causes intracellular transport disorder and congenital hypothyroidism

Molecular and cellular endocrinology, 2023-07, Vol.572, p.111948-111948, Article 111948

2023

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A novel mutation in intron 11 donor splice site, responsible of a rare genotype in thyroglobulin gene by altering the pre-mRNA splincing process. Cell expression and bioinformatic analysis

Molecular and cellular endocrinology, 2021-02, Vol.522, p.111124, Article 111124

2021

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Curating the gnomAD database: Report of novel variants in the globin‐coding genes and bioinformatics analysis

Human mutation, 2020-01, Vol.41 (1), p.81-102

2020

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Control of dendritic cell maturation and function by triiodothyronine

The FASEB journal, 2008-04, Vol.22 (4), p.1032-1042

2008

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Molecular analysis of thyroglobulin mutations found in patients with goiter and hypothyroidism

Molecular and cellular endocrinology, 2018-09, Vol.473, p.1-16

2018

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

Molecular and cellular endocrinology, 2015-03, Vol.404, p.9-15

2015

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The p.Pro2232Leu variant in the ChEL domain of thyroglobulin gene causes intracellular transport disorder and congenital hypothyroidism

Endocrine, 2023-04, Vol.80 (1), p.47-53

2023

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Three Mutations (p.Q36H, p.G418fsX482, and g.IVS19-2A>C) in the Dual Oxidase 2 Gene Responsible for Congenital Goiter and Iodide Organification Defect

Clinical chemistry (Baltimore, Md.), 2006-02, Vol.52 (2), p.182-191

2006

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p.L571P in the linker domain of rat thyroglobulin causes intracellular retention

Molecular and cellular endocrinology, 2020-04, Vol.505, p.110719, Article 110719

2020

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Extractive purification of recombinant peroxidase isozyme c from insect larvae in aqueous two-phase systems

Separation and purification technology, 2012-09, Vol.98, p.199-205

2012

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Thyroid hormone synthesis continues despite biallelic thyroglobulin mutation with cell death

JCI insight, 2021-06, Vol.6 (11)

2021

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The Chaperones Involved in Hemoglobin Synthesis Take the Spotlight: Analysis of AHSP in the Argentinean Population and Review of the Literature

Hemoglobin, 2018-11, Vol.42 (5-6), p.310-314

2018

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Thyroglobulin Gene Mutations in Congenital Hypothyroidism

Hormone research in paediatrics, 2011-01, Vol.75 (5), p.311-321

2011

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

Endocrine, 2022-06, Vol.77 (1), p.86-101

2022

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Improved Expression of SARS-CoV-2 Spike RBD Using the Insect Cell-Baculovirus System

Viruses, 2022-12, Vol.14 (12), p.2794

2022

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Congenital goitrous hypothyroidism: mutation analysis in the thyroid peroxidase gene

Clinical endocrinology (Oxford), 2012-04, Vol.76 (4), p.568-576

2012

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The role of thyroglobulin in thyroid hormonogenesis

Iodide Handling Disorders (NIS, TPO, TG, IYD)

Defects in protein folding in congenital hypothyroidism

Structure and genetic variants of thyroglobulin: Pathophysiological implications

Genetics and phenomics of hypothyroidism and goiter due to thyroglobulin mutations

Engineering of the baculovirus expression system for optimized protein production

Solutions against emerging infectious and noninfectious human diseases through the application of baculovirus technologies

Curating the gnomAD database: Report of novel variants in the thyrogobulin gene using in silico bioinformatics algorithms

Curating the gnomAD database: Report of novel variants in the thyroid peroxidase gene using in silico bioinformatics algorithms and a literature review

The p.Cys1281Tyr variant in the hinge module/flap region of thyroglobulin causes intracellular transport disorder and congenital hypothyroidism

A novel mutation in intron 11 donor splice site, responsible of a rare genotype in thyroglobulin gene by altering the pre-mRNA splincing process. Cell expression and bioinformatic analysis

Curating the gnomAD database: Report of novel variants in the globin‐coding genes and bioinformatics analysis

Control of dendritic cell maturation and function by triiodothyronine

Molecular analysis of thyroglobulin mutations found in patients with goiter and hypothyroidism

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

The p.Pro2232Leu variant in the ChEL domain of thyroglobulin gene causes intracellular transport disorder and congenital hypothyroidism

Three Mutations (p.Q36H, p.G418fsX482, and g.IVS19-2A>C) in the Dual Oxidase 2 Gene Responsible for Congenital Goiter and Iodide Organification Defect

p.L571P in the linker domain of rat thyroglobulin causes intracellular retention

Extractive purification of recombinant peroxidase isozyme c from insect larvae in aqueous two-phase systems

Thyroid hormone synthesis continues despite biallelic thyroglobulin mutation with cell death

The Chaperones Involved in Hemoglobin Synthesis Take the Spotlight: Analysis of AHSP in the Argentinean Population and Review of the Literature

Thyroglobulin Gene Mutations in Congenital Hypothyroidism

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

Improved Expression of SARS-CoV-2 Spike RBD Using the Insect Cell-Baculovirus System

Congenital goitrous hypothyroidism: mutation analysis in the thyroid peroxidase gene

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