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Frontiers in Endocrinology|May 23, 2022
Silent but Not Harmless: A Synonymous <i>SLC5A5</i> Gene Variant Leading to Dyshormonogenic Congenital HypothyroidismRomina Celeste Geysels, Carlos Eduardo Bernal Barquero, Mariano Martín, et al.
International Journal of Molecular Sciences|August 26, 2022
Targeted Next-Generation Sequencing of Congenital Hypothyroidism-Causative Genes Reveals Unexpected Thyroglobulin Gene Variants in Patients with Iodide Transport DefectCarlos Eduardo Bernal Barquero, Romina Celeste Geysels, Virginie Jacques, et al.
Molecular Cancer Research : MCR|March 11, 2018
Functional Toll-like Receptor 4 Overexpression in Papillary Thyroid Cancer by MAPK/ERK-Induced ETS1 Transcriptional ActivityVictoria Peyret, Magalí Nazar, Mariano Martín, et al.
Frontiers in Endocrinology|January 3, 2025
Functional characterization of novel compound heterozygous missense <i>SLC5A5</i> gene variants causing congenital dyshormonogenic hypothyroidismGerardo Hernán Carro, Mariano Martín, Sofía Savy, et al.
The Journal of Clinical Endocrinology and Metabolism|April 29, 2021
A Novel SLC5A5 Variant Reveals the Crucial Role of Kinesin Light Chain 2 in Thyroid HormonogenesisMariano Martín, Carlos Pablo Modenutti, Mauco Lucas Gil Rosas, et al.
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