INVESTIGADORES
CITTERIO Cintia Eliana
artículos
CITTERIO, CINTIA E.; TARGOVNIK, HÉCTOR M; ARVAN, PETER
The role of thyroglobulin in thyroid hormonogenesis
Nature reviews. Endocrinology; Año: 2019 vol. 15 p. 323 - 338
CINTIA E. CITTERIO; YOSHIAKI MORISHITA; NADA DAKKA; BALAJI VELUSWAMY; PETER ARVAN
Relationship Between the Dimerization of Thyroglobulin and its Ability to Form Triiodothyronine
JOURNAL OF BIOLOGICAL CHEMISTRY (ONLINE); Año: 2018 vol. 293 p. 4860 - 4869
CINTIA E. CITTERIO; BALAJI VELUSWAMY; SARAH J. MORGAN; VALERIE A. GALTON; J. PAUL BANGA; STEPHEN ATKINS; YOSHIAKI MORISHITA; SUSANNE NEUMANN; RAUF LATIF; MARVIN C. GERSHENGORN; TERRY J. SMITH; PETER ARVAN
De novo triiodothyronine formation from thyrocytes activated by Thyroid Stimulating Hormone
JOURNAL OF BIOLOGICAL CHEMISTRY (ONLINE); Año: 2017 vol. 292 p. 15434 - 15444
HECTOR M. TARGOVNIK; CINTIA E. CITTERIO; CARINA M. RIVOLTA
Iodide Handling Disorders (NIS, TPO, TG, IYD)
BEST PRACTICE & RESEARCH CLINICAL ENDOCRINOLOGY & METABOLISM; Lugar: Amsterdam; Año: 2017 vol. 31 p. 195 - 212
SOFÍA SIFFO; EZEQUIELA ADROVER; CINTIA E. CITTERIO; MIRTA B. MIRAS; VIVIANA A. BALBI; ANA CHIESA; JACQUES WEILL; GABRIELA SOBRERO; VERONICA G. GONZÁLEZ; PATRICIA PAPENDIECK; ELENA BUENO MARTINEZ; ROGELIO GONZÁLEZ-SARMIENTO; CARINA M. RIVOLTA; HÉCTOR M. TARGOVNIK
Molecular Analysis of Thyroglobulin Mutations Found in Patients with Goiter and Hypothyroidism.
MOLECULAR AND CELLULAR ENDOCRINOLOGY.; Lugar: Amsterdam; Año: 2017
FIORELLA S. BELFORTE; CINTIA E. CITTERIO; GRACIELA TESTA; MARÍA C. OLCESE; GABRIELA SOBRERO; MIRTA B. MIRAS; HÉCTOR M. TARGOVNIK; CARINA M. RIVOLTA
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.; Lugar: Amsterdam; Año: 2016 vol. 419 p. 172 - 184
HÉCTOR M. TARGOVNIK; CINTIA E. CITTERIO; SOFÍA SIFFO; CARINA M. RIVOLTA
Advances and Perspectives in Genetics of Congenital Thyroid Disorders
Journal of Clinical and Molecular Endocrinology; Lugar: Londres; Año: 2016 vol. 1 p. 1 - 3
HÉCTOR M. TARGOVNIK; CINTIA E. CITTERIO; SOFÍA SIFFO; CARINA M. RIVOLTA
Advances and Perspectives in Genetics of Congenital Thyroid Disorders Associated with Thyroglobulin Gene Mutations
Peertechz Journal of Biological Research and Development; Año: 2016 vol. 1 p. 62 - 70
CINTIA E. CITTERIO; CECILIA M. MORALES; NATACHA BOUHOURS-NOUET; GLORIA A. MACHIAVELLI; ELENA BUENO; FREDERIQUE GATELAIS; REGIS COUNTANT; ROGELIO GONZÁLEZ-SARMIENTO; CARINA M. RIVOLTA; HÉCTOR M. TARGOVNIK
Novel compound heterozygous Thyroglobulin mutations c.745+1G>A/c.7036+2T>A associated with congenital goiter and hypothyroidism in a Vietnamese family. Identification of a new cryptic 5´ splice site in the exon 6
MOLECULAR AND CELLULAR ENDOCRINOLOGY.; Lugar: Amsterdam; Año: 2015 vol. 404 p. 102 - 112
FIORELLA S. BELFORTE; ALEXANDRA M. TARGOVNIK; RODOLFO M. GONZÁLEZ-LEBRERO; CAROLINA OSORIO LARROCHE; CINTIA E. CITTERIO; ROGELIO GONZÁLEZ-SARMIENTO; MARÍA V. MIRANDA; HÉCTOR M. TARGOVNIK; CARINA M. RIVOLTA
Kinetic characterization of human thyroperoxidase. Normal and pathological enzyme expression in Baculovirus System: A molecular model of functional expression
MOLECULAR AND CELLULAR ENDOCRINOLOGY.; Lugar: Amsterdam; Año: 2015 vol. 404 p. 9 - 15
CINTIA E. CITTERIO; LILIANA C. ROSSETTI; PIERRE F. SOUCHON; CECILIA MORALES; MATHILDE THOUVARD-VIPREY; ANNE S. SALMON-MUSIAL; PIERRE L.A. MAURAN; MARTINE DOCO-FENZY; ROGELIO GONZÁLEZ-SARMIENTO; CARINA M. RIVOLTA; CARLOS D. DE BRASI; HÉCTOR M. TARGOVNIK
Novel Mutational Mechanism in the Thyroglobulin Gene: Imperfect DNA Inversion as a Cause for Hereditary Hypothyroidism
MOLECULAR AND CELLULAR ENDOCRINOLOGY.; Lugar: Amsterdam; Año: 2013 vol. 381 p. 220 - 229
CINTIA E. CITTERIO; GLORIA A. MACHIAVELLI; MIRTA B. MIRAS; LAURA GRUÑEIRO PAPENDIECK; KATHERINE LACHLAN; GABRIELA SOBRERO; ANA CHIESA; JOANNA WALKER; LILIANA MUÑOZ; GRACIELA TESTA; FIORELLA S. BELFORTE; ROGELIO GONZÁLEZ-SARMIENTO; CARINA M. RIVOLTA; HÉCTOR M. TARGOVNIK
New insights into thyroglobulin gene: Molecular analysis of seven novel mutations associated with goiter and hypothyroidism
MOLECULAR AND CELLULAR ENDOCRINOLOGY.; Lugar: Amsterdam; Año: 2013 vol. 365 p. 277 - 291
HÉCTOR M. TARGOVNIK; THOMAS EDUARD; VIVIANA VARELA; MAITHÉ TAUBER; CINTIA E. CITTERIO; ROGELIO GONZÁLEZ-SARMIENTO; CARINA M. RIVOLTA
Two novel mutations in the thyroglobulin gene as cause of congenital hypothyroidism: Identification a cryptic donor splice site in the exon 19
MOLECULAR AND CELLULAR ENDOCRINOLOGY.; Lugar: Amsterdam; Año: 2012 vol. 348 p. 313 - 321
TARGOVNIK. HÉCTOR MANUEL; CITTERIO, CINTIA ELIANA; RIVOLTA, CARINA MARCELA
Thyroglobulin Gene Mutations in Congenital Hypothyroidism
HORMONE RESERCH IN PAEDIATRICS; Lugar: Basilea; Año: 2011 vol. 75 p. 311 - 321
CINTIA E. CITTERIO; REGIS COUNTANT; STEPHANIE ROULEAU; JOSÉ M. MIRALLES-GARCÍA; ROGELIO GONZÁLEZ-SARMIENTO; CARINA M. RIVOLTA; HÉCTOR M. TARGOVNIK
A new compound heterozygous for c.886C>T/c.2206C>T [p.R277X/p.Q717X] mutations in the thyroglobulin gene as a cause of foetal goitrous hypothyroidism
CLINICAL ENDOCRINOLOGY; Lugar: Oxford; Año: 2011 vol. 74 p. 533 - 535