Héctor M. Targovnik

Identification of a mutation in the coding sequence of the human thyroid peroxidase gene causing congenital goiter.

Marc Abramowicz, Héctor M. Targovnik, Viviana Varela et al. · Journal of Clinical Investigation · 1992 · 192 citations · Full text

Biology, Mendelian Disorder, Genetic Disorder +13

A 3' splice site mutation in the thyroglobulin gene responsible for congenital goiter with hypothyroidism.

Tamio Ieiri, Pascale Cochaux, Héctor M. Targovnik et al. · Journal of Clinical Investigation · 1991 · 169 citations · Full text

Thyroglobulin Gene, Genetics, Molecular Biology +17

Congenital hypothyroid goiter with deficient thyroglobulin. Identification of an endoplasmic reticulum storage disease with induction of molecular chaperones.

Geraldo Medeiros‐Neto, Pan Suk Kim, Sung Eun Yoo et al. · Journal of Clinical Investigation · 1996 · 132 citations · Full text

Molecular Chaperones, Developmental Biology, Congenital Hypothyroid Goiter +11

An unusually long poly(purine)-poly(pyrimidine) sequence is located upstream from the human thyroglobulin gene

Daniel Christophe, Bartolomé Cabrer, Albino Bacolla et al. · Nucleic Acids Research · 1985 · 118 citations · Full text

Control of dendritic cell maturation and function by triiodothyronine

Iván Mascanfroni, María M. Montesinos, Sebastián Susperreguy et al. · The FASEB Journal · 2007 · 87 citations · Full text