Report for Papendieck P

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References (2)

Title : Targeted Next-Generation Sequencing of Congenital Hypothyroidism-Causative Genes Reveals Unexpected Thyroglobulin Gene Variants in Patients with Iodide Transport Defect - Bernal Barquero_2022_Int.J.Mol.Sci_23_9251
Author(s) : Bernal Barquero CE , Geysels RC , Jacques V , Carro GH , Martin M , Peyret V , Abregu MC , Papendieck P , Masini-Repiso AM , Savagner F , Chiesa AE , Citterio CE , Nicola JP
Ref : Int J Mol Sci , 23 :9251 , 2022
Abstract : Bernal Barquero_2022_Int.J.Mol.Sci_23_9251
ESTHER : Bernal Barquero_2022_Int.J.Mol.Sci_23_9251
PubMedSearch : Bernal Barquero_2022_Int.J.Mol.Sci_23_9251
PubMedID: 36012511
Gene_locus related to this paper: human-TG

Title : Molecular analysis of thyroglobulin mutations found in patients with goiter and hypothyroidism - Siffo_2018_Mol.Cell.Endocrinol_473_1
Author(s) : Siffo S , Adrover E , Citterio CE , Miras MB , Balbi VA , Chiesa A , Weill J , Sobrero G , Gonzalez VG , Papendieck P , Martinez EB , Gonzalez-Sarmiento R , Rivolta CM , Targovnik HM
Ref : Mol Cell Endocrinol , 473 :1 , 2018
Abstract : Siffo_2018_Mol.Cell.Endocrinol_473_1
ESTHER : Siffo_2018_Mol.Cell.Endocrinol_473_1
PubMedSearch : Siffo_2018_Mol.Cell.Endocrinol_473_1
PubMedID: 29275168
Gene_locus related to this paper: human-TG