Molina MF

References (4)

Title : The p.Cys1281Tyr variant in the hinge module\/flap region of thyroglobulin causes intracellular transport disorder and congenital hypothyroidism - Gomes_2023_Mol.Cell.Endocrinol_572_111948
Author(s) : Gomes Pio M , Adrover E , Miras MB , Sobrero G , Molina MF , Scheps KG , Rivolta CM , Targovnik HM
Ref : Mol Cell Endocrinol , 572 :111948 , 2023
Abstract :
PubMedSearch : Gomes_2023_Mol.Cell.Endocrinol_572_111948
PubMedID: 37164149

Title : 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 - Pio_2021_Mol.Cell.Endocrinol_522_111124
Author(s) : Pio MG , Molina MF , Siffo S , Chiesa A , Rivolta CM , Targovnik HM
Ref : Mol Cell Endocrinol , 522 :111124 , 2021
Abstract :
PubMedSearch : Pio_2021_Mol.Cell.Endocrinol_522_111124
PubMedID: 33321114

Title : Curating the gnomAD database: Report of novel variants in the thyrogobulin gene using in silico bioinformatics algorithms - Pio_2021_Mol.Cell.Endocrinol_534_111359
Author(s) : Pio MG , Siffo S , Scheps KG , Molina MF , Adrover E , Abelleyro MM , Rivolta CM , Targovnik HM
Ref : Mol Cell Endocrinol , 534 :111359 , 2021
Abstract :
PubMedSearch : Pio_2021_Mol.Cell.Endocrinol_534_111359
PubMedID: 34119605

Title : p.L571P in the linker domain of rat thyroglobulin causes intracellular retention - Citterio_2020_Mol.Cell.Endocrinol_505_110719
Author(s) : Citterio CE , Siffo S , Moya CM , Pio MG , Molina MF , Scheps KG , Rey OA , Arvan P , Rivolta CM , Targovnik HM
Ref : Mol Cell Endocrinol , 505 :110719 , 2020
Abstract :
PubMedSearch : Citterio_2020_Mol.Cell.Endocrinol_505_110719
PubMedID: 31972331