| Functional toll-like receptor 4 overexpression in papillary thyroid cancer by MAPK/ERK–induced ETS1 transcriptional activity V Peyret, M Nazar, M Martín, AA Quintar, EA Fernandez, RC Geysels, ... Molecular Cancer Research 16 (5), 833-845, 2018 | 35 | 2018 |
| A Carboxy-Terminal Monoleucine-Based Motif Participates in the Basolateral Targeting of the Na+/I− Symporter M Martín, CP Modenutti, V Peyret, RC Geysels, E Darrouzet, T Pourcher, ... Endocrinology 160 (1), 156-168, 2019 | 31 | 2019 |
| Implications of Na+/I- Symporter Transport to the Plasma Membrane for Thyroid Hormonogenesis and Radioiodide Therapy M Martín, RC Geysels, V Peyret, CE Bernal Barquero, AM Masini-Repiso, ... Journal of the Endocrine Society 3 (1), 222-234, 2019 | 30 | 2019 |
| Novel sodium/iodide symporter compound heterozygous pathogenic variants causing dyshormonogenic congenital hypothyroidism M Martín, CE Bernal Barquero, RC Geysels, P Papendieck, V Peyret, ... Thyroid 29 (7), 1023-1026, 2019 | 22 | 2019 |
| A Novel SLC5A5 Variant Reveals the Crucial Role of Kinesin Light Chain 2 in Thyroid Hormonogenesis M Martín, CP Modenutti, ML Gil Rosas, V Peyret, RC Geysels, ... The Journal of Clinical Endocrinology & Metabolism 106 (7), 1867-1881, 2021 | 16 | 2021 |
| The PDZ protein SCRIB regulates sodium/iodide symporter (NIS) expression at the basolateral plasma membrane M Martín, L Salleron, V Peyret, RC Geysels, E Darrouzet, S Lindenthal, ... The FASEB Journal 35 (8), e21681, 2021 | 14 | 2021 |
| Congenital iodide transport defect: recent advances and future perspectives M Martín, JP Nicola iMedPub Journals, 2016 | 14 | 2016 |
| The transcription factor NF-κB mediates thyrotropin-stimulated expression of thyroid differentiation markers RC Geysels, V Peyret, M Martín, M Nazar, C Reale, CE Bernal Barquero, ... Thyroid 31 (2), 299-314, 2021 | 10 | 2021 |
| Silent but Not Harmless: A Synonymous SLC5A5 Gene Variant Leading to Dyshormonogenic Congenital Hypothyroidism RC Geysels, CE Bernal Barquero, M Martín, V Peyret, M Nocent, ... Frontiers in Endocrinology 13, 868891, 2022 | 8 | 2022 |
| Transcription factor CREB3L1 regulates the expression of the sodium/iodide symporter (NIS) in rat thyroid follicular cells P Di Giusto, M Martín, M Funes Chabán, L Sampieri, JP Nicola, C Alvarez Cells 11 (8), 1314, 2022 | 8 | 2022 |
| An intramolecular ionic interaction linking defective sodium/iodide symporter transport to the plasma membrane and dyshormonogenic congenital hypothyroidism CE Bernal Barquero, M Martín, RC Geysels, V Peyret, P Papendieck, ... Thyroid 32 (1), 19-27, 2022 | 5 | 2022 |
| Efficient calculation of enzyme reaction free energy profiles using a hybrid differential relaxation algorithm: Application to mycobacterial zinc hydrolases JM Romero, M Martin, CL Ramirez, VG Dumas, MA Marti Advances in Protein Chemistry and Structural Biology 100, 33-65, 2015 | 5 | 2015 |
| MotSASi: Functional short linear motifs (SLiMs) prediction based on genomic single nucleotide variants and structural data M Martín, FG Brunello, CP Modenutti, JP Nicola, MA Marti Biochimie 197, 59-73, 2022 | 4 | 2022 |
| Impact of the mutational landscape of the sodium/iodide symporter in congenital hypothyroidism M Martín, JP Nicola Thyroid 31 (12), 1776-1785, 2021 | 4 | 2021 |
| A Novel Iodide Transport Defect-Causing NA plus/I-Symporter (NIS) Carboxy-Terminus Mutant Uncovers a Critical Tryptophan-Acid Motif Plasma Membrane Transport Required for M Martin, C Modenutti, R Geysels, V Peyret, M Signorino, G Testa, ... HORMONE RESEARCH IN PAEDIATRICS 90, 9-9, 2018 | 3 | 2018 |
| Gp29 LysA of mycobacteriophage TM4 can hydrolyze peptidoglycan through an N-acetyl-muramoyl-L-alanine amidase activity E Urdániz, M Martín, F Payaslián, LA Defelipe, M Dodes, M Martinez, ... Biochimica et Biophysica Acta (BBA)-Proteins and Proteomics 1870 (2), 140745, 2022 | 2 | 2022 |
| Targeted next-generation sequencing of congenital hypothyroidism-causative genes reveals unexpected thyroglobulin gene variants in patients with iodide transport defect CE Bernal Barquero, RC Geysels, V Jacques, GH Carro, M Martín, ... International Journal of Molecular Sciences 23 (16), 9251, 2022 | 1 | 2022 |
| Deep mutagenesis reveals the distinct mutational landscape of ADan and ABri amyloid nucleation M Martín, B Bolognesi bioRxiv, 2023.09. 15.557952, 2023 | | 2023 |
| A NOVEL MUTATION IN THE SODIUM/IODIDE SYMPORTER CARBOXY-TERMINUS UNCOVERS A CRITICAL TRYPTOPHAN-ACID DOMAIN REQUIRED FOR PLASMA MEMBRANE TARGETING M Martin, V Peyret, M Signorino, G Testa, C Modenutti, G Sobrero, ... HORMONE RESEARCH IN PAEDIATRICS 88, 586-587, 2017 | | 2017 |
| Iodide Transport Defect: Identification of a Novel Mutation in the Carboxy-terminus of the Sodium/iodide Symporter in a Pediatric Patient with Congenital Hypothyroidism J Pablo Nicola, M Martin, M Signorino, G Testa, G Sobrero, L Munoz, ... HORMONE RESEARCH IN PAEDIATRICS 86, 485-486, 2016 | | 2016 |
