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Mariano Martín
Mariano Martín
Unknown affiliation
Verified email at ibecbarcelona.eu
Title
Cited by
Cited by
Year
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
352018
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
312019
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
302019
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
212019
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
162021
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
142021
Congenital iodide transport defect: recent advances and future perspectives
M Martín, JP Nicola
iMedPub Journals, 2016
142016
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
102021
Algunas preguntas sobre la historia del concepto" crisis"
R Koselleck, MF Martín
Philosophia 76 (2), 101-115, 2016
92016
Introducción a una lógica del absurdo (apuntes sobre el primer Vázquez Montalbán)
M Martín
Les Langues Néo-latines, 258-259, 1986
91986
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
82022
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
82022
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
52022
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
52015
Impact of the mutational landscape of the sodium/iodide symporter in congenital hypothyroidism
M Martín, JP Nicola
Thyroid 31 (12), 1776-1785, 2021
42021
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
32022
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
32018
NOTAS SOBRE LA COLECCIÓN ESTUDIOS ALEMANES: Aportes e hipótesis para la historia de las ideas¹
M Martín
Revista de historia americana y argentina 52 (2), 125-150, 2017
32017
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
22022
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
12022
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