Stebėti
Mariano Martín
Mariano Martín
Nežinomas ryšys
Patvirtintas el. paštas ibecbarcelona.eu
Pavadinimas
Cituota
Cituota
Metai
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
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
342019
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
322019
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
242019
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
192021
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
152021
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
122021
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
112022
Congenital iodide transport defect: recent advances and future perspectives
M Martín, JP Nicola
iMedPub Journals, 2016
112016
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
102022
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
62022
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
62022
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
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
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
42022
Impact of the mutational landscape of the sodium/iodide symporter in congenital hypothyroidism
M Martín, JP Nicola
Thyroid 31 (12), 1776-1785, 2021
42021
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
Massive experimental quantification of amyloid nucleation allows interpretable deep learning of protein aggregation
M Thompson, M Martín, TS Olmo, C Rajesh, PK Koo, B Bolognesi, ...
bioRxiv, 2024
2*2024
Amyloids at the border: deep mutagenesis and random sequence extension reveal an incomplete amyloid-forming motif in Bri2 that turns amyloidogenic upon C-terminal extension
M Martín, B Bolognesi
bioRxiv, 2023.09. 15.557952, 2024
12024
Functional characterization of novel compound heterozygous missense SLC5A5 gene variants causing congenital dyshormonogenic hypothyroidism
GH Carro, M Martín, S Savy, V Peyret, RC Geysels, FA Montes, ...
Frontiers in Endocrinology 15, 1465176, 2024
2024
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