E-LIB Suche - Ergebnisse für: Leton, R. (Rocío)

1

Co-occurrence of mutations in NF1 and other susceptibility ..:

Mellid, S. (Sandra) ; Gil, E. (Eduardo) ; Leton, R. (Rocío)...
info:eu-repo/grantAgreement/ISCIII/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016 (ISCIII)/PI18%2F00454/ES/CARACTERIZACION MOLECULAR, OMICA Y FUNCIONAL DE MUTACIONES EN EL GEN DLST EN PACIENTES CON FEOCROMOCITOMA/PARAGANGLIOMA. , 2023

Link: https://hdl.handle.net/1..

2

Integrative multi-omics analysis identifies a prognostic mi..:

Calsina, B. (Bruna) ; Castro-Vega, L.-J. (Luis-Jaime) ; Torres-Pérez, R. (Rafael)...
info:eu-repo/grantAgreement/EC/FP7/259735. , 2019

Link: http://repub.eur.nl/pub/..

3

Gain-of-function mutations in DNMT3A in patients with parag..:

Remacha, Laura ; Currás-Freixes, Maria ; Torres-Ruiz, Raúl...
Genetics in Medicine. 20 (2018) 12 - p. 1644-1651 , 2018

Link: https://doi.org/10.1038/..

4

Role of MDH2 pathogenic variant in pheochromocytoma and par..:

Calsina, Bruna ; Currás-Freixes, Maria ; Buffet, Alexandre...
Genetics in Medicine. 20 (2018) 12 - p. 1652-1662 , 2018

Link: https://doi.org/10.1038/..

5

Tumoral EPAS1 (HIF2A) mutations explain sporadic pheochromo..:

Comino-Méndez, Iñaki ; de Cubas, Aguirre A. ; Bernal, Carmen...
Human Molecular Genetics. 22 (2013) 11 - p. 2169-2176 , 2013

Link: https://doi.org/10.1093/..

6

MAX mutations cause hereditary and sporadic pheochromocytom..:

Burnichon, N. (Nelly) ; Cascoń, A. (Alberto) ; Schiavi, F. (Francesca)...
http://repub.eur.nl/pub/65878. , 2012

Link: http://repub.eur.nl/pub/..

7

Gain-of-function mutations in DNMT3A in patients with parag..:

Remacha, Laura ; Currás-Freixes, Maria ; Torres-Ruiz, Raúl...
http://hdl.handle.net/10668/12435. , 2018

Link: http://hdl.handle.net/10..

8

REGISTRI: Regorafenib in first-line of KIT/PDGFRA wild type..:

Martin-Broto, Javier ; Valverde, Claudia ; Hindi, Nadia...
Molecular Cancer. 22 (2023) 1 - p. , 2023

Link: https://doi.org/10.1186/..

9

DLST mutations in pheochromocytoma and paraganglioma cause ..:

Mellid, Sara ; García, Fernando ; Leandro‐García, Luis Javier...
Cancer Communications. 43 (2023) 7 - p. 838-843 , 2023

Link: https://doi.org/10.1002/..

10

Genomic and immune landscape Of metastatic pheochromocytoma..:

Calsina, Bruna ; Piñeiro-Yáñez, Elena ; Martínez-Montes, Ángel M....
Nature Communications. 14 (2023) 1 - p. , 2023

Link: https://doi.org/10.1038/..

11

Co-occurrence of mutations in NF1 and other susceptibility ..:

Mellid, Sara ; Gil, Eduardo ; Letón, Rocío...
Frontiers in Endocrinology. 13 (2023) - p. , 2023

Link: https://doi.org/10.3389/..

12

Comprehensive molecular analysis of immortalization hallmar..:

Montero‐Conde, Cristina ; Leandro‐García, Luis Javier ; Martínez‐Montes, Ángel M....
Clinical and Translational Medicine. 12 (2022) 8 - p. , 2022

Link: https://doi.org/10.1002/..

13

Considerations on diagnosis and surveillance measures of PT..:

Pena-Couso, Laura ; Ercibengoa, María ; Mercadillo, Fátima...
Orphanet Journal of Rare Diseases. 17 (2022) 1 - p. , 2022

Link: https://doi.org/10.1186/..

14

Analysis of Telomere Maintenance Related Genes Reveals NOP1..:

Monteagudo, María ; Martínez, Paula ; Leandro-García, Luis J....
Cancers. 13 (2021) 19 - p. 4758 , 2021

Link: https://doi.org/10.3390/..

15

Molecular characterization of chromophobe renal cell carcin..:

Roldan-Romero, Juan María ; Santos, María ; Lanillos, Javier...
Modern Pathology. 33 (2020) 12 - p. 2580-2590 , 2020

Link: https://doi.org/10.1038/..