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Luis Javier Leandro-García
Luis Javier Leandro-García
在 cnio.es 的电子邮件经过验证 - 首页
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Exome sequencing identifies MAX mutations as a cause of hereditary pheochromocytoma
I Comino-Méndez, FJ Gracia-Aznárez, F Schiavi, I Landa, ...
Nature genetics 43 (7), 663-667, 2011
5842011
Tumoral and tissue‐specific expression of the major human β‐tubulin isotypes
LJ Leandro‐García, S Leskelä, I Landa, C Montero‐Conde, ...
Cytoskeleton 67 (4), 214-223, 2010
3112010
Single nucleotide polymorphism associations with response and toxic effects in patients with advanced renal-cell carcinoma treated with first-line sunitinib: a multicentre …
J Garcia-Donas, E Esteban, LJ Leandro-García, DE Castellano, ...
The lancet oncology 12 (12), 1143-1150, 2011
2872011
The miR-200 family controls β-tubulin III expression and is associated with paclitaxel-based treatment response and progression-free survival in ovarian cancer patients
S Leskelä, LJ Leandro-García, M Mendiola, J Barriuso, L Inglada-Pérez, ...
Endocrine-related cancer 18 (1), 85-95, 2011
2392011
Research resource: transcriptional profiling reveals different pseudohypoxic signatures in SDHB and VHL-related pheochromocytomas
E López-Jiménez, G Gómez-López, LJ Leandro-García, I Muñoz, ...
Molecular endocrinology 24 (12), 2382-2391, 2010
2252010
Tumoral EPAS1 (HIF2A) mutations explain sporadic pheochromocytoma and paraganglioma in the absence of erythrocytosis
I Comino-Méndez, AA de Cubas, C Bernal, C Álvarez-Escolá, ...
Human molecular genetics 22 (11), 2169-2176, 2013
1792013
Genetics of pheochromocytoma and paraganglioma in Spanish patients
A Cascon, G Pita, N Burnichon, I Landa, E Lopez-Jimenez, ...
The Journal of Clinical Endocrinology & Metabolism 94 (5), 1701-1705, 2009
1652009
Polymorphisms in cytochromes P450 2C8 and 3A5 are associated with paclitaxel neurotoxicity
S Leskelä, C Jara, LJ Leandro-Garcia, A Martinez, J Garcia-Donas, ...
The pharmacogenomics journal 11 (2), 121-129, 2011
1632011
Overexpression and activation of EGFR and VEGFR2 in medullary thyroid carcinomas is related to metastasis
C Rodríguez-Antona, J Pallares, C Montero-Conde, L Inglada-Pérez, ...
Endocrine-Related Cancer 17 (1), 7-16, 2010
1412010
Molecular characterisation of a common SDHB deletion in paraganglioma patients
A Cascon, I Landa, E Lopez-Jimenez, A Díez-Hernández, M Buchta, ...
Journal of medical genetics 45 (4), 233-238, 2008
892008
Prospective study assessing hypoxia-related proteins as markers for the outcome of treatment with sunitinib in advanced clear-cell renal cell carcinoma
J Garcia-Donas, LJ Leandro-Garcia, AG Del Alba, M Morente, I Alemany, ...
Annals of oncology 24 (9), 2409-2414, 2013
882013
Genome-wide association study identifies ephrin type A receptors implicated in paclitaxel induced peripheral sensory neuropathy
LJ Leandro-García, L Inglada-Pérez, G Pita, E Hjerpe, S Leskelä, C Jara, ...
Journal of medical genetics 50 (9), 599-605, 2013
812013
Whole-Exome Sequencing Reveals Defective CYP3A4 Variants Predictive of Paclitaxel Dose-Limiting Neuropathy
M Apellániz-Ruiz, MY Lee, L Sánchez-Barroso, G Gutiérrez-Gutiérrez, ...
Clinical Cancer Research 21 (2), 322-328, 2015
802015
Regulatory polymorphisms in β-tubulin IIa are associated with paclitaxel-induced peripheral neuropathy
LJ Leandro-García, S Leskelä, C Jara, H Gréen, E Åvall-Lundqvist, ...
Clinical Cancer Research 18 (16), 4441-4448, 2012
792012
SWI/SNF complex mutations promote thyroid tumor progression and insensitivity to redifferentiation therapies
M Saqcena, LJ Leandro-Garcia, JLV Maag, V Tchekmedyian, ...
Cancer Discovery 11 (5), 1158-1175, 2021
662021
Integrative analysis of miRNA and mRNA expression profiles in pheochromocytoma and paraganglioma identifies genotype-specific markers and potentially regulated pathways
AA De Cubas, LJ Leandro-García, F Schiavi, V Mancikova, ...
Endocrine-related cancer 20 (4), 477-493, 2013
622013
Rationalization of genetic testing in patients with apparently sporadic pheochromocytoma/paraganglioma
A Cascon, E Lopez-Jimenez, I Landa, S Leskelä, LJ Leandro-García, ...
Hormone and metabolic research 41 (09), 672-675, 2009
532009
SDHC mutation in an elderly patient without familial antecedents
E López‐Jiménez, JM De Campos, EM Kusak, I Landa, S Leskelä, ...
Clinical Endocrinology 69 (6), 906-910, 2008
492008
Deep sequencing reveals microRNAs predictive of antiangiogenic drug response
J García-Donas, B Beuselinck, L Inglada-Pérez, O Graña, P Schöffski, ...
JCI insight 1 (10), 2016
472016
Allelic variant at− 79 (C> T) in CDKN1B (p27Kip1) confers an increased risk of thyroid cancer and alters mRNA levels
I Landa, C Montero-Conde, D Malanga, S De Gisi, G Pita, ...
Endocrine-Related Cancer 17 (2), 317-328, 2010
462010
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