MicroRNAs as B-cell lymphoma biomarkers by Manterola L, Fernandez-Mercado M, Larrea E, Goicoechea I, Arestin M, Armesto M, Hernandez L, Lawrie CH

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Why some tumours trigger neovascularisation and others don’t: the story thus far by Adighibe, O, Leek, R, Fernandez-Mercado, M, Hu, J, Snell, C, Gatter, K, Harris, A, Pezzella, F

Silencing of ASXL1 impairs the granulomonocytic lineage potential of human CD34⁺ progenitor cells. by Davies, C, Yip, B, Fernandez-Mercado, M, Woll, P, Agirre, X, Prosper, F, Jacobsen, SE, Wainscoat, J, Pellagatti, A, Boultwood, J

Silencing of ASXL1 impairs the granulomonocytic lineage potential of human CD34+ progenitor cells by Davies, C, Yip, B, Fernandez-Mercado, M, Woll, P, Agirre, X, Prosper, F, Jacobsen, SE, Wainscoat, J, Pellagatti, A, Boultwood, J

Frequent Mutation of the Polycomb-Associated Gene ASXL1 In Acute Myeloid Leukemia Secondary to Myelodysplastic Syndrome or Chronic Myelomonocytic Leukemia by Fernandez-Mercado, M, Pellagatti, A, Perry, J, Fernandez-Santamaria, C, Calasanz, M, Larrayoz, M, Odero, MD, Killick, S, Wainscoat, J, Boultwood, J

Whole-exome sequencing in del(5q) myelodysplastic syndromes in transformation to acute myeloid leukemia by Pellagatti, A, Fernandez-Mercado, M, Di Genua, C, Larrayoz, M, Killick, S, Dolatshad, H, Burns, A, Calasanz, M, Schuh, A, Boultwood, J

Whole-exome sequencing in del(5q) myelodysplastic syndromes in transformation to acute myeloid leukemia. by Pellagatti, A, Fernandez-Mercado, M, Di Genua, C, Larrayoz, M, Killick, S, Dolatshad, H, Burns, A, Calasanz, M, Schuh, A, Boultwood, J

Targeted re-sequencing analysis of 25 genes commonly mutated in myeloid disorders in del(5q) myelodysplastic syndromes. by Fernandez-Mercado, M, Burns, A, Pellagatti, A, Giagounidis, A, Germing, U, Agirre, X, Prosper, F, Aul, C, Killick, S, Wainscoat, J, Schuh, A, Boultwood, J

Mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression. by Fernandez-Mercado, M, Pellagatti, A, Di Genua, C, Larrayoz, M, Winkelmann, N, Aranaz, P, Burns, A, Schuh, A, Calasanz, M, Cross, N, Boultwood, J

Mutations in SETBP1 are recurrent in myelodysplastic syndromes and often coexist with cytogenetic markers associated with disease progression by Fernandez-Mercado, M, Pellagatti, A, Di Genua, C, Larrayoz, M, Winkelmann, N, Aranaz, P, Burns, A, Schuh, A, Calasanz, M, Cross, N, Boultwood, J

Effects of L-leucine in 5q- syndrome and other RPS14-deficient erythroblasts. by Yip, B, Pellagatti, A, Vuppusetty, C, Giagounidis, A, Germing, U, Lamikanra, A, Roberts, D, Fernandez-Mercado, M, McDonald, E, Killick, S, Wainscoat, J, Boultwood, J

Effects of L-leucine in 5q-syndrome and other RPS14-deficient erythroblasts by Yip, B, Pellagatti, A, Vuppusetty, C, Giagounidis, A, Germing, U, Lamikanra, A, Roberts, D, Fernandez-Mercado, M, McDonald, E, Killick, S, Wainscoat, J, Boultwood, J

Activation of the mTOR Signaling Pathway by L-Leucine in RPS14-Deficient Erythroid Cells by Yip, B, Vuppusetty, C, Pellagatti, A, Giagounidis, A, Germing, U, Lamikanra, A, Roberts, D, Fernandez-Mercado, M, McDonald, E, Mecucci, C, Killick, S, Wainscoat, J, Boultwood, J

Mutation patterns of 16 genes in primary and secondary acute myeloid leukemia (AML) with normal cytogenetics by Fernandez-Mercado, M, Yip, B, Pellagatti, A, Davies, C, Larrayoz, M, Kondo, T, Pérez, C, Killick, S, McDonald, E, Odero, MD, Agirre, X, Prósper, F, Calasanz, M, Wainscoat, J, Boultwood, J

TET2 mutations are associated with specific 5-methylcytosine and 5-hydroxymethylcytosine profiles in patients with chronic myelomonocytic leukemia by Pérez, C, Martínez-Calle, N, Martín-Subero, J, Segura, V, Delabesse, E, Fernandez-Mercado, M, Garate, L, Alvarez, S, Rifon, J, Varea, S, Boultwood, J, Wainscoat, J, Cruz Cigudosa, J, Calasanz, M, Cross, N, Prósper, F, Agirre, X

Frequent mutation of the polycomb-associated gene ASXL1 in the myelodysplastic syndromes and in acute myeloid leukemia. by Boultwood, J, Perry, J, Pellagatti, A, Fernandez-Mercado, M, Fernandez-Santamaria, C, Calasanz, M, Larrayoz, M, Garcia-Delgado, M, Giagounidis, A, Malcovati, L, Della Porta, MG, Jädersten, M, Killick, S, Hellström-Lindberg, E, Cazzola, M, Wainscoat, J

The transporter ABCB7 is a mediator of the phenotype of acquired refractory anemia with ring sideroblasts. by Nikpour, M, Scharenberg, C, Liu, A, Conte, S, Karimi, M, Mortera-Blanco, T, Giai, V, Fernandez-Mercado, M, Papaemmanuil, E, Högstrand, K, Jansson, M, Vedin, I, Stephen Wainscoat, J, Campbell, P, Cazzola, M, Boultwood, J, Grandien, A, Hellström-Lindberg, E

The transporter ABCB7 is a mediator of the phenotype of acquired refractory anemia with ring sideroblasts by Nikpour, M, Scharenberg, C, Scharenberg, C, Liu, A, Conte, S, Karimi, M, Mortera-Blanco, T, Giai, V, Fernandez-Mercado, M, Papaemmanuil, E, Högstrand, K, Jansson, M, Vedin, I, Stephen Wainscoat, J, Campbell, P, Campbell, P, Cazzola, M, Cazzola, M, Boultwood, J, Grandien, A, Hellström-Lindberg, E