Zobrazeno 1 - 10
of 188
pro vyhledávání: '"Lahortiga, I"'
Autor:
Vazquez, I.1,2, Lahortiga, I.2, Agirre, X.2, Larrayoz, M. J.1, Vizmanos, J. L.1, Ardanaz, M. T.3, Zeleznik-Le, N. J.4, Calasanz, M. J.1, Odero, M. D.1,2 modero@unav.es
Publikováno v:
Leukemia (08876924). Dec2004, Vol. 18 Issue 12, p2041-2044. 4p.
Autor:
Baxter, EJ, Kulkarni, S, Vizmanos, JL, Jaju, R, Martinelli, G, Testoni, N, Hughes, G, Salamanchuk, Z, Calasanz, MJ, Lahortiga, I, Pocock, CF, Dang, R, Fidler, C, Wainscoat, JS, Boultwood, J, Cross, NC
The BCR-ABL-negative chronic myeloproliferative disorders (CMPD) and myelodysplastic/myeloproliferative diseases (MDS/MPD) are a spectrum of related conditions for which the molecular pathogenesis is poorly understood. Translocations that disrupt and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::2ab4bbe9f08cddb2ca96c7062df0c53e
https://doi.org/10.1046/j.1365-2141.2003.04051.x
https://doi.org/10.1046/j.1365-2141.2003.04051.x
Autor:
Pauwels D, Klaassen H, Lahortiga I, Kilonda A, Jacobs K, Sweron B, Corbau R, Chaltin P, Marchand A, Cools J
Publikováno v:
Identification of novel FLT3 kinase inhibitors..
Autor:
De Keersmaecker, K.1,2, Lahortiga, I.1,2, Graux, C.3, Marynen, P.1, Maertens, J.4, Cools, J.1, Vandenberghe, P.5 Peter.Vandenberghe@med.kuleuven.be
Publikováno v:
Leukemia (08876924). Dec2006, Vol. 20 Issue 12, p2202-2204. 3p. 1 Graph.
Publikováno v:
ecancermedicalscience
Autor:
Saez, B. (Borja), Martin-Subero, J.I. (Jose Ignacio), Lahortiga, I. (Idoya), Largo, C. (Cristina), Larrayoz, M.J. (María J.), Odero, M.D. (Maria Dolores), Prosper, F. (Felipe), Cigudosa, J.C. (Juan Cruz), Siebert, R. (Reiner), Calasanz-Abinzano, M.J. (Maria Jose)
The simultaneous occurrence of two different translocations affecting both alleles of the IGH gene has rarely been reported in multiple myeloma. In such a case, two different oncogenes might become transcriptionally deregulated. To investigate this h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1111::3a3b125bdc012b2e4d7ee36cc92fc731
https://hdl.handle.net/10171/18361
https://hdl.handle.net/10171/18361
Autor:
Agirre-Ena, X. (Xabier), Roman-Gomez, J. (José), Vazquez, I. (Iria), Jimenez-Velasco, A. (A.), Garate, L. (Leire), Montiel-Duarte, C. (Cristina), Artieda, P. (P.), Cordeu, L. (Lucía), Lahortiga, I. (Idoya), Calasanz-Abinzano, M.J. (Maria Jose), Heiniger, A. (A.), Torres, A. (Antonio), Minna, J.D. (John D.), Prosper, F. (Felipe)
The PARK2 gene, previously identified as a mutated target in patients with autosomal recessive juvenile parkinsonism (ARJP), has recently been found to be a candidate tumor suppressor gene in ovarian, breast, lung and hepatocellular carcinoma that ma
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1111::77940fe37561f41e130457fe27a35909
https://hdl.handle.net/10171/18363
https://hdl.handle.net/10171/18363
Autor:
Lahortiga, I. (Idoya), Belloni, E. (E.), Vazquez, I. (Iria), Agirre-Ena, X. (Xabier), Larrayoz, M.J. (María J.), Vizmanos-Pérez, J.L. (José Luis), Valgañon, M. (Mikel), Zudaire, I. (Isabel), Saez, B. (Borja), Mateos, M.C. (María C.), Di-Fiore, P.P. (Pier Paolo), Calasanz-Abinzano, M.J. (Maria Jose), Odero, M.D. (Maria Dolores)
Publikováno v:
Dadun. Depósito Académico Digital de la Universidad de Navarra
instname
instname
The t(7;11)(p15;p15.4) has been reported to fuse the NUP98 gene (11p15), a component of the nuclear pore complex, with the class-1 homeobox gene HOXA9 at 7p15. This translocation has been associated with myeloid leukemias, predominantly acute myeloid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::202e60c1465e6addac65f2ae805d8ed1
https://hdl.handle.net/10171/19526
https://hdl.handle.net/10171/19526
Autor:
Agirre-Ena, X. (Xabier), Roman-Gomez, J. (José), Vazquez, I. (Iria), Jimenez-Velasco, A. (A.), Larrayoz, M.J. (María J.), Lahortiga, I. (Idoya), Andreu, E.J. (Enrique José), Marquez, J. (José), Beltran-de-Heredia, J. (J.M.), Odero, M.D. (Maria Dolores), Prosper, F. (Felipe), Calasanz-Abinzano, M.J. (Maria Jose)
In this study, we report the case of a Philadelphia (Ph) positive chronic myelogenous leukemia (CML) patient with the presence of p190 and p210 BCR-ABL1 mRNA fusion transcripts derived from e1a2 and b3a2 BCR-ABL1 genomic rearrangements, respectively.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1111::806d08100120a8b254c5b5a7cde48f5a
https://hdl.handle.net/10171/18561
https://hdl.handle.net/10171/18561
Autor:
Lahortiga, I. (Idoya), Vazquez, I. (Iria), Belloni, E. (E.), Roman, J.P. (José P.), Gasparini, P. (P.), Novo-Villaverde, F. J. (Francisco Javier), Zudaire, I. (Isabel), Pelicci, P.G. (Pier G.), Hernandez, J.M. (J. M.), Calasanz-Abinzano, M.J. (Maria Jose), Odero, M.D. (Maria Dolores)
Publikováno v:
Dadun. Depósito Académico Digital de la Universidad de Navarra
instname
instname
Rearrangements in the distal region of the short arm of chromosome 1 are recurrent aberrations in a broad spectrum of human neoplasias. However, neither the location of the breakpoints (BP) on 1p36 nor the candidate genes have been fully determined.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::51eff3a77fd65417f1c10df6d17b8cd9
https://hdl.handle.net/10171/19455
https://hdl.handle.net/10171/19455