Villa O - Search Results

1

Methotrexate resistance in vitro is achieved by a dynamic selectionprocess of tumor cell variants emerging during treatment.

de Anta JM, Mayo C, Solé F, Salido M, Espinet B, Corzo C, Petzold M, Villa O, Serrano S, Real FX, Mayol X. de Anta JM, et al. Among authors: villa o. Int J Cancer. 2006 Oct 1;119(7):1607-15. doi: 10.1002/ijc.22028. Int J Cancer. 2006. PMID: 16671091 Free article.

2

Insertion (8;11) in a renal oncocytoma with multifocal transformation to chromophobe renal cell carcinoma.

Salido M, Lloreta J, Melero C, García M, Placer J, Espinet B, Villa O, Bielsa O, Gelabert-Mas A, Serrano S, Solé F. Salido M, et al. Among authors: villa o. Cancer Genet Cytogenet. 2005 Dec;163(2):160-3. doi: 10.1016/j.cancergencyto.2005.04.016. Cancer Genet Cytogenet. 2005. PMID: 16337860

3

Blast cells with nuclear extrusions in the form of micronuclei are associated with MYC amplification in acute myeloid leukemia.

Villa O, Salido M, Pérez-Vila ME, Ferrer A, Arenillas L, Pedro C, Espinet B, Corzo C, Serrano S, Woessner S, Florensa L, Solé F. Villa O, et al. Cancer Genet Cytogenet. 2008 Aug;185(1):32-6. doi: 10.1016/j.cancergencyto.2008.04.014. Cancer Genet Cytogenet. 2008. PMID: 18656691

4

Detection of abnormalities of PRV-1, TPO, and c-MPL genes detected by fluorescence in situ hybridization in essential thrombocythemia.

Puigdecanet E, Espinet B, Villa O, Florensa L, Besses C, Serrano S, Solé F. Puigdecanet E, et al. Among authors: villa o. Cancer Genet Cytogenet. 2006 May;167(1):39-42. doi: 10.1016/j.cancergencyto.2005.08.016. Cancer Genet Cytogenet. 2006. PMID: 16682284

5

Small supernumerary marker chromosome causing partial trisomy 6p in a child with craniosynostosis.

Villa O, Del Campo M, Salido M, Gener B, Astier L, Del Valle J, Gallastegui F, Pérez-Jurado LA, Solé F. Villa O, et al. Am J Med Genet A. 2007 May 15;143A(10):1108-13. doi: 10.1002/ajmg.a.31709. Am J Med Genet A. 2007. PMID: 17431916

6

Mosaic uniparental disomies and aneuploidies as large structural variants of the human genome.

Rodríguez-Santiago B, Malats N, Rothman N, Armengol L, Garcia-Closas M, Kogevinas M, Villa O, Hutchinson A, Earl J, Marenne G, Jacobs K, Rico D, Tardón A, Carrato A, Thomas G, Valencia A, Silverman D, Real FX, Chanock SJ, Pérez-Jurado LA. Rodríguez-Santiago B, et al. Among authors: villa o. Am J Hum Genet. 2010 Jul 9;87(1):129-38. doi: 10.1016/j.ajhg.2010.06.002. Am J Hum Genet. 2010. PMID: 20598279 Free PMC article.

7

Deletion of TET2 gene in an acute myeloid leukemia case with a t(4;15)(q24;q26) characterized by glass needle based chromosome microdissection and oligonucleotide array.

Villa O, Mallo M, Kosyakova N, Salido M, Liehr T, Martínez-Avilés L, Pedro C, García-Aragonés M, Espinet B, Bellosillo B, Florensa L, Arenillas L, Cuscó I, Jurado LA, Solé F. Villa O, et al. Leuk Res. 2011 Sep;35(9):e161-3. doi: 10.1016/j.leukres.2011.05.027. Epub 2011 Jun 17. Leuk Res. 2011. PMID: 21684005 No abstract available.

8

Duplication dup(1)(q41q44) defined by fluorescence in situ hybridization: delineation of the 'trisomy 1q42-->qter syndrome'.

Coccé MC, Villa O, Obregon MG, Salido M, Barreiro C, Solé F, Gallego MS. Coccé MC, et al. Among authors: villa o. Cytogenet Genome Res. 2007;118(1):84-6. doi: 10.1159/000106446. Cytogenet Genome Res. 2007. PMID: 17901705

9

Complex chromosome 8;21 translocation with associated hyperdiploidy in acute myeloid leukemia (FAB-M2).

Corral Mdel P, Villa O, Alfaro EM, Alonso CN, Baro C, Felice MS, Rossi J, Solé F, Gallego MS. Corral Mdel P, et al. Among authors: villa o. Pediatr Blood Cancer. 2008 Mar;50(3):651-4. doi: 10.1002/pbc.21192. Pediatr Blood Cancer. 2008. PMID: 17405156

10

Euchromatic variant 16p+. Implications in prenatal diagnosis.

López Pajares I, Villa O, Salido M, Mori MA, Gonzalez A, Lapunzina P, De Torres ML, Vallcorba I, Palomares M, Fernández L, Delicado A. López Pajares I, et al. Among authors: villa o. Prenat Diagn. 2006 Jun;26(6):535-8. doi: 10.1002/pd.1454. Prenat Diagn. 2006. PMID: 16634122

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