Sole F - Search Results

1

TERT and AURKA gene copy number gains enhance the detection of acral lentiginous melanomas by fluorescence in situ hybridization.

Diaz A, Puig-Butillé JA, Valera A, Muñoz C, Costa D, Garcia-Herrera A, Carrera C, Sole F, Malvehy J, Puig S, Alos L. Diaz A, et al. Among authors: sole f. J Mol Diagn. 2014 Mar;16(2):198-206. doi: 10.1016/j.jmoldx.2013.10.009. Epub 2013 Dec 27. J Mol Diagn. 2014. PMID: 24374110 Free article.

2

Chimeric BCR/ABL gene detected by fluorescence in situ hybridization in three new cases of Philadelphia chromosome-negative chronic myelocytic leukemia.

Costa D, Espinet B, Queralt R, Carrió A, Solé F, Colomer D, Cervantes F, Hernández JA, Besses C, Campo E. Costa D, et al. Among authors: sole f. Cancer Genet Cytogenet. 2003 Mar;141(2):114-9. doi: 10.1016/s0165-4608(02)00662-3. Cancer Genet Cytogenet. 2003. PMID: 12606128

3

Type I MOZ/CBP (MYST3/CREBBP) is the most common chimeric transcript in acute myeloid leukemia with t(8;16)(p11;p13) translocation.

Rozman M, Camós M, Colomer D, Villamor N, Esteve J, Costa D, Carrió A, Aymerich M, Aguilar JL, Domingo A, Solé F, Gomis F, Florensa L, Montserrat E, Campo E. Rozman M, et al. Among authors: sole f. Genes Chromosomes Cancer. 2004 Jun;40(2):140-5. doi: 10.1002/gcc.20022. Genes Chromosomes Cancer. 2004. PMID: 15101047

4

New chromosomal alterations in a series of 23 splenic marginal zone lymphoma patients revealed by Spectral Karyotyping (SKY).

Baró C, Salido M, Espinet B, Astier L, Domingo A, Granada I, Millà F, Carrió A, Costa D, Luño E, Hernández JM, Campo E, Florensa L, Ferrer A, Salar A, Bellosillo B, Besses C, Serrano S, Solé F. Baró C, et al. Among authors: sole f. Leuk Res. 2008 May;32(5):727-36. doi: 10.1016/j.leukres.2007.09.012. Epub 2007 Nov 19. Leuk Res. 2008. PMID: 18023866

5

Multiple recurrent chromosomal breakpoints in mantle cell lymphoma revealed by a combination of molecular cytogenetic techniques.

Salaverria I, Espinet B, Carrió A, Costa D, Astier L, Slotta-Huspenina J, Quintanilla-Martinez L, Fend F, Solé F, Colomer D, Serrano S, Miró R, Beà S, Campo E. Salaverria I, et al. Among authors: sole f. Genes Chromosomes Cancer. 2008 Dec;47(12):1086-97. doi: 10.1002/gcc.20609. Genes Chromosomes Cancer. 2008. PMID: 18709664

6

FOXP1 molecular cytogenetics and protein expression analyses in primary cutaneous large B cell lymphoma, leg-type.

Espinet B, García-Herrera A, Gallardo F, Baró C, Salgado R, Servitje O, Estrach T, Colomo L, Romagosa V, Barranco C, Serrano S, Campo E, Pujol RM, Solé F. Espinet B, et al. Among authors: sole f. Histol Histopathol. 2011 Feb;26(2):213-21. doi: 10.14670/HH-26.213. Histol Histopathol. 2011. PMID: 21154235 Free article.

7

Application of FISH 7q in MDS patients without monosomy 7 or 7q deletion by conventional G-banding cytogenetics: does -7/7q- detection by FISH have prognostic value?

Ademà V, Hernández JM, Abáigar M, Lumbreras E, Such E, Calull A, Dominguez E, Arenillas L, Mallo M, Cervera J, Marugán I, Tormo M, García F, González T, Luño E, Sanzo C, Martín ML, Fernández M, Costa D, Blázquez B, Barreña B, Marco F, Batlle A, Buño I, Martínez-Laperche C, Noriega V, Collado R, Ivars D, Carbonell F, Vallcorba I, Melero J, Delgado E, Vargas MT, Grau J, Salido M, Espinet B, Melero C, Florensa L, Pedro C, Solé F. Ademà V, et al. Among authors: sole f. Leuk Res. 2013 Apr;37(4):416-21. doi: 10.1016/j.leukres.2012.12.010. Epub 2013 Jan 18. Leuk Res. 2013. PMID: 23337401

8

Reciprocal translocations in myelodysplastic syndromes and chronic myelomonocytic leukemias: review of 5,654 patients with an evaluable karyotype.

Costa D, Muñoz C, Carrió A, Nomdedeu M, Calvo X, Solé F, Luño E, Cervera J, Vallespí T, Berneaga D, Gómez C, Arias A, Such E, Sanz G, Grau J, Insunza A, Calasanz MJ, Ardañaz MT, Hernández JM, Azaceta G, Álvarez S, Sánchez J, Martín ML, Bargay J, Gómez V, Cervero CJ, Allegue MJ, Collado R, Campo E, Nomdedeu B; Spanish Group of Myelodysplastic Syndromes (GESMD). Costa D, et al. Among authors: sole f. Genes Chromosomes Cancer. 2013 Aug;52(8):753-63. doi: 10.1002/gcc.22071. Epub 2013 May 19. Genes Chromosomes Cancer. 2013. PMID: 23686965

9

TERT gene amplification is associated with poor outcome in acral lentiginous melanoma.

Diaz A, Puig-Butillé JA, Muñoz C, Costa D, Díez A, Garcia-Herrera A, Carrera C, Badenas C, Solé F, Malvehy J, Puig S, Alos L. Diaz A, et al. Among authors: sole f. J Am Acad Dermatol. 2014 Oct;71(4):839-41. doi: 10.1016/j.jaad.2014.05.035. J Am Acad Dermatol. 2014. PMID: 25219713 No abstract available.

10

Refining the Breakpoints of Three New Translocations Identified in Myelodysplastic Syndromes.

Costa D, Muñoz C, Carrió A, Arias A, Gómez C, Solé F, Espinet B, Azaceta G, Calasanz MJ, Nomdedeu M, Calvo X, Campo E, Nomdedeu B. Costa D, et al. Among authors: sole f. Acta Haematol. 2016;135(2):94-100. doi: 10.1159/000439161. Epub 2015 Oct 28. Acta Haematol. 2016. PMID: 26509426

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Article Language

Species

Sex

Age

Other

396 results

Search Page

Filters