Concha Muñoz
University of Barcelona
18 Papers
199 Citations
Concha Muñoz is an academic researcher from University of Barcelona. The author has contributed to research in topics: Gene & Fluorescence in situ hybridization. The author has an hindex of 10, co-authored 18 publications.
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Papers
Different distribution of NOTCH1 mutations in chronic lymphocytic leukemia with isolated trisomy 12 or associated with other chromosomal alterations.
Cristina López,Julio Delgado,Dolors Costa,Laura Conde,Gabriela Ghita,Neus Villamor,Alba Navarro,Maite Cazorla,Cándida Gómez,Amparo Arias,Concha Muñoz,Tycho Baumann,María Rozman,Marta Aymerich,Dolors Colomer,Francesc Cobo,Elias Campo,Armando López-Guillermo,Emili Montserrat,Ana Carrió +19 more
TL;DR: The findings indicate that the distribution of NOTCH1 mutations in CLL with trisomy 12 is heterogeneous and that the presence of additional chromosomal abnormalities such astrisomy 18 could change the prognosis of these patients.
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miR-328 mediates a metabolic shift in colon cancer cells by targeting SLC2A1/GLUT1.
Sandra Santasusagna,I. Moreno,Alfons Navarro,Concha Muñoz,Francisco Ramos Martínez,Raquel Hernández,Joan J. Castellano,Mariano Monzo +7 more
TL;DR: It is suggested that miR-328 may be involved in the orchestration of the Warburg effect in colon cancer cells and thus inversely correlates with the classically reported upregulated SLC2A1/GLUT1 expression in tumors.
Identification and characterization of novel uroporphyrinogen decarboxylase gene mutations in a large series of porphyria cutanea tarda patients and relatives
Celia Badenas,Jordi To-Figueras,John D. Phillips,Christy A. Warby,Concha Muñoz,Carmen Herrero +5 more
TL;DR: The role of UROD mutations as a strong risk factor for PCT even in areas where environmental factors have been shown to be highly associated with the disease is emphasized.
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TERT gene amplification is associated with poor outcome in acral lentiginous melanoma
Alba Díaz,Joan Anton Puig-Butille,Joan Anton Puig-Butille,Concha Muñoz,Dolors Costa,Anna Díez,Adriana García-Herrera,Cristina Carrera,Cristina Carrera,Celia Badenas,Celia Badenas,Francesc Solé,Josep Malvehy,Josep Malvehy,Susana Puig,Susana Puig,Llucia Alos +16 more
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Do we need to do fluorescence in situ hybridization analysis in myelodysplastic syndromes as often as we do
Dolors Costa,Sandra Valera,Ana Carrió,Amparo Arias,Concha Muñoz,María Rozman,Mohamed Belkaid,Rita Coutinho,Benet Nomdedeu,Elias Campo +9 more
TL;DR: The results indicate that FISH studies provide relevant information in MSD in which the conventional cytogenetic analysis was unsuccessful but add little value to a normal katyotype in conventional cytognetic analysis.
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