Video Experimental Relacionado

Updated: Sep 9, 2025

Chromosomics: Detection of Numerical and Structural Alterations in All 24 Human Chromosomes Simultaneously Using a Novel OctoChrome FISH Assay
06:25

Chromosomics: Detection of Numerical and Structural Alterations in All 24 Human Chromosomes Simultaneously Using a Novel OctoChrome FISH Assay

Published on: February 6, 2012

19.0K

Cromoplejía

Franck Pellestor1,2, Jean Baptiste Gaillard3, Benjamin Ganne3,4

  • 1Unit of Chromosomal Genetics and Research Platform Chromostem, Department of Molecular Genetics and Cytogenomics, Site Unique de Biologie (SUB), Montpellier CHU, Montpellier Cedex 5, France. f-pellestor@chu-montpellier.fr.

Methods in molecular biology (Clifton, N.J.)
|August 30, 2025
PubMed
Resumen

La cromoplejía, un reordenamiento cromosómico complejo, causa fusiones genéticas y trastornos en el cáncer. Este evento genómico masivo, que ocurre al principio de la oncogénesis, impulsa la evolución y la progresión del tumor.

Palabras clave:
La cromogénesisCromoplejíaSe suprimiránFusión genéticaCáncer de próstataEvolución puntuadaLa translocaciónEl tumor

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