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Genética, Patología Molecular y Enfermedades Raras
Capacidades I+D
Genómica:
-Habilidades clínicas de diagnóstico de síndromes clínicos, genéticos y dismórficos
-Consejo genético
-Cariotipado
-Extracción de ácidos nucleicos
-Electroforesis en gel de ácidos nucleicos
-PCR
-Secuenciación electroforesis capilar
-Cuantificación de ácidos nucleicos mediante espectrofotometría
-Microscopia optica de fluorescencia
Patología Molecular:
-Identificación de marcadores con valor diagnóstico, pronóstico en lesiones precursoras de cáncer
-Caracterización histológica, inmunohistoquímica y molecular de cánceres, fundamentalmente colorrectal
-Evaluación de variantes genéticas relacionadas con variaciones interindividuales en la respuesta a fármacos basados en el concepto de terapia molecular dirigida, con especial atención a los tratamientos con anticuerpos monoclonales en enfermedad inflamatoria crónica
-Identificación de polimorfismos relacionados con susceptibilidad genética a
enfermedades neoplásicas
Instrumentos / Equipos disponibles
No hay información disponible.