Inicio > Matemáticas y ciencia > Biologia, ciencias de la vida > Ciencias de la vida: cuestiones generales > Genética (no médica) > Hydroxyméthylation de l’ADN dans les troubles liés à l’expansion des répétitions non codantes
Hydroxyméthylation de l’ADN dans les troubles liés à l’expansion des répétitions non codantes

Hydroxyméthylation de l’ADN dans les troubles liés à l’expansion des répétitions non codantes

Rustam Esanov

81,42 €
IVA incluido
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Editorial:
KS OmniScriptum Publishing
Año de edición:
2024
Materia
Genética (no médica)
ISBN:
9786208407094
81,42 €
IVA incluido
Disponible

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Sobre IBD

Mes recherches portent sur les troubles liés à l’expansion des répétitions, une famille de troubles qui résultent de la séquence microsatellite répétitive à l’intérieur du gène. En particulier, cette thèse porte sur deux maladies à expansion de répétitions non codantes : La sclérose latérale amyotrophique associée à C9orf72 (C9-ALS) et le syndrome de l’X fragile (FXS). Notre groupe a été le premier à signaler la présence de 5-hydroxyméthylcytosine, une nouvelle marque épigénétique et un intermédiaire actif de déméthylation de l’ADN, dans les loci étendus des patients atteints de C9-ALS et de FXS.

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