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Genbearbeitung, Zell- und Gentherapie

Genbearbeitung, Zell- und Gentherapie

Anisha Manju Amuthalekha / Rekha Beularani / Sunithakumari Minialphonse

98,63 €
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Editorial:
KS OmniScriptum Publishing
Año de edición:
2024
Materia
Genética (no médica)
ISBN:
9786208164652
98,63 €
IVA incluido
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Beim Gene Editing werden präzise Veränderungen an der DNA eines Organismus vorgenommen, um Mutationen zu korrigieren, schädliche Gene zu deaktivieren oder neues genetisches Material einzuführen. Techniken wie CRISPR-Cas9 ermöglichen gezielte genetische Veränderungen und damit potenzielle Behandlungen für ein breites Spektrum von Krankheiten, einschließlich genetischer Störungen und Krebserkrankungen. Bei der Zelltherapie werden gesunde, funktionsfähige Zellen in einen Patienten verpflanzt, um geschädigtes Gewebe zu ersetzen oder zu reparieren. Stammzellen, insbesondere induzierte pluripotente Stammzellen (iPSC), werden häufig zur Regeneration von Geweben und zur Behandlung von Krankheiten wie Blutkrankheiten und degenerativen Erkrankungen eingesetzt. Die Gentherapie zielt darauf ab, Krankheiten zu behandeln oder zu verhindern, indem veränderte oder neue Gene in die Zellen eines Patienten eingebracht werden. Mit Hilfe viraler Vektoren können therapeutische Gene genetische Defekte korrigieren, fehlende Proteine wiederherstellen oder das Fortschreiten von Krankheiten verlangsamen. Dieser Ansatz ist vielversprechend für die Behandlung von Erbkrankheiten, Krebs und seltenen genetischen Erkrankungen.

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