CRISPR/Cas9 genome editing to treat sickle cell disease

CRISPR/Cas9 genome editing to treat sickle cell disease

This thesis is submitted in partial fulfillment of the requirements for the degree of Bachelor of Pharmacy, 2022.

التفاصيل البيبلوغرافية
المؤلف الرئيسي:	Ullah, Mohammad
مؤلفون آخرون:	Islam, Farzana
التنسيق:	أطروحة
اللغة:	English
منشور في:	Brac University 2023
الموضوعات:	SCD CRISPR/Cas9 Hematopoietic stem/progenitor cells Fetal hemoglobin Gene editing tools Genetic engineering > Research Gene therapy > Research Biotechnology
الوصول للمادة أونلاين:	http://hdl.handle.net/10361/19355

مواد مشابهة

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Biased acquisition of spacers by the CRISPR System of the V. cholerae
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