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.

গ্রন্থ-পঞ্জীর বিবরন
প্রধান লেখক:	Ullah, Mohammad
অন্যান্য লেখক:	Islam, Farzana
বিন্যাস:	গবেষণাপত্র
ভাষা:	English
প্রকাশিত:	Brac University 2023
বিষয়গুলি:	SCD CRISPR/Cas9 Hematopoietic stem/progenitor cells Fetal hemoglobin Gene editing tools Genetic engineering > Research Gene therapy > Research Biotechnology
অনলাইন ব্যবহার করুন:	http://hdl.handle.net/10361/19355

অনুরূপ উপাদানগুলি

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National Gene Bank, Ganakbari, Ashulia
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Stem cell in cancer disease cure vs cause
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Potential use of mesenchymal stem cells in regenerative medicines: a review
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Genotyping of a Clinically Important SNP rs1799853 Present in the CYP2C9 Gene Using Tetra-primer ARMS PCR Method
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CRISPR-Cas Systems
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