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.

Մատենագիտական մանրամասներ
Հիմնական հեղինակ:	Ullah, Mohammad
Այլ հեղինակներ:	Islam, Farzana
Ձևաչափ:	Թեզիս
Լեզու:	English
Հրապարակվել է:	Brac University 2023
Խորագրեր:	SCD CRISPR/Cas9 Hematopoietic stem/progenitor cells Fetal hemoglobin Gene editing tools Genetic engineering > Research Gene therapy > Research Biotechnology
Առցանց հասանելիություն:	http://hdl.handle.net/10361/19355

Նմանատիպ նյութեր

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Distribution of complete CRISPR-Cas systems in vibrio cholerae and its effect on presence of plasmid derived contigs in complete genome assemblies
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Qualitative classification of the breast cancer genome and clustering of the cancer gene network
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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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Biased acquisition of spacers by the CRISPR System of the V. cholerae
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Correlation between the prevalence of plasmids and AMR genes in the environmental isolates of different bacterial species
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RNA drugs and RNA targets for small molecules: Prospects and challenges
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Study of antibiotic resistance gene transfer between isolates from patients with urinary tract infection via conjugation
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Determination of transfer of Azithromycin resistance gene though Conjugation, among Enterobacteriaceae, isolated from Urinary Tract Infected patients
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Isolation of cellulolytic bacteria from soil and identification by 16S rRNA gene sequencing
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CRISPR-Cas Systems
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