Results 1 to 10 of about 152,507 (240)

A review on genome editing by CRISPR-Cas9 technique for cancer treatment [PDF]

open access: yesWorld Cancer Research Journal, 2020
In this review, we summarize CRISPR-Cas9 system-based gene modification for the therapeutic treatment of cancer. Cancer is a group of diseases involving anomalous cell growth with the potential to invade or blow out to other parts of the body, which is ...
M. Niuz Morshed Khan   +3 more
doaj   +1 more source

Gene Editing to Tackle Facioscapulohumeral Muscular Dystrophy

open access: yesFrontiers in Genome Editing, 2022
Facioscapulohumeral dystrophy (FSHD) is a skeletal muscle disease caused by the aberrant expression of the DUX4 gene in the muscle tissue. To date, different therapeutic approaches have been proposed, targeting DUX4 at the DNA, RNA or protein levels. The
Virginie Mariot, Julie Dumonceaux
doaj   +1 more source

Entering the post-epigenomic age: back to epigenetics [PDF]

open access: yesOpen Biology, 2018
It is undeniably one of the greatest findings in biology that (with some very minor exceptions) every cell in the body possesses the whole genetic information needed to generate a complete individual.
Sebastian Bultmann, Stefan H. Stricker
doaj   +1 more source

Prospects for using CRISPR-Cas9 system in the treatment of human viral diseases

open access: yesActa Biomedica Scientifica, 2023
The aim. To analyze the possibility of using the genetic mechanisms of CRISPR-Cas9 technology in the prevention and treatment of certain viral diseases.Materials and methods.
A. M. Ziganshin   +4 more
doaj   +1 more source

A genomic sequence of the type II-A clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated system in Mycoplasma salivarium strain ATCC 29803

open access: yesJournal of Oral Microbiology, 2022
Introduction Clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated systems are RNA-mediated adaptive immune systems that actagainst invading genetic elements such as phages or plasmids.
Harumi Mizuki   +3 more
doaj   +1 more source

Tunable Transcriptional Interference at the Endogenous Alcohol Dehydrogenase Gene Locus in Drosophila melanogaster

open access: yesG3: Genes, Genomes, Genetics, 2020
Neighboring sequences of a gene can influence its expression. In the phenomenon known as transcriptional interference, transcription at one region in the genome can repress transcription at a nearby region in cis. Transcriptional interference occurs at a
Victoria Jorgensen   +12 more
doaj   +1 more source

The Involvement of the Cas9 Gene in Virulence of Campylobacter jejuni

open access: yesFrontiers in Cellular and Infection Microbiology, 2018
Campylobacter jejuni is considered as the leading cause of gastroenteritis all over the world. This bacterium has the CRISPR–cas9 system, which is used as a gene editing technique in different organisms.
Muhammad A. B. Shabbir   +11 more
doaj   +1 more source

Optimizing CRISPR Cas9 Genome Editing System: A Review

open access: yesInternational Journal of Endorsing Health Science Research, 2017
CRISPR Cas9 is highly advanced genome editing technology extensively used for the modifications of genetic components in various sectors of living organisms. This technology has been adapted from the prokaryotic immune system, where it plays a vital role
Meen Bahadur Budhthoki   +5 more
doaj   +1 more source

Evaluating the feasibility of Cas9 overexpression in 3T3-L1 cells for generation of genetic knock-out adipocyte cell lines

open access: yesAdipocyte, 2021
Cell lines recapitulating physiological processes can represent alternatives to animal or human studies. The 3T3-L1 cell line is used to mimic adipocyte function and differentiation. Since transfection of 3T3-L1 cells is difficult, we used a modified 3T3-
Tomás Suchý   +6 more
doaj   +1 more source

Debating CRISPR/cas9 and Mitochondrial Donation: Continuity and Transition Performances at Scientific Conferences

open access: yesEngaging Science, Technology, and Society, 2016
Conferences are important performative sites. Here we detail a UK science policy conference debating the novel biomedical techniques CRISPR/cas9 and mitochondrial donation.
Neil Stephens, Rebecca Dimond
doaj   +1 more source

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