Results 121 to 130 of about 14,674 (226)
CrRNA sequences used for LDLR/PCSK9 targeting cleavage.
CrRNA sequences used for LDLR/PCSK9 targeting cleavage.
Hiroki Shiomi (718724) +13 more
core +1 more source
ABSTRACT Background More than 1000 genes have been identified as predominantly expressed in the human testis. Advances in gene editing technologies have enabled the rapid and efficient generation of genetically engineered mice. This approach facilitates the screening of genes essential for spermatogenesis by analyzing knockout mouse models.
Yumiao Qiu +2 more
wiley +1 more source
Construction of Erwinia amylovora mutants via crRNA expression
Abstract Genome editing is essential for studying gene function for pathogens such as Erwinia amylovora , which causes devastating fire blight in fruit trees of the family Rosaceae. CRISPR/Cas genome editing technology has been widely used in various model organisms, but
Yu Dong +7 more
openaire +1 more source
Abstract A recent study showed that female medaka lacking the estrogen receptor gene esr2b are unreceptive to male courtship and instead court other females. In this study, we investigated the brain transcriptome of esr2b‐deficient females to explore the underlying mechanisms of this behavioral phenotype, and identified npyb, one of the two ...
Yuki Homan +9 more
wiley +1 more source
ABSTRACT The single crossover occurring via homologous recombination is a common phenomenon existing among microbes like Escherichia coli, Bacillus subtilis, Vibrio natriegens, Gluconobacter oxydans and most cyanobacteria species, threatening the stability of engineered strains and challenging iterative genetic engineering. Among them, we take the fast‐
Shubin Li +5 more
wiley +1 more source
Mappingin vivogenetic interactomics through Cpf1 crRNA array screening
Genetic interactions lay the foundation of biological networks in virtually all organisms. Due to the complexity of mammalian genomes and cellular architectures, unbiased mapping of genetic interactionsin vivois challenging. Cpf1 is a single effector RNA-
Guangchuan Wang +4 more
core +1 more source
SWITCHER, a CRISPR-inducible floxed wild-type Cre regulating CRISPR activity
Although several Cre-regulated CRISPR/Cas platforms exist, a CRISPR/Cas-controlled Cre-system remains a challenge. Here, we present a genetic switch we term SWITCHER based on a floxed wild-type Cre-construct representing a CRISPR-inducible and self ...
Björn Schuster +5 more
doaj +1 more source
‘Splice-at-will’ Cas12a crRNA engineering enabled direct quantification of ultrashort RNAs
Abstract We present a robust ‘splice-at-will’ CRISPR RNA (crRNA) engineering mechanism that overcomes the limitations of clustered regularly interspaced short palindromic repeats (CRISPR)/Cas system in directly detecting ultrashort RNAs.
Xinrui Fei +3 more
openaire +2 more sources
A minimum crRNA guide length of 17 nucleotides is necessary to engage Cas9 target cleavage.
A. Sequence of crRNA guides of variable length used in the current study. B. EMSA (left) and cleavage assay (right) of Cas9/tracrRNA/crRNA combinations using p53 [Exon 7] as probe and resolved on a 5% native polyacrylamide gel and 10% polyacrylamide/8M ...
Hisashi Miura (638238) +7 more
core +1 more source
The CRISPR-Cas13 system exhibits potent RNA cleavage activity and has been widely utilized for RNA-targeting applications. However, its collateral cleavage of bystander RNAs limits in vivo therapeutic applications. In this study, we generated a series of
Wenxia Zhang +9 more
doaj +1 more source

