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Genetic Engineering Market Size, Trends and Insights By Product (Biochemical, Genetic Markers), By Devices (PCR, Gene Gun, Gel Assemblies), By Techniques (Gene Splicing, Artificial Selection, Recombinant DNA Technology, Synthesizing DNA, Gene Editing, Other), …
datacite
Sirsat, Nitin
2024
置信度 0.79
Genetic Engineering MarketGenetic Engineering Market SizeGenetic Engineering Market ShareGenetic Engineering Market TrendsGenetic Engineering Market Report
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The discovery of the CRISPR/Cas9 system in 2012 has opened up new possibilities for targeted, inexpensive, and reproducible genetic modification of human cells. One of these possibilities is the targeted modification of induced pluripotent stem cells (iPS) for…
datacite
Nießing, Bastian
2024
置信度 0.76
Hochschulschriftgenome editing , CRISPR/Cas9 , automation , StemCellFactory , induced pluripotent stem cells , iPS cells
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Alzheimer's disease (AD) is the most prevalent neurodegenerative disorder, accounting for 60-70% of dementia cases diagnosed worldwide. The impact of AD is rapidly increasing, with deaths more than doubling from 2000 to 2021. As populations age, especially in …
datacite
Gonzalez Diaz, Alicia
2024
置信度 0.79
Amyloid-βiPSCOligomersPhase separationPreclinical models
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Эффективность и точность подходов редактирования генома растений совершенствуются с каждым годом, благодаря чему значительно расширяются возможности улучшения различных характеристик сельскохозяйственных культур. Картофель – важнейшая овощная и техническая кул…
datacite
Дегтярёва, Влада, Долгов, Сергей, Мирошниченко, Дмитрий
2024
置信度 0.75
genome editingpotatoCRISPR/Cas9TALENгеномное редактирование
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This repository contains extended and underlying data for "Improved gene editing and fluorescent-protein tagging in Aspergillus nidulans using a Golden Gate-based CRISPR-Cas9 plasmid system". Modaffari et al., 2024.
datacite
Modaffari, Domenico
2024
置信度 0.75
Cell biologyMicrobiologyFOS: Biological sciences
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This repository contains extended and underlying data for "Improved gene editing and fluorescent-protein tagging in Aspergillus nidulans using a Golden Gate-based CRISPR-Cas9 plasmid system". Modaffari et al., 2024.
datacite
Modaffari, Domenico
2024
置信度 0.75
Cell biologyMicrobiologyFOS: Biological sciences
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This repository contains extended and underlying data for "Improved gene editing and fluorescent-protein tagging in Aspergillus nidulans using a Golden Gate-based CRISPR-Cas9 plasmid system". Modaffari et al., 2024.
datacite
Modaffari, Domenico
2024
置信度 0.75
Cell biologyMicrobiologyFOS: Biological sciences
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Since the advent of CRISPR-Cas9, a groundbreaking gene-editing technology that enables precise genomic modifications via a short RNA guide sequence, there has been a marked increase in the accessibility and application of this technology across various fields.…
datacite
Bao, Condy, Liu, Fuxiao
2024
置信度 0.79
Quantitative Methods (q-bio.QM)Artificial Intelligence (cs.AI)Machine Learning (cs.LG)FOS: Biological sciencesFOS: Biological sciences
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Phi-3-MLX is a versatile AI framework that leverages both the Phi-3-Vision multimodal model and the recently updated (July 2, 2024) Phi-3-Mini-128K language model, optimized for Apple Silicon using the MLX framework. This project provides an easy-to-use interf…
datacite
JosefAlbers, Rémi
2024
置信度 0.72
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Genetic engineering of primary hematopoietic cells is essential for mechanistic immunology studies, however the development of cell-based therapies yet remains constrained by two major factors: the fragility of many primary lineages and challenges of viral del…
preprints
2026
置信度 0.81
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Background: /Objectives: Despite the success of statin and PCSK9 inhibitor therapies, significant residual cardiovascular risk persists, driven by atherogenic triglyceride-rich lipoproteins (TRLs) and the independent, causal risk factor, lipoprotein(a) [Lp(a)]…
preprints
2025
置信度 0.81
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Endogenous protein tagging in Caenorhabditis elegans enables direct visualization and manipulation of proteins in vivo, providing native readouts of expression, localization, and dynamics. No coordinated effort currently exists to comprehensively tag proteins …
preprints
2025
置信度 0.81
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Durable resistance to soil-borne pathogens remains elusive in cereals, partly because susceptibility (S) genes that facilitate root infection have not been identified in monocots. In the model legume Medicago truncatula , the SCAR/WAVE complex member MtAPI fun…
preprints
2026
置信度 0.81
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Engineered deletions are a powerful probe for studying genome architecture, function, and regulation. Yet, the lack of effective methods to create them in large numbers and at multi-kilobase scale has rendered interrogating all the gigabases of human DNA elusi…
preprints
2025
置信度 0.81
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Background Investigating the subcellular distribution of proteins is crucial for understanding complex cell behaviours and disease mechanisms, and fluorescence microscopy has become a key tool for visualising protein localisation. Endogenous protein tagging, w…
preprints
2025
置信度 0.81
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Abstract Colorectal cancer (CRC) tumours with high stromal content have a worse outcome, but the mechanisms governing this are unclear. Using high-throughput single-cell perturbation analysis of CRC patient-derived organoids (PDOs) and cancer-associated fibrob…
preprints
2026
置信度 0.81
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The liverwort Marchantia polymorpha is a widely used model organism for studying land plant biology, which has also proven to be a promising testbed for bioengineering. CRISPR/Cas9 technology has emerged as a transformative tool for precise genome modification…
preprints
2025
置信度 0.81
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Abstract Age-related macular degeneration (AMD) is a leading cause of central vision loss. Immunofluorescence and gene expression studies in human donor eyes have shown that choriocapillaris endothelial cells (CECs) are lost before retinal pigment epithelium (…
preprints
2026
置信度 0.86
biologyneurosciencecell biologymedicinecancer
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ABSTRACT Genetic defects of the gene encoding the ubiquitin ligase UBE3A cause a severe neurodevelopmental disorder, the Angelman syndrome (AS). The pathophysiology of AS remains unclear, hindering the development of effective therapies. Using AS animal models…
preprints
2026
置信度 0.81
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CRISPR-based therapeutics rely on guide RNAs (gRNAs) and the Cas9 endonuclease for precise gene editing. Ensuring gRNA purity and base-level sequence integrity is essential for clinical translation. While industry-standard practice relies on liquid chromatogra…
preprints
2025
置信度 0.81
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CRISPR–Cas9 gene editing holds transformative promise for genetic therapies, but is hindered by off-target effects that undermine its precision and safety. To address this, we developed CRISMER, a hybrid deep-learning architecture that uses multi-branch convol…
preprints
2025
置信度 0.81
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Objective The accumulation of DNA damage and mutations is a key contributor to aging. Recent studies have shown that disrupting the Beclin 1-BCL2 autophagy regulatory complex through gene editing can extend lifespan in mice. The precise application of gene edi…
preprints
2025
置信度 0.86
cancermedicinescience policymicrobiologydata science
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Wolman disease (WD), the severe infantile form of lysosomal acid lipase deficiency, is a rare metabolic disorder caused by inactivating mutations in the LIPA gene. Although WD is characterized by profound hepatic dysfunction, experimental human systems capable…
preprints
2025
置信度 0.81
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Programmed with an RNA guide, Cas9 nuclease directs double-strand DNA cleavage via its two nuclease domains. However, Cas9 sometimes falsely identifies DNA targets by binding and cleaving DNA that does not match its PAM and guide RNA sequence requirements. Cas…
preprints
2026
置信度 0.81
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Human retinal organoids are in vitro 3D structures that recapitulate key molecular and structural characteristics of the in vivo retina. They include the presence of all essential retinal cell types including photoreceptors, making them relevant models for pre…
preprints
2024
置信度 0.81
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Accurate prediction of CRISPR-based gene editing remains challenging since existing models often fail to generalize across experimental and cellular contexts. We introduce CRISPRzip, a mechanistic kinetic model that quantitatively links nucleotide sequence and…
preprints
2025
置信度 0.81
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Light is essential for photosynthetic organisms, but excess light can generate toxic levels of reactive oxygen species (ROS). To neutralize these ROS, plants and algae produce a variety of antioxidants like carotenoids, tocopherols, and glutathione. However, t…
preprints
2026
置信度 0.81
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The transcription factor ATF6 has a central role in adapting mammalian cells to endoplasmic reticulum (ER) stress via the Unfolded Protein Response (UPR). This has driven efforts to identify modulators of ATF6 signalling. Here, an unbiased genome-wide CRISPR-C…
preprints
2025
置信度 0.81
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The production of overwintering eggs is a critical adaptation for winter survival among many insects. Melanization contributes to eggshell pigmentation and hardening, consequently enhancing resistance to environmental stress. The complex life cycle of the pea …
preprints
2024
置信度 0.81
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Background Macrophages adopt activation states along a spectrum from pro- to anti-inflammatory, enabling appropriate responses to pathogens and environmental cues. Dysregulated inflammatory macrophage activation contributes to diseases including sepsis, rheuma…
preprints
2025
置信度 0.81
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Summary Plants can propagate their own clones through asexual reproduction. Genetic and hormonal factors regulating asexual reproduction have begun to be elucidated in the liverwort Marchantia polymorpha , which produce asexual propagules called gemmae within …
preprints
2026
置信度 0.81
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The possibility of CRISPR/Cas gene editing system regulation is an important point for creation of effective molecular biological instrument. Allosteric regulation at the level of guide RNAs is one of possible approach to regulate gene editing system. In this …
preprints
2024
置信度 0.81
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The CRISPR/Cas9 system has become a powerful tool for molecular design breeding in livestock such as sheep. However, the efficiency of the Cas9 system combined with zygote microinjection remains suboptimal. In this study, mature sheep oocytes were used for mic…
preprints
2024
置信度 0.81
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Multiplex genome editing via CRISPR enables simultaneous gene knockout, activation, and repression, but current toolkits often rely on repetitive and lengthy Pol III promoters, limiting construct diversity and genetic stability. Here, we present a diverse coll…
preprints
2024
置信度 0.81
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Ethylene glycol (EG), one of the main monomers of polyethylene terephthalate (PET), is an attractive target for microbial upcycling. Despite this interest, there is a limited number of described organisms that can efficiently metabolise EG. Here, we report the…
preprints
2025
置信度 0.81
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During collective cell invasion, epithelial-to-mesenchymal transition (EMT) and morphogen signalling-mediated cell fate specification are traditionally viewed as a linear cascade: morphogens drive cell fates that activate EMT programs. Here, we uncover recipro…
preprints
2025
置信度 0.81
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Genetic biocontrol systems have broad applications in population control of insects implicated in both disease spread and food security. In this study we establish and characterise a novel split-CRISPR/Cas9 system we term Sex Conversion Induced by CRISPR (SCIC…
preprints
2024
置信度 0.81
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CRISPR-Cas9 systems can be used for precise genome editing in filamentous fungi, including Aspergillus nidulans . However, current CRISPR-Cas9 systems for A. nidulans rely on relatively complex or multi-step cloning methods to build a plasmid expressing both C…
preprints
2024
置信度 0.81
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The ability to efficiently make precise genome edits in somatic tissues will have profound implications for gene therapy and basic science. CRISPR/Cas9 mediated homology-directed repair (HDR) is one approach that is commonly used to achieve precise and efficie…
preprints
2024
置信度 0.81
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Abstract Background Pancreatic cancer is one of the main causes of cancer-related deaths, especially pancreatic ductal adenocarcinoma and it’s characterized by a poor prognosis. The KRAS gene mutation is prevalent in about 85% of pancreatic cancer cases which …
preprints
2024
置信度 0.81
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Improving the efficiency of germplasm innovation has always been the aim of rice breeders. Tra-ditional hybrid breeding methods for variety selection rarely meet the practical needs of rice pro-duction. The emergence of genome editing technologies, such as CRI…
preprints
2024
置信度 0.81
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Nitric oxide (NO) is an important signaling molecule in flowering plant immunity. It rapidly accumulates in response to pathogen perception. In addition to it’s direct response to microbes, NO controls a range of defence responses primarily through S -nitrosyl…
preprints
2025
置信度 0.81
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CRISPR/Cas9 based genome editing has advanced our understanding of a myriad of important biological phenomena. Important challenges to multiplex genome editing in maize include assembly of large complex DNA constructs, few genotypes with efficient transformati…
preprints
2024
置信度 0.81
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ABSTRACT Inactivation of disease alleles by allele-specific editing is a promising approach to treat dominant-negative genetic disorders, provided the causative gene is haplo-sufficient. We previously edited a dominant NEFL missense mutation with inactivating …
preprints
2024
置信度 0.81
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To assist in the establishment of an efficient CRISPR/Cas9 gene editing workflow in bovine cells, we compared the efficiency of four Streptococcus pyogenes Cas9 (SpCas9) nuclease variants (produced in-house or commercially) and two different Cas9/sgRNA ribonuc…
preprints
2024
置信度 0.81
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The CRISPR-Cas system has revolutionized gene editing, while its outcome prediction remains unsatisfactory, especially in new cell states due to their distinct DNA repair preferences. In this study, we introduce inDecay, a flexible system for predicting CRISPR…
preprints
2024
置信度 0.81
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Programmable epigenome editors modify gene expression in mammalian cells by altering the local chromatin environment at target loci without inducing DNA breaks. However, the large size of CRISPR-based epigenome editors poses a challenge to their broad use in b…
preprints
2024
置信度 0.81
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Targeted gene editing can be achieved using CRISPR/Cas9-assisted recombineering. However, high-efficiency editing requires careful optimization for each locus to be modified which can be tedious and time-consuming. In this work, we developed a simple, fast and…
preprints
2025
置信度 0.86
biologysynthetic biologycomputational biologygeneticsmodular design
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The receptor-like cytoplasmic kinase BIK1 and its close homolog PBL1 have been widely recognized as central components of plant immunity. However, most genetic studies of BIK1 and PBL1 functions were carried out with single T-DNA insertional mutant alleles. So…
preprints
2025
置信度 0.81
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Summary CRISPR-Cas9 (clustered, regularly interspaced, short palindromic repeats with CRISPR-associated protein 9) is a powerful, versatile, and cost-effective molecular tool that can be used for genetic engineering purposes and beyond 1 and is especially suit…
preprints
2024
置信度 0.81
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With the groundbreaking advancements in genome editing technologies, particularly CRISPR-Cas9, creating knockout mutants has become highly efficient. However, the CRISPR-Cas9 system introduces DNA double-strand breaks, which can increase the risk of chromosoma…
preprints
2024
置信度 0.81
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Genetic modifications using CRISPR-Cas9 have revolutionized cancer research and other pre-clinical studies. Exceptionally, these efficient tools are inadequate in a few disease models and cell lines due to the aberrant differentiation states and the accumulati…
preprints
2024
置信度 0.81
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Abstract Background Livestock, particularly cattle, are crucial for biotechnology fields, such as genetic breeding, infectious diseases, bioreactors, and specific disease models. However, genetic engineering in cattle has lagged due to long gestation periods, …
preprints
2024
置信度 0.81
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SUMMARY The distribution and level of epigenetic (chromatin) marks have implications for differential regulatory effects at specific gene loci. Herein, we applied a protocol which combines in vivo electroporation and a CRISPR-dead (d)Cas9 system to probe and e…
preprints
2024
置信度 0.81
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The class 1 HDACs 1, 2 and 3 form seven families of distinct large multiprotein complexes that regulate gene expression via deacetylation of lysines in histone tails. The degree of redundancy and functional overlap between complexes and their primary gene targ…
preprints
2025
置信度 0.86
biologycomputational biologygeneticssynthetic biologyq-bio.gn
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CRISPR/Cas9 technologies provide unique capabilities for modeling disease and understanding gene-to-phenotype connections. In cultured cells, chemical-mediated control of Cas9 activity can limit off-target effects and enable mechanistic study of essential gene…
preprints
2024
置信度 0.81
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Genome editing enables sequence-function profiling of endogenous cis-regulatory elements, driving understanding of their mechanisms and the development of gene therapies. However, these approaches cannot be combined with direct scalable readouts of chromatin s…
preprints
2024
置信度 0.81
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ABSTRACT Improper disposal of potato peels harms the environment, wasting nutrient-rich resources that could be used for beneficial enzyme production like lipase. This study aimed to edit the lacZ gene in Escherichia coli using utilizing the CRISPR Cas9 techno…
preprints
2024
置信度 0.81
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Streptomycetes hold immense potential for discovering novel bioactive molecules for applications in medicine or sustainable agriculture. However, high-throughput exploration is hampered by the current Streptomyces genetic engineering methods that involve the m…
preprints
2024
置信度 0.81
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As members of the α-proteobacteria group, Caulobacter crescentus and its relatives are known for their asymmetric life cycle and comprehensive applications in gene delivery, agricultural biotechnology, and the production of high-value compounds. However, genet…
preprints
2024
置信度 0.81
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Abstract The parthenogenetic life cycle of the stick insect Medauroidea extradentata offers unique advantages for the generation of transgenic lines, as an isogenic and stable transgenic line can in principle be achieved already in the first generation. Howeve…
preprints
2024
置信度 0.81
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Verification of genome editing in human pluripotent stem cells (hPSCs), particularly in silent locus is desirable but challenging because it often requires complex and time-intensive lineage-specific or tissue-specific differentiation to induce their expressio…
preprints
2024
置信度 0.81
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Genome editing has become a routine tool for functionally characterizing plant and animal genomes. However, stable genome editing in plants remains limited by the time- and labor- intensive process of generating transgenic plants, as well as by the efficient i…
preprints
2024
置信度 0.81
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The advent of CRISPR-based technologies has enabled the rapid advancement of programmable gene manipulation in cells, tissues, and whole organisms. An emerging platform for targeted gene perturbation is epigenetic editing, the direct editing of chemical modifi…
preprints
2024
置信度 0.81
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Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR), an exceptionally potent genome-editing technique developed in 2012, is the ideal tool of the future for treating diseases by permanently correcting deleterious base mutations or disrupting dis…
preprints
2024
置信度 0.86
nanotechnologybiologypharmacologygeneticsvariety
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ABSTRACT ARGONAUTE (AGO) proteins associate with small RNAs to form RNA-induced silencing complexes (RISCs). Arabidopsis AGO1 effects post-transcriptional silencing by microRNAs (miRNAs) and small interfering RNAs (siRNAs) and is necessary for siRNA amplificat…
preprints
2025
置信度 0.72
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Mutations in the MECP2 gene cause the severe neurological disorder Rett syndrome. A cluster of frameshift-causing C-terminal deletions (CTDs) lead to loss of ∼100 amino acids at the C-terminus of the MeCP2 protein, and account for approximately 10% of RTT-caus…
preprints
2025
置信度 0.81
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SUMMARY The SAGA transcriptional co-activator complex regulates gene expression through histone acetylation at promoters, mediated by its histone acetyl transferase, KAT2A. While its structure and function have been extensively investigated, how the stability …
preprints
2025
置信度 0.81
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Lung cancer treatment has long been a major field of study in research due to the com-plexity and variability of cancer. Because drug resistance is a major hurdle for lung cancer treat-ment, in this article, we will review the epidermal growth factor receptor …
preprints
2024
置信度 0.81
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CRISPR-Cas systems are transformative tools for gene editing which can be tuned or controlled by anti-CRISPRs (Acrs) - phage derived inhibitors that regulate CRISPR-Cas activity. However, Acrs that are capable of inhibiting biotechnologically relevant CRISPR s…
preprints
2024
置信度 0.81
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CRISPR-Cas systems are transforming precision medicine with engineered probiotics as next-generation diagnostics and therapeutics. To promote human health and treat disease, engineering probiotic bacteria demands maximal versatility to enable non-natural funct…
preprints
2024
置信度 0.81
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Recent advancements in cancer treatment, including targeted therapy, personalized vaccines, immunotherapy, and bacteriotherapy have shown promising potential in the curing of many kinds of cancer. The pursuit of innovative therapeutic approaches is impeded by …
preprints
2024
置信度 0.81
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Familial dysautonomia (FD) is a fatal autosomal recessive sensory and autonomic neuropathy. FD is caused by a T-to-C point mutation in intron 20 of the Elongator acetyltransferase complex subunit 1 ( ELP1 ) gene, which results in tissue-specific skipping of ex…
preprints
2024
置信度 0.81
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The use of CRISPR-associated enzymes in iPSC-derived neurons for precise gene targeting and high-throughput gene perturbation screens offers great potential but presents unique challenges compared to dividing cell lines. CRISPRi screens in iPSC-derived neurons…
preprints
2024
置信度 0.81
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CRISPR nuclease-mediated gene knock-out is limited by suboptimal sgRNAs, inaccessible target sites, and silent mutations. Here, we present a Cas12a-based system that targets each gene with four sgRNAs to overcome these limitations, using Drosophila as a tracta…
preprints
2024
置信度 0.81
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Poly (ADP-Ribose) Polymerase inhibitors (PARPi) induce cytotoxicity in homologous recombination repair (HRR)-deficient cancers by causing PARP1 to become trapped on chromatin, resulting in irreparable replication-associated DNA damage. Although increased clear…
preprints
2025
置信度 0.81
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Cas9 from Streptococcus pyogenes (SpCas9) revolutionized genome editing by enabling programmable DNA cleavage guided by an RNA. However, SpCas9 tolerates mismatches in the DNA-RNA duplex, which can lead to deleterious off-target editing. Here, we reveal that C…
preprints
2024
置信度 0.81
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Adaptive Laboratory Evolution (ALE) is a powerful approach for mining genetic data to engineer industrial microorganisms. This evolution-informed design requires robust genetic tools to incorporate the discovered alleles into target strains. Here, we introduce…
preprints
2024
置信度 0.81
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Single-cell transcriptomic and proteomic technologies enable molecular profiling of immune cells at scale but provide limited access to cellular phenotypes shaped by spatial organisation, organelle architecture and cytoskeletal remodelling. Here we present TGl…
preprints
2026
置信度 0.81
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The use and publication of research utilising CRISPR/cas9 in gene editing and knock outs (KOs) within cell lines is now widespread and has proved extremely powerful in the interrogation of gene function. However, the potential of experimental artefacts resulti…
preprints
2024
置信度 0.81
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Abstract Background Due to its ability to grow fast on CO 2 , CO and H 2 at high temperatures and with high energy efficiency, the thermophilic acetogen Thermoanaerobacter kivui could become an attractive host for industrial biotechnology. In a circular carbon…
preprints
2025
置信度 0.81
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Astrocytes, which are increasingly recognized as pivotal constituents of brain circuits governing a wide range of functions, express GABA transporter 3 (Gat3), an astrocyte-specific GABA transporter responsible for maintenance of extra-synaptic GABA levels. He…
preprints
2024
置信度 0.81
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Plant gene editing technology has significantly advanced in recent years, thereby transforming both biotechnological research and agricultural practices. This review provides a comprehensive summary of recent advancements in this rapidly evolving field, showca…
preprints
2024
置信度 0.81
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Abstract Background CRISPR/Cas9 is used for editing of non-coding sequence. This study tested the involvement of downstream cis-element in regulating CD44 expression and the possibility of using CRISPR/Cas9 system to manipulate the transcription factor binding…
preprints
2024
置信度 0.81
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Systemic lupus erythematosus (SLE) is a complex autoimmune disorder characterized by widespread inflammation and autoantibody production. Its development and progression involve genetic, epigenetic, and environmental factors. Although genome-wide association s…
preprints
2024
置信度 0.81
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Crops obtained by genome editing (GE) technologies represent a notable and disruptive shift from genetically modified or transgenic plants, outpacing public perception and regulatory frame-works. Multiple aspects of GE are contributing to the advancement of mo…
preprints
2024
置信度 0.81
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Summary Since their discovery, CRISPR/Cas9 systems have been repurposed for programmable targeted genomic editing. This has led to unprecedented advancement of gene editing for therapeutic benefit. Initial uses of CRISPR/Cas9 were focused on gene disruption vi…
preprints
2024
置信度 0.81
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ABSTRACT Predicting how changes in human DNA sequence impact gene expression remains challenging. Here, we present PETRA ( P rime E diting of T ranscribed R egulatory elements to A ssay expression), a multiplexed genome editing method to quantify the effects o…
preprints
2025
置信度 0.81
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CRISPR gene editing strategies are shaping cell therapies through precise and tunable control over gene expression. However, achieving reliable therapeutic effects with improved safety and efficacy requires informed target gene selection. This depends on a tho…
preprints
2024
置信度 0.81
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CRISPR technology has revolutionized fungal genetic engineering by accelerating the pace and expanding the feasible scope of experiments in this field. Among various CRISPR-Cas systems, Cas9 and Cas12a are widely used in genetic and metabolic engineering. In f…
preprints
2024
置信度 0.81
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ABSTRACT Nucleic acid nanostructures offer unique opportunities for biomedical applications due to their sequence-programmable structures and functions, which enable the design of complex responses to molecular cues. Control of the biological activity of thera…
preprints
2024
置信度 0.81
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Abstract Background Pseudomonas putida KT2440, a non-pathogenic soil bacterium, is a key platform strain in synthetic biology and industrial applications due to its robustness and metabolic versatility. Various systems have been developed for genome editing in…
preprints
2024
置信度 0.81
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Abstract In the post-COVID-19 era, drug-resistant bacterial infections emerge as one of major death causes, where multidrug-resistant Acinetobacter baumannii (MRAB) and drug-resistant Pseudomonas aeruginosa (DRPA) represent primary pathogens. However, the clas…
preprints
2024
置信度 0.81
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Gene editing has been revolutionised by the CRISPR-Cas9 technology. The versatility and ease-of-use of the technology far exceeds its predecessors, however, the selection of a high-quality guide RNA (gRNA) is critical to directing it to a target site. Selectin…
preprints
2024
置信度 0.81
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Abstract The combination of isothermal amplification and CRISPR-Cas12a system is a valuable tool for detecting nucleic acids, especially in emergency situations or disease outbreaks. However, achieving compatibility between these technologies has been a challe…
preprints
2024
置信度 0.81
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Background: and Objectives. Cartilage repair remains a critical challenge in orthopaedic medicine due to the tissue's limited self-healing ability, contributing to degenerative joint conditions such as osteoarthritis (OA). In response, regenerative medici…
preprints
2024
置信度 0.81
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Abstract The transition from well-fed to food-deprived conditions in C. elegans triggers a stereotypic exploration behaviour in C. elegans characterised by a temporal decrease in cumulative reorientations. We conducted a screen of neuropeptide mutants and iden…
preprints
2025
置信度 0.77
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Abstract Staphylococcus aureus Cas9 (SaCas9), which is smaller than the widely-used Streptococcus pyogenes Cas9 (SpCas9), has been harnessed for gene therapy using an adeno-associated virus vector. However, SaCas9 requires an NNGRRT (where N is any nucleotide …
preprints
2024
置信度 0.81
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The identification of novel antimalarials with activity against both the liver and blood stages of the parasite lifecycle would have the dual benefit of prophylactic and curative potential. However, one challenge of leveraging chemical hits from phenotypic scr…
preprints
2025
置信度 0.81
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Malaria is caused by protozoan parasites of the genus Plasmodium and remains a global health concern. The parasite has a highly adaptable life cycle comprising successive rounds of asexual replication in a vertebrate host and sexual maturation in the mosquito …
preprints
2024
置信度 0.81