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Efficient introduction of specific homozygous and heterozygous mutations using CRISPR/Cas9
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Outgoing claims: the papers this work cites, builds on, or argues with.
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Donor DNA Utilization During Gene Targeting with Zinc-Finger Nucleases
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Enhanced homology-directed human genome engineering by controlled timing of CRISPR/Cas9 delivery
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Functional characterisation of rare variants in genes encoding the MAPK/ERK signalling pathway identified in long-lived Leiden Longevity Study participants
inferred← citeshttps://doi.org/10.1007/s11481-019-09844-3openalex-snapshot
Utilization of the CRISPR-Cas9 Gene Editing System to Dissect Neuroinflammatory and Neuropharmacological Mechanisms in Parkinson’s Disease
inferred← citeshttps://doi.org/10.1007/s11626-022-00655-0openalex-snapshot
Generation of NPHP1 knockout human pluripotent stem cells by a practical biallelic gene deletion strategy using CRISPR/Cas9 and ssODN
inferred← citeshttps://doi.org/10.1007/s11920-020-01148-1openalex-snapshot
Modeling Psychiatric Disorder Biology with Stem Cells
inferred← citeshttps://doi.org/10.1007/s11926-017-0671-7openalex-snapshot
Recent Advances in Tissue Engineering Strategies for the Treatment of Joint Damage
inferred← citeshttps://doi.org/10.1007/s12015-021-10254-3openalex-snapshot
Human iPSC-Derived Neural Models for Studying Alzheimer’s Disease: from Neural Stem Cells to Cerebral Organoids
inferred← citeshttps://doi.org/10.1007/s12015-023-10585-3openalex-snapshot
Recent Advances in CRISPR/Cas9 Delivery Approaches for Therapeutic Gene Editing of Stem Cells
inferred← citeshttps://doi.org/10.1007/s12015-023-10602-5openalex-snapshot
Using Ribonucleoprotein-based CRISPR/Cas9 to Edit Single Nucleotide on Human Induced Pluripotent Stem Cells to Model Type 3 Long QT Syndrome (SCN5A±)
inferred← citeshttps://doi.org/10.1007/s12015-026-11221-6openalex-snapshot
From Design to Single-Cell Cloning: A Complete RNP-Based CRISPR-Cas9 Protocol for Precision Gene Correction in Human iPSCs
inferred← citeshttps://doi.org/10.1007/s12033-019-00185-3openalex-snapshot
CRISPR–Cas9 System for Genome Engineering of Photosynthetic Microalgae
inferred← citeshttps://doi.org/10.1007/s12035-018-1123-8openalex-snapshot
Are Tanycytes the Missing Link Between Type 2 Diabetes and Alzheimer’s Disease?
inferred← citeshttps://doi.org/10.1007/s12035-019-01665-yopenalex-snapshot
Autophagy Induction by Bexarotene Promotes Mitophagy in Presenilin 1 Familial Alzheimer’s Disease iPSC-Derived Neural Stem Cells
inferred← citeshttps://doi.org/10.1007/s12041-025-01493-1openalex-snapshot
Generation of albino C57BL/6J mice by CRISPR embryo editing of the mouse tyrosinase locus
inferred← citeshttps://doi.org/10.1007/s12185-026-04251-wopenalex-snapshot
Gene editing of hematopoietic stem cells: applications and advances
inferred← citeshttps://doi.org/10.1007/s12272-020-01226-1openalex-snapshot
Role of RS-1 derivatives in homology-directed repair at the human genome ATG5 locus
inferred← citeshttps://doi.org/10.1007/s13205-021-03041-xopenalex-snapshot
Application of CRISPR–Cas9 in plant–plant growth-promoting rhizobacteria interactions for next Green Revolution
inferred← citeshttps://doi.org/10.1007/s13238-021-00838-7openalex-snapshot
Homology-based repair induced by CRISPR-Cas nucleases in mammalian embryo genome editing
inferred← citeshttps://doi.org/10.1007/s13238-021-00862-7openalex-snapshot
Precise genome editing without exogenous donor DNA via retron editing system in human cells
inferred← citeshttps://doi.org/10.1007/s13273-022-00256-8openalex-snapshot
CRISPR-Cas9-generated mouse model of neurofibromatosis type 1
inferred← citeshttps://doi.org/10.1007/s40120-020-00218-zopenalex-snapshot
CRISPR-Cas9: A Promising Genome Editing Therapeutic Tool for Alzheimer’s Disease—A Narrative Review
inferred← citeshttps://doi.org/10.1007/s42247-019-00049-1openalex-snapshot
Rich-color visual genotyping of single-nucleotide polymorphisms based on platinum nanoparticle–induced etching of gold nanorods
inferred← citeshttps://doi.org/10.1007/s42994-019-00009-7openalex-snapshot
Precise gene replacement in plants through CRISPR/Cas genome editing technology: current status and future perspectives
inferred← citeshttps://doi.org/10.1007/s42994-021-00051-4openalex-snapshot
Expanding the range of CRISPR/Cas9-directed genome editing in soybean
inferred← citeshttps://doi.org/10.1016/b978-0-12-809880-6.00005-9openalex-snapshot
Scarless Wound Healing
inferred← citeshttps://doi.org/10.1016/b978-0-12-813669-0.00009-9openalex-snapshot
Small RNA-mediated prevention, diagnosis and therapies of cancer
inferred← citeshttps://doi.org/10.1016/b978-0-12-816573-7.00002-xopenalex-snapshot
Disease in a Dish: Cellular Models to Understand Human Conditions
inferred← citeshttps://doi.org/10.1016/b978-0-12-817876-8.00002-4openalex-snapshot
Targeting Alzheimer’s disease and related dementias with CRISPR and human pluripotent stem cell technologies
inferred← citeshttps://doi.org/10.1016/b978-0-12-818084-6.00011-8openalex-snapshot
Gene editing and central nervous system regeneration
inferred← citeshttps://doi.org/10.1016/b978-0-12-818422-6.00095-2openalex-snapshot
Induced pluripotent stem cell technology: venturing into the second decade
inferred← citeshttps://doi.org/10.1016/b978-0-12-821044-4.00024-8openalex-snapshot
Genetically Engineered Animal Models in Toxicologic Research
inferred← citeshttps://doi.org/10.1016/b978-0-12-821477-0.00006-4openalex-snapshot
Corynebacterium glutamicum as a robust microbial factory for production of value-added proteins and small molecules: fundamentals and applications
inferred← citeshttps://doi.org/10.1016/b978-0-12-822003-0.00012-7openalex-snapshot
Autophagic processes in early- and late-onset Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/b978-0-12-822277-5.00016-xopenalex-snapshot
Advantages and limitations of hiPSC-derived neurons for the study of neurodegeneration
inferred← citeshttps://doi.org/10.1016/b978-0-323-85764-2.00008-9openalex-snapshot
Induced pluripotent stem cells for modeling of X-linked dystonia-parkinsonism
inferred← citeshttps://doi.org/10.1016/b978-0-323-85765-9.00008-4openalex-snapshot
Human induced pluripotent stem cell modeling of neurofibromatosis type 1
inferred← citeshttps://doi.org/10.1016/b978-0-323-85766-6.00007-3openalex-snapshot
Combining bioscaffolds and iPSCs in the treatment of neural trauma and Alzheimer’s disease
inferred← citeshttps://doi.org/10.1016/b978-0-323-85767-3.00007-4openalex-snapshot
The application of iPSC-derived kidney organoids and genome editing in kidney disease modeling
inferred← citeshttps://doi.org/10.1016/b978-0-323-85767-3.00009-8openalex-snapshot
Application of CRISPR/Cas system in iPSC-based disease model of hereditary deafness
inferred← citeshttps://doi.org/10.1016/b978-0-443-23841-3.00014-5openalex-snapshot
CRISPR/Cas9 gene editing: A new hope for Alzheimer's disease
inferred← citeshttps://doi.org/10.1016/b978-0-443-23841-3.00023-6openalex-snapshot
CRISPR/Cas9 gene editing: A new hope for Parkinson's disease
inferred← citeshttps://doi.org/10.1016/b978-0-443-27414-5.00002-6openalex-snapshot
Applying innovative genome editing technologies (e.g., CRISPR/Cas9 systems) in stem cell engineering and neurological disorders and diseases
inferred← citeshttps://doi.org/10.1016/b978-0-443-33877-9.00015-xopenalex-snapshot
Cellular models of chronic diseases: From bench to bedside
inferred← citeshttps://doi.org/10.1016/b978-0-443-43920-9.00010-5openalex-snapshot
CRISPR-edited plants for enhanced secondary metabolism: Methods and applications
inferred← citeshttps://doi.org/10.1016/bs.irn.2026.08.026openalex-snapshot
Novel therapies in Alzheimer’s disease
inferred← citeshttps://doi.org/10.1016/bs.mcb.2025.03.020openalex-snapshot
Mouse and human T cell Cas9-RNP/nucleofection-mediated gene-editing
inferred← citeshttps://doi.org/10.1016/bs.mie.2018.10.021openalex-snapshot
A pipeline for characterization of novel Cas9 orthologs
inferred← citeshttps://doi.org/10.1016/bs.mie.2018.10.028openalex-snapshot
Preparation and electroporation of Cas12a/Cpf1-guide RNA complexes for introducing large gene deletions in mouse embryonic stem cells
inferred← citeshttps://doi.org/10.1016/bs.mie.2025.01.003openalex-snapshot
Bacterial directed evolution of CRISPR base editors
inferred← citeshttps://doi.org/10.1016/bs.pmbts.2017.09.002openalex-snapshot
CRISPR/Cas9 Technology: Applications and Human Disease Modeling
inferred← citeshttps://doi.org/10.1016/bs.pmbts.2017.09.003openalex-snapshot
Dynamics of Indel Profiles Induced by Various CRISPR/Cas9 Delivery Methods
inferred← citeshttps://doi.org/10.1016/bs.pmbts.2021.01.018openalex-snapshot
CRISPR-Cas9 based genome editing for defective gene correction in humans and other mammals
inferred← citeshttps://doi.org/10.1016/j.ab.2017.03.016openalex-snapshot
Simple quantitative PCR analysis for allelic Pten loss in tumor progression
inferred← citeshttps://doi.org/10.1016/j.addr.2020.05.001openalex-snapshot
Advances in genome editing for genetic hearing loss
inferred← citeshttps://doi.org/10.1016/j.addr.2020.09.004openalex-snapshot
Non-viral strategies for delivering genome editing enzymes
inferred← citeshttps://doi.org/10.1016/j.addr.2024.115346openalex-snapshot
Exploring the potential of cell-derived vesicles for transient delivery of gene editing payloads
inferred← citeshttps://doi.org/10.1016/j.bbadis.2017.11.027openalex-snapshot
FTO demethylase activity is essential for normal bone growth and bone mineralization in mice
inferred← citeshttps://doi.org/10.1016/j.bioelechem.2020.107486openalex-snapshot
A low-cost smartphone controlled portable system with accurately confined on-chip 3D electrodes for flow-through cell electroporation
inferred← citeshttps://doi.org/10.1016/j.biopha.2023.115046openalex-snapshot
CRISPR-Cas12b enables a highly efficient attack on HIV proviral DNA in T cell cultures
inferred← citeshttps://doi.org/10.1016/j.biotechadv.2021.107737openalex-snapshot
Paving the way towards precise and safe CRISPR genome editing
inferred← citeshttps://doi.org/10.1016/j.brainres.2019.146458openalex-snapshot
Modeling cell-cell interactions in the brain using cerebral organoids
inferred← citeshttps://doi.org/10.1016/j.ceb.2016.10.001openalex-snapshot
CNS disease models with human pluripotent stem cells in the CRISPR age
inferred← citeshttps://doi.org/10.1016/j.cell.2016.10.044openalex-snapshot
CRISPR-Based Technologies for the Manipulation of Eukaryotic Genomes
inferred← citeshttps://doi.org/10.1016/j.cell.2017.01.002openalex-snapshot
Endogenous DNA Damage as a Source of Genomic Instability in Cancer
inferred← citeshttps://doi.org/10.1016/j.cell.2017.06.049openalex-snapshot
A Genetic Variant Associated with Five Vascular Diseases Is a Distal Regulator of Endothelin-1 Gene Expression
inferred← citeshttps://doi.org/10.1016/j.cell.2017.10.034openalex-snapshot
Precise Editing at DNA Replication Forks Enables Multiplex Genome Engineering in Eukaryotes
inferred← citeshttps://doi.org/10.1016/j.cell.2018.09.010openalex-snapshot
Stem Cells, Genome Editing, and the Path to Translational Medicine
inferred← citeshttps://doi.org/10.1016/j.cell.2020.02.020openalex-snapshot
Initiation of Parental Genome Reprogramming in Fertilized Oocyte by Splicing Kinase SRPK1-Catalyzed Protamine Phosphorylation
inferred← citeshttps://doi.org/10.1016/j.cell.2020.03.039openalex-snapshot
Pooled Knockin Targeting for Genome Engineering of Cellular Immunotherapies
inferred← citeshttps://doi.org/10.1016/j.cell.2020.05.037openalex-snapshot
Determinants of Base Editing Outcomes from Target Library Analysis and Machine Learning
inferred← citeshttps://doi.org/10.1016/j.cell.2021.04.035openalex-snapshot
Efficient embryonic homozygous gene conversion via RAD51-enhanced interhomolog repair
inferred← citeshttps://doi.org/10.1016/j.cell.2022.05.017openalex-snapshot
Cholesterol and matrisome pathways dysregulated in astrocytes and microglia
inferred← citeshttps://doi.org/10.1016/j.cell.2024.01.042openalex-snapshot
Past, present, and future of CRISPR genome editing technologies
inferred← citeshttps://doi.org/10.1016/j.cellin.2022.100067openalex-snapshot
Current advances of CRISPR-Cas technology in cell therapy
inferred← citeshttps://doi.org/10.1016/j.cellin.2024.100226openalex-snapshot
Precision epitope editing: A path to advanced immunotherapies
inferred← citeshttps://doi.org/10.1016/j.cellin.2026.100323openalex-snapshot
Capicua mediates interleukin-2 withdrawal–induced death of activated CD8+ T cells
inferred← citeshttps://doi.org/10.1016/j.celrep.2018.12.046openalex-snapshot
Base-Editing-Mediated R17H Substitution in Histone H3 Reveals Methylation-Dependent Regulation of Yap Signaling and Early Mouse Embryo Development
inferred← citeshttps://doi.org/10.1016/j.celrep.2019.06.038openalex-snapshot
In Vivo Single-Cell Genotyping of Mouse Cortical Neurons Transfected with CRISPR/Cas9
inferred← citeshttps://doi.org/10.1016/j.celrep.2020.107689openalex-snapshot
Detection of Deleterious On-Target Effects after HDR-Mediated CRISPR Editing
inferred← citeshttps://doi.org/10.1016/j.celrep.2021.109494openalex-snapshot
Optimized CRISPR-mediated gene knockin reveals FOXP3-independent maintenance of human Treg identity
inferred← citeshttps://doi.org/10.1016/j.celrep.2022.111775openalex-snapshot
Human iPSC-hepatocyte modeling of alpha-1 antitrypsin heterozygosity reveals metabolic dysregulation and cellular heterogeneity
inferred← citeshttps://doi.org/10.1016/j.celrep.2025.115777openalex-snapshot
Astrocyte induction of disease-associated microglia is suppressed by acute exposure to fAD neurons in human iPSC triple cultures
inferred← citeshttps://doi.org/10.1016/j.coisb.2017.08.002openalex-snapshot
Mapping a diversity of genetic interactions in yeast
inferred← citeshttps://doi.org/10.1016/j.conb.2020.01.008openalex-snapshot
Neurodegeneration in a dish: advancing human stem-cell-based models of Alzheimer’s disease
inferred← citeshttps://doi.org/10.1016/j.copbio.2022.102724openalex-snapshot
New synthetic biology tools for metabolic control
inferred← citeshttps://doi.org/10.1016/j.cpb.2025.100540openalex-snapshot
Gene editing tools promote the development of chloroplast gene engineering
inferred← citeshttps://doi.org/10.1016/j.cr.2019.08.001openalex-snapshot
Methods and applications of CRISPR/Cas system for genome editing in stem cells
inferred← citeshttps://doi.org/10.1016/j.crmeth.2022.100389openalex-snapshot
Precise and heritable gene targeting in rice using a sequential transformation strategy
inferred← citeshttps://doi.org/10.1016/j.crmeth.2022.100393openalex-snapshot
Highly selective transgene expression through the flip-excision switch system by using a unilateral spacer sequence
inferred← citeshttps://doi.org/10.1016/j.crphys.2023.100101openalex-snapshot
Precise CRISPR-Cas9-mediated mutation of a membrane trafficking domain in the Drosophila vesicular monoamine transporter gene
inferred← citeshttps://doi.org/10.1016/j.csbj.2022.03.031openalex-snapshot
The use of base editing technology to characterize single nucleotide variants
inferred← citeshttps://doi.org/10.1016/j.ddtec.2016.09.007openalex-snapshot
Endonuclease mediated genome editing in drug discovery and development: promises and challenges
inferred← citeshttps://doi.org/10.1016/j.ddtec.2018.02.001openalex-snapshot
Developing precision medicine using scarless genome editing of human pluripotent stem cells
inferred← citeshttps://doi.org/10.1016/j.ddtec.2018.06.002openalex-snapshot
CRISPR/Cas9-mediated genome editing in human stem cell-derived cardiomyocytes: Applications for cardiovascular disease modelling and cardiotoxicity screening
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