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Generation of knock-in primary human T cells using Cas9 ribonucleoproteins

Proceedings of the National Academy of Sciences - PNAS, 2015-08, Vol.112 (33), p.10437-10442

2015

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The Loss of Profilin 1 Causes Early Onset Paget's Disease of Bone

Journal of bone and mineral research, 2020-08, Vol.35 (8), p.1387-1398

2020

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Engineered Staphylococcus auricularis Cas9 with high‐fidelity

The FASEB journal, 2023-08, Vol.37 (8), p.e23060-n/a

2023

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NanoBiT‐ and NanoBiT/BRET‐based assays allow the analysis of binding kinetics of Wnt‐3a to endogenous Frizzled 7 in a colorectal cancer model

British journal of pharmacology, 2024-10, Vol.181 (20), p.3819-3835

2024

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MicroRNA

Journal of allergy and clinical immunology, 2018-04, Vol.141 (4), p.1202-1207

2018

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Multiple genetic variants at the SLC30A8 locus affect local super‐enhancer activity and influence pancreatic β‐cell survival and function

The FASEB journal, 2024-04, Vol.38 (8), p.e23610-n/a

2024

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Society for Maternal-Fetal Medicine Special Statement: Beyond the scalpel: in utero fetal gene therapy and curative medicine

American journal of obstetrics and gynecology, 2021-12, Vol.225 (6), p.B9-B18

2021

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Novel RPL13 Variants and Variable Clinical Expressivity in a Human Ribosomopathy With Spondyloepimetaphyseal Dysplasia

Journal of bone and mineral research, 2021-02, Vol.36 (2), p.283-297

2021

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Frequent loss of heterozygosity in CRISPR-Cas9–edited early human embryos

Proceedings of the National Academy of Sciences - PNAS, 2021-06, Vol.118 (22), p.1-9

2021

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Nonviral gene editing via CRISPR/Cas9 delivery by membrane-disruptive and endosomolytic helical polypeptide

Proceedings of the National Academy of Sciences - PNAS, 2018-05, Vol.115 (19), p.4903-4908

2018

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Single-cell RNA-seq reveals novel regulators of human embryonic stem cell differentiation to definitive endoderm

Genome Biology, 2016-08, Vol.17 (1), p.173-173, Article 173

2016

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Identification of CYP46A1 as a new regulator of lipid metabolism through CRISPR‐based whole‐genome screening

The FASEB journal, 2020-10, Vol.34 (10), p.13776-13791

2020

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A scalable strategy for high-throughput GFP tagging of endogenous human proteins

Proceedings of the National Academy of Sciences - PNAS, 2016-06, Vol.113 (25), p.E3501-E3508

2016

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Efficient delivery of genome-editing proteins using bioreducible lipid nanoparticles

Proceedings of the National Academy of Sciences - PNAS, 2016-03, Vol.113 (11), p.2868-2873

2016

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RNA-directed gene editing specifically eradicates latent and prevents new HIV-1 infection

Proceedings of the National Academy of Sciences - PNAS, 2014-08, Vol.111 (31), p.11461-11466

2014

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CASFISH: CRISPR/Cas9-mediated in situ labeling of genomic loci in fixed cells

Proceedings of the National Academy of Sciences - PNAS, 2015-09, Vol.112 (38), p.11870-11875

2015

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CRISPR-Cas9 off-targeting assessment with nucleic acid duplex energy parameters

Genome Biology, 2018-10, Vol.19 (1), p.177-177, Article 177

2018

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Generation of Knock-out Primary and Expanded Human NK Cells Using Cas9 Ribonucleoproteins

Journal of visualized experiments, 2018-06 (136)

2018

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Cas9-mediated targeting of viral RNA in eukaryotic cells

Proceedings of the National Academy of Sciences - PNAS, 2015-05, Vol.112 (19), p.6164-6169

2015

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Patient-iPSC-Derived Kidney Organoids Show Functional Validation of a Ciliopathic Renal Phenotype and Reveal Underlying Pathogenetic Mechanisms

American journal of human genetics, 2018-05, Vol.102 (5), p.816-831

2018

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Live‐cell screening platform using human‐induced pluripotent stem cells expressing fluorescence‐tagged cytochrome P450 1A1

The FASEB journal, 2020-07, Vol.34 (7), p.9141-9155

2020

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Depletion of Abundant Sequences by Hybridization (DASH): using Cas9 to remove unwanted high-abundance species in sequencing libraries and molecular counting applications

Genome Biology, 2016-03, Vol.17 (1), p.41-41, Article 41

2016

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A CRISPR view of development

Genes & development, 2014-09, Vol.28 (17), p.1859-1872

2014

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Siglec-9 is an inhibitory receptor on human mast cells in vitro

Journal of allergy and clinical immunology, 2023-09, Vol.152 (3), p.711-724.e14

2023

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Acceleration of cancer science with genome editing and related technologies

Cancer science, 2018-12, Vol.109 (12), p.3679-3685

2018

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Generation of knock-in primary human T cells using Cas9 ribonucleoproteins

The Loss of Profilin 1 Causes Early Onset Paget's Disease of Bone

Engineered Staphylococcus auricularis Cas9 with high‐fidelity

NanoBiT‐ and NanoBiT/BRET‐based assays allow the analysis of binding kinetics of Wnt‐3a to endogenous Frizzled 7 in a colorectal cancer model

MicroRNA

Multiple genetic variants at the SLC30A8 locus affect local super‐enhancer activity and influence pancreatic β‐cell survival and function

Society for Maternal-Fetal Medicine Special Statement: Beyond the scalpel: in utero fetal gene therapy and curative medicine

Novel RPL13 Variants and Variable Clinical Expressivity in a Human Ribosomopathy With Spondyloepimetaphyseal Dysplasia

Frequent loss of heterozygosity in CRISPR-Cas9–edited early human embryos

Nonviral gene editing via CRISPR/Cas9 delivery by membrane-disruptive and endosomolytic helical polypeptide

Single-cell RNA-seq reveals novel regulators of human embryonic stem cell differentiation to definitive endoderm

Identification of CYP46A1 as a new regulator of lipid metabolism through CRISPR‐based whole‐genome screening

A scalable strategy for high-throughput GFP tagging of endogenous human proteins

Efficient delivery of genome-editing proteins using bioreducible lipid nanoparticles

RNA-directed gene editing specifically eradicates latent and prevents new HIV-1 infection

CASFISH: CRISPR/Cas9-mediated in situ labeling of genomic loci in fixed cells

CRISPR-Cas9 off-targeting assessment with nucleic acid duplex energy parameters

Generation of Knock-out Primary and Expanded Human NK Cells Using Cas9 Ribonucleoproteins

Cas9-mediated targeting of viral RNA in eukaryotic cells

Patient-iPSC-Derived Kidney Organoids Show Functional Validation of a Ciliopathic Renal Phenotype and Reveal Underlying Pathogenetic Mechanisms

Live‐cell screening platform using human‐induced pluripotent stem cells expressing fluorescence‐tagged cytochrome P450 1A1

Depletion of Abundant Sequences by Hybridization (DASH): using Cas9 to remove unwanted high-abundance species in sequencing libraries and molecular counting applications

A CRISPR view of development

Siglec-9 is an inhibitory receptor on human mast cells in vitro

Acceleration of cancer science with genome editing and related technologies

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