Pointing fingers at the limiting step in gene targeting

Insulin facilitates entry of calcium ions into human and murine erythrocytes via Piezo1: a newly identified mechanism with implications for type 2 diabetes.

The FEBS journal·2025

Utilization of Prognosis Assignment: A Cross-Sectional Survey of Military Periodontists.

Military medicine·2024

Subcellular localization of mutant P23H rhodopsin in an RFP fusion knock-in mouse model of retinitis pigmentosa.

Disease models & mechanisms·2022

Histone deacetylase knockouts modify transcription, CAG instability and nuclear pathology in Huntington disease mice.

eLife·2020

Soy Protein Nanofiber Scaffolds for Uniform Maturation of Human Induced Pluripotent Stem Cell-Derived Retinal Pigment Epithelium.

Tissue engineering. Part C, Methods·2020

Esthetic Management of a Recurrent Peripheral Ossifying Fibroma.

Clinical advances in periodontics·2019

Characterization of microbial dark matter at scale with MetaSBT and taxonomy-aware Sequence Bloom Trees.

Nature biotechnology·2026

Proteome-wide identification of the druggable CRBN interactome.

Nature biotechnology·2026

Discovery and design of potent cell surface display elements.

Nature biotechnology·2026

Mechanistic machine learning for prediction of prime editing outcomes.

Nature biotechnology·2026

Simultaneous single-cell profiling of chromatin, transcriptome and surface markers with OneCell CUT&Tag captures epigenomic reprogramming.

Nature biotechnology·2026

Non-invasive nanoparticle barcoding in nonhuman primates.

Nature biotechnology·2026

Integrated genetic identification and molecular dynamics simulations in a novel LOXL3 genetic mutation associated with Stickler syndrome.

Frontiers in genetics·2026

The ZBTB16/CUL3/ROC1 ubiquitin ligase drives the degradation of pathogenic pendrin (SLC26A4) protein variants.

Journal of biomedical science·2026

Identification and functional characterization of a SUZ12 frameshift variant in a Chinese family with Imagawa-Matsumoto syndrome.

BMC medical genomics·2026

The first 25 years of the NICHD Structural Birth Defects Initiative.

Developmental biology·2026

Neurovascular Involvement in Arterial Tortuosity Syndrome Associated with a Homozygous SLC2A10 p.(Trp162Ter) Variant: Clinical, Molecular, and In Silico Characterization.

International journal of molecular sciences·2026

NAM-BSA: A Bulked Segregant Analysis Method Using a NAM Population.

Plants (Basel, Switzerland)·2026

Related Experiment Videos

Pointing fingers at the limiting step in gene targeting

Related Concept Videos

Insulin facilitates entry of calcium ions into human and murine erythrocytes via Piezo1: a newly identified mechanism with implications for type 2 diabetes.

Utilization of Prognosis Assignment: A Cross-Sectional Survey of Military Periodontists.

Subcellular localization of mutant P23H rhodopsin in an RFP fusion knock-in mouse model of retinitis pigmentosa.

Histone deacetylase knockouts modify transcription, CAG instability and nuclear pathology in Huntington disease mice.

Soy Protein Nanofiber Scaffolds for Uniform Maturation of Human Induced Pluripotent Stem Cell-Derived Retinal Pigment Epithelium.

Esthetic Management of a Recurrent Peripheral Ossifying Fibroma.

Characterization of microbial dark matter at scale with MetaSBT and taxonomy-aware Sequence Bloom Trees.

Proteome-wide identification of the druggable CRBN interactome.

Discovery and design of potent cell surface display elements.

Mechanistic machine learning for prediction of prime editing outcomes.

Simultaneous single-cell profiling of chromatin, transcriptome and surface markers with OneCell CUT&Tag captures epigenomic reprogramming.

Non-invasive nanoparticle barcoding in nonhuman primates.

Integrated genetic identification and molecular dynamics simulations in a novel LOXL3 genetic mutation associated with Stickler syndrome.

The ZBTB16/CUL3/ROC1 ubiquitin ligase drives the degradation of pathogenic pendrin (SLC26A4) protein variants.

Identification and functional characterization of a SUZ12 frameshift variant in a Chinese family with Imagawa-Matsumoto syndrome.

The first 25 years of the NICHD Structural Birth Defects Initiative.

Neurovascular Involvement in Arterial Tortuosity Syndrome Associated with a Homozygous SLC2A10 p.(Trp162Ter) Variant: Clinical, Molecular, and In Silico Characterization.

NAM-BSA: A Bulked Segregant Analysis Method Using a NAM Population.

Related Experiment Videos

Pointing fingers at the limiting step in gene targeting

Related Concept Videos

Related Articles