Jiahai Shi

16 Medical Drive
Singapore, Singapore

Last Updated: 09/26/2026

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Found 56 publications

Engineering red cells across scales: Red Blood Cells (RBCs) and RBC-derived extracellular vesicles.

Engineering red cells across scales: Red Blood Cells (RBCs) and RBC-derived extracellular vesicles.

Journal: Current opinion in biotechnology

Published: April 01, 2026

Recessive variants in WSB2 encoding a substrate receptor of E3 ubiquitin ligase underlie a neurodevelopmental syndrome.

Recessive variants in WSB2 encoding a substrate receptor of E3 ubiquitin ligase underlie a neurodevelopmental syndrome.

Journal: European journal of human genetics : EJHG

Published: November 20, 2024

The solute carrier family 26 member 9 modifies rapidly progressing cystic fibrosis associated with homozygous F508del CFTR mutation.

The solute carrier family 26 member 9 modifies rapidly progressing cystic fibrosis associated with homozygous F508del CFTR mutation.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: March 26, 2024

Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsy.

Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsy.

Journal: American journal of human genetics

Published: March 03, 2023

De Novo Designed Self-Assembling Rhodamine Probe for Real-Time, Long-Term and Quantitative Live-Cell Nanoscopy.

De Novo Designed Self-Assembling Rhodamine Probe for Real-Time, Long-Term and Quantitative Live-Cell Nanoscopy.

Journal: ACS nano

Published: February 06, 2023

De novo missense variants in phosphatidylinositol kinase PIP5KIγ underlie a neurodevelopmental syndrome associated with altered phosphoinositide signaling.

De novo missense variants in phosphatidylinositol kinase PIP5KIγ underlie a neurodevelopmental syndrome associated with altered phosphoinositide signaling.

Journal: American journal of human genetics

Published: January 24, 2023

Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsy.

Rare EIF4A2 variants are associated with a neurodevelopmental disorder characterized by intellectual disability, hypotonia, and epilepsy.

Journal: American journal of human genetics

Published: April 15, 2022

Enhancing Circulation and Tumor Accumulation of Carboplatin via an Erythrocyte-Anchored Prodrug Strategy.

Enhancing Circulation and Tumor Accumulation of Carboplatin via an Erythrocyte-Anchored Prodrug Strategy.

Journal: Angewandte Chemie (International ed. in English)

Published: March 14, 2022

An RNA G-Quadruplex Structure within the ADAR 5'UTR Interacts with DHX36 Helicase to Regulate Translation.

An RNA G-Quadruplex Structure within the ADAR 5'UTR Interacts with DHX36 Helicase to Regulate Translation.

Journal: Angewandte Chemie (International ed. in English)

Published: March 08, 2022

Grab regulates transferrin receptor recycling and iron uptake in developing erythroblasts.

Grab regulates transferrin receptor recycling and iron uptake in developing erythroblasts.

Journal: Blood

Published: December 16, 2021

Surface-engineered extracellular vesicles for targeted delivery of therapeutic RNAs and peptides for cancer therapy.

Surface-engineered extracellular vesicles for targeted delivery of therapeutic RNAs and peptides for cancer therapy.

Journal: Theranostics

Published: November 02, 2021

Reanalysis of Exome Data Identifies Novel SLC25A46 Variants Associated with Leigh Syndrome.

Reanalysis of Exome Data Identifies Novel SLC25A46 Variants Associated with Leigh Syndrome.

Journal: Journal of personalized medicine

Published: October 26, 2021

Showing 1-12 of 56

Last Updated: 09/26/2026