Toru Sengoku

Yokohama, Japan

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 26 publications

De Novo Discovery of Nonstandard Thioisoindole-Bridged Bicyclic Peptides Targeting Traf2- and NCK-Interacting Kinase.

De Novo Discovery of Nonstandard Thioisoindole-Bridged Bicyclic Peptides Targeting Traf2- and NCK-Interacting Kinase.

Journal: Angewandte Chemie (International ed. in English)

Published: January 20, 2026

De novo GNAS-Gsα variant (p.Thr55Ala) with constitutive gain-of-function effects on AVPR2 and PTH1R signalings.

De novo GNAS-Gsα variant (p.Thr55Ala) with constitutive gain-of-function effects on AVPR2 and PTH1R signalings.

Journal: Journal of human genetics

Published: August 25, 2025

Structural insights into inhibition mechanism of the helicase-primase complex from human herpesvirus 1.

Structural insights into inhibition mechanism of the helicase-primase complex from human herpesvirus 1.

Journal: Cell chemical biology

Published: June 19, 2025

Germline-derived GNAS-Gsα variants associated with both gain-of-function and loss-of-function phenotypes.

Germline-derived GNAS-Gsα variants associated with both gain-of-function and loss-of-function phenotypes.

Journal: European journal of endocrinology

Published: December 06, 2024

Clinical and genetic spectrum of patients with IRF2BPL syndrome.

Clinical and genetic spectrum of patients with IRF2BPL syndrome.

Journal: Journal of human genetics

Published: August 08, 2024

De Novo Discovery of Pseudo-Natural Prenylated Macrocyclic Peptide Ligands.

De Novo Discovery of Pseudo-Natural Prenylated Macrocyclic Peptide Ligands.

Journal: Angewandte Chemie (International ed. in English)

Published: May 27, 2024

Genetic and functional diversity of β-N-acetylgalactosamine-targeting glycosidases expanded by deep-sea metagenome analysis.

Genetic and functional diversity of β-N-acetylgalactosamine-targeting glycosidases expanded by deep-sea metagenome analysis.

Journal: Nature communications

Published: August 23, 2023

Structure of the human Bre1 complex bound to the nucleosome.

Structure of the human Bre1 complex bound to the nucleosome.

Journal: Nature communications

Published: June 07, 2023

Biallelic structural variations within FGF12 detected by long-read sequencing in epilepsy.

Biallelic structural variations within FGF12 detected by long-read sequencing in epilepsy.

Journal: Life science alliance

Published: March 06, 2023

Brain monoamine vesicular transport disease caused by homozygous SLC18A2 variants: A study in 42 affected individuals.

Brain monoamine vesicular transport disease caused by homozygous SLC18A2 variants: A study in 42 affected individuals.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: April 07, 2022

Structural basis of transcription regulation by CNC family transcription factor, Nrf2.

Structural basis of transcription regulation by CNC family transcription factor, Nrf2.

Journal: Nucleic acids research

Published: October 26, 2021

Pathogenic variants in the survival of motor neurons complex gene GEMIN5 cause cerebellar atrophy.

Pathogenic variants in the survival of motor neurons complex gene GEMIN5 cause cerebellar atrophy.

Journal: Clinical genetics

Published: June 07, 2021

Showing 1-12 of 26

Last Updated: 09/26/2026