Taiki Abe

Sendai, 9808574, Japan

Last Updated: 09/26/2026

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Found 22 publications

Elaidic acid drives cellular senescence and inflammation via lipid raft-mediated IL-1R signaling.

Elaidic acid drives cellular senescence and inflammation via lipid raft-mediated IL-1R signaling.

Journal: iScience
Published: December 09, 2024

Phenotypic Analysis of Embryos in a Noonan Syndrome Model Mouse With the Rit1 A57G Mutation.

Phenotypic Analysis of Embryos in a Noonan Syndrome Model Mouse With the Rit1 A57G Mutation.

Journal: Molecular genetics & genomic medicine
Published: November 23, 2024

Missense and truncated variants in ERF in individuals with a Noonan-like phenotype without craniosynostosis.

Missense and truncated variants in ERF in individuals with a Noonan-like phenotype without craniosynostosis.

Journal: Scientific reports
Published: September 29, 2024

Dysregulation of RAS proteostasis by autosomal-dominant LZTR1 mutation induces Noonan syndrome-like phenotypes in mice.

Dysregulation of RAS proteostasis by autosomal-dominant LZTR1 mutation induces Noonan syndrome-like phenotypes in mice.

Journal: JCI insight
Published: April 26, 2024

Lymphatic endothelial cell-specific NRAS p.Q61R mutant embryos show abnormal lymphatic vessel morphogenesis.

Lymphatic endothelial cell-specific NRAS p.Q61R mutant embryos show abnormal lymphatic vessel morphogenesis.

Journal: Human molecular genetics
Published: January 28, 2024

LZTR1 deficiency exerts high metastatic potential by enhancing sensitivity to EMT induction and controlling KLHL12-mediated collagen secretion.

LZTR1 deficiency exerts high metastatic potential by enhancing sensitivity to EMT induction and controlling KLHL12-mediated collagen secretion.

Journal: Cell death & disease
Published: February 14, 2023

Mecom mutation related to radioulnar synostosis with amegakaryocytic thrombocytopenia reduces HSPCs in mice.

Mecom mutation related to radioulnar synostosis with amegakaryocytic thrombocytopenia reduces HSPCs in mice.

Journal: Blood advances
Published: June 29, 2022

Duplications in the G3 domain or switch II region in HRAS identified in patients with Costello syndrome.

Duplications in the G3 domain or switch II region in HRAS identified in patients with Costello syndrome.

Journal: Human mutation
Published: April 29, 2021

Prepulse inhibition predicts subjective hearing in rats.

Prepulse inhibition predicts subjective hearing in rats.

Journal: Scientific reports
Published: April 23, 2021

Chronic Hypercapnic Respiratory Failure in an Adult Patient with Silver-Russell Syndrome.

Chronic Hypercapnic Respiratory Failure in an Adult Patient with Silver-Russell Syndrome.

Journal: Internal medicine (Tokyo, Japan)
Published: February 01, 2021

Phenotypic heterogeneity in individuals with MECOM variants in 2 families.

Phenotypic heterogeneity in individuals with MECOM variants in 2 families.

Journal: Blood advances
Published: November 23, 2020

PXR Functionally Interacts with NF-κB and AP-1 to Downregulate the Inflammation-Induced Expression of Chemokine CXCL2 in Mice.

PXR Functionally Interacts with NF-κB and AP-1 to Downregulate the Inflammation-Induced Expression of Chemokine CXCL2 in Mice.

Journal: Cells
Published: August 21, 2020
Showing 1-12 of 22

Last Updated: 09/26/2026