Publications by authors named "Tomoki Togashi"

Claim this Profile
T
Therapeutic base editing to generate a gain-of-function F9 variant for hemophilia B.
Nemekhbayar Baatartsogt, Yuji Kashiwakura, Takafumi Hiramoto, Rina Ito, Rikako Sato, Tomoki Togashi

Blood· October 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mechanism of antithrombin deficiency due to the novel variant C32W in the C-terminus of the signal peptide.
Yuika Kikuchi, Satomi Nagaya, Tomoki Togashi, Yuta Imai, Maki Togashi

Int J Hematol· July 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The novel protein C variant p.C101F results in early intracellular degradation that drives type I protein C deficiency.
Rikuto Yui, Satomi Nagaya, Ibuki Yasuda, Tomoki Togashi, Yuika Kikuchi

Int J Hematol· June 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Cure of Congenital Purpura Fulminans via Expression of Engineered Protein C Through Neonatal Genome Editing in Mice.
Tomoki Togashi, Nemekhbayar Baatartsogt, Yasumitsu Nagao, Yuji Kashiwakura, Morisada Hayakawa

Arterioscler Thromb Vasc Biol· December 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Identification of two de novo variants causing inherited antithrombin deficiency by quantitative analysis of variant alleles.
Tomoki Togashi, Satomi Nagaya, Makiko Meguro-Horike, Haruto Matsumoto, Yuta Imai

Thromb Res· January 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
Functional analysis of two abnormal antithrombin proteins with different intracellular kinetics.
Yuta Imai, Satomi Nagaya, Yuhei Araiso, Makiko Meguro-Horike, Tomoki Togashi

Thromb Res· October 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
An AsCas12f-based compact genome-editing tool derived by deep mutational scanning and structural analysis.
Tomohiro Hino, Satoshi N Omura, Ryoya Nakagawa, Tomoki Togashi, Satoru N Takeda

Cell· October 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Protein S deficiency caused by cryptic splicing due to the novel intron variant c.346+5G>C in PROS1.
Satomi Nagaya, Tomoki Togashi, Masaharu Akiyama, Yuta Imai, Haruto Matsumoto

Thromb Res· September 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Identification and functional analysis of three novel genetic variants resulting in premature termination codons in three unrelated patients with hereditary antithrombin deficiency.
Yuta Imai, Satomi Nagaya, Yuhei Araiso, Makiko Meguro-Horike, Tomoki Togashi

Int J Hematol· April 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Molecular genetic analysis of inherited protein C deficiency caused by the novel large deletion across two exons of PROC.
Tomoki Togashi, Makiko Meguro-Horike, Satomi Nagaya, Sayaka Sugihara, Tatsuo Ichinohe

Thromb Res· April 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
G
Genetic analysis of a compound heterozygous patient with congenital factor X deficiency and regular replacement therapy with a prothrombin complex concentrate.
Tomoki Togashi, Satomi Nagaya, Masayuki Nagasawa, Makiko Meguro-Horike, Keiji Nogami

Int J Hematol· January 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis