Masahiro Yoda
Nagano, Japan
Last Updated: 09/26/2026
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Found 13 publications
Ribosome-engineered Lacticaseibacillus rhamnosus GG with enhanced adhesion and immune activation via surface moonlighting proteins.
Journal: Microbiology spectrum
Published: October 27, 2025
Construction of genetically modified lactic acid bacteria producing an Anti-Interleukin-31 receptor A Single-chain variable fragment.
Journal: Molecular biology reports
Published: August 11, 2025
Genetically Modified Lactococcus lactis Hypersecreting IL-1Ra Improves Glucose Metabolism and Modulates the Gut Microbiota in an Obese Mouse Model.
Journal: Journal of diabetes research
Published: August 08, 2025
Development of a Genetically Modified Lactococcus lactis Strain that Produces a Single-Chain Variable Fragment Targeting Interleukin-6 Receptor α to Suppress Serum Amyloid A.
Journal: Current microbiology
Published: June 09, 2025
Development of engineered IL-36γ-hypersecreting Lactococcus lactis to improve the intestinal environment.
Journal: World journal of microbiology & biotechnology
Published: July 31, 2024
A novel variant fibrinogen, AαE11del, demonstrating the importance of AαE11 residue in thrombin binding.
Journal: International journal of hematology
Published: June 14, 2021
Automated screening procedure for the phenotypes of congenital fibrinogen disorders using novel parameters, |min1|c and Ac/|min1|c, obtained from clot waveform analysis using the Clauss method.
Journal: Clinica chimica acta; international journal of clinical chemistry
Published: June 07, 2021
Novel variant fibrinogen γp.C352R produced hypodysfibrinogenemia leading to a bleeding episode and failure of infertility treatment.
Journal: International journal of hematology
Published: April 14, 2021
Recombinant γY278H Fibrinogen Showed Normal Secretion from CHO Cells, but a Corresponding Heterozygous Patient Showed Hypofibrinogenemia.
Journal: International journal of molecular sciences
Published: April 12, 2021
A Novel Amino Acid Substitution, Fibrinogen Bβp.Pro234Leu, Associated with Hypofibrinogenemia Causing Impairment of Fibrinogen Assembly and Secretion.
Journal: International journal of molecular sciences
Published: November 27, 2020
Congenital fibrinogen disorder with a compound heterozygote possessing two novel FGB mutations, one qualitative and the other quantitative.
Journal: Thrombosis research
Published: June 04, 2020
Comparison of molecular structure and fibrin polymerization between two Bβ-chain N-terminal region fibrinogen variants, Bβp.G45C and Bβp.R74C.
Journal: International journal of hematology
Published: April 16, 2020
Last Updated: 09/26/2026