Author

S. Wada

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Biochemistry· 2 Microbiology· 2 Physiology· 2 Bioengineering· 1 Cell Biology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 7 Research Focus:cell type annotation· 3 Organism:mouse· 3 Research Focus:host-pathogen & immune response· 2 Assay:proteomics· 2 Organism:rat· 2 Assay:bulk RNA-seq· 1 Organism:C. elegans· 1

Frequent Co-Authors

C. L. Mendias· 2 shared J. B. Swanson· 2 shared S. A. Rodeo· 2 shared A. C. Konja· 1 shared A. C. Noah· 1 shared A. N. Piacentini· 1 shared A. Okamoto· 1 shared A. Shimoda· 1 shared

Activity by Year

2016-2024 · peak 3/yr

Co-Author Collaboration Network

10 top collaborators · 14 mutual co-author links

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2 shared papersPhysiology

C. L. Mendias

Mutual co-authors in cluster

Author profile →

8 papers

Recent·Most cited

Fetal Kidney Transplantation for In Utero Fetuses

K. Morimoto, S. Yamanaka, K. Matsui, Y. Kinoshita, Y. Inage, S. Yamamoto, N. Koda, N. Matsumoto, Y. Saito, T. Takamura, T. Fujimoto, S. Fukunaga, S. Tajiri, K. Matsumoto, K. Ozawa, , T. Yokoo

This paper describes a novel fetal therapy approach using transplanted fetal kidneys from different species to provide a bridge to dialysis in affected fetuses, demonstrating successful urine production and long-term function without immunosuppressants.

bioRxiv · Apr 15, 2024 · PreprintBioengineering

A case of mycobacteriosis associated with Mycobacterium pseudoshottsii in aquarium-reared fish in Japan

T. Komine, I. Hyogo, O. Kentaro, M. Yoshida, Y. Sugimoto, M. Inohana, H. Fukano, O. Kurata, S. Wada

The paper reports the first isolation of Mycobacterium pseudoshottsii from aquarium-reared fish in Japan, identified through microbiological and genetic analyses.

bioRxiv · Jul 14, 2022Microbiology

Classification of Extracellular Vesicles based on Surface Glycan Structures by Spongy-like Separation Media

E. Kanao, S. Wada, H. Nishida, T. Kubo, T. Tanigawa, K. Imami, A. Shimoda, K. Umezaki, Y. Sasaki, K. Akiyoshi, J. Adachi, K. Otsuka, Y. Ishihama

This paper introduces a novel lectin-based affinity chromatography method using spongy monoliths to classify extracellular vesicles based on surface glycan structures and demonstrates subpopulations through proteome profiling.

bioRxiv · May 10, 2022Biochemistry

High-performance GPCR optogenetics based on molecular properties of animal opsins, MosOpn3 and LamPP

M. Koyanagi, B. Shen, T. Nagata, L. Sun, S. Wada, S. Kamimura, E. Kage-Nakadai, A. Terakita

This study evaluates two animal opsins, MosOpn3 and LamPP, for GPCR optogenetics in C. elegans, showing high sensitivity and color-dependent behavioral control.

bioRxiv · Feb 7, 2022 · PreprintBiochemistry

Adaptive and Innate Immune Cell Responses in Tendons and Lymph Nodes After Tendon Injury and Repair

A. C. Noah, T. M. Li, L. M. Martinez, S. Wada, J. B. Swanson, N. P. Disser, K. B. Sugg, S. A. Rodeo, T. T. Lu, C. L. Mendias

This study investigates adaptive and innate immune cell responses in tendons and lymph nodes after tendon injury, finding a coordinated adaptive immune response that may regulate healing.

bioRxiv · Oct 2, 2019Physiology

The MRL/MpJ Mouse Strain Is Not Protected From Muscle Atrophy And Weakness After Rotator Cuff Tear

J. R. Talarek, A. N. Piacentini, A. C. Konja, S. Wada, J. B. Swanson, S. C. Nussenzweig, J. S. Dines, S. A. Rodeo, C. L. Mendias

This study shows that MRL/MpJ mice, previously thought to be protected from muscle atrophy after rotator cuff tear, actually experience similar force loss and pathological changes as C57Bl/6 mice.

bioRxiv · Jul 14, 2019Physiology

CAT1/SLC7A1 acts as a cellular receptor for bovine leukemia virus infection

L. Bai, H. Sato, Y. Kubo, S. Wada, Y. Aida

This paper identifies CAT1/SLC7A1 as the cellular receptor for bovine leukemia virus (BLV) infection, showing it mediates viral entry and is essential for BLV susceptibility across species.

bioRxiv · Jun 10, 2019Microbiology

Fetal therapy model of myelomeningocele with three-dimensional skin using amniotic fluid cell-derived induced pluripotent stem cells

K. Kajiwara, T. Tanemoto, S. Wada, J. Karibe, N. Ihara, Y. Ikemoto, T. Kawasaki, Y. Ohishi, O. Samura, K. Okamura, S. Takada, H. Akutsu, H. Sago, A. Okamoto, A. UMEZAWA

This study uses iPSC-derived artificial skin to treat a rat model of myelomeningocele during pregnancy, showing potential for antenatal therapy.

bioRxiv · Dec 19, 2016Cell Biology