70,867 results match your criteria: "Fukuoka University; 8-19-1 Nanakuma[Affiliation]"
Intern Med
December 2024
Department of Cardiovascular Medicine, St. Luke's International Hospital, Japan.
Magn Reson Med Sci
December 2024
Advanced Imaging Research Center, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Eur J Obstet Gynecol Reprod Biol
February 2025
Medical Information Center, Kyushu University Hospital, Fukuoka City, Japan. Electronic address:
Expert Rev Clin Pharmacol
December 2024
Department of Post-Infectious Diseases Therapeutics, Graduate School of Medicine, Osaka University, Suita, Japan.
J Urol
December 2024
Department of Urology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Circ Res
January 2025
Department of Health Development and Medicine (S.Y., H.H., J.S., S.B., H.N.), Osaka University Graduate School of Medicine, Japan.
Eng Microbiol
June 2024
Department of Bioscience and Biotechnology, Graduate school of Bioresource and Bioenvironmental Sciences, Kyushu University, Fukuoka 819-0395, Japan.
Geroscience
December 2024
Center for Liberal Arts, Fukuoka Institute of Technology, 3-30-1 Wajiro-Higashi, Higashi-Ku, Fukuoka, 811-0295, Japan.
Sci Rep
December 2024
Laboratory of Drug Informatics, Gifu Pharmaceutical University, 1-25-4, Daigaku-nishi, Gifu, 501-1196, Japan.
Sci Rep
December 2024
School of Chemical Engineering, Yeungnam University, Gyeongsan, 38541, Republic of Korea.
Anticancer Res
December 2024
Project division of ALA advanced medical research, Institute of Medical Science, University of Tokyo, Tokyo, Japan.
Anticancer Res
December 2024
Department of Gastroenterological Surgery, Osaka Metropolitan University Graduate School of Medicine, Osaka, Japan.
Anticancer Res
December 2024
Department of Medical Physics, Graduate School of Medical Sciences, Kindai University, Osaka, Japan.
Blood Adv
February 2025
Ragon Institute of Mass General, Massachusetts Institute of Technology, and Harvard, Cambridge, MA.
Patients with cytotoxic T-lymphocyte-associated protein 4 (CTLA4) deficiency exhibit profound humoral immune dysfunction, yet the basis for the B-cell defect is not known. We observed a marked reduction in transitional-to-follicular (FO) B-cell development in patients with CTLA4 deficiency, correlating with decreased CTLA4 function in regulatory T cells, increased CD40L levels in effector CD4+ T cells, and increased mammalian target of rapamycin complex 1 (mTORC1) signaling in transitional B cells (TrBs). Treatment of TrBs with CD40L was sufficient to induce mTORC1 signaling and inhibit FO B-cell maturation in vitro.
View Article and Find Full Text PDFJ Am Chem Soc
December 2024
Research Institute for Electronic Science, Hokkaido University, Kita 20 Nishi 10, Kita-ku, Sapporo, Hokkaido 001-0020, Japan.
Proc Natl Acad Sci U S A
December 2024
National Institute of Advanced Industrial Science and Technology, Research Center for Computational Design of Advanced Functional Materials, Tsukuba, Ibaraki 305-8568, Japan.
Cytotherapy
November 2024
Department of Hematology/Oncology, The Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Genes Cells
January 2025
Division of Transcriptomics, Medical Institute of Bioregulation, Kyushu University, Fukuoka, Japan.
FEBS J
January 2025
Research Center for Pharmaceutical Development, Graduate School of Pharmaceutical Sciences, Tohoku University, Sendai, Japan.
J Appl Gerontol
December 2024
Department of Occupational Therapy, Kyoto Tachibana University, Kyoto, Japan.
J Gastroenterol Hepatol
December 2024
Division of Gastroenterology, Department of Medicine, Jichi Medical University, Shimotsuke, Tochigi, Japan.
Cancer Sci
December 2024
Department of Surgery and Oncology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.
Zoological Lett
December 2024
Evolutionary Neurobiology Unit, Okinawa Institute of Science and Technology Graduate University, Okinawa, Japan.
Beta-catenin is essential for diverse biological processes, such as body axis determination and cell differentiation, during metazoan embryonic development. Beta-catenin is thought to exert such functions through complexes formed with various proteins. Although β-catenin complex proteins have been identified in several bilaterians, little is known about the structural and functional properties of β-catenin complexes in early metazoan evolution.
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