Zobrazeno 1 - 10
of 194
pro vyhledávání: '"Yukie, Yamaguchi"'
Autor:
Chika Asai, Naoko Takamura, Tomoya Watanabe, Miho Asami, Noriko Ikeda, Charles F. Reese, Stanley Hoffman, Yukie Yamaguchi
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-11 (2024)
Abstract The plasma membrane protein caveolin-1 (CAV-1) regulates signaling by inhibiting a wide range of kinases and other enzymes. Our previous study demonstrated that the downregulation of CAV-1 in psoriatic epidermal cells contributes to inflamma
Externí odkaz:
https://doaj.org/article/50b06ae0e3d641a0b9317dcdb509a433
Autor:
Tomoya Watanabe, Yasushi Ototake, Asami Akita, Mao Suzuki, Miwa Kanaoka, Jun Tamura, Yusuke Saigusa, Yukie Yamaguchi
Publikováno v:
Arthritis Research & Therapy, Vol 26, Iss 1, Pp 1-8 (2024)
Abstract Background Anti-SS-A/Ro antibody (anti-SSA), the diagnostic marker of Sjögren’s syndrome (SS), is often detected in systemic sclerosis (SSc). Some patients are diagnosed with SSc/SS overlap syndromes, while there are anti-SSA-positive SSc
Externí odkaz:
https://doaj.org/article/24ebe46e88b14bb1bfd0f3cb82e970bc
Autor:
Akimichi Morita, Yukari Okubo, Shinichi Imafuku, Yayoi Tada, Keiichi Yamanaka, Kazumitsu Sugiura, Yukie Yamaguchi, Masahito Yasuda, Hitoshi Tsuchihashi, Morihisa Saitoh, Wataru Sakamoto, Ryuhei Okuyama, the study investigators
Publikováno v:
JEADV Clinical Practice, Vol 2, Iss 2, Pp 261-272 (2023)
Abstract Background Generalized pustular psoriasis (GPP) is a rare and often refractory disease, and GPP flares can be life threatening. The rarity of GPP prevents the development and evaluation of effective GPP‐specific treatments and obstructs di
Externí odkaz:
https://doaj.org/article/318927d3bab444da8a4fed58d243b566
Publikováno v:
Journal of Cutaneous Immunology and Allergy, Vol 6, Iss 5, Pp 175-176 (2023)
Externí odkaz:
https://doaj.org/article/f89ba2d67b0f496098bfa172ef29bf2c
Autor:
Yuko Watanabe, Yukie Yamaguchi
Publikováno v:
Allergology International, Vol 71, Iss 2, Pp 179-184 (2022)
Systemic autoimmune diseases are reportedly associated with a high frequency of drug allergies. In particular, systemic lupus erythematosus (SLE), Sjögren's syndrome (SS), and adult-onset Still's disease (AOSD) have recently drawn attention. Based o
Externí odkaz:
https://doaj.org/article/9727a14f8a684c538c5cb5f000f9888a
Publikováno v:
Journal of Cutaneous Immunology and Allergy, Vol 6, Iss 3, Pp 108-109 (2023)
Externí odkaz:
https://doaj.org/article/3cb95fd548c2474090c07765daf87c7e
Autor:
Tomoya Watanabe, Yukie Yamaguchi
Publikováno v:
Frontiers in Immunology, Vol 14 (2023)
Immune checkpoint inhibitors (ICIs) are monoclonal antibodies that block key mediators of tumor-mediated immune evasion. The frequency of its use has increased rapidly and has extended to numerous cancers. ICIs target immune checkpoint molecules, suc
Externí odkaz:
https://doaj.org/article/3c05c9fd5dad4256a7a71ff7b956b0b0
Autor:
Naoko Takamura, Yukie Yamaguchi
Publikováno v:
Frontiers in Immunology, Vol 13 (2022)
The skin is the outermost layer and largest organ in the human body. Since the skin interfaces with the environment, it has a variety of roles, including providing a protective barrier against external factors, regulating body temperature, and retain
Externí odkaz:
https://doaj.org/article/feb58eddb5c64bb8b07dbca883dfb4c4
Mortality and risk factors on admission in toxic epidermal necrolysis: A cohort study of 59 patients
Autor:
Tomoya Watanabe, Hirofumi Go, Yusuke Saigusa, Naoko Takamura, Yuko Watanabe, Yumiko Yamane, Michiru Totsuka, Hideyuki Ishikawa, Kazuko Nakamura, Setsuko Matsukura, Takeshi Kambara, Shunsuke Takaki, Yukie Yamaguchi, Michiko Aihara
Publikováno v:
Allergology International, Vol 70, Iss 2, Pp 229-234 (2021)
Background: Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are rare but life-threatening disorders characterized by widespread epidermal necrosis of the skin and mucosa. The severity-of-illness scoring system for TEN (SCORTEN) wa
Externí odkaz:
https://doaj.org/article/8e2ba05fc7a0423589eade9f207b46a9
Autor:
Tomohito Yoshihara, Yasuhiro Nanri, Satoshi Nunomura, Yukie Yamaguchi, Carol Feghali-Bostwick, Keiichi Ajito, Shoichi Murakami, Masaaki Mawatari, Kenji Izuhara
Publikováno v:
Respiratory Research, Vol 21, Iss 1, Pp 1-12 (2020)
Abstract Background Idiopathic pulmonary fibrosis (IPF) is a devastating disease with a median survival of only three to 5 years. Fibroblast proliferation is a hallmark of IPF as is secretion of extracellular matrix proteins from fibroblasts. However
Externí odkaz:
https://doaj.org/article/a8557acc33d84671b1e7c326e746aa7f