Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Ryo Nagahama"'
Autor:
Yoshiro Saito, Atsushi Yamada, Dai Suzuki, Junichi Tanaka, Ryo Nagahama, Tamaki Kurosawa, Koutaro Maki, Kenji Mishima, Tatsuo Shirota, Ryutaro Kamijo
Publikováno v:
Genomics Data, Vol 5, Iss C, Pp 115-119 (2015)
Aging, also called senescence, is thought to be a physiological phenomenon that commonly occurs in various organs and tissues (Enoki et al., 2007 [1]). Many older adults experience dysfunction in their salivary glands, for example xerostomia, which i
Externí odkaz:
https://doaj.org/article/96897f9ce52d428fa58fc85011ab5a6e
Autor:
Tetsutaro Yamaguchi, Tatsuo Shirota, Mohamed Adel, Masahiro Takahashi, Shugo Haga, Ryo Nagahama, Misato Nakashima, Mayu Furuhata, Takaaki Kamatani, Koutaro Maki
Publikováno v:
Case Reports in Dentistry, Vol 2017 (2017)
Williams–Beuren syndrome (WBS) is a rare multisystem disorder caused by a hemizygous deletion of the elastin gene on chromosome 7q11.23. WBS patients have characteristic skeletal features and dental anomalies accompanied by mental retardation, a fr
Externí odkaz:
https://doaj.org/article/72ba67e1acd74853a4f89ad287507742
Publikováno v:
Clinical and Investigative Orthodontics. :1-10
Three‐dimensional assessment of the pharyngeal airway in Japanese preschoolers with orofacial clefts
Autor:
Tetsutaro Yamaguchi, Mary L. Marazita, Seth M. Weinberg, Mayu Furuhata, Hiroshi Yoshida, Daisuke Tomita, Misato Tsuneoka, Yu Hikita, Myoung Keun Lee, Mohamed Adel, Koutaro Maki, Ryo Nagahama, Masahiro Takahashi, Takatoshi Nakawaki, Yoko Suzuki
Publikováno v:
The Laryngoscope. 130:533-540
Objectives/hypothesis Individuals with orofacial clefts often experience respiratory problems because of nasopharyngeal abnormalities. Pharyngeal airway morphology is thought to differ among the various cleft types. We measured three-dimensional (3D)
Autor:
Ryo Nagahama, Matsuo Yamamoto, Akiko Sakashita, Ryo Aizawa, Hiroaki Ogata, Tadashi Kato, Koutaro Maki, Ryutaro Kamijo, Mikiko Ikehata, Daichi Chikazu, Junichi Tanaka, Atsushi Yamada, Kenji Mishima, Tatsuaki Seki
Publikováno v:
Biochemical and biophysical research communications. 512(2)
Cdc42 (cell division cycle 42) is ubiquitously expressed small GTPases belonging to the Rho family of proteins. Previously, we generated limb bud mesenchyme-specific Cdc42 inactivated mice (Cdc42 conditional knockout mice; Cdc42 fl/fl; Prx1-Cre), whi
Autor:
Matsuo Yamamoto, Atsushi Yamada, Takehiko Iijima, Naoko Morimura, Ryo Nagahama, Masayuki Tsukasaki, Mikiko Ikehata, Tatsuo Shirota, Ryutaro Kamijo, Yoshiro Saito, Dai Suzuki, Ryo Aizawa, Koutaro Maki, Daichi Chikazu, Katsuhiro Hiranuma, Masamichi Takami, Tamaki Kurosawa
Publikováno v:
FEBS Open Bio
The extracellular matrix protein nephronectin (Npnt), also called POEM, is considered to play critical roles as an adhesion molecule in development and functions of various tissues, such as the kidneys, liver, and bone. In the present study, we exami
Autor:
Ryo Nagahama, Masahiro Takahashi, Koutaro Maki, Kazuyoshi Hosomichi, Tetsutaro Yamaguchi, Hiroshi Yoshida, Seth M. Weinberg, Mary L. Marazita, Atsushi Tajima
Publikováno v:
Archives of oral biology. 96
Objective The aim of the present study is to explore genetic factors determining difference of cleft side using whole-genome sequencing and evaluation of craniofacial morphology using cephalometric analysis between Japanese monozygotic (MZ) twins wit
Whole-genome sequencing in a pair of monozygotic twins with discordant cleft lip and palate subtypes
Autor:
Masahiro Takahashi, Hiroshi Yoshida, Seth M. Weinberg, Kazuyoshi Hosomichi, Mary L. Marazita, Tetsutaro Yamaguchi, Atsushi Tajima, Koutaro Maki, Ryo Nagahama
Publikováno v:
Oral diseases. 24(7)
Objective Orofacial clefts (OFCs) are common and etiologically complex birth defects. This study explored potential genetic differences in a pair of Japanese monozygotic (MZ) twins with different forms of OFC using whole-genome sequencing. Subjects a
Autor:
Koutaro Maki, Dai Suzuki, Atsushi Yamada, Takeshi Harada, Matsuo Yamamoto, Mutsuko Nakayama, Shu Takeda, Hidetoshi Kassai, Ryo Aizawa, Ryo Nagahama, Kazuyoshi Baba, Wataru Suzuki, Ryutaro Kamijo, Atsu Aiba
Publikováno v:
Endocrinology. 156:314-322
Cdc42 is a widely expressed protein that belongs to the family of Rho GTPases and controls a broad variety of signal transduction pathways in a variety of cell types. To investigate the physiological functions of Cdc42 during cartilage development, w
Autor:
Matsuo Yamamoto, Ryutaro Kamijo, Kenji Mishima, Koutaro Maki, Dai Suzuki, Junichi Tanaka, Ryo Nagahama, Atsu Aiba, Hidetoshi Kassai, Atsushi Yamada, Ryo Aizawa
Publikováno v:
Biochemical and biophysical research communications. 470(4)
Cdc42, a small Rho GTPase family member, has been shown to regulate multiple cellular functions in vitro, including actin cytoskeletal reorganization, cell migration, proliferation, and gene expression. However, its tissue-specific roles in vivo rema