Zobrazeno 1 - 10
of 72
pro vyhledávání: '"Shinichiro Sano"'
Autor:
Kaori Hara-Isono, Keiko Matsubara, Akie Nakamura, Shinichiro Sano, Takanobu Inoue, Sayaka Kawashima, Tomoko Fuke, Kazuki Yamazawa, Maki Fukami, Tsutomu Ogata, Masayo Kagami
Publikováno v:
Clinical Epigenetics, Vol 15, Iss 1, Pp 1-11 (2023)
Abstract Background Our previous study suggested that assisted reproductive technology (ART) may be a possible risk factor for the development of epimutation-mediated imprinting disorders (epi-IDs) for mothers aged ≥ 30 years. However, whether ART
Externí odkaz:
https://doaj.org/article/275e16ae7540475282e1ab546e79f968
Autor:
Eiko Nagata, Yasuharu Kashiwagura, Eisaku Okada, Shimako Tanaka, Shinichiro Sano, Mitsuhiro Nishida, Satoshi Hayano, Satoru Iwashima, Akio Hakamata, Keiichi Odagiri, Naoki Inui, Hiroshi Watanabe, Kazuo Umemura, Shinya Uchida
Publikováno v:
Journal of Pharmacological Sciences, Vol 149, Iss 2, Pp 60-65 (2022)
Infantile hemangioma (IH) is a common tumor in infants that gradually resolves and is often untreated. However, for cosmetic reasons, parents often opt for treatment. Oral propranolol, the first-line therapy for IH, is sometimes associated with sever
Externí odkaz:
https://doaj.org/article/404d9011c9ce4387ba110666ea8d50c3
Autor:
Takanobu Inoue, Akie Nakamura, Tomoko Fuke, Kazuki Yamazawa, Shinichiro Sano, Keiko Matsubara, Seiji Mizuno, Yoshika Matsukura, Chie Harashima, Tatsuji Hasegawa, Hisakazu Nakajima, Kumi Tsumura, Zenro Kizaki, Akira Oka, Tsutomu Ogata, Maki Fukami, Masayo Kagami
Publikováno v:
Clinical Epigenetics, Vol 9, Iss 1, Pp 1-10 (2017)
Abstract Background Silver-Russell syndrome (SRS) is a rare congenital disorder characterized by pre- and postnatal growth failure and dysmorphic features. Recently, pathogenic copy number variations (PCNVs) and imprinting defects other than hypometh
Externí odkaz:
https://doaj.org/article/7eca2377d6064342b9054fb0551c24b9
Autor:
Tomoko Fuke, Seiji Mizuno, Toshiro Nagai, Tomonobu Hasegawa, Reiko Horikawa, Yoko Miyoshi, Koji Muroya, Tatsuro Kondoh, Chikahiko Numakura, Seiji Sato, Kazuhiko Nakabayashi, Chiharu Tayama, Kenichiro Hata, Shinichiro Sano, Keiko Matsubara, Masayo Kagami, Kazuki Yamazawa, Tsutomu Ogata
Publikováno v:
PLoS ONE, Vol 8, Iss 3, p e60105 (2013)
BackgroundRecent studies have revealed relative frequency and characteristic phenotype of two major causative factors for Silver-Russell syndrome (SRS), i.e. epimutation of the H19-differentially methylated region (DMR) and uniparental maternal disom
Externí odkaz:
https://doaj.org/article/8288174ccaaa4443a29a1247cb62d067
Autor:
Shinichiro Sano1,2 sanosin2u@yahoo.co.jp, Shotaro Iwamoto3, Rie Matsushita4, Yohei Masunaga2, Yasuko Fujisawa2, Tsutomu Ogata2,5
Publikováno v:
Clinical Pediatric Endocrinology. Apr2024, Vol. 33 Issue 2, p66-70. 5p.
Autor:
Shinichiro Sano1,2 sanosin2u@yahoo.co.jp, Yohei Masunaga2, Fumiko Kato3, Yasuko Fujisawa2, Hirotomo Saitsu4, Tsutomu Ogata2,3,5
Publikováno v:
Clinical Pediatric Endocrinology. 2022, Vol. 31 Issue 3, p172-177. 6p.
Autor:
Tatsuki Urakawa, Shinichiro Sano, Sayaka Kawashima, Akie Nakamura, Hirohito Shima, Motoki Ohta, Yuki Yamada, Ai Nishida, Hiromune Narusawa, Yoshiaki Ohtsu, Keiko Matsubara, Sumito Dateki, Yoshihiro Maruo, Maki Fukami, Tsutomu Ogata, Masayo Kagami
Publikováno v:
European Journal of Endocrinology; Dec2023, Vol. 189 Issue 6, p590-600, 11p
Autor:
Tomoko Fuke, Akie Nakamura, Takanobu Inoue, Sayaka Kawashima, Kaori Hara-Isono, Keiko Matsubara, Shinichiro Sano, Kazuki Yamazawa, Maki Fukami, Tsutomu Ogata, Masayo Kagami
Publikováno v:
Journal of Human Genetics. 67:607-611
Silver-Russel syndrome (SRS) is a representative imprinting disorder (ID) characterized by growth failure and diagnosed by clinical features. Recently, international consensus has recommended using the Netchine-Harbison clinical scoring system (NH-CS
Autor:
Sayaka Kawashima, Akiko Yuno, Shinichiro Sano, Akie Nakamura, Keisuke Ishiwata, Tomoyuki Kawasaki, Kazuyoshi Hosomichi, Kazuhiko Nakabayashi, Hidenori Akutsu, Hirotomo Saitsu, Maki Fukami, Takeshi Usui, Tsutomu Ogata, Masayo Kagami
Publikováno v:
Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral ResearchReferences. 37(10)
Loss of methylation (LOM) at GNAS-A/B:TSS-differentially methylated regions (DMRs) in the GNAS locus is observed in pseudohypoparathyroidism type 1B (PHP1B). Many PHP1B cases are sporadic, but autosomal dominant-PHP1B has a deletion involving NESP55
Autor:
null Sayaka Kawashima, null Akiko Yuno, null Shinichiro Sano, null Akie Nakamura, null Keisuke Ishiwata, null Tomoyuki Kawasaki, null Kazuyoshi Hosomichi, null Kazuhiko Nakabayashi, null Hidenori Akutsu, null Hirotomo Saitsu, null Maki Fukami, null Takeshi Usui, null Tsutomu Ogata, null Masayo Kagami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84bbecb7218172fa90f6e08c5b225ad7
https://doi.org/10.1002/jbmr.4652/v2/response1
https://doi.org/10.1002/jbmr.4652/v2/response1