Zobrazeno 1 - 10
of 42
pro vyhledávání: '"Hideto Imura"'
Autor:
Loc Nguyen Gia Pham, Teruyuki Niimi, Satoshi Suzuki, Minh Duc Nguyen, Linh Cao Hoai Nguyen, Tuan Duc Nguyen, Kien Ai Hoang, Duc Minh Nguyen, Chisato Sakuma, Toko Hayakawa, Makino Hiyori, Nagana Natsume, Hiroo Furukawa, Hideto Imura, Junko Akashi, Tohru Ohta, Nagato Natsume
Publikováno v:
Genes, Vol 14, Iss 11, p 1995 (2023)
This study aims to identify potential variants in the TP63–IRF6 pathway and GREM1 for the etiology of non-syndromic orofacial cleft (NSOFC) among the Vietnamese population. By collecting 527 case–parent trios and 527 control samples, we conducted
Externí odkaz:
https://doaj.org/article/858c475a19b044a28c1b3451463d7936
Autor:
Harumi Ejiri, Hideto Imura, Reizo Baba, Akiko Sumi, Akiko Koga, Kaoru Kanno, Miho Kunimoto, Kayo Hayami, Teruyuki Niimi, Shuji Nomoto, Nagato Natsume
Publikováno v:
Healthcare, Vol 11, Iss 16, p 2289 (2023)
Background: We believe that parental presence before the induction of anesthesia for surgery among children with a cleft palate/lip would be effective in mitigating their preoperative anxiety. Objective: We assessed the states of patients with a clef
Externí odkaz:
https://doaj.org/article/f6a669f8764f424ca1b52fbc9fd99c65
Autor:
Duc Minh Nguyen, Satoshi Suzuki, Hideto Imura, Teruyuki Niimi, Hiroo Furukawa, Thanh‐Van Ta, Son Minh Tong, Tra Thu Nguyen, Loc Nguyen Gia Pham, Duy Le Tran, Nagato Natsume
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 9, Iss 9, Pp n/a-n/a (2021)
Abstract Aims Dozens of causative genes and their mechanisms of nonsyndromic cleft lip with or without cleft palate (NSCL/P) were revealed through genome‐wide association and linkage studies. Results were, however, not always replicated in differen
Externí odkaz:
https://doaj.org/article/d4092d537aec48f3ae425680e1e9edcc
Autor:
Chisato Sakuma, Hideto Imura, Tomohiro Yamada, Azumi Hirata, Yayoi Ikeda, Masaaki Ito, Nagato Natsume
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 4, p 2069 (2022)
Rupture of the basement membrane in fused palate tissue can cause the palate to separate after fusion in mice, leading to the development of cleft palate. Here, we further elucidate the mechanism of palatal separation after palatal fusion in 8–10-w
Externí odkaz:
https://doaj.org/article/d6d14f674d8b44c6a95d9955ea30ffdc
Autor:
Masaaki Ito, Taku Toriumi, Takahiro Hiratsuka, Hideto Imura, Yasunori Akiyama, Ichinnorov Chimedtseren, Yoshinori Arai, Kazuhiro Yamaguchi, Akihiko Azuma, Ken-ichiro Hata, Nagato Natsume, Masaki Honda
Publikováno v:
Materials, Vol 14, Iss 9, p 2306 (2021)
This study aimed to examine the optimal cross-link density of recombinant peptide (RCP) particles, based on human collagen type I, for bone reconstruction in human alveolar cleft. Low- (group 1), medium- (group 2), and high- (group 3) cross-linked RC
Externí odkaz:
https://doaj.org/article/9a5c7f4f87944da682a855cfa366f661
Autor:
Nagato Natsume, Kayo Hayami, Junko Akashi, Chisato Sakuma, Kumiko Fujiwara, Hiroo Furukawa, Kazuo Takeuchi, Teruyuki Niimi, Nagana Natsume, Hideto Imura, Waka Yoshida
Publikováno v:
Congenital Anomalies. 62:11-17
We have been conducting a survey on the birth prevalence of orofacial clefts, including cleft lip with or without cleft palate and cleft palate, in the Tokai area in central Japan every year for 37 years. Along with the yearly trends in the birth pre
Publikováno v:
Japanese Journal of Oral and Maxillofacial Surgery. 67:359-364
Publikováno v:
Cureus.
Autor:
Aiji Sato (Boku), Izumi Kuroda, Hideto Imura, Mayumi Hashimoto, Yoko Okumura, Naoko Tachi, Nagato Natsume, Masahiro Okuda
Von Recklinghausen’s disease is characterized by skin pigmentation, multiple neurofibromatosis, and osseous changes. In the management of anesthesia, a variety of pathologies need to be taken into account. This case describes the perioperative mana
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::16623363be274df18ae5752cfee01969
https://doi.org/10.22541/au.164327535.52775849/v1
https://doi.org/10.22541/au.164327535.52775849/v1
Publikováno v:
Congenital Anomalies. 61:105-107