Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Hanna Mochida"'
Autor:
Dina Husein, Ahmed Alamoudi, Yoshio Ohyama, Hanna Mochida, Brigitte Ritter, Yoshiyuki Mochida
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-15 (2022)
Abstract Amelogenesis Imperfecta (AI) represents a group of hereditary conditions that manifest tooth enamel defects. Several causative mutations in the WDR72 gene have been identified and patients with WDR72 mutations have brown (or orange-brown) di
Externí odkaz:
https://doaj.org/article/6b5ad1ac633b4111a10b9cc0d066d9e6
Autor:
I-Ping Lin, Hanna Mochida, Prasit Pavasant, Yoshio Ohyama, Nattanan Govitvattana, Yoshiyuki Mochida, Masaru Kaku, Haytham Jaha
Publikováno v:
Calcif Tissue Int
It is widely accepted that cellular processes are controlled by protein phosphorylation and has become increasingly clear that protein degradation, localization and conformation as well as protein-protein interaction are the examples of subsequent ce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e117d8ad74b209ce789ece054c1a087b
https://doi.org/10.1007/s00223-021-00847-y
https://doi.org/10.1007/s00223-021-00847-y
Autor:
Dina Husein, Ahmed Alamoudi, Yoshio Ohyama, Hanna Mochida, Brigitte Ritter, Yoshiyuki Mochida
Publikováno v:
Scientific reports. 12(1)
Amelogenesis Imperfecta (AI) represents a group of hereditary conditions that manifest tooth enamel defects. Several causative mutations in the WDR72 gene have been identified and patients with WDR72 mutations have brown (or orange-brown) discolored
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2d4e10e0cc7f12fbf5ce775fc1a4f59
https://pubmed.ncbi.nlm.nih.gov/35301423
https://pubmed.ncbi.nlm.nih.gov/35301423