Zobrazeno 1 - 10
of 284
pro vyhledávání: '"Jung-Wook Kim"'
Publikováno v:
Journal of Personalized Medicine, Vol 14, Iss 2, p 191 (2024)
Hypodontia, i.e., missing one or more teeth, is a relatively common human disease; however, oligodontia, i.e., missing six or more teeth, excluding the third molars, is a rare congenital disorder. Many genes have been shown to cause oligodontia in no
Externí odkaz:
https://doaj.org/article/5e73c4896777415496c8d784736128a1
Autor:
Tian Liang, Shih-Kai Wang, Charles Smith, Hong Zhang, Yuanyuan Hu, Figen Seymen, Mine Koruyucu, Yelda Kasimoglu, Jung-Wook Kim, Chuhua Zhang, Thomas L. Saunders, James P. Simmer, Jan C.-C. Hu
Publikováno v:
Scientific Reports, Vol 12, Iss 1, Pp 1-20 (2022)
Abstract Human ACP4 (OMIM*606362) encodes a transmembrane protein that belongs to histidine acid phosphatase (ACP) family. Recessive mutations in ACP4 cause non-syndromic hypoplastic amelogenesis imperfecta (AI1J, OMIM#617297). While ACP activity has
Externí odkaz:
https://doaj.org/article/b1ed9c32d099421cbc3e834f910de5b2
Publikováno v:
Journal of Personalized Medicine, Vol 13, Iss 10, p 1494 (2023)
Hereditary conditions that affect tooth enamel in quantity and/or quality are called amelogenesis imperfecta (AI). AI can occur as an isolated condition or as a symptom of a syndrome. An OMIM search with the term “AI” yielded 79 result entries. M
Externí odkaz:
https://doaj.org/article/d68d7c9668c041638196e45d3464f697
Autor:
Tian Liang, Yuanyuan Hu, Hong Zhang, Qian Xu, Charles E. Smith, Chuhua Zhang, Jung-Wook Kim, Shih-Kai Wang, Thomas L. Saunders, Yongbo Lu, Jan C.-C. Hu, James P. Simmer
Publikováno v:
Scientific Reports, Vol 11, Iss 1, Pp 1-14 (2021)
Abstract Non-syndromic inherited defects of tooth dentin are caused by two classes of dominant negative/gain-of-function mutations in dentin sialophosphoprotein (DSPP): 5′ mutations affecting an N-terminal targeting sequence and 3′ mutations that
Externí odkaz:
https://doaj.org/article/8cc6c2e7bcd84aac8371c3b57be3059c
Autor:
Youn Jung Kim, Hong Zhang, Yejin Lee, Figen Seymen, Mine Koruyucu, Yelda Kasimoglu, James P. Simmer, Jan C.-C. Hu, Jung-Wook Kim
Publikováno v:
Journal of Personalized Medicine, Vol 13, Iss 2, p 326 (2023)
Amelogenesis imperfecta (AI) is a heterogeneous collection of hereditary enamel defects. The affected enamel can be classified as hypoplastic, hypomaturation, or hypocalcified in form. A better understanding of normal amelogenesis and improvements in
Externí odkaz:
https://doaj.org/article/e260c2489f714da1ab7191a3b0d6252d
Autor:
Young Woon Chang, Yoo Min Park, Chi Hyuk Oh, Shin Ju Oh, Jun-Hyung Cho, Jung-Wook Kim, Jae-Young Jang
Publikováno v:
The Korean Journal of Internal Medicine, Vol 35, Iss 3, Pp 574-581 (2020)
Background/Aims The eradication failure rate of standard triple therapy (proton pump inhibitor, clarithromycin, and amoxicillin) for Helicobacter pylori infection has increased owing to antibiotic resistance in Korea. We assessed whether Saccharomyce
Externí odkaz:
https://doaj.org/article/d7fd13caba1a4a549c4a2d7e53cb4b53
Autor:
Young Woon Chang, Weon Jin Ko, Chi Hyuk Oh, Yoo Min Park, Shin Ju Oh, Jung Rock Moon, Jun-Hyung Cho, Jung-Wook Kim, Jae-Young Jang
Publikováno v:
The Korean Journal of Internal Medicine, Vol 34, Iss 5, Pp 1022-1029 (2019)
Background/Aims The eradication rate of the first-line triple therapy (a proton pump inhibitor, clarithromycin, and amoxicillin) for Helicobacter pylori infection has gradually decreased in Korea. We evaluated whether clinical parameters, clarithromy
Externí odkaz:
https://doaj.org/article/75e59568bb1547b886b7f82bb8232182
Publikováno v:
Journal of Personalized Medicine, Vol 12, Iss 9, p 1401 (2022)
The process of tooth formation is a series of reciprocal interactions between the ectoderm and mesoderm, and it is believed that many genetic factors are involved in this complex process. More than a dozen genes have been identified in non-syndromic
Externí odkaz:
https://doaj.org/article/006f15883bf14fcdaf15f207c272b769
Autor:
Youn Jung Kim, Yejin Lee, Hong Zhang, Figen Seymen, Mine Koruyucu, Sule Bayrak, Nuray Tuloglu, James P. Simmer, Jan C.-C. Hu, Jung-Wook Kim
Publikováno v:
Journal of Personalized Medicine, Vol 12, Iss 6, p 1002 (2022)
Hereditary dentin defects are conventionally classified into three types of dentinogenesis imperfecta (DGI) and two types of dentin dysplasia (DD). Mutations in the dentin sialophosphoprotein (DSPP) gene have been identified to cause DGI type II and
Externí odkaz:
https://doaj.org/article/ef404692779247ca9bedeaa237f28907
Autor:
Tae Hee Lee, Seong-Eun Kim, Kyung Sik Park, Jeong Eun Shin, Seon-Young Park, Han Seung Ryu, Jung-Wook Kim, Yoo Jin Lee, Young Sin Cho, Suyeon Park, Constipation Research Group of The Korean Society of Neurogastroenterology, Motility
Publikováno v:
The Korean Journal of Gastroenterology, Vol 72, Iss 6, Pp 295-303 (2018)
Background/Aims: The primary aims of this study were to evaluate the content quality of YouTube videos on exercises to help relieve constipation and to assess whether the video source, exercise types, and popularity affected their quality. Methods: E
Externí odkaz:
https://doaj.org/article/364404da16a94867abc09d819ca5fb36