Zobrazeno 1 - 10
of 51
pro vyhledávání: '"Yelda KASIMOGLU"'
Autor:
Sabiha Ceren İlisulu, Sinem Birant, Yelda Kasimoglu, Mine Koruyucu, Elif Bahar Tuna İnce, Figen Seymen
Publikováno v:
Journal of Dental Sciences, Vol 18, Iss 4, Pp 1859-1866 (2023)
Abstract Background/purpose: Twin studies are crucial to assess the relative contribution of genetic and environmental factors. This study was conducted to evaluate association between deleterious oral habits and dental caries–periodontal parameter
Externí odkaz:
https://doaj.org/article/f3d314cf4cb24e67b3f00b000138156d
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
Autor:
Derya TABAKCILAR, Kadriye PEKER, Dilek Ozge YILMAZ, Yelda KASIMOGLU, Elif Bahar TUNA-INCE, Koray GENCAY, Figen SEYMEN
Publikováno v:
Brazilian Oral Research, Vol 36 (2023)
Abstract This study evaluated the influence of socio-demographic, clinical, and parental psychological factors on oral health-related quality of life (OHRQoL) and determined their predictors in preschool-aged children with traumatic dental injury (TD
Externí odkaz:
https://doaj.org/article/7e236aa0fb7746658088386ed290a5df
Autor:
Mengqi Zhou, Hong Zhang, Heather Camhi, Figen Seymen, Mine Koruyucu, Yelda Kasimoglu, Jung-Wook Kim, Hera Kim-Berman, Ninna M. R. Yuson, Paul J. Benke, Yiqun Wu, Feng Wang, Yaqin Zhu, James P. Simmer, Jan C-C. Hu
Publikováno v:
International Journal of Oral Science, Vol 13, Iss 1, Pp 1-11 (2021)
Abstract Oligodontia is the congenital absence of six or more teeth and comprises the more severe forms of tooth agenesis. Many genes have been implicated in the etiology of tooth agenesis, which is highly variable in its clinical presentation. The p
Externí odkaz:
https://doaj.org/article/b4fae4e706cc42399f6b5e82f45aca92
Publikováno v:
Children, Vol 10, Iss 4, p 683 (2023)
The timing of primary tooth eruption is critical for children’s health planning and the diagnosis of specific growth disorders. The purpose of this study is to assess the relationship between twin pairs’ birth weight, gestational age, and gender,
Externí odkaz:
https://doaj.org/article/78fecde8b67442f8ac8362d7afe4d3d6
Autor:
Shih‐Kai Wang, Hong Zhang, Michael B. Chavez, Yuanyuan Hu, Figen Seymen, Mine Koruyucu, Yelda Kasimoglu, Connor D. Colvin, Tamara N. Kolli, Michelle H. Tan, Yin‐Lin Wang, Pei‐Ying Lu, Jung‐Wook Kim, Brian L. Foster, John D. Bartlett, James P. Simmer, Jan C.‐C. Hu
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 8, Iss 8, Pp n/a-n/a (2020)
Abstract Background Matrix metallopeptidase 20 (MMP20) is an evolutionarily conserved protease that is essential for processing enamel matrix proteins during dental enamel formation. MMP20 mutations cause human autosomal recessive pigmented hypomatur
Externí odkaz:
https://doaj.org/article/89d3f87d0001415bb348c887bd7e7fc1
Autor:
Mengqi Zhou, Hong Zhang, Heather Camhi, Figen Seymen, Mine Koruyucu, Yelda Kasimoglu, Jung-Wook Kim, Hera Kim-Berman, Ninna M. R. Yuson, Paul J. Benke, Yiqun Wu, Feng Wang, Yaqin Zhu, James P. Simmer, Jan C-C. Hu
Publikováno v:
International Journal of Oral Science, Vol 13, Iss 1, Pp 1-1 (2021)
Externí odkaz:
https://doaj.org/article/69aca93b9fdf4733af20c92ca8e7c19f
Autor:
Hong Zhang, Yuanyuan Hu, Figen Seymen, Mine Koruyucu, Yelda Kasimoglu, Shih‐Kai Wang, John Timothy Wright, Michael W. Havel, Chuhua Zhang, Jung‐Wook Kim, James P. Simmer, Jan C.‐C. Hu
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 10, Pp n/a-n/a (2019)
Abstract Background ENAM mutations cause autosomal dominant or recessive amelogenesis imperfecta (AI) and show a dose effect: enamel malformations are more severe or only penetrant when both ENAM alleles are defective. Methods Whole exome sequences o
Externí odkaz:
https://doaj.org/article/7b61b9235588451f9c86615f3eaad46c
Publikováno v:
Dental Research Journal, Vol 13, Iss 2, Pp 145-150 (2016)
Background: Talon cusp is a rare dental anomaly characterized by a cusp-like projection, often including the palatal surface of the affected tooth. The aim of the present study was to investigate the prevalence and characteristics of talon cusps in a
Externí odkaz:
https://doaj.org/article/f6e0e6e0071b41b78c2b24cfab519e5b
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
Volume 13
Issue 2
Pages: 326
Volume 13
Issue 2
Pages: 326
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::61daeb27ffa77168a6f7a2feb31ceda1