Zobrazeno 1 - 10
of 125
pro vyhledávání: '"Hailan, Feng"'
Publikováno v:
International Journal of Oral Science, Vol 16, Iss 1, Pp 1-11 (2024)
Abstract Human with bi-allelic WNT10A mutations and epithelial Wnt10a knockout mice present enlarged pulp chamber and apical displacement of the root furcation of multi-rooted teeth, known as taurodontism; thus, indicating the critical role of Wnt10a
Externí odkaz:
https://doaj.org/article/7fe5a86b509c47c6887e8b8fd0c7af52
Publikováno v:
ACS Omega, Vol 9, Iss 6, Pp 6994-7002 (2024)
Externí odkaz:
https://doaj.org/article/8dabd4456c4d4948b72f2f6d6c4e4228
Autor:
Liutao Zhang, Miao Yu, Kai Sun, Zhuangzhuang Fan, Haochen Liu, Hailan Feng, Yang Liu, Dong Han
Publikováno v:
npj Genomic Medicine, Vol 6, Iss 1, Pp 1-8 (2021)
Abstract Low-density lipoprotein receptor-related protein 6 (LRP6) is a pathogenic gene of selective tooth agenesis-7 (OMIM#616724). Although the malformation of the digits and fore- and hindlimbs has been reported in Lrp6-deficient mice, it has been
Externí odkaz:
https://doaj.org/article/0f5f01fad42d4d5981731dcaf8e1df2b
Autor:
Fang Li, Miao Yu, Zhuangzhuang Fan, Junyi Wu, Hua Tian, Hailan Feng, Yang Liu, Haochen Liu, Dong Han
Publikováno v:
Frontiers in Physiology, Vol 13 (2022)
Junctional epidermolysis bullosa (JEB) is a group of autosomal recessive disorders characterized by amelogenesis imperfecta (AI) and fragility of the skin and mucous membranes. The purpose of this study was to identify pathogenic gene variants and in
Externí odkaz:
https://doaj.org/article/c4fd850980d04ffe9eab2d71fb3e2ed6
Publikováno v:
International Journal of Oral Science, Vol 13, Iss 1, Pp 1-10 (2021)
Abstract The goal of this study was to identify MSX1 gene variants in multiple Chinese families with nonsyndromic oligodontia and analyse the functional influence of these variants. Whole-exome sequencing (WES) and Sanger sequencing were performed to
Externí odkaz:
https://doaj.org/article/86f097bfba6142429fb0f71b67739205
Publikováno v:
Diagnostics, Vol 12, Iss 12, p 3087 (2022)
The goal of this study was to identify the pathogenic gene variants in patients with odonto-onycho-dermal dysplasia syndrome (OODD) or nonsyndromic tooth agenesis. Four unrelated individuals with tooth agenesis and their available family members were
Externí odkaz:
https://doaj.org/article/86fbb2dc6137458bb159b553ced2c03c
Publikováno v:
Diagnostics, Vol 12, Iss 12, p 2936 (2022)
The goal of the current study was to identify the pathogenic gene variant in a Chinese family with Blepharocheilodontic (BCD) syndrome. Whole-exome sequencing (WES) and Sanger sequencing were used to identify the pathogenic gene variant. The harmfuln
Externí odkaz:
https://doaj.org/article/5e979b39fd8d49d8b7f8025dd14f16d8
Publikováno v:
Diagnostics, Vol 12, Iss 10, p 2300 (2022)
The goal of this study was to identify the pathogenic gene variants in female patients with severe X-linked hypohidrotic ectodermal dysplasia (XLHED). Whole-exome sequencing (WES) and Sanger sequencing were used to screen for the pathogenic gene vari
Externí odkaz:
https://doaj.org/article/fa9d2c5bcbde4565868acdadfa80f07e
Autor:
Jiechen Song, Yuxing Xu, Yuncheng Zhou, Pengfei Wang, Hailan Feng, Jun Yang, Fuchang Zhuge, Qiangqiang Tan
Publikováno v:
ACS Applied Materials & Interfaces. 15:20897-20908
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7f249a87ee1e523a64fbdc79c697dd2
https://doi.org/10.1021/acsami.2c22562
https://doi.org/10.1021/acsami.2c22562
Autor:
Jinglei Zheng, Haochen Liu, Yuan Zhan, Yang Liu, Sing‐Wai Wong, Tao Cai, Hailan Feng, Dong Han
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 7, Iss 6, Pp n/a-n/a (2019)
Abstract Background Ectrodactyly‐Ectodermal dysplasia‐Cleft lip/palate (EEC) syndrome and Ankyloblepharon‐Ectodermal defects‐Cleft lip/palate (AEC) syndrome belong to p63 syndromes, a group of rare disorders exhibiting a wide variety of clini
Externí odkaz:
https://doaj.org/article/f526f4478e254972b25c3a1bc9f66374