Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Jinglei Zheng"'
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
Autor:
Jinglei Zheng, Haochen Liu, Miao Yu, Bichen Lin, Kai Sun, Hangbo Liu, Hailan Feng, Yang Liu, Dong Han
Publikováno v:
International Journal of Molecular Sciences, Vol 24, Iss 2, p 1648 (2023)
Oligodontia manifests as a congenital reduction in the number of permanent teeth. Despite the major efforts that have been made, the genetic etiology of oligodontia remains largely unknown. Bone morphogenetic protein receptor type 2 (BMPR2) variants
Externí odkaz:
https://doaj.org/article/4a62899e83de4eab8330ccfd4e8d6efe
Autor:
Miao Yu, Hangbo Liu, Yang Liu, Jinglei Zheng, Junyi Wu, Kai Sun, Hailan Feng, Haochen Liu, Dong Han
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 20, p 12465 (2022)
Keratinocyte differentiation factor 1 (KDF1) is a recently identified and rare candidate gene for human tooth agenesis; however, KDF1-related morphological characteristics and pathological changes in dental tissue and the oral epithelium remain large
Externí odkaz:
https://doaj.org/article/d1cf8beca05f4b6d981edf7198f56ac9
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
Publikováno v:
International Journal of Molecular Sciences, Vol 23, Iss 15, p 8142 (2022)
The purpose of this research was to investigate and identify PAX9 gene variants in four Chinese families with non-syndromic tooth agenesis. We identified pathogenic gene variants by whole-exome sequencing (WES) and Sanger sequencing and then studied
Externí odkaz:
https://doaj.org/article/4abe59003b2e41f5bd32b1596679a38c
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
Autor:
Haochen, Liu, Hangbo, Liu, Lanxin, Su, Jinglei, Zheng, Hailan, Feng, Yang, Liu, Miao, Yu, Dong, Han
Publikováno v:
International journal of molecular sciences. 23(15)
The purpose of this research was to investigate and identify
Publikováno v:
International Journal of Oral Science, Vol 13, Iss 1, Pp 1-10 (2021)
International Journal of Oral Science
International Journal of Oral Science
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 identify
Publikováno v:
Archives of oral biology. 141
To identify DLX3 variants in a Chinese family with typical clinical manifestations of tricho-dento-osseous syndrome (TDO).Sanger sequencing was performed to detect DLX3 variants in the TDO family. Three-dimensional laser scanning microscopy, bioinfor
Publikováno v:
International journal of food microbiology. 374
To investigate new disposal methods for agricultural waste from tea plantations, the dynamics of chemical composition and microbial populations of tea plant pruning waste during 60 days of ensiling were studied. The results showed that the pH value d