Zobrazeno 1 - 10
of 16
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
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:
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:
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; Volume 23; Issue 20; Pages: 12465
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1edcdbdc062ac40d2eb4faf9c209968
Publikováno v:
International Journal of Molecular Sciences; Volume 23; Issue 15; Pages: 8142
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://explore.openaire.eu/search/publication?articleId=doi_dedup___::217ee5095d3de698744df9399c46d9d2
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::1c22d3651b437f4d0daa64a5ad1d50e0
https://pubmed.ncbi.nlm.nih.gov/35897718
https://pubmed.ncbi.nlm.nih.gov/35897718
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23fedde956720d71f2ec5ab6178605e3
https://doaj.org/article/86f097bfba6142429fb0f71b67739205
https://doaj.org/article/86f097bfba6142429fb0f71b67739205
Autor:
Tao Cai, Miao Yu, Hong Qu, Liutao Zhang, Jinglei Zheng, Yang Liu, Dong Han, Yongsheng Zhou, Haochen Liu, Hailan Feng, Sing-Wai Wong, Zhuangzhuang Fan
Publikováno v:
Human Mutation. 41:1957-1966
Nonsyndromic oligodontia is a rare congenital anomaly. Mutations in the ectodysplasin A receptor (EDAR) gene are the primary cause of hypohidrotic ectodermal dysplasia but are rarely reported in nonsyndromic oligodontia. This study investigated EDAR
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::02f2114ac973dad1f2e501100658ce12
https://doi.org/10.1002/humu.24104
https://doi.org/10.1002/humu.24104
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e4db5df7c8110e1cc1c8dc7e1e33f495
https://pubmed.ncbi.nlm.nih.gov/35714441
https://pubmed.ncbi.nlm.nih.gov/35714441
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ea55ff6af5de3956fabacecdaa7a672
https://pubmed.ncbi.nlm.nih.gov/35643036
https://pubmed.ncbi.nlm.nih.gov/35643036