Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Hangbo Liu"'
Publikováno v:
Mathematics, Vol 12, Iss 22, p 3505 (2024)
This research focuses on how market sentiment affects corporate governance in the Chinese market. The sample covers the years from 2014 to 2023. Market sentiment is estimated using a cross-sectional absolute deviation (CSAD) model, and earnings quali
Externí odkaz:
https://doaj.org/article/b126f60d416b4167b5862e7acf8bf3e3
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
Publikováno v:
Frontiers in Oncology, Vol 8 (2018)
Head and neck cancer is the 6th most common malignancy worldwide and urgently requires novel therapy methods to change the situation of low 5-years survival rate and poor prognosis. Targeted therapy provides more precision, higher efficiency while lo
Externí odkaz:
https://doaj.org/article/b28d9bbe953948828f218dc5c5abad06
Publikováno v:
Diagnostics (Basel, Switzerland). 12(12)
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://explore.openaire.eu/search/publication?articleId=pmid________::76920517064766cfc55fdd05376cd1cb
https://pubmed.ncbi.nlm.nih.gov/36552944
https://pubmed.ncbi.nlm.nih.gov/36552944
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:
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