Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Lanxin Su"'
Publikováno v:
Frontiers in Psychiatry, Vol 15 (2024)
BackgroundIn an era marked by increasing loneliness, understanding the impact of parenting practices on adolescent well-being and resilience is crucial. This study investigates the relationship between parental democratic communication and key indica
Externí odkaz:
https://doaj.org/article/9e927487f0c0474283f499b14f9fbdd0
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:
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
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:
Journal of Information Hiding and Privacy Protection. 3:69-82
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eba10fa2d485c8924dde928be6d19537
https://doi.org/10.32604/jihpp.2021.014108
https://doi.org/10.32604/jihpp.2021.014108
Autor:
Lanxin Su, Huiyong Liu
Publikováno v:
2021 7th International Conference on Computer and Communications (ICCC).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9eaeb142b05db3cc3f679562219cf03c
https://doi.org/10.1109/iccc54389.2021.9674243
https://doi.org/10.1109/iccc54389.2021.9674243
Publikováno v:
Frontiers in Cell and Developmental Biology, Vol 12 (2024)
Bone defect is a common clinical symptom which can arise from various causes. Currently, bone tissue engineering has demonstrated positive therapeutic effects for bone defect repair by using seeding cells such as mesenchymal stem cells and precursor
Externí odkaz:
https://doaj.org/article/15e0908e46814fd19ee285a1ed0df66c