Fu Xiong

Publication Activity (10 Years)

Years Active: 2021-2023
Publications (10 Years): 8

Top Topics

Transcription Factor

Intellectual Disability

Top Venues

European journal of oral sciences

International journal of oral science

Stem cells international

Clinical oral investigations

This page only lists publications with an associated author ORCID identifier.

Publications

Buling Wu, Wanyu Lu, Weidong Meng, Wenxiao Liao, Aiqin Hu, Buling Wu, Fu Xiong
A novel single-base deletion of the RUNX Family Transcription Factor 2 gene associated with cleidocranial dysplasia. European journal of oral sciences (2023)
Buling Wu, Wanyu Lu, Weidong Meng, Wenxiao Liao, Aiqin Hu, Buling Wu, Fu Xiong
A novel single-base deletion of the RUNX Family Transcription Factor 2 gene associated with cleidocranial dysplasia. European journal of oral sciences 131 (1) (2023)
Buling Wu, Wanyu Lu, Weidong Meng, Wenxiao Liao, Aiqin Hu, Buling Wu, Fu Xiong
A novel single-base deletion of the RUNX Family Transcription Factor 2 gene associated with cleidocranial dysplasia. European journal of oral sciences 131 (1) (2023)
Yanxia Zhang, Hongting Xie, Guanxia Liang, Yunrong Qin, Xiaofeng Wei, Sisi Ning, Yi Liang, Xiongda Liang, Yuling Xie, Zezhang Lin, Dina Zhu, Jiaqiong Lin, Fu Xiong, Xiangming Xu, Xuan Shang
A novel gain-of-function PIP4K2A mutation elevates the expression of β-globin and aggravates the severity of α-thalassemia. British journal of haematology (2023)
Buling Wu, Wanyu Lu, Weidong Meng, Wenxiao Liao, Aiqin Hu, Buling Wu, Fu Xiong
A novel single-base deletion of the RUNX Family Transcription Factor 2 gene associated with cleidocranial dysplasia. European journal of oral sciences 131 (1) (2023)
Jianfan Chen, Xueqing Xu, Song Chen, Ting Lu, Yingchun Zheng, Zhongzhi Gan, Zongrui Shen, Shunfei Ma, Duocai Wang, Leyi Su, Fei He, Xuan Shang, Huiyong Xu, Dong Chen, Leitao Zhang, Fu Xiong
Double heterozygous pathogenic mutations in KIF3C and ZNF513 cause hereditary gingival fibromatosis. International journal of oral science 15 (1) (2023)
Yuhua Pan, Sheng Yi, Dong Chen, Xinya Du, Xinchen Yao, Fei He, Fu Xiong
Identification of a novel missense heterozygous mutation in the KDF1 gene for non-syndromic congenital anodontia. Clinical oral investigations 26 (8) (2022)
Buling Wu, Ting Lu, Ling Peng, Qi Zeng, Xiangyu Huang, Xinchen Yao, Buling Wu, Fu Xiong
Functional Analysis of Ectodysplasin-A Mutations in X-Linked Nonsyndromic Hypodontia and Possible Involvement of X-Chromosome Inactivation. Stem cells international 2021 (2021)