H. Feng

发表

Functional analysis of novel RUNX2 mutations in cleidocranial dysplasia

Li Zeng, Jiahui Wei, Dong Han, 2017, Mutagenesis.

Mutations in WNT10B Are Identified in Individuals with Oligodontia.

Zhongsheng Sun, Jinchen Li, Dong Han, 2016, American journal of human genetics.

Tooth defects of EEC and AEC syndrome caused by heterozygous TP63 mutations in three Chinese families and genotype‐phenotype correlation analyses of TP63‐related disorders

Dong Han, Haochen Liu, Yang Liu, 2019, Molecular genetics & genomic medicine.

A novel inhibitor of nuclear factor kappa-B kinase subunit gamma mutation identified in an incontinentia pigmenti patient with syndromic tooth agenesis.

Li Zeng, Dong Han, Haochen Liu, 2019, Archives of oral biology.

Novel DLX3 variant identified in a family with tricho-dento-osseous syndrome.

Dong Han, Haochen Liu, Yang Liu, 2022, Archives of oral biology.

Distinct impacts of bi‐allelic WNT10A mutations on the permanent and primary dentitions in odonto‐onycho‐dermal dysplasia

Dong Han, Haochen Liu, Yang Liu, 2019, American journal of medical genetics. Part A.

Association between rs11001553 of DKK1 and non-syndromic tooth agenesis in the Chinese Han population.

H. Feng, D. Han, J. Zhang, 2014, Genetics and molecular research : GMR.

Novel missense mutations in the AXIN2 gene associated with non-syndromic oligodontia.

Dong Han, Haochen Liu, Yixiang Wang, 2014, Archives of oral biology.

Epithelial Wnt10a Is Essential for Tooth Root Furcation Morphogenesis

Y. Wang, Yang Liu, H. Feng, 2020, Journal of dental research.

Lrp6 Dynamic Expression in Tooth Development and Mutations in Oligodontia

H. Feng, D. Han, M. Yu, 2020, Journal of dental research.

DLX3 regulates osteogenic differentiation of bone marrow mesenchymal stem cells via Wnt/β-catenin pathway mediated histone methylation of DKK4.

Haochen Liu, S. Sun, H. Feng, 2019, Biochemical and biophysical research communications.

DLX3 promotes bone marrow mesenchymal stem cell proliferation through H19/miR-675 axis.

Jian Xu, Haochen Liu, Yang Liu, 2017, Clinical science.

Senescence: novel insight into DLX3 mutations leading to enhanced bone formation in Tricho-Dento-Osseous syndrome

Jian Xu, Haochen Liu, N. Zhao, 2016, Scientific Reports.

Nine Novel PAX9 Mutations and a Distinct Tooth Agenesis Genotype-Phenotype

H. Feng, X. Zhang, B. Bai, 2018, Journal of dental research.

Phenotype and genotype analyses in seven families with dentinogenesis imperfecta or dentin dysplasia.

H. Feng, J. Yang, F. Li, 2017, Oral diseases.

A novel 18-bp in-frame deletion mutation in RUNX2 causes cleidocranial dysplasia.

Jiahui Wei, N. Zhao, S. Sun, 2017, Archives of oral biology.

Functional Study of Ectodysplasin-A Mutations Causing Non-Syndromic Tooth Agenesis

Wenjing Shen, Guozhong Zhang, Haochen Liu, 2016, PloS one.

A case-control study of the association between tooth-development gene polymorphisms and non-syndromic hypodontia in the Chinese Han population.

Haochen Liu, H. Feng, Dong Han, 2012, European journal of oral sciences.

Novel Identification of a Four-base-pair Deletion Mutation in PITX2 in a Rieger Syndrome Family

Y. Wang, H. Feng, X. Zhang, 2003, Journal of dental research.

A novel non-stop mutation in MSX1 causing autosomal dominant non-syndromic oligodontia.

H. Feng, D. Han, Sing-Wai Wong, 2014, Mutagenesis.

rs929387 of GLI3 Is Involved in Tooth Agenesis in Chinese Han Population

Haochen Liu, H. Feng, Dong Han, 2013, PloS one.

Comparative analysis of rare EDAR mutations and tooth agenesis pattern in EDAR‐ and EDA‐associated nonsyndromic oligodontia

Haochen Liu, Yang Liu, H. Feng, 2020, Human mutation.

Functional study of novel PAX9 variants: the paired domain and non-syndromic oligodontia.

Haochen Liu, Yang Liu, H. Feng, 2020, Oral diseases.

Occlusal Rehabilitation in a Patient with Oligodontia and Microdontia using Implants and Full-Ceramic Restorations: A Clinical Report.

H. Feng, Sing-Wai Wong, Iting Yeh, 2019, The Chinese journal of dental research : the official journal of the Scientific Section of the Chinese Stomatological Association.

A Novel AXIN2 Missense Mutation Is Associated with Non-Syndromic Oligodontia

Haochen Liu, H. Feng, Yuan Zhan, 2015, PloS one.

EDA Gene Mutations Underlie Non-syndromic Oligodontia

H. Feng, H. Qu, D. Han, 2009, Journal of dental research.

Novel EDA mutation resulting in X-linked non-syndromic hypodontia and the pattern of EDA-associated isolated tooth agenesis.

H. Feng, H. Qu, Xiao-xia Zhang, 2008, European journal of medical genetics.

Identification and Functional Analysis of Two Novel PAX9 Mutations

H. Feng, R. D'Souza, G. Mues, 2008, Cells Tissues Organs.

Association between EDAR Polymorphisms and Non-Syndromic Tooth Agenesis in the Chinese Han Population.

Haochen Liu, Yang Liu, H. Feng, 2017, The Chinese journal of dental research : the official journal of the Scientific Section of the Chinese Stomatological Association.

Long non-coding RNA H19/SAHH axis epigenetically regulates odontogenic differentiation of human dental pulp stem cells.

Haochen Liu, Yang Liu, S. Sun, 2018, Cellular signalling.

miR‐675 promotes odontogenic differentiation of human dental pulp cells by epigenetic regulation of DLX3

Haochen Liu, Yang Liu, N. Zhao, 2018, Experimental cell research.

BMPR2 Variants Underlie Nonsyndromic Oligodontia

Haochen Liu, Yang Liu, H. Feng, 2023, International journal of molecular sciences.

Correlation between the phenotypes and genotypes of X-linked hypohidrotic ectodermal dysplasia and non-syndromic hypodontia caused by ectodysplasin-A mutations.

H. Feng, S. Pan, Dong Han, 2011, European journal of medical genetics.

mmu‐miR‐1963 negatively regulates the ameloblast differentiation of LS8 cell line by directly targeting Smoc2 3'UTR

Haochen Liu, Yang Liu, H. Feng, 2018, Experimental cell research.

Mutant Runx2 regulates amelogenesis and osteogenesis through a miR-185-5p-Dlx2 axis

H. Feng, Yajuan Gu, Hongshan Zhao, 2017, Cell Death & Disease.

ameloblast differentiation of LS 8 cell line by directly targeting Smoc 2 3 ’ UTR

Jinhao, Haochen Liu, Yang Liu, 2017 .

Dose Dependence Effect in Biallelic WNT10A Variant-Associated Tooth Agenesis Phenotype

Yang Liu, H. Feng, Miao Yu, 2022, Diagnostics.

KDF1 Novel Variant Causes Unique Dental and Oral Epithelial Defects

Yang Liu, H. Feng, Jinglei Zheng, 2022, International journal of molecular sciences.

BMP4 mutations in tooth agenesis and low bone mass.

Hao Wang, Yang Liu, H. Feng, 2019, Archives of oral biology.

Novel MSX1 variants identified in families with nonsyndromic oligodontia

Yang Liu, H. Feng, T. Cai, 2021, International journal of oral science.

DLX3 epigenetically regulates odontoblastic differentiation of hDPCs through H19/miR-675 axis.

Haochen Liu, Yang Liu, S. Sun, 2019, Archives of oral biology.

Morphological analyses and a novel de novo DLX3 mutation associated with tricho-dento-osseous syndrome in a Chinese family.

Hailan Feng, Lixin Qiu, Haochen Liu, 2015, European journal of oral sciences.

A Novel CDH1 Variant Identified in a Chinese Family with Blepharocheilodontic Syndrome

Yang Liu, H. Feng, Miao Yu, 2022, Diagnostics.

Down-regulation of Wnt10a affects odontogenesis and proliferation in mesenchymal cells.

Lei Wang, Yang Liu, H. Feng, 2013, Biochemical and biophysical research communications.

Rare phenotype: Hand preaxial polydactyly associated with LRP6-related tooth agenesis in humans

Yang Liu, H. Feng, Miao Yu, 2021, NPJ genomic medicine.

DLX3 negatively regulates osteoclastic differentiation through microRNA-124.

Yang Liu, N. Zhao, Yixiang Wang, 2016, Experimental cell research.

Mutant Runx2 regulates amelogenesis and osteogenesis through a miR-185-5p-Dlx2 axis

H. Feng, Yajuan Gu, Hongshan Zhao, 2017, Cell Death & Disease.

[Mutation detection in ED1 gene in hypohidrotic ectodermal dysplasia (HED) families].

H. Feng, Ying Wang, Xiao-xia Zhang, 2003, Beijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences.

Novel PITX2 mutations identified in Axenfeld-Rieger syndrome and the pattern of PITX2-related tooth agenesis.

Yang Liu, S. Sun, H. Feng, 2019, Oral diseases.

Four Novel PAX9 Variants and the PAX9-Related Non-Syndromic Tooth Agenesis Patterns

Haochen Liu, Yang Liu, H. Feng, 2022, International journal of molecular sciences.

Rare compound heterozygous variants of LAMB3 and histological features of enamel and oral mucosa

Haochen Liu, Yang Liu, H. Feng, 2022, Frontiers in Physiology.

Rare X-Linked Hypohidrotic Ectodermal Dysplasia in Females Associated with Ectodysplasin-A Variants and the X-Chromosome Inactivation Pattern

Yang Liu, H. Feng, Jinglei Zheng, 2022, Diagnostics.

Restorative treatment strategies for patients with cleidocranial dysplasia

Jiahui Wei, H. Feng, Xuemei Gao, 2015, Acta Odontologica Scandinavica.

Mutations in WNT10B Are Identified in Individuals with Oligodontia.

Zhongsheng Sun, Jinchen Li, H. Feng, 2016, American journal of human genetics.

DLX3 mutation negatively regulates odontogenic differentiation of human dental pulp cells.

Haochen Liu, Yang Liu, Yixiang Wang, 2017, Archives of oral biology.