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European Journal of Medical Genetics|April 5, 2011
Correlation between the phenotypes and genotypes of X-linked hypohidrotic ectodermal dysplasia and non-syndromic hypodontia caused by ectodysplasin-A mutationsJin Zhang, Dong Han, Shujuan Song, et al.Archives of Oral Biology|June 17, 2022
Novel DLX3 variant identified in a family with tricho-dento-osseous syndromeHaochen Liu, Yue Wang, Hangbo Liu, et al.ACS Applied Materials & Interfaces|April 19, 2023
Cellulose-Assisted Vertically Heterostructured PEO-Based Solid Electrolytes Mitigating Li-Succinonitrile Corrosion for Lithium Metal BatteriesJiechen Song, Yuxing Xu, Yuncheng Zhou, et al.Molecular Genetics & Genomic Medicine|May 4, 2019
Tooth defects of EEC and AEC syndrome caused by heterozygous TP63 mutations in three Chinese families and genotype-phenotype correlation analyses of TP63-related disordersJinglei Zheng, Haochen Liu, Yuan Zhan, et al.Archives of Oral Biology|April 29, 2019
DLX3 epigenetically regulates odontoblastic differentiation of hDPCs through H19/miR-675 axisLi Zeng, Shichen Sun, Liying Dong, et al.European Journal of Medical Genetics|July 29, 2008
Novel EDA mutation resulting in X-linked non-syndromic hypodontia and the pattern of EDA-associated isolated tooth agenesisDong Han, Yu Gong, Hua Wu, et al.International Journal of Molecular Sciences|January 21, 2023
<i>BMPR2</i> Variants Underlie Nonsyndromic OligodontiaJinglei Zheng, Haochen Liu, Miao Yu, et al.Frontiers in Physiology|October 27, 2022
Rare compound heterozygous variants of <i>LAMB3</i> and histological features of enamel and oral mucosaFang Li, Miao Yu, Zhuangzhuang Fan, et al.Oral Diseases|June 9, 2024
A novel WNT10A variant impairs the homeostasis of alveolar bone mesenchymal stem cellsBichen Lin, Haochen Liu, Hangbo Liu, et al.International Journal of Molecular Sciences|October 27, 2022
<i>KDF1</i> Novel Variant Causes Unique Dental and Oral Epithelial DefectsMiao Yu, Hangbo Liu, Yang Liu, et al.Pageof 9