[图书][B] Perspectives in Genetic and Epigenetic Regulatory Mechanisms in Dental and Craniofacial Biology
W Lin, D Jing, Y Wu, L Guo - 2023 - books.google.com
Genetic factors have been proved to be involved in almost all dental and craniomaxillofacial
diseases. Typical dental and craniomaxillofacial hereditary diseases refer to hereditary …
diseases. Typical dental and craniomaxillofacial hereditary diseases refer to hereditary …
Crucial roles of microRNA-16-5p and microRNA-27b-3p in ameloblast differentiation through regulation of genes associated with amelogenesis imperfecta
A Suzuki, H Yoshioka, T Liu, A Gull, N Singh… - Frontiers in …, 2022 - frontiersin.org
Amelogenesis imperfecta is a congenital disorder within a heterogeneous group of
conditions characterized by enamel hypoplasia. Patients suffer from early tooth loss, social …
conditions characterized by enamel hypoplasia. Patients suffer from early tooth loss, social …
[PDF][PDF] Integrative Organismal Biology
… Further, we examine the complex underlying genetic and … for dental alveoli, which is why
reduction of teeth (oligodontia, either congenial or acquired due to high prevalence of dental …
reduction of teeth (oligodontia, either congenial or acquired due to high prevalence of dental …
一个非综合征型先天缺牙家系的MSX1 基因突变分析
丁婷婷， 邹东， 刘浩辰 - 山东大学学报(医学版), 2022 - yxbwk.njournal.sdu.edu.cn
… Methods A family with non-syndromic tooth agenesis was recruited from Beijing Childrens …
novo MSX1 missense mutation is identified in a patient with non-syndromic tooth agenesis, …
novo MSX1 missense mutation is identified in a patient with non-syndromic tooth agenesis, …
Studio genetico e molecolare su pazienti con anomalie dentarie
G Padalino - 2024 - iris.uniroma1.it
… Mutations in the human homeobox MSX1 gene in the congenital lack of permanent teeth. …
agenesis: mutations of MSX1 and PAX9 reflect their role in patterning human dentition. …
agenesis: mutations of MSX1 and PAX9 reflect their role in patterning human dentition. …
6-12 yaş grubu çocuklarda diş anomalileri ve daimi 1. büyük azı dişlerin endodontik tedavi gereksinimlerinin radyografik değerlendirilmesi
HZ Bodur Güney - acikbilim.yok.gov.tr
… MSX1 ve PAX9 genler transkripsiyon faktörlerini kodlar ve bu genlerin her ikisindeki
mutasyonlar otozomal dominant arka diş eksikliğine neden olur45, 46. Ectodysplasin A (EDA) …
mutasyonlar otozomal dominant arka diş eksikliğine neden olur45, 46. Ectodysplasin A (EDA) …