[HTML][HTML] Functional mechanisms of TRPS1 in disease progression and its potential role in personalized medicine
L Yang, X Gong, J Wang, Q Fan, J Yuan, X Yang… - … -Research and Practice, 2022 - Elsevier
The gene of transcriptional repressor GATA binding 1 (TRPS1), as an atypical GATA
transcription factor, has received considerable attention in a plethora of physiological and …
transcription factor, has received considerable attention in a plethora of physiological and …
The genes involved in dentinogenesis
S Chen, H Xie, S Zhao, S Wang, X Wei, S Liu - Organogenesis, 2022 - Taylor & Francis
The development and repair of dentin are strictly regulated by hundreds of genes. Abnormal
dentin development is directly caused by gene mutations and dysregulation. Understanding …
dentin development is directly caused by gene mutations and dysregulation. Understanding …
[PDF][PDF] Features of the course of enamel biomineralization processes in various anatomical areas of the tooth
The aim: To establish the features of the structural organization of enamel in various
anatomical areas of the tooth and determine their influence on the characteristics of the …
anatomical areas of the tooth and determine their influence on the characteristics of the …
Expression and function of the P2X7 receptor in human osteoblasts: The role of NFATc1 transcription factor
LS Bergamin, L Penolazzi, E Lambertini… - Journal of Cellular …, 2021 - Wiley Online Library
Bone mineralization is an orchestrated process by which mineral crystals are deposited by
osteoblasts; however, the detailed mechanisms remain to be elucidated. The presence of …
osteoblasts; however, the detailed mechanisms remain to be elucidated. The presence of …
[HTML][HTML] Trps1 transcription factor represses phosphate-induced expression of SerpinB2 in osteogenic cells
M Socorro, A Shinde, H Yamazaki, S Khalid, D Monier… - Bone, 2020 - Elsevier
Serine protease inhibitor SerpinB2 is one of the most upregulated proteins following cellular
stress. This multifunctional serpin has been attributed a number of pleiotropic activities …
stress. This multifunctional serpin has been attributed a number of pleiotropic activities …
Deficiency of mineralization-regulating transcription factor trps1 compromises quality of dental tissues and increases susceptibility to dental caries
M Socorro, P Hoskere, C Roberts… - Frontiers in dental …, 2022 - frontiersin.org
Dental caries is the most common chronic disease in children and adults worldwide. The
complex etiology of dental caries includes environmental factors as well as host genetics …
complex etiology of dental caries includes environmental factors as well as host genetics …
Deficiency of Trps1 in Cementoblasts Impairs Cementogenesis and Tooth Root Formation
K Fujikawa, M Socorro, L Lukashova, P Hoskere… - Calcified Tissue …, 2024 - Springer
Cementum is the least studied of all mineralized tissues and little is known about
mechanisms regulating its formation. Therefore, the goal of this study was to provide new …
mechanisms regulating its formation. Therefore, the goal of this study was to provide new …
Cut out that YAPping: Mechanisms to reduce scar formation
V Horsley - Cell Stem Cell, 2022 - cell.com
Tissue repair in adult mammals lacks the regenerative ability of many tissues in other adult
organisms like axolotl and newts. In this issue of Cell Stem Cell, Mascharak et al. use multi …
organisms like axolotl and newts. In this issue of Cell Stem Cell, Mascharak et al. use multi …
Analysis of the function, mechanism and clinical application prospect of TRPS1, a new marker for breast cancer
X He, H Huang, Y Liu, H Li, H Ren - Gene, 2024 - Elsevier
It has been discovered that Trichorhinophalangeal Syndrome-1 (TRPS1), a novel member of
the GATA transcription factor family, participates in both normal physiological processes and …
the GATA transcription factor family, participates in both normal physiological processes and …
Recombinant human growth hormone therapy for childhood trichorhinophalangeal syndrome type I: a case report
D Huang, J Zhao, FL Xia, CC Zou - Children, 2022 - mdpi.com
Trichorhinophalangeal syndrome type I (TRPS I; MIM 190350) is a rare autosomal dominant
disorder of congenital malformations due to variants of the gene TRPS1. We reported on an …
disorder of congenital malformations due to variants of the gene TRPS1. We reported on an …