Results 171 to 180 of about 6,450 (193)
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FGFs and BMP4 induce both Msx1-independent and Msx1-dependent signaling pathways in early tooth development

Development, 1998
ABSTRACT During early tooth development, multiple signaling molecules are expressed in the dental lamina epithelium and induce the dental mesenchyme. One signal, BMP4, has been shown to induce morphologic changes in dental mesenchyme and mesenchymal gene expression via Msx1, but BMP4 cannot substitute for all the inductive functions of ...
M, Bei, R, Maas
openaire   +2 more sources

Msx1 Cooperates with Histone H1b for Inhibition of Transcription and Myogenesis

Science, 2004
During embryogenesis, differentiation of skeletal muscle is regulated by transcription factors that include members of the Msx homeoprotein family. By investigating Msx1 function in repression of myogenic gene expression, we identified a physical interaction between Msx1 and H1b, a specific isoform of mouse histone H1.
Hansol, Lee   +2 more
openaire   +2 more sources

Msx1 disruption leads to diencephalon defects and hydrocephalus

Developmental Dynamics, 2004
AbstractWe have analyzed the expression of the Msx1 gene in the developing mouse brain and examined the brain phenotype in homozygotes. Msx1 is expressed in every cerebral vesicle throughout development, particularly in neuroepithelia, such as those of the fimbria and the medulla.
Casto, Ramos   +4 more
openaire   +2 more sources

Bioinformatic Analysis of Msx1 and Msx2 Involved in Craniofacial Development

Journal of Craniofacial Surgery, 2014
Msx1 and Msx2 were revealed to be candidate genes for some craniofacial deformities, such as cleft lip with/without cleft palate (CL/P) and craniosynostosis. Many other genes were demonstrated to have a cross-talk with MSX genes in causing these defects. However, there is no systematic evaluation for these MSX gene-related factors.
Jiewen, Dai   +5 more
openaire   +2 more sources

[Msx1 and its influence on craniofacial growth].

L' Orthodontie francaise, 2007
Many genes that interact in a complex and interdependent manner participate in the development of the craniofacial complex. One of them, the Msxl homeobox gene, a transcription factor, is expressed from early developmental stages to adulthood in accordance with specific spatio-temporal patterns.
Brigitte, Vi-Fane   +2 more
openaire   +1 more source

Orodental malformations associated with human MSX1 sequence variants

The Journal of the American Dental Association
MSX1 sequence variants have been known to cause human tooth agenesis (TA) with or without orofacial clefts. However, their roles during the whole processes of tooth development are not fully understood. This study aimed to characterize a 4-membered family with TA carrying a novel MSX1 pathogenic variant and investigate the disease mechanism.The authors
Yin-Lin Wang   +6 more
openaire   +2 more sources

A novelMSX1 mutation in hypodontia

American Journal of Medical Genetics Part A, 2004
Gert Matthijs, A Verdonck, C Carels
exaly  

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