Results 111 to 120 of about 6,450 (193)
Msx1 and Msx2 act as essential activators of Atoh1 expression in the murine spinal cord
, 2014 International audienceDorsal spinal neurogenesis is orchestrated by the combined action of signals secreted from the roof plate organizer and a downstream transcriptional cascade. Within this cascade, Msx1 and Msx2, two homeodomain transcription factors (
Daubas, Philippe +7 more
core +1 more source
Extracting fluorescent reporter time courses of cell lineages from high-throughput microscopy at low temporal resolution [PDF]
Live Cell Imaging and High Throughput Screening are rapidly evolving techniques and have found many applications in recent years. Modern microscopy enables the visualisation of internal changes in the cell through the use of fluorescently tagged ...
Downey, Mike J.
core
Endothelial Msx1 transduces hemodynamic changes into an arteriogenic remodeling response
, 2015 Collateral remodeling is critical for blood flow restoration in peripheral arterial disease and is triggered by increasing fluid shear stress in preexisting collateral arteries.
Sander Craps +34 more
core +1 more source
The Msx1 Homeoprotein Recruits Polycomb to the Nuclear Periphery during Development
, 2011 Control of gene expression during development requires the concerted action of sequence-specific transcriptional regulators and epigenetic modifiers, which are spatially coordinated within the nucleus through mechanisms that are poorly understood.
Michael H. Kagey +15 more
core +1 more source
, 2018 Figure S1. ERK activity is not required for MSX1 expression. (A) Immunolocalization of flag-tagged MSX1 protein in U0126-treated DPSCs. Wild-type MSX1 located exclusively in the nucleus, while mutant MSX1 was distributed over the entire cytoplasm.
Ruili Yang (4927636) +6 more
core +1 more source
MSX1 gene in the etiology orofacial deformities.
Postepy higieny i medycyny doswiadczalnej (Online), 2016 The muscle segment homeobox (MSX1) gene plays a crucial role in epithelial-mesenchymal tissue interactions in craniofacial development. It plays a regulative role in cellular proliferation, differentiation and cell death. The human MSX1 domain was also found in cow (Bt 302906), mouse (Mm 123311), rat (Rn13592001), chicken (Gg 170873) and clawed toad ...
openaire +1 more source
A MISSENSE MUTATION OF MSX1 GENE IN PAKISTANI FAMILIES WITH HYPODONTIA
Pakistan Armed Forces Medical Journal, 2019 Objective: To understand the role of MSX1 gene in Pakistani families with hypodontia. Study Design: Descriptive study. Place and Duration of Study: This descriptive study was performed in Human Molecular Genetics (HMG) Laboratory of Baluchistan ...
Muhammad Nawaz +5 more
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Análisis mutacional del gen MSX1 en pacientes con FLPNS e hipodoncia
Revista Universitas Medica, 2009 Introducción. La etiología de la hendidura labio-palatina es compleja e involucra factores genéticos y ambientales. Además de la hendidura, numerosos estudios han reportado la presencia de anomalías dentales en asociación con varias formas de hendidura ...
SANDRA JANETH GUTIÉRREZ PRIETO +3 more
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