Results 181 to 190 of about 130,744 (316)

Loss of Twist1 leads to disruption of ciliary length, endocytic vesicle dynamics, and cell–cell junctions during neural tube formation

Developmental Dynamics, EarlyView.
Abstract Background Endocytosis constitutes a fundamental cellular process governing development through coordinated regulation of plasma membrane remodeling and ciliogenesis, processes essential for cell shape changes and tissue development. Although Twist1 null embryos display complete cranial neural tube (NT) closure defects and conditional knockout
Derrick Thomas, Brittany M. Hufft‐Martinez, Zarna Lalwani, Vi Pham, Mary Elmeniawi, An J. Tran, Jianming Xu, Irfan Saadi, Walid D. Fakhouri   +8 more
wiley   +1 more source

RNA Polymerase III subunit Polr3a is required for craniofacial cartilage and bone development in zebrafish. [PDF]

PLoS Genet
Lubash BT, Gutierrez R, Hansen NA, Fink K, Hopkins CA, Sands LB, Nelson JC, Watt KEN.   +7 more
europepmc   +1 more source

Role of SoxE transcription factors in development and disease

Developmental Dynamics, EarlyView.
Abstract Sox8, Sox9, and Sox10 arose by multiple rounds of genome duplications from a single SoxE gene in ancestral vertebrates. In this review, we will briefly discuss the molecular structure and function of SoxE transcription factors and their evolutionary origin. We will then discuss their expression, function, and developmental disorders.
Merin Lawrence, Gerhard Schlosser
wiley   +1 more source

Smart Hydrogels for Craniofacial Regeneration. [PDF]

Cells
Omidian H, Gill EJ, Kandalam U.
europepmc   +1 more source

Mesenchymal Chondrosarcoma Presenting as Atypical Brown–Sequard Syndrome

Annals of the Child Neurology Society, EarlyView.
Naman D. Shah, Adam Z. Kalawi, Rachel Pearson, Ali Nael, John R. Crawford   +4 more
wiley   +1 more source

Secretopathies emerge as a new class of neurocristopathies

Developmental Dynamics, EarlyView.
Abstract Neural crest cells are a transient embryonic population of cells that give rise to a wide range of structures, including craniofacial cartilage and bone, peripheral neurons and glia, as well as components of the cardiac outflow tract, among others.
Amanda Teixeira, Cassandra Millet‐Boureima, Joshua A. Moore, Loydie A. Jerome‐Majewska   +3 more
wiley   +1 more source

Long-term CPAP treatment for OSA in pycnodysostosis: A 15-year longitudinal follow-up of a patient. [PDF]

Respir Med Case Rep
Bouhamdi A, Chefchaou Y, Benjelloun M, Labyad S, Abida A, Souirti Z, Abourazzak S, Tizniti S, Serraj M, Amara B, Benjelloun MC, Elbiaze M.   +11 more
europepmc   +1 more source

Proteomic profiling of Elp1‐deficient trigeminal ganglia reveals disruption of neurotrophic and metabolic pathways in a familial dysautonomia mouse model

Developmental Dynamics, EarlyView.
Abstract Background Elp1, a subunit of the Elongator complex, is essential for tRNA modification and neuronal development. Mutations in ELP1 underlie familial dysautonomia (FD), a disorder marked by sensory and autonomic neuropathy. While loss of Elp1 disrupts trigeminal ganglion formation and survival, the downstream molecular consequences remain ...
Carrie E. Leonard, Lauren Clarissa Tang, Beatrix Ueberheide, Lisa A. Taneyhill   +3 more
wiley   +1 more source

IoMT-enabled implant sensors for early detection of neurovascular complications in craniofacial distraction osteogenesis. [PDF]

Ann Med Surg (Lond)
Ali T, Khan SA, Shahbaz Z, Haider R, Tahir A, Qamar MA.   +5 more
europepmc   +1 more source

Craniofacial dysostosis.

Journal of the All-India Ophthalmological Society, 1966
Garg K, Saxena R, Bisaria K
openaire   +2 more sources