Competence, specification and commitment to an olfactory placode fate [PDF]
, 2008 The nasal placode shares a common origin with other sensory placodes within a pre-placodal domain at the cranial neural plate border. However, little is known about early events in nasal placode development as it segregates from prospective lens, neural ...
Bhattacharyya, Sujata +1 more
core +2 more sources
Journal of Indian Academy of Oral Medicine and Radiology, 2008 Treacher Collin′s syndrome is a rare syndrome that is characterized primarily by defects of the structures derived from first and second branchial arches. It is a group of closely related defects of head and face; often hereditary/familial in pattern. We
Y Samata +3 more
doaj +1 more source
Rhombomere of origin determines autonomous versus environmentally regulated expression of Hoxa3 in the avian embryo [PDF]
, 1996 We have investigated the pattern and regulation of Hoxa3 expression in the hindbrain and associated neural crest cells in the chick embryo, using whole mount in situ hybridization in conjunction with DiI labeling of neural crest cells and microsurgical ...
Ariza-McNaughton, Linda +4 more
core
Goldenhar's Syndrome (A Case Report)
Indian Journal of Plastic Surgery, 1987 Goldenhar's syndrome or occulo-auriculo-vertebral dysplasia is characterized by the presence of abnormalities of the first and second branchial arches accompanied by apibulbar dermoids or lipodermoids and vertebral anomaties.
S. Bhattacharya +2 more
doaj +1 more source
In ovo time-lapse analysis after dorsal neural tube ablation shows rerouting of chick hindbrain neural crest [PDF]
, 2000 Previous analyses of single neural crest cell trajectories have suggested important roles for interactions between neural crest cells and the environment, and amongst neural crest cells. To test the relative contribution of intrinsic versus extrinsic
Bronner-Fraser, Marianne +2 more
core
A 22-Week-Old Fetus with Nager Syndrome and Congenital Diaphragmatic Hernia due to a Novel SF3B4 Mutation. [PDF]
, 2014 Nager syndrome, or acrofacial dysostosis type 1 (AFD1), is a rare multiple malformation syndrome characterized by hypoplasia of first and second branchial arches derivatives and appendicular anomalies with variable involvement of the radial/axial ray. In
BOTTILLO, IRENE +7 more
core +1 more source
Goldenhar syndrome with rare clinical features
Indian Journal of Paediatric Dermatology, 2017 Goldenhar syndrome is an uncommon syndrome with malformations of first and second branchial arches. Accessory tragus is a constant feature of this syndrome but may be associated with other syndromes as well.
Vineet Relhan +3 more
doaj +1 more source
Phylogeny, expression patterns and regulation of DNA Methyltransferases in early development of the flatfish, Solea senegalensis [PDF]
, 2017 Background: The identification of DNA methyltransferases (Dnmt) expression patterns during development and their regulation is important to understand the epigenetic mechanisms that modulate larval plasticity in marine fish.
Armesto, Paula +5 more
core +2 more sources
Branchial Cysts in Quito, Ecuador
International Archives of Otorhinolaryngology, 2020 Introduction Branchial cleft anomalies are the second most common congenital anomaly in children. However, some lesions may not develop clinically and are not diagnosed until adulthood.
Luis Pacheco-Ojeda +2 more
doaj +1 more source
A new transgenic reporter line reveals Wnt-dependent Snai2 re-expression and cranial neural crest differentiation in Xenopus [PDF]
, 2019 During vertebrate embryogenesis, the cranial neural crest (CNC) forms at the neural plate border and subsequently migrates and differentiates into many types of cells.
Duncan, Melinda K. +7 more
core +1 more source