Results 21 to 30 of about 76,690 (303)
Craniofacial Features in Richieri-Costa-Pereira Syndrome
, 2021 Objective: Patients with Richieri-Costa-Pereira syndrome (RCPS) present severe craniofacial alterations and frequently require orthodontic and surgical procedures.
Pardo, Milena P. +3 more
core +1 more source
Progress in Orthodontics, 2021 Background A systematic review of the evidence should be undertaken to support the justification for undertaking a clinical trial. The aim of this study was to examine whether reports of orthodontic Randomised Clinical Trials (RCTs) cite prior systematic
Kishan Patel +3 more
doaj +1 more source
A gene network regulated by FGF signalling during ear development
Scientific Reports, 2017 During development cell commitment is regulated by inductive signals that are tightly controlled in time and space. In response, cells activate specific programmes, but the transcriptional circuits that maintain cell identity in a changing signalling ...
Maryam Anwar +4 more
doaj +1 more source
Q&A: Morphological insights into evolution
BMC Biology, 2017 In this question and answer article we discuss how evolution shapes morphology (the shape and pattern of our bodies) but also how learning about morphology, and specifically how that morphology arises during development, can shed light on mechanisms that
Neal Anthwal, Abigail S. Tucker
doaj +1 more source
egfl6 expression in the pharyngeal pouch is dispensable for craniofacial development
Animal Cells and Systems, 2021 Epidermal growth factor-like domain multiple 6 (Egfl6) is a basement membrane protein and plays an important role in hair follicle morphogenesis, angiogenesis, notochord development in vertebrates.
Sil Jin +4 more
doaj +1 more source
Craniofacial Growth Analysis of Individuals With and Without Cleft Lip and Palate in Colombia [PDF]
, 2021 Introducción: El crecimiento craneofacial es un proceso dinámico e impredecible influenciado por factores genéticos y ambientales, presentando diferencias fenotípicas y de género.
González Carrera, María Clara +6 more
core +1 more source
Stem Cells International, 2022 Objectives. Kabuki syndrome (KS) is a rare genetic disorder characterized by developmental delay, retarded growth, and cardiac, gastrointestinal, neurocognitive, renal, craniofacial, dental, and skeletal defects.
Badam Enkhmandakh +6 more
doaj +1 more source
Craniofacial development: making faces [PDF]
Journal of Anatomy, 2005 Craniofacial development has traditionally been a field of research in which many divergent views are expressed and novel theories put forward to explain observed normal and abnormal phenomena. Decades of investigation have shown that craniofacial development is an intricate and complex series of events that require inductive and directive cell and ...
Evans, D J, Francis-West, P H
openaire +2 more sources
The ribosome biogenesis factor Nol11 is required for optimal rDNA transcription and craniofacial development in Xenopus. [PDF]
PLoS Genetics, 2015 The production of ribosomes is ubiquitous and fundamental to life. As such, it is surprising that defects in ribosome biogenesis underlie a growing number of symptomatically distinct inherited disorders, collectively called ribosomopathies. We previously
John N Griffin +4 more
doaj +1 more source
, 2020 Objective: A diagnosis of a congenital craniofacial condition can have a significant impact on the psychological wellbeing of the affected family. As the first health professionals likely to come into contact with families, non-specialists, such as ...
Costa, Bruna, Stock, Nicola Marie
core +1 more source