Results 51 to 60 of about 3,948 (205)
Regulation of PHOX2B gene expression by the long non‐coding natural antisense RNA PHOX2B‐AS1
The FEBS Journal, EarlyView.PHOX2B is a transcription factor essential for autonomic nervous system development. We identify and characterize PHOX2B‐AS1, a human long non‐coding antisense transcript at the PHOX2B locus, along with its murine counterpart. Our findings reveal bidirectional transcription and reciprocal regulation: PHOX2B activates PHOX2B‐AS1, whereas PHOX2B‐AS1 ...
Simona Di Lascio +12 more
wiley +1 more source
Mandibular condyle: structure properties and growth regulation [PDF]
, 2014 Malocclusion is a developmental condition. In most instances, malocclusion and dentofacial deformity arise from variations in the normal development, and so it must be evaluated against a perspective of natural growth.
Ren, C, Yang, Y
core +1 more source
Orthodontics &Craniofacial Research, EarlyView.ABSTRACT Objective To explore the effect of personalised titanium plate Bone‐anchored maxillary protraction (BAMP) on the maxillofacial structure of adolescents with skeletal Class III malocclusion. Methods A total of 20 patients with skeletal Class III malocclusion were selected as the treatment group 1 (TG1) with treatment using individualised BAMP ...
Yang Liu +7 more
wiley +1 more source
Cleidocranial dysplasia: A report of two cases
Journal of Indian Society of Pedodontics and Preventive Dentistry, 2011 Cleidocranial dysplasia (CCD) is an autosomal dominant disorder that presents with skeletal dysplasia. It commonly presents with significant dental problems such as retention of multiple deciduous teeth, impaction or delay in eruption of permanent teeth,
D N Mehta, R V Vachhani, M B Patel
doaj +1 more source
The applications of stereolithography in facial reconstructive surgery [PDF]
, 2001 The development of rapid prototyping has evolved from the crude milled models to the laser polymerised stereolithographic models of excellent accuracy. The technology was advanced further with the recent introduction of fused deposition modelling and the
Cheung, LK, Wong, LLS, Wong, MCM
core +1 more source
Pathways to enhancing prenatal diagnosis of skeletal dysplasias
Pregnancy, Volume 2, Issue 3, May 2026.Abstract Skeletal dysplasias are a group of Mendelian disorders that variably alter the development of the musculoskeletal system and phenotypically range from mild short stature syndromes to severe perinatal or neonatal morbidity. Prenatal diagnosis of these conditions can be challenging due to the lack of precision with ultrasound imaging compared to
Michelle Joy Wang +4 more
wiley +1 more source
Cone-beam computed tomography: An inevitable investigation in cleidocranial dysplasia
Contemporary Clinical Dentistry, 2015 Cleidocranial dysplasia is a heritable skeletal dysplasia and one of the most common features of this syndrome is multiple impacted supernumerary teeth.
Nandita S Gupta +3 more
doaj +1 more source
Clinical Case Reports, Volume 14, Issue 4, April 2026.ABSTRACT Pycnodysostosis is a rare autosomal recessive skeletal dysplasia resulting from pathogenic variants in the CTSK gene, which encodes cathepsin K, a lysosomal cysteine protease expressed in osteoclasts. Deficiency of this enzyme leads to defective bone resorption and generalized osteosclerosis.
Meghana Krishna Kesineni +6 more
wiley +1 more source
Clinical Spectrum of Cleidocranial Dysplasia: A Case Report
National Journal of Community Medicine, 2010 Background: The developmental anomaly involving skeleton and teeth is Cleidocranial dysplasia. It is an autosomal disorder with equal sex distribution.
P Sakhi +5 more
doaj
Late-Developing Supernumerary Premolars: Analysis of Different Therapeutic Approaches [PDF]
, 2016 This case series describes the different potential approaches to late-developing supernumerary premolars (LDSP). LDSP are supernumerary teeth (ST) formed after the eruption of the permanent dentition; usually they develop in the premolar region of the ...
Aiello, Domenico +5 more
core +3 more sources