Results 201 to 210 of about 68,059 (240)

Intergenerational Dental Fear and Anxiety: Children's Pattern of Dental Service Use

Community Dentistry and Oral Epidemiology, EarlyView.
ABSTRACT Objectives Dental care‐related fear and anxiety, involving emotional reactions to dental situations, can negatively impact children's quality of life, oral and systemic health. Recognising maternal characteristics as key determinants of child health, this study examined the intergenerational relationship between dental fear/anxiety and early ...
Helena Silveira Schuch, Cinthia Fonseca Araujo, Giulia Tarquinio Demarco, Mariana Gonzalez Cademartori, Marília Leão Goettems, Andréa Dâmaso Bertoldi, Daniel W. McNeil, Flávio Fernando Demarco   +7 more
wiley   +1 more source

FAM20B Related Skeletal Dysplasia: Expanding the Prenatal Phenotype

Clinical Genetics, EarlyView.
FAM20B encodes glycosaminoglycan xylosylkinase, a key enzyme in proteoglycan biosynthesis. We report compound heterozygous FAM20B variants causing severe, lethal skeletal dysplasia in three fetuses from two pregnancies. Disrupted glycosaminoglycan chain formation leads to abnormal cartilage and bone development, illustrating the essential role of ...
Arda Arduç, Linda C. Zuurbier, Merel C. van Maarle, Peter Lauffer, Jonathan I. M. L. Verbeke, Caroline J. Bax, Minke van Tuyl, Ron Hochstenbach, Eva Pajkrt   +8 more
wiley   +1 more source

Prevalence and Spectrum of Congenital Heart Disease in Individuals With Distal Chromosome 22q11.22–23 Deletions

Clinical Genetics, EarlyView.
The frequency and severity of congenital heart disease vary extensively in individuals with 22q11.22–23 distal deletions. Reduced gene dosage particularly within the low copy repeat (LCR22) D–E region including MAPK1 and HIC2 conveys risk for these defects.
Tanner J. Nelson, Daniel E. McGinn, T. Blaine Crowley, Lydia Rockart, Audrey Green, Victoria Giunta, Oanh Tran, Daniella Miller, Jeroen Breckpot, Ann Swillen, M. Cristina Digilio, Marta Unolt, Carolina Putotto, Federica Pulvirenti, Bruno Marino, Beverly S. Emanuel, Elaine H. Zackai, Zhengdong D. Zhang, Elizabeth Goldmuntz, Erik Boot, Anne S. Bassett, Bernice E. Morrow, Donna M. McDonald‐McGinn   +22 more
wiley   +1 more source

Expanding the Phenotypic Spectrum Associated With Loss‐of‐Function SMARCA4 Variants to Eye Developmental Anomalies

Clinical Genetics, EarlyView.
This study expands the clinical spectrum of SMARCA4 by describing a novel phenotype in three unrelated individuals with truncating variants. Distinct from Coffin–Siris syndrome and rhabdoid tumor predisposition, this new association is characterized by ocular malformations, specifically microphthalmia and coloboma.
Bertrand Chesneau, Marjolaine Willems, Abdelhakim Bouazzaoui, Léopoldine Lequeux, Julie Plaisancié, Salima El Chehadeh, Hélène Dollfus, Nicolas Chassaing   +7 more
wiley   +1 more source

Selective Targeting of IL‐1RAP‐Dependent Eosinophilic Inflammation in Allergic Fungal Airway Disease

Allergy, EarlyView.
Thomas J. Williams, James S. Griffiths, Luis E. Gonzales‐Huerta, David Bell, Anna K. Reed, Anand Shah, Julian R. Naglik, Darius Armstrong‐James   +7 more
wiley   +1 more source

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Craniofacial Muscle Development

2015
The developmental mechanisms that control head muscle formation are distinct from those that operate in the trunk. Head and neck muscles derive from various mesoderm populations in the embryo and are regulated by distinct transcription factors and signaling molecules.
Inbal, Michailovici, Tamar, Eigler, Eldad, Tzahor   +2 more
openaire   +2 more sources

Evolving maps in craniofacial development

Seminars in Cell & Developmental Biology, 2010
The shaping of the vertebrate head results from highly dynamic integrated processes involving the growth and exchange of signals between the ectoderm, the endoderm, the mesoderm and Cephalic Neural Crest Cells (CNCCs). During embryonic development, these tissues change their shape and relative position rapidly and come transiently in contact with each ...
Gitton, Yorick, Heude, Eglantine, Vieux-Rochas, Maxence, Benouaiche, Laurence, Fontaine, Anastasia, Sato, Takahiro, Kurihara, Yukiko, Kurihara, Hiroki, Couly, Gérard, Levi, Giovanni   +9 more
openaire   +3 more sources

Craniofacial Syndromes Part I: Craniofacial Growth and Development, Craniosynostosis Syndromes, Craniofacial Microsomia, and Craniofacial Dysostoses

DeckerMed Plastic Surgery, 2020
Craniofacial syndromes are a diverse group of congenital disorders primarily affecting structures of the head and face.  Recent genetic advances have improved our ability to diagnosis specific syndromes, understand the molecular basis for abnormal embryogenesis, and anticipate future treatment needs. This is the first of a two-part series exploring the
Carolyn R. Rogers-Vizena, Cory M. Resnick, Francesca Saldanha   +2 more
openaire   +1 more source

Craniofacial and upper airway development

Paediatric Respiratory Reviews, 2010
Development of the craniofacial and upper airway structures is a complex choreography of mesenchymal and epithelial tissues responding to soluble growth factors and transcription factors in a tightly regulated sequence. Interruption of the development process or mutation of required transcription or growth factors leads to congenital anomalies of the ...
Leila A, Mankarious, Steven L, Goudy
openaire   +2 more sources

Craniofacial Development in Myotonic Dystrophy

The Cleft Palate Craniofacial Journal, 1992
Anthropometric, cephalometric, and dental data from 23 subjects (12 males and 11 females) afflicted with myotonic dystrophy were compared to similar data from normal subjects who participated in the Iowa Facial Growth Study. A two by two analysis of variance showed that myotonic subjects differed from normal subjects in headlength, head breadth ...
R N, Staley, S E, Bishara, J W, Hanson, A J, Nowak   +3 more
openaire   +2 more sources