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craniofacial biology/genetics (29) 29
index medicus (23) 23
dentistry (21) 21
dentistry, oral surgery & medicine (21) 21
humans (16) 16
craniofacial anomalies (15) 15
animals (14) 14
genetics (12) 12
cleft lip/palate (9) 9
craniofacial biology (9) 9
cleft palate (8) 8
mutation (7) 7
proteins (7) 7
studies (7) 7
surgery (7) 7
craniofacial abnormalities - genetics (6) 6
female (6) 6
growth/development (6) 6
mandible (6) 6
cartilage (5) 5
cell differentiation (5) 5
congenital defects (5) 5
data analysis (5) 5
developmental biology (5) 5
expression (5) 5
genomes (5) 5
male (5) 5
mice (5) 5
morphogenesis (5) 5
orthodontic (5) 5
cell proliferation (4) 4
cleft lip - genetics (4) 4
cleft palate - genetics (4) 4
defects (4) 4
etiology (4) 4
gene expression (4) 4
genes (4) 4
genetic predisposition to disease (4) 4
genotype (4) 4
jaw (4) 4
kinases (4) 4
maxillofacial surgery (4) 4
muscles (4) 4
neural crest (4) 4
patients (4) 4
phenotype (4) 4
phenotypes (4) 4
research reports (4) 4
signal transduction (4) 4
tooth development (4) 4
age (3) 3
animal models (3) 3
bone (3) 3
bone growth (3) 3
bones (3) 3
cell biology (3) 3
cell growth (3) 3
child (3) 3
children (3) 3
chondrocyte (3) 3
chondrocytes (3) 3
cleft palate - embryology (3) 3
craniofacial growth (3) 3
development (3) 3
endochondral ossification (3) 3
evolution (3) 3
face (3) 3
gene (3) 3
growth (3) 3
growth factor (3) 3
immunohistochemistry (3) 3
mineralization (3) 3
mouth (3) 3
muscle biology (3) 3
orofacial cleft (3) 3
single-nucleotide polymorphism (3) 3
skeletal-muscle (3) 3
skull (3) 3
stem cells (3) 3
stomatognathic diseases (3) 3
transcription factors (3) 3
zebrafish (3) 3
abnormalities (2) 2
abnormalities, multiple - genetics (2) 2
acid phosphatase (2) 2
adult (2) 2
alveolar bone (2) 2
anatomy (2) 2
anormalidades (2) 2
association (2) 2
c-type natriuretic peptide (2) 2
cara (2) 2
cell adhesion & migration (2) 2
cell culture techniques (2) 2
cell-matrix interactions (2) 2
cleft lip - embryology (2) 2
cleft-lip (2) 2
clonal deletion (2) 2
collagen (2) 2
complications (2) 2
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1. Full Text Neonatal Satellite Cells Form Small Myotubes in Vitro
by Carvajal Monroy, P.L and Grefte, S and Kuijpers-Jagtman, A.M and Den Hoff, Von, J.W and Wagener, F.A.D.T.G
Journal of Dental Research, ISSN 0022-0345, 2017, Volume 96, Issue 3, pp. 331 - 338
Although palatal muscle reconstruction in patients with cleft palate takes place during early childhood, normal speech development is often not achieved. We... 
craniofacial biology/genetics | muscle biology | stem cells | cranio-maxillofacial surgery | cleft palate | craniofacial anomalies
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2. Full Text Deregulated Adhesion Program in Palatal Keratinocytes of Orofacial Cleft Patients
by Mammadova and Carels and Zhou and Gilissen and Helmich and Bian and Von den Hoff
Genes, ISSN 2073-4425, 10/2019, Volume 10, Issue 11, p. 836
Orofacial clefts (OFCs) are the most frequent craniofacial birth defects. An orofacial cleft (OFC) occurs as a result of deviations in palatogenesis. Cell... 
molecular biology | craniofacial biology/genetics | cell biology | craniofacial anomalies | gene expression
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3. Full Text Identification and Functional Studies of MYO1H for Mandibular Prognathism
by Sun, R and Wang, Y and Jin, M and Chen, L and Cao, Y and Chen, F
Journal of Dental Research, ISSN 0022-0345, 12/2018, Volume 97, Issue 13, pp. 1501 - 1509
Mandibular prognathism (MP) is regarded as a craniofacial deformity resulting from the combined effects of environmental and genetic factors, while the... 
craniofacial biology/genetics | genetics | craniofacial anomalies | zebrafish | developmental biology | orthodontic(s) | CARTILAGE | POLYMORPHISMS | GENE | DENTISTRY, ORAL SURGERY & MEDICINE | SEGREGATION ANALYSIS | LINKAGE | ASSOCIATION
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4. Full Text Deviating dental arch morphology in mild coronal craniosynostosis syndromes
by Choi, T.M and Kragt, Lea and Goos, Jacqueline and Mathijssen, I.M.J and Wolvius, Eppo and Ongkosuwito, Edwin
Clinical Oral Investigations, ISSN 1432-6981, 01/2018
textabstractObjectives: To determine whether the intramaxillary relationship of patients with Muenke syndrome and Saethre-Chotzen syndrome or TCF12-related... 
Craniofacial anomalies | Jaw relationship | Tooth development | Jaw biomechanics | Syndromic craniosynostosis | Dental arch dimensions | Orthodontic(s) | Growth/development | Craniofacial biology/genetics
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5. Full Text Three-dimensional palatal anatomic characteristics' correlation with dermatoglyphic heterogeneity in Angle malocclusions
by AlShahrani, I and Dawasaz, AA and Syed, S and Ibrahim, M and Togoo, RA
ANGLE ORTHODONTIST, ISSN 0003-3219, 07/2019, Volume 89, Issue 4, pp. 643 - 650
Objectives: To assess correlation of dermatoglyphic (DG) pattern with quantitative palatal anatomic parameters measured using three-dimensional (3D) scanning... 
ARCH WIDTHS | Oral diagnosis | Dental anatomy | DENTISTRY, ORAL SURGERY & MEDICINE | Orthodontic(s) | GENES | Growth/development | DENTAL ARCH | EXPRESSION | CLASS-II | OCCLUSION | Craniofacial biology/genetics
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6. Full Text Protein Arginine Methyltransferase PRMT1 Is Essential for Palatogenesis
by Gou, Y and Li, J and Jackson-Weaver, O and Wu, J and Zhang, T and Gupta, R and Cho, I and Ho, T.V and Chen, Y and Li, M and Richard, S and Wang, J and Chai, Y and Xu, J
Journal of Dental Research, ISSN 0022-0345, 12/2018, Volume 97, Issue 13, pp. 1510 - 1518
Cleft palate is among the most common birth defects. Currently, only 30% of cases have identified genetic causes, whereas the etiology of the majority remains... 
craniofacial biology/genetics | cleft palate | posttranslational modifications | craniofacial anomalies | signal transduction | epigenetics | METHYLATION | CLEFT-LIP | REGULATOR | DENTISTRY, ORAL SURGERY & MEDICINE | IN-VIVO | CRANIOFACIAL DEVELOPMENT | HISTONE H4 | MOLECULAR-MECHANISMS
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7. Full Text Deviating dental arch morphology in mild coronal craniosynostosis syndromes
by Choi, T.M and Kragt, L and Goos, J.A.C and Mathijssen, I.M.J and Wolvius, E.B and Ongkosuwito, E.M
Clinical Oral Investigations, ISSN 1432-6981, 2019, Volume 23, Issue 7, pp. 2995 - 3003
To determine whether the intramaxillary relationship of patients with Muenke syndrome and Saethre-Chotzen syndrome or TCF12-related craniosynostosis are... 
Jaw relationship | Craniofacial anomalies | Tooth development | Syndromic craniosynostosis | Jaw biomechanics | Dental arch dimensions | Orthodontic(s) | Growth/development | Dentistry | Craniofacial biology/genetics | Biomechanics | Advertising executives | Orthodontics
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8. Full Text Disruption of FOXF2 as a Likely Cause of Absent Uvula in an Egyptian Family
by Seselgyte, R and Bryant, D and Demetriou, C and Ishida, M and Peskett, E and Moreno, N and Morrogh, D and Sell, D and Lees, M and Farrall, M and Moore, G.E and Sommerlad, B and Pauws, E and Stanier, P
Journal of Dental Research, ISSN 0022-0345, 6/2019, Volume 98, Issue 6, pp. 659 - 665
This study investigated the genetic basis of an unusual autosomal dominant phenotype characterized by familial absent uvula, with a short posterior border of... 
craniofacial biology/genetics | cleft palate | transcription factor(s) | speech pathology | oral pathology | gene expression
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9. Full Text Selective Role of Discoidin Domain Receptor 2 in Murine Temporomandibular Joint Development and Aging
by Ge, C and Mohamed, F and Binrayes, A and Kapila, S and Franceschi, R.T
Journal of Dental Research, ISSN 0022-0345, 3/2018, Volume 97, Issue 3, pp. 321 - 328
Temporomandibular joint (TMJ) disorders are often associated with development of osteoarthritis-like changes in the mandibular condyle. Discoidin domain... 
cell-matrix interactions | craniofacial biology/genetics | joint disease | growth/development | temporomandibular disorders (TMD) | cartilage | ACTIVATION | OSTEOBLAST DIFFERENTIATION | COLLAGEN | MOUSE | MODEL | ARTICULAR-CARTILAGE | DENTISTRY, ORAL SURGERY & MEDICINE | OSTEOARTHRITIS | cellmatrix interactions | EPIDEMIOLOGY | MODULATION | KINASES | craniofacial biology | development | genetics | growth | Research Reports
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10. Full Text BMP1 and TLL1 Are Required for Maintaining Periodontal Homeostasis
by Wang, J and Massoudi, D and Ren, Y and Muir, A.M and Harris, S.E and Greenspan, D.S and Feng, J.Q
Journal of Dental Research, ISSN 0022-0345, 5/2017, Volume 96, Issue 5, pp. 578 - 585
Mutations in bone morphogenetic protein 1 (BMP1) in humans or deletion of BMP1 and related protease tolloid like 1 (TLL1) in mice lead to osteogenesis... 
craniofacial biology/genetics | mineralized tissue/development | matrix biology | inflammation | ECM | periodontal tissues/periodontium | PROCOLLAGEN C-PROTEINASE | TOLLOID-LIKE 1 | BONE MORPHOGENETIC PROTEIN-1 | DMP1 | DENTIN MATRIX PROTEIN-1 | GENE | ROLES | DENTISTRY, ORAL SURGERY & MEDICINE | MOUSE MODEL | OSTEOGENESIS IMPERFECTA | MICE | Bone Morphogenetic Protein 1 - deficiency | Immunohistochemistry | Mandible | Extracellular Matrix Proteins - biosynthesis | Tolloid-Like Metalloproteinases - physiology | Extracellular Matrix - metabolism | Homeostasis | Tolloid-Like Metalloproteinases - deficiency | Bone Morphogenetic Protein 1 - physiology | X-Ray Microtomography | Matrix Metalloproteinase 13 - metabolism | Mice, Knockout | Microscopy, Confocal | Periodontal Ligament - physiology | Periodontitis - physiopathology | Phenotype | Animals | Tartrate-Resistant Acid Phosphatase - metabolism | Anti-Bacterial Agents - pharmacology | Mice | Procollagen - biosynthesis | craniofacial biology | development | genetics | periodontium | mineralized tissue | periodontal tissues | Research Reports
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11. Full Text The Mighty Chondrocyte
: No Bones about It
by Purcell, P and Trainor, P.A
Journal of Dental Research, ISSN 0022-0345, 12/2015, Volume 94, Issue 12, pp. 1625 - 1627
craniofacial biology/genetics | osteoblast(s) | cell differentiation | bone biology | cartilage | mandibular condyle | DENTISTRY, ORAL SURGERY & MEDICINE | OSTEOBLASTS | HYPERTROPHIC CHONDROCYTES | GROWTH-PLATE | FATE | Animals | Chondrocytes - physiology | Mandibular Condyle - growth & development | Bone Development - physiology | craniofacial biology | Departments | genetics
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12. Full Text The Use of Variant Maps to Explore Domain-Specific Mutations of FGFR1
by Lansdon, L.A and Bernabe, H.V and Nidey, N and Standley, J and Schnieders, M.J and Murray, J.C
Journal of Dental Research, ISSN 0022-0345, 10/2017, Volume 96, Issue 11, pp. 1339 - 1345
Here we describe the genotype-phenotype correlations of diseases caused by variants in Fibroblast Growth Factor Receptor 1 (FGFR1) and report a novel, de novo... 
craniofacial biology/genetics | clinical phenotypes | genetics | craniofacial anomalies | protein modeling | Hartsfield syndrome | GENOTYPE | PHENOTYPE | GROWTH-FACTOR RECEPTORS | GENETIC-VARIATION | ISOLATED HYPOGONADOTROPIC HYPOGONADISM | SIGNALING PATHWAY | DENTISTRY, ORAL SURGERY & MEDICINE | KALLMANN-SYNDROME | SPECTRUM | ASSOCIATION | Genetic Association Studies | Humans | Genotype | Male | Cleft Palate - genetics | Holoprosencephaly - genetics | Mutation, Missense | Receptor, Fibroblast Growth Factor, Type 1 - genetics | Intellectual Disability - genetics | Genetic Variation | Cleft Lip - genetics | Phenotype | Hand Deformities, Congenital - genetics | Adult | Fingers - abnormalities | Craniofacial Abnormalities - genetics | craniofacial biology | Research Reports
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13. Full Text Anti-EDAR Agonist Antibody Therapy Resolves Palate Defects in Pax9-/- Mice
by Jia, S and Zhou, J and Wee, Y and Mikkola, M.L and Schneider, P and D’Souza, R.N
Journal of Dental Research, ISSN 0022-0345, 10/2017, Volume 96, Issue 11, pp. 1282 - 1289
To date, surgical interventions are the only means by which craniofacial anomalies can be corrected so that function, esthetics, and the sense of well-being... 
craniofacial biology/genetics | therapeutic treatment | cleft palate | morphogenesis | developmental biology | gene expression | LINKED ECTODERMAL DYSPLASIA | CLEFT-LIP | ECTODYSPLASIN | KAPPA-B | BMP4 | RECEPTOR EDAR | DENTISTRY, ORAL SURGERY & MEDICINE | HAIR FOLLICLE INDUCTION | PAX9 | MSX1 | Signal Transduction | Antibodies, Monoclonal - pharmacology | PAX9 Transcription Factor - metabolism | Cleft Palate - embryology | Cleft Palate - drug therapy | Mice, Inbred Strains | Morphogenesis | Phenotype | Animals | In Situ Hybridization | Edar Receptor - agonists | Gene Expression Regulation, Developmental | Mice | Real-Time Polymerase Chain Reaction | craniofacial biology | genetics | Research Reports
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14. Full Text The ADAMTS1 Gene Is Associated with Familial Mandibular Prognathism
by Guan, X and Song, Y and Ott, J and Zhang, Y and Li, C and Xin, T and Li, Z and Gan, Y and Li, J and Zhou, S and Zhou, Y
Journal of Dental Research, ISSN 0022-0345, 9/2015, Volume 94, Issue 9, pp. 1196 - 1201
Mandibular prognathism is a facial skeletal malocclusion. Until now, the genetic mechanism has been unclear. The goal of this study was to identify candidate... 
craniofacial biology/genetics | molecular genetics | SNV | whole genome analysis | orthodontic(s) | bioinformatics | JAW | TOOTH | CONDYLAR CARTILAGE | MALOCCLUSION | DENTISTRY, ORAL SURGERY & MEDICINE | GROWTH | OSTEOBLASTS | EXPRESSION | Humans | Middle Aged | Male | Mutation, Missense | Young Adult | Asian Continental Ancestry Group | Pedigree | Adolescent | Adult | Female | Aged | Polymorphism, Single Nucleotide | ADAM Proteins - genetics | Child | Prognathism - genetics | ADAMTS1 Protein
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15. Full Text Circulatory CNP Rescues Craniofacial Hypoplasia in Achondroplasia
by Yamanaka, S and Nakao, Kazumasa and Koyama, N and Isobe, Y and Ueda, Y and Kanai, Y and Kondo, E and Fujii, T and Miura, M and Yasoda, A and Nakao, Kazuwa and Bessho, K
Journal of Dental Research, ISSN 0022-0345, 12/2017, Volume 96, Issue 13, pp. 1526 - 1534
Achondroplasia is the most common genetic form of human dwarfism, characterized by midfacial hypoplasia resulting in occlusal abnormality and foramen magnum... 
craniofacial biology/genetics | maxillofacial surgery | chondrocyte(s) | growth factor(s) | craniofacial anomalies | growth/development | ENDOCHONDRAL OSSIFICATION | PARATHYROID-HORMONE 1-34 | UPPER AIRWAY-OBSTRUCTION | SKELETAL DYSPLASIAS | NASAL SEPTAL CARTILAGE | GLYCOSAMINOGLYCAN SYNTHESIS | SPHENO-OCCIPITAL SYNCHONDROSIS | NATRIURETIC-PEPTIDE | DENTISTRY, ORAL SURGERY & MEDICINE | MANDIBULAR CONDYLAR CARTILAGE | TRANSGENIC MICE | In Situ Nick-End Labeling | Natriuretic Peptide, C-Type - blood | Osteogenesis - drug effects | Achondroplasia - pathology | Reverse Transcriptase Polymerase Chain Reaction | X-Ray Microtomography | Jaw Abnormalities - pathology | Animals | Achondroplasia - diagnostic imaging | Mice | Jaw Abnormalities - drug therapy | Achondroplasia - drug therapy | Natriuretic Peptide, C-Type - pharmacology | Jaw Abnormalities - diagnostic imaging
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16. Full Text Face Forward: Gene Variants, Pathways, and Therapies for Craniofacial Anomalies
by Richman, J.M and Schutte, B.C
Journal of Dental Research, ISSN 0022-0345, 10/2017, Volume 96, Issue 11, pp. 1181 - 1183
craniofacial biology/genetics | tooth development | genetic variation | orofacial cleft(s) | epithelium/adhesion | palate embryology | DENTISTRY, ORAL SURGERY & MEDICINE | Genetic Variation | Cleft Lip - genetics | Animals | Tooth Abnormalities - genetics | Cleft Lip - embryology | Humans | Cleft Palate - surgery | Tooth Abnormalities - therapy | Cleft Palate - embryology | Tooth Abnormalities - embryology | Cleft Palate - genetics | Cleft Lip - surgery
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17. Full Text Molecular and Cellular Regulatory Mechanisms of Tongue Myogenesis
by Parada, C and Han, D and Chai, Y
Journal of Dental Research, ISSN 0022-0345, 6/2012, Volume 91, Issue 6, pp. 528 - 535
The tongue exerts crucial functions in our daily life. However, we know very little about the regulatory mechanisms of mammalian tongue development. In this... 
craniofacial biology/genetics | muscle biology myoblasts | tongue | developmental biology | neural crest | C-MET RECEPTOR | SATELLITE CELLS | NEURAL CREST CELLS | CRANIOFACIAL MUSCLES | SKELETAL-MUSCLE | GENE | TENDON FIBROBLASTS | DENTISTRY, ORAL SURGERY & MEDICINE | MUSCLE PROGENITOR CELLS | PRECURSOR CELLS | EXPRESSION | Paired Box Transcription Factors - genetics | Neural Crest - cytology | Humans | Muscle Development - physiology | Wnt Signaling Pathway - physiology | Cell Movement - genetics | Intercellular Signaling Peptides and Proteins - physiology | Somites - cytology | Somites - embryology | Animals | Branchial Region - cytology | Gene Expression Regulation, Developmental | Neural Crest - embryology | Muscle Development - genetics | Tongue - innervation | Tongue - anatomy & histology | Tongue - embryology | Branchial Region - embryology | craniofacial biology | Reviews | genetics
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18. Full Text Neonatal Satellite Cells Form Small Myotubes In Vitro
by Carvajal Monroy, P.L and Grefte, S and Kuijpers-Jagtman, A.M and Hoff, J.W. Von den and Wagener, F.A.D.T.G
Journal of Dental Research, ISSN 0022-0345, 2017, Volume 96, Issue 3, pp. 331 - 338
Although palatal muscle reconstruction in patients with cleft palate takes place during early childhood, normal speech development is often not achieved. We... 
craniofacial biology/genetics | muscle biology | stem cells | cleft palate | cranio-maxillofacial surgery | craniofacial anomalies | SURVIVAL | CLEFT-PALATE | SOFT PALATE | PROLIFERATION | MYOFIBERS | HETEROGENEITY | SKELETAL-MUSCLE | REPAIR | FIBER TYPES | DENTISTRY, ORAL SURGERY & MEDICINE | DIFFERENTIATION | Animals, Newborn | Immunohistochemistry | Cell Proliferation | Age Factors | Satellite Cells, Skeletal Muscle - cytology | Rats | Muscle, Skeletal - metabolism | Muscle, Skeletal - cytology | Myosin Heavy Chains - metabolism | Animals | Muscle Fibers, Skeletal - cytology | Cell Differentiation | Cell Culture Techniques | In Vitro Techniques
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