X
Search Filters
Format Format
Format Format
X
Sort by Item Count (A-Z)
Filter by Count
Journal Article (1770) 1770
Book Review (196) 196
Publication (129) 129
Magazine Article (15) 15
Book Chapter (11) 11
Conference Proceeding (8) 8
Book / eBook (2) 2
Dissertation (2) 2
more...
Subjects Subjects
Subjects Subjects
X
Sort by Item Count (A-Z)
Filter by Count
cleidocranial dysplasia (1204) 1204
index medicus (1186) 1186
humans (1185) 1185
female (519) 519
male (516) 516
animals (502) 502
osteoblast differentiation (371) 371
mice (367) 367
dentistry (355) 355
cleidocranial dysplasia - genetics (320) 320
cbfa1 (277) 277
adult (274) 274
child (262) 262
runx2 (256) 256
biochemistry & molecular biology (250) 250
adolescent (234) 234
core binding factor alpha 1 subunit - genetics (227) 227
cell biology (224) 224
radiography (211) 211
cleidocranial dysplasia - diagnostic imaging (199) 199
genetics & heredity (193) 193
cleidocranial dysplasia - complications (192) 192
transcription factors - genetics (190) 190
transcription factor (178) 178
expression (169) 169
core binding factor alpha 1 subunit (156) 156
gene (156) 156
osteoblasts - metabolism (153) 153
mutation (151) 151
core binding factor alpha 1 subunit - metabolism (148) 148
bone-formation (141) 141
child, preschool (139) 139
transcription factors - metabolism (137) 137
osteoblasts - cytology (134) 134
cleidocranial dysplasia - diagnosis (131) 131
old medline (127) 127
cleidocranial dysplasia - pathology (124) 124
dysplasia (120) 120
neoplasm proteins (120) 120
phenotype (114) 114
differentiation (113) 113
cell differentiation (106) 106
cell line (105) 105
transcription factors (103) 103
gene-expression (101) 101
bone (100) 100
cells, cultured (98) 98
endocrinology & metabolism (98) 98
middle aged (95) 95
dentistry, oral surgery & medicine (94) 94
osteoblast (93) 93
stomatognathic system (93) 93
genetic aspects (92) 92
infant (92) 92
pedigree (90) 90
gene expression (89) 89
developmental biology (86) 86
osteogenesis (83) 83
analysis (82) 82
molecular sequence data (81) 81
base sequence (79) 79
musculoskeletal diseases (79) 79
research (79) 79
osteoblasts (77) 77
diagnosis, differential (72) 72
gene expression regulation, developmental (72) 72
mutations (72) 72
cell differentiation - physiology (71) 71
abridged index medicus (70) 70
article (70) 70
gene expression regulation (68) 68
bone morphogenetic protein-2 (67) 67
embryonic structures (67) 67
infant, newborn (67) 67
osteoblasts - physiology (67) 67
dna-binding proteins - genetics (66) 66
chondrocyte differentiation (64) 64
mice, transgenic (64) 64
protein binding (64) 64
teeth (64) 64
binding (63) 63
signal transduction (63) 63
cells (62) 62
promoter regions, genetic (62) 62
bone-development (61) 61
genes (61) 61
mice, knockout (61) 61
osteocalcin gene (61) 61
bones (60) 60
osteogenesis - physiology (60) 60
transcription factors - physiology (60) 60
dna-binding (59) 59
musculoskeletal, neural, and ocular physiology (58) 58
acute myeloid-leukemia (57) 57
in-vivo (56) 56
proteins (56) 56
surgery (56) 56
family (55) 55
oncology (54) 54
reverse transcriptase polymerase chain reaction (53) 53
more...
Library Location Library Location
Language Language
Language Language
X
Sort by Item Count (A-Z)
Filter by Count
English (1428) 1428
German (72) 72
Italian (53) 53
French (46) 46
Spanish (39) 39
Japanese (30) 30
Polish (28) 28
Russian (17) 17
Chinese (16) 16
Hungarian (9) 9
Portuguese (9) 9
Croatian (8) 8
Dutch (8) 8
Korean (7) 7
Romanian (6) 6
Danish (4) 4
Serbian (4) 4
Czech (3) 3
Greek (3) 3
Turkish (3) 3
Bulgarian (1) 1
Slovak (1) 1
Swedish (1) 1
more...
Publication Date Publication Date
Click on a bar to filter by decade
Slide to change publication date range


The Cleft Palate-Craniofacial Journal, ISSN 1055-6656, 7/2018, Volume 55, Issue 6, pp. 891 - 894
Objective: The aim of this article is to publish a literature review and report on a new case of cleidocranial dysplasia syndrome with 6p21.1-p12.3... 
Chromosomal anomaly | 6p21.1-p12.3 microdeletion | Cleidocranial dysplasia | Skeletal dysplasia | SURGERY | chromosomal anomaly | UBIQUITIN LIGASE | cleidocranial dysplasia | skeletal dysplasia | DEFICIENCY | FAMILY | EPSILON | DENTISTRY, ORAL SURGERY & MEDICINE | BIOLOGY | DIFFERENTIATION | MUTATIONS | ENDOTHELIAL GROWTH-FACTOR | KAPPA-B ACTIVITY | REVEALS
Journal Article
Annals of Plastic Surgery, ISSN 0148-7043, 07/2019, Volume 83, Issue 1, pp. 112 - 117
ABSTRACTCleidocranial dysplasia (CCD) is a rare hereditary disorder characterized by skeletal malformations and dental abnormalities. Mutations of the... 
orthodontic | supernumerary teeth | combined sequential treatment | RUNX2 | cleidocranial dysplasia | SYSTEM | SURGERY | PATIENT | MUTATIONS | Case studies | Care and treatment | Cleidocranial dysplasia | Patient outcomes | Methods | Oral surgery
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 6/2014, Volume 111, Issue 23, pp. 8482 - 8487
The pathogenesis of cleidocranial dysplasia (CCD) as well as the specific role of core binding factor β (Cbfβ) and the Runt-related transcription factor... 
Phenotypes | Bone formation | Chondrocytes | Bones | Skull | Skeletal development | Mice | Promoter regions | Epiphyses | Osteoblasts | Endochondral bone formation | Growth plate formation | Chondrocyte differentiation | Ossification | Osteoblast differentiation | OSTEOBLAST | MULTIDISCIPLINARY SCIENCES | endochondral bone formation | BINDING-FACTOR-BETA | BONE-DEVELOPMENT | RUNX2 | growth plate formation | TOOTH DEVELOPMENT | osteoblast differentiation | INTERACTS | chondrocyte differentiation | ossification | DIFFERENTIATION | Osteogenesis - physiology | Protein Multimerization | Core Binding Factor beta Subunit - genetics | Mice, 129 Strain | Core Binding Factor Alpha 1 Subunit - metabolism | Promoter Regions, Genetic - genetics | Collagen Type I - genetics | Chondrocytes - physiology | Gene Expression Regulation, Developmental | Cleidocranial Dysplasia - physiopathology | Cleidocranial Dysplasia - metabolism | Chondrocytes - metabolism | Osteogenesis - genetics | Core Binding Factor beta Subunit - metabolism | Animals, Newborn | Skull - metabolism | Collagen Type I - metabolism | Mice, Inbred C57BL | Osteoblasts - physiology | Cells, Cultured | Activating Transcription Factor 4 - genetics | Core Binding Factor beta Subunit - physiology | Mice, Transgenic | Transcription Factors - genetics | Reverse Transcriptase Polymerase Chain Reaction | Blotting, Western | Mice, Knockout | Transcription Factors - metabolism | Microscopy, Confocal | Animals | Activating Transcription Factor 4 - metabolism | Cleidocranial Dysplasia - genetics | Skull - cytology | Sp7 Transcription Factor | Protein Binding | Osteoblasts - metabolism | Core Binding Factor Alpha 1 Subunit - genetics | Microscopy, Fluorescence | Index Medicus | Biological Sciences
Journal Article
National journal of maxillofacial surgery, ISSN 0975-5950, 07/2014, Volume 5, Issue 2, pp. 206 - 208
Cleidocranial dysplasia (CCD) is an autosomal dominant disorder resulting in the skeletal and dental abnormalities due to the disturbance in ossification of... 
Case studies | Rare diseases | Genetic disorders | Cleidocranial dysplasia | Clavicular hypoplasia | cleidocranial dysostosis | cleidocranial dysplasia | Case Report
Journal Article
Journal Article
by Ma, YM and Zhao, FM and Yu, D
BMC PEDIATRICS, ISSN 1471-2431, 04/2019, Volume 19, Issue 1, pp. 97 - 97
BackgroundCleidocranial dysplasia is a rare autosomal dominant disorder resulting in skeletal and dental abnormalities due to the disturbance in ossification... 
PEDIATRICS | Cleidocranial dysplasia | RUNX2 | CHILDREN | Care and treatment | Diagnosis | Epilepsy | Cases | Proteins | Convulsions & seizures | Laboratories | Teeth | Electroencephalography | Mutation
Journal Article
Revista Chilena de Pediatria, ISSN 0370-4106, 07/2017, Volume 88, Issue 4, pp. 517 - 523
Journal Article
The Journal of craniofacial surgery, ISSN 1049-2275, 05/2015, Volume 26, Issue 3, pp. 792 - 795
The aim of this study was to report the orthodontic-surgical approach of a 21-year-old female patient diagnosed with cleidocranial dysplasia. An orthognathic... 
SURGERY | orthodontics | MANAGEMENT | MALOCCLUSION | ABNORMALITIES | MODALITY | CLEIDO-CRANIAL DYSPLASIA | DEFORMITIES | orthognathic surgery | mandibular advancement | Cleidocranial dysplasia | OSTEOTOMY | Orthognathic Surgery - methods | Young Adult | Cleidocranial Dysplasia - surgery | Female | Humans | Dentistry
Journal Article
Bone, ISSN 8756-3282, 03/2019, Volume 120, pp. 176 - 186
Cleidocranial dysplasia (CCD) is an autosomal dominant disorder caused by heterozygous mutations in . Affected individuals exhibit delayed maturation or... 
Secondary cartilage | Cleidocranial dysplasia | Sphenoid bone | Osterix | Runx2 | CONDYLAR CARTILAGE | OSTEOBLAST DIFFERENTIATION | GENE | BIOLOGY | ENDOCRINOLOGY & METABOLISM | CBFA1 | MUTATIONS
Journal Article
Journal of Dental Research, ISSN 0022-0345, 4/2015, Volume 94, Issue 4, pp. 577 - 583
Cleidocranial dysplasia (CCD) is a skeletal dysplasia caused by heterozygous mutations of RUNX2, a gene that is essential for the mineralization of bone and... 
craniofacial biology/genetics | cell biology | craniofacial anomalies | osteogenesis | osteoclasts | bone remodeling/regeneration | craniofacial biology | OSTEOBLAST DIFFERENTIATION | RESORPTION | regeneration | RUNX2 GENE | ALTERED GENE-EXPRESSION | PERIODONTAL-LIGAMENT CELLS | genetics | TOOTH DEVELOPMENT | OSTEOCLAST FORMATION | DENTISTRY, ORAL SURGERY & MEDICINE | CBFA1 | bone remodeling | DECIDUOUS TEETH | BONE | Isoenzymes - analysis | Cell Proliferation | Dental Pulp - pathology | Coculture Techniques | Humans | Tartrate-Resistant Acid Phosphatase | Core Binding Factor Alpha 1 Subunit - analysis | Bone Remodeling - physiology | Extracellular Matrix Proteins - analysis | Phosphoproteins - analysis | Cathepsin K - analysis | Alkaline Phosphatase - analysis | Cell Differentiation - physiology | Child | Osteocalcin - analysis | Osteoclasts - pathology | Acid Phosphatase - analysis | Cells, Cultured | Calcification, Physiologic - physiology | Matrix Metalloproteinase 9 - analysis | RANK Ligand - analysis | Osteoprotegerin - analysis | Cleidocranial Dysplasia - pathology | Leukocytes, Mononuclear - pathology | Osteoblasts - pathology | Cation Transport Proteins - analysis | Cleidocranial Dysplasia - genetics | Sialoglycoproteins - analysis | Odontoblasts - pathology | Core Binding Factor Alpha 1 Subunit - genetics | Index Medicus | Dentistry
Journal Article
PLoS ONE, ISSN 1932-6203, 07/2017, Volume 12, Issue 7, pp. e0181653 - e0181653
Journal Article