Keyphrases
Mouse Model
100%
Neural Crest Cells
70%
Treacher Collins Syndrome
54%
CblC
54%
Caenorhabditis Elegans
54%
Epithelial Cells
54%
Craniofacial Disorders
52%
Ribosome Biogenesis
51%
Homocystinuria
48%
Methylmalonic Acidemia
48%
Craniofacial Development
47%
Pathophysiology
45%
Zebrafish Model
40%
Ronin
40%
Ribosomopathy
37%
Cobalamin Metabolism
36%
Craniofacial Skeleton
32%
Apical Junction
31%
Junction Proteins
29%
Antioxidant Supplementation
27%
Craniofacial Anomalies
27%
Cell Discovery
27%
Cell Properties
27%
RNA Polymerase III
27%
RNA Polymerase I
27%
SKI-II
27%
Cardiac Neural Crest
27%
Neural Crest Cell Migration
27%
Ventricle
27%
Cell Potential
27%
Inborn Errors
27%
Rare Diseases
27%
Outflow Tract Septation
27%
Migration Outflow
27%
Axial Elongation
27%
Somitogenesis
27%
MBTPS1
27%
Proprotein Convertase
27%
Vertebral Development
27%
ECM Signaling
27%
FOXC2
27%
Cell Polarization
27%
Precursor Cells
27%
Polarity Proteins
27%
Apicobasal
27%
Junction Formation
27%
Intestinal Epithelial Cells
27%
Cell Population
25%
Embryogenesis
25%
Cell Death
24%
Medicine and Dentistry
Neural Crest Cell
93%
Disease
72%
Mandibulofacial Dysostosis
54%
Craniofacial Development
47%
Biogenesis
40%
Ribosome
40%
Neural Crest
39%
Progenitor Cell
33%
Cell Population
33%
Skeleton
32%
Craniofacial Malformation
27%
Supplementation
27%
Rare Disease
27%
Stem Cell
27%
Cell Migration
27%
Stem Cell
27%
Ventricle of Heart
27%
DNA Directed RNA Polymerase III
27%
RNA Polymerase I
27%
Antioxidant
27%
Caenorhabditis Elegans
27%
Cell Death
24%
Embryo Development
24%
Neuroepithelial Cell
17%
Pathophysiology
13%
Pigment Cell
13%
Connective Tissue Cell
13%
Tissue (Anatomy)
13%
Glia
13%
Endocrine Cell
13%
Facial Bone
13%
Transcription Factors
13%
Ribosome RNA
10%
Coenzyme
9%
Diet Supplementation
6%
Neuroepithelium
6%
Maternal Treatment
6%
Cell Maturation
6%
Neurocristopathy
6%
DNA Damage
6%
Connective Tissue
6%
Haploinsufficiency
6%
Genotype Phenotype Correlation
6%
Autosomal Dominant Inheritance
6%
Infant Mortality
6%
Oxidative Stress
6%
Congenital Malformation
6%
Craniofacial Syndrome
5%
Ciliopathy
5%
Orphan Disorder
5%
Biochemistry, Genetics and Molecular Biology
Mouse Model
87%
Neural Crest
67%
Cobalamin
54%
Homocystinuria
54%
Metabolic Pathway
45%
Methylmalonic Acidemia
33%
Treacher Collins Syndrome
27%
Ribosome Biogenesis
27%
Caenorhabditis Elegans
27%
Somitogenesis
27%
Proprotein Convertase
27%
Stem Cell
27%
Animal Model
22%
Craniofacial Development
20%
Embryogenesis
20%
Progenitor Cell
20%
Transcription Factors
20%
Somite
20%
Protein Kinase C
18%
Zebra Fish
13%
Cell Death
13%
Genetics
13%
Molecular Biology
13%
Genetic Approach
13%
Protein Catabolism
9%
Allele
9%
Maternal Effect
9%
CRISPR/Cas9
9%
Succinyl-CoA
9%
Genome Editing
9%
Methylcobalamin
9%
Coenzyme
9%
Diptera
9%
Anabolism
9%
Transgenic Mouse
9%
Cadherin
9%
Methionine
9%
Protein Tertiary Structure
9%
Precursor
6%
Neuroepithelial Cell
6%
Infant Mortality
6%
Dietary Antioxidants
6%
Cell Maturation
6%
Genotype Phenotype Correlation
6%
Loss of Function Mutation
6%
Protein Subunit
6%
Haploinsufficiency
6%
DNA Damage
6%
Endocrine Cell
6%
Connective Tissue Cell
6%
