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