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Keyphrases
Autosomal Recessive Congenital Ichthyosis
100%
Ichthyosis
60%
Congenital Ichthyosis
57%
Skin Diseases
56%
Epidermis
46%
Keratinization Disorder
36%
Letter to Editor
30%
Gain-of-function mutation
30%
ALOXE3
30%
Skin Model
29%
Allelic Heterogeneity
26%
Lipoxygenase
26%
ALOX12
26%
Disease Model
25%
3D Skin Model
24%
Transglutaminase
22%
In Vitro Model
19%
Epidermal Barrier
19%
Autosomal Recessive
19%
Turkey
18%
Cystatin A
18%
Three-dimensional (3D)
17%
Skin Barrier Function
17%
Epidermal Differentiation
17%
CYP4F22
16%
Palmoplantar Keratoderma
16%
Keratinocytes
16%
Treatment Strategy
15%
Reconstructed Human Skin
15%
Hyperkeratotic
15%
Clinical Characteristics
15%
Three-dimensional Skin Model
15%
Nanotransport
15%
Core-multishell
15%
Gene Knockout
14%
Cornification Disorder
14%
TGM1
14%
Vitamin D Status
14%
Functional Analysis
14%
Peeling Skin Disease
13%
Germany
13%
Ichthyosis Syndrome
13%
Barrier Function
12%
Psoriasis
12%
Growth Factor Binding
12%
Binding Protein
12%
Insulin-like
12%
Life Characteristics
12%
Putative Drug Targets
12%
Self-improving
12%
Biochemistry, Genetics and Molecular Biology
Autosomal Recessive Inheritance
84%
Keratinocyte
37%
Lipoxygenase
29%
Genetics
19%
Protease Inhibitor
15%
Loss of Function Mutation
15%
Vitamin D
14%
Missense Mutation
13%
Cathepsin L
12%
Transglutaminase
12%
Cystatin
12%
Ceramide
12%
Adipocyte
12%
Insulin-Like Growth Factor-Binding Protein
12%
Autosomal Dominant Inheritance
12%
Cell Adhesion
12%
Cystatin A
12%
Hypovitaminosis D
12%
Genotype Phenotype Correlation
12%
Human Induced Pluripotent Stem Cell
12%
Cell Culture
12%
Albinism
12%
Hermansky-Pudlak Syndrome
12%
Consanguinity
12%
Morphology
12%
Maturation
12%
Exome Sequencing
9%
Ceramide Synthase
9%
Lipid
8%
Chromosome
8%
Parathyroid Hormone
8%
Missense
7%
Keratinization
7%
Causal Relationship
6%
ABCA12
6%
Inheritance
6%
Arginine
6%
Candidate Gene
6%
Mutagenesis
6%
in Vitro Gene Transfer
6%
Pedigree
6%
Translation Initiation
6%
Amino Acids
6%
Infancy
6%
Genodermatosis
6%
Codon
6%
Nonsense Mutation
5%
Homozygosity
5%
Splice Site Mutation
5%
