Keyphrases
Pigmentary Disorders
100%
Mutant Protein
100%
SOX10
100%
Phenotypic Variation
100%
Endothelin B Receptor
57%
Microphthalmia-associated Transcription Factor
42%
Megacolon
42%
Transactivation
28%
Hypopigmentation
28%
Waardenburg Syndrome
28%
Deafblindness
28%
Transcription Factor
14%
Non-associated
14%
DNA-binding Domain
14%
Modifier Genes
14%
Inherited Disorders
14%
Transcription Factor Sp1
14%
Syndrome Type
14%
Impaired Function
14%
SOX10 Gene
14%
Pigmentary Abnormalities
14%
Medicine and Dentistry
Mutant Protein
100%
Pigmentary Disorder
100%
Promoter Region
80%
Endothelin Receptor
80%
Microphthalmia Associated Transcription Factor
60%
Megacolon
60%
Transactivation
40%
Waardenburg Syndrome
40%
Hypopigmentation
40%
Deafblindness
40%
Disease
20%
Transcription Factors
20%
Carboxy Terminal Sequence
20%
DNA Binding
20%
Transcription Factor Sp1
20%
Modifier Gene
20%
Biochemistry, Genetics and Molecular Biology
Mutant Protein
100%
SOX10
100%
Promoter Region
50%
Endothelin Receptor Type B
50%
Microphthalmia-Associated Transcription Factor
37%
Transactivation
25%
Transcription Factors
12%
C-Terminus
12%
DNA-binding Domain
12%
Modifier Gene
12%
Sp1 Transcription Factor
12%
Neuroscience
Mutant Protein
100%
SOX10
100%
Promoter Region
50%
Endothelin Receptor Type B
50%
Microphthalmia-Associated Transcription Factor
37%
Transactivation
25%
Transcription Factors
12%
C-Terminus
12%
DNA Binding
12%
Sp1 Transcription Factor
12%
Modifier Gene
12%