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In-vitro characterization of androgen receptor mutations associated with complete androgen insensitivity syndrome reveals distinct functional deficits
R. Werner
, J. Zhan, J. Gesing, D. Struve,
O. Hiort
*
*
Corresponding author for this work
Clinic of Pediatric and Adolescent Medicine
Children's Hospital Zhejiang
11
Citations (Scopus)
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Dive into the research topics of 'In-vitro characterization of androgen receptor mutations associated with complete androgen insensitivity syndrome reveals distinct functional deficits'. Together they form a unique fingerprint.
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Immunology and Microbiology
Amino Acid
100%
Carboxy Terminal Sequence
100%
Medical Decision Making
100%
Genotype Phenotype Correlation
100%
Amino Terminal Sequence
100%
Deletion Mutant
100%
Karyotype 46,XY
100%
Neuroscience
Androgen
100%
In Vitro
100%
Androgen Receptor
100%
Medical Decision Making
12%
Missense Mutation
12%
Transactivation
12%
Amino Terminal Sequence
12%
Amino Acid
12%
Karyotype 46,XY
12%
Biochemistry, Genetics and Molecular Biology
Androgen Receptor
100%
Dissociation Constant
14%
C-Terminus
14%
N-Terminus
14%
Transactivation
14%
Karyotype 46,XY
14%
Missense Mutation
14%
Amino Acid
14%
Genotype Phenotype Correlation
14%