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Publications by B C Chung
Mutations of P450c21 (Steroid 21-Hydroxylase) at Cys428, Val281, and Ser268 Result in Complete, Partial, or No Loss of Enzymatic Activity, Respectively.
Journal of Clinical Investigation
Medicine
Related publications
Why Human Cytochrome P450c21 Is a Progesterone 21-Hydroxylase
Biochemistry
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Analysis of Steroid 21-Hydroxylase Gene in Five Unrelated Japanese Patients With 21-Hydroxylase Deficiency
Endocrinologia Japonica
Steroid 21-Hydroxylase Deficiency in Mice. An Animal Model for Congenital Adrenal Hyperplasia.
Proceedings of The Japanese Association of Animal Models for Human Diseases
The Orphan Nuclear Receptor NGFI-B Regulates Expression of the Gene Encoding Steroid 21-Hydroxylase.
Molecular and Cellular Biology
Cell Biology
Molecular Biology
HLA Class I-, Complement C4- And 21-Hydroxylase Probes in the Genetic Analysis of 21-Hydroxylase Deficiency
Clinical Chemistry and Laboratory Medicine
Biochemistry
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Clinical Biochemistry
Alanine-Scanning Mutations in the “Primer Grip” of P66 HIV-1 Reverse Transcriptase Result in Selective Loss of RNA Priming Activity
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
Molecular Pathology of 21-Hydroxylase Deficiency
Pediatric Research
Child Health
Pediatrics
Perinatology
Two Genes Encoding Steroid 21-Hydroxylase Are Located Near the Genes Encoding the Fourth Component of Complement in Man.
Proceedings of the National Academy of Sciences of the United States of America
Multidisciplinary
Pathogenic Mutations in Retinitis Pigmentosa 2 Predominantly Result in Loss of RP2 Protein Stability in Humans and Zebrafish
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
