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Publications by Manisha K. Gupta
Why Human Cytochrome P450c21 Is a Progesterone 21-Hydroxylase
Biochemistry
Biochemistry
Related publications
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
Analysis of Steroid 21-Hydroxylase Gene in Five Unrelated Japanese Patients With 21-Hydroxylase Deficiency
Endocrinologia Japonica
Molecular Pathology of 21-Hydroxylase Deficiency
Pediatric Research
Child Health
Pediatrics
Perinatology
HLA Class I-, Complement C4- And 21-Hydroxylase Probes in the Genetic Analysis of 21-Hydroxylase Deficiency
Clinical Chemistry and Laboratory Medicine
Biochemistry
Medicine
Clinical Biochemistry
Thermostable Cytochrome P450 Steroid Hydroxylase From a Thermophilic Bacillus Strain
Biochemical Society Transactions
Biochemistry
Dna Hybridization Analysis of 21-Hydroxylase Deficiency
Pediatric Research
Child Health
Pediatrics
Perinatology
Location of the Gene for 21-Hydroxylase Deficiency
Pediatric Research
Child Health
Pediatrics
Perinatology
Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency
Apparent Activities of 21-Hydroxylase, 17alpha-Hydroxylase and 17,20-Lyase Are Impaired in Adrenal Incidentalomas
European Journal of Endocrinology
Medicine
Endocrinology
Metabolism
Diabetes
