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Publications by Anurupa Maitra
A Novel 9-Bp Insertion Detected in Steroid 21-Hydroxylase Gene (CYP21A2): Prediction of Its Structural and Functional Implications by Computational Methods
Journal of Biomedical Science
Cell Biology
Pharmacology
Biochemistry
Endocrinology
Clinical Biochemistry
Molecular Biology
Medicine
Metabolism
Diabetes
Related publications
Identification of a Novel Compound Heterozygous Mutation of the CYP21A2 Gene Causing 21‑hydroxylase Deficiency in a Chinese Pedigree
Molecular Medicine Reports
Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine
Analysis of Steroid 21-Hydroxylase Gene in Five Unrelated Japanese Patients With 21-Hydroxylase Deficiency
Endocrinologia Japonica
Functional Studies of Novel CYP21A2 Mutations Detected in Norwegian Patients With Congenital Adrenal Hyperplasia
Endocrine Connections
Internal Medicine
Endocrinology
Metabolism
Diabetes
The Orphan Nuclear Receptor NGFI-B Regulates Expression of the Gene Encoding Steroid 21-Hydroxylase.
Molecular and Cellular Biology
Cell Biology
Molecular Biology
Novel Involvement of a Mitochondrial Steroid Hydroxylase (P450c11) in Xenobiotic Metabolism
Journal of Biological Chemistry
Biochemistry
Cell Biology
Molecular Biology
The Combination of a Novel 2 Bp Deletion Mutation and p.D63H in CYP11B1 Cause Congenital Adrenal Hyperplasia Due to Steroid 11β-Hydroxylase Deficiency
Endocrine Journal
Endocrinology
Metabolism
Diabetes
Location of the Gene for 21-Hydroxylase Deficiency
Pediatric Research
Child Health
Pediatrics
Perinatology
Steroid 21-Hydroxylase Deficiency in Mice. An Animal Model for Congenital Adrenal Hyperplasia.
Proceedings of The Japanese Association of Animal Models for Human Diseases
Deletion of the 21-Hydroxylase Gene in Congenital Adrenal Hyperplasia
Pediatric Research
Child Health
Pediatrics
Perinatology
