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Publications by Ivan Dedov

Partial Deficiency of 17 -Hydroxylase/17,20-Lyase Caused by a Novel Missense Mutation in the Canonical Cytochrome Heme-Interacting Motif

European Journal of Endocrinology

English

A Glucokinase Gene Mutation in a Young Boy With Diabetes Mellitus, Hyperinsulinemia, and Insulin Resistance

International Medical Case Reports Journal

Medicine

2017

English

Related publications

The Regulation of Steroidogenesis by 17.alpha.-Hydroxylase/17,20-Lyase (P450c17).

Folia Pharmacologica Japonica

Pharmacology

1998

English

Metabolic Evidence for Impaired 17 -Hydroxylase Activity in a Kindred Bearing the E305G Mutation for Isolate 17,20-Lyase Activity

European Journal of Endocrinology

English

Apparent Activities of 21-Hydroxylase, 17alpha-Hydroxylase and 17,20-Lyase Are Impaired in Adrenal Incidentalomas

European Journal of Endocrinology

English

Characterization of Testicular Expression of P450 17α-Hydroxylase, 17,20-Lyase in Zebrafish and Its Perturbation by the Pharmaceutical Fungicide Clotrimazole

General and Comparative Endocrinology

English

17 Hydroxylase Deficiency in an Adolescent Girl

English

17 -Hydroxylase/17,20 Lyase Inhibitor VN/124-1 Inhibits Growth of Androgen-Independent Prostate Cancer Cells via Induction of the Endoplasmic Reticulum Stress Response

Molecular Cancer Therapeutics

Cancer Research

Oncology

2008

English

IDENTIFICATION OF a NEW MUTATION IN STEROID 11β-Hydroxylase DEFICIENCY

English

Identification of a Novel Compound Heterozygous Mutation of the CYP21A2 Gene Causing 21‑hydroxylase Deficiency in a Chinese Pedigree

Molecular Medicine Reports

English

Long QT Syndrome With Nocturnal Cardiac Events Caused by a KCNH2 Missense Mutation (G604S)

Internal Medicine

Medicine

2012

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by Ivan Dedov

Partial Deficiency of 17 -Hydroxylase/17,20-Lyase Caused by a Novel Missense Mutation in the Canonical Cytochrome Heme-Interacting Motif

A Glucokinase Gene Mutation in a Young Boy With Diabetes Mellitus, Hyperinsulinemia, and Insulin Resistance

Related publications

The Regulation of Steroidogenesis by 17.alpha.-Hydroxylase/17,20-Lyase (P450c17).

Metabolic Evidence for Impaired 17 -Hydroxylase Activity in a Kindred Bearing the E305G Mutation for Isolate 17,20-Lyase Activity

Apparent Activities of 21-Hydroxylase, 17alpha-Hydroxylase and 17,20-Lyase Are Impaired in Adrenal Incidentalomas

Characterization of Testicular Expression of P450 17α-Hydroxylase, 17,20-Lyase in Zebrafish and Its Perturbation by the Pharmaceutical Fungicide Clotrimazole

17 Hydroxylase Deficiency in an Adolescent Girl

17 -Hydroxylase/17,20 Lyase Inhibitor VN/124-1 Inhibits Growth of Androgen-Independent Prostate Cancer Cells via Induction of the Endoplasmic Reticulum Stress Response

IDENTIFICATION OF a NEW MUTATION IN STEROID 11β-Hydroxylase DEFICIENCY

Identification of a Novel Compound Heterozygous Mutation of the CYP21A2 Gene Causing 21‑hydroxylase Deficiency in a Chinese Pedigree

Long QT Syndrome With Nocturnal Cardiac Events Caused by a KCNH2 Missense Mutation (G604S)