V. Dhir

发表

A bioinformatic analysis of the RAB genes of Trypanosoma brucei.

Mark C. Field, Mark C Field, J. Ackers, 2005, Molecular and biochemical parasitology.

Premature adrenarche: novel lessons from early onset androgen excess.

T. Barrett, G. Lavery, P. Stewart, 2011, European journal of endocrinology.

Concomitant Mutations in the P450 Oxidoreductase and Androgen Receptor Genes Presenting with 46,XY Disordered Sex Development and Androgenization at Adrenarche

I. Hughes, C. Shackleton, N. Krone, 2010, The Journal of clinical endocrinology and metabolism.

at Adrenarche Genes Presenting with 46,XY Disordered Sex Development and Androgenization Concomitant Mutations in the P450 Oxidoreductase and Androgen Receptor

I. Hughes, N. Krone, W. Arlt, 2010 .

Genes Presenting with 46 , XY Disordered Sex Development and Androgenization Concomitant Mutations in the P 450 Oxidoreductase and Androgen Receptor

I. Hughes, N. Krone, W. Arlt, 2010 .

Differential inhibition of CYP17A1 and CYP21A2 activities by the P450 oxidoreductase mutant A287P.

A. Doherty, C. Shackleton, P. Stewart, 2007, Molecular endocrinology.

Congenital adrenal hyperplasia and P450 oxidoreductase deficiency

N. Krone, W. Arlt, V. Dhir, 2007, Clinical endocrinology.

Inactivating PAPSS2 mutations in a patient with premature pubarche.

N. Hanley, J. Smeitink, R. Smeets, 2009, The New England journal of medicine.

Human DHEA sulfation requires direct interaction between PAPS synthase 2 and DHEA sulfotransferase SULT2A1

E. Rosta, S. Knauer, W. Arlt, 2018, The Journal of Biological Chemistry.

University of Birmingham Human DHEA sulfation requires direct interaction between PAPS synthase 2 and DHEA

E. Rosta, J. Jez, S. Knauer, 2018 .

Perturbation of local endogenous expression by insertion of Pol I expression constructs into the genome of Trypanosoma brucei.

Mark C. Field, C. Allen, V. Dhir, 2005, Experimental parasitology.

A novel entity of clinically isolated adrenal insufficiency caused by a partially inactivating mutation of the gene encoding for P450 side chain cleavage enzyme (CYP11A1).

J. Grötzinger, N. Krone, W. Arlt, 2011, The Journal of clinical endocrinology and metabolism.

Steroid 17alpha-hydroxylase deficiency: functional characterization of four mutations (A174E, V178D, R440C, L465P) in the CYP17A1 gene.

J. Grötzinger, H. Schwarz, W. Sippell, 2009, The Journal of clinical endocrinology and metabolism.

Effects of castration and androgen replacement on erectile function in a rabbit model.

Kwangsung Park, A. Traish, Noel N Kim, 1999, Endocrinology.

New Approaches to the Microscopic Imaging of Trypanosoma brucei

Mark C. Field, D. Goulding, G. Morgan, 2004, Microscopy and Microanalysis.

Sunitinib Inhibits Cell Proliferation and Alters Steroidogenesis by Down-Regulation of HSD3B2 in Adrenocortical Carcinoma Cells

M. Fassnacht, M. Zink, B. Allolio, 2011, Front. Endocrin..

EVALUATION OF CHRONIC CONSTRICTION INJURY INDUCED NEUROPATHIC PAIN USING FLAVONOID NARINGENIN IN RATS

J. Kaur, V. Dhir, Deepak Kumar, 2020 .

Functional characterization of three CYP21A2 sequence variants (p.A265V, p.W302S, p.D322G) employing a yeast co‐expression system

F. Domínguez, J. Grötzinger, W. Sippell, 2009, Human mutation.

Alternative pathway androgen biosynthesis and human fetal female virilization

N. Hanley, R. Auchus, C. Shackleton, 2019, Proceedings of the National Academy of Sciences.

University of Birmingham Human DHEA sulfation requires direct interaction between PAPS synthase 2 and DHEA

E. Rosta, S. Knauer, W. Arlt, 2018 .

Collagen XXVII Is Developmentally Regulated and Forms Thin Fibrillar Structures Distinct from Those of Classical Vertebrate Fibrillar Collagens*

R. Poulsom, R. Boot-Handford, K. Kadler, 2007, Journal of Biological Chemistry.

TbRAB23; a nuclear-associated Rab protein from Trypanosoma brucei.

Mark C. Field, V. Dhir, 2004, Molecular and biochemical parasitology.

TbRAB1 and TbRAB2 mediate trafficking through the early secretory pathway of Trypanosoma brucei.

Mark C. Field, D. Goulding, V. Dhir, 2004, Molecular and biochemical parasitology.

The Genus Alternanthera: Phytochemical and Ethnopharmacological Perspectives

Rajeev K. Singla, Bairong Shen, R. Madaan, 2022, Frontiers in Pharmacology.

Prenatal Diagnosis of Congenital Adrenal Hyperplasia Caused by P450 Oxidoreductase Deficiency

O. Abdul-Rahman, R. Harrison, E. Blair, 2013, Journal of Clinical Endocrinology and Metabolism.

Prenatal Diagnosis of Congenital Adrenal Hyperplasia Caused by P450 Oxidoreductase Deficiency

O. Abdul-Rahman, R. Harrison, E. Blair, 2013, The Journal of clinical endocrinology and metabolism.

Genotype-Phenotype Analysis in Congenital Adrenal Hyperplasia due to P450 Oxidoreductase Deficiency

M. Dattani, P. Hindmarsh, M. Kempers, 2011, The Journal of clinical endocrinology and metabolism.

Delayed diagnosis of adrenal insufficiency in a patient with severe penoscrotal hypospadias due to two novel P450 side-change cleavage enzyme (CYP11A1) mutations (p.R360W; p.R405X)

N. Krone, W. Arlt, A. Taylor, 2012, European journal of endocrinology.

A diagnosis not to be missed: nonclassic steroid 11β-hydroxylase deficiency presenting with premature adrenarche and hirsutism.

N. Krone, W. Arlt, W. Högler, 2013, The Journal of clinical endocrinology and metabolism.

University of Birmingham Functional Consequences of Seven Novel Mutations in the CYP11B1 Gene: Four Mutations Associated with Nonclassic and Three Mutations Causing Classic 11 beta-Hydroxylase Deficiency

G. Conway, T. Cole, M. Quinkler, 2010 .

A Missense Mutation in the Human Cytochrome b5 Gene causes 46,XY Disorder of Sex Development due to True Isolated 17,20 Lyase Deficiency

C. Shackleton, N. Taylor, N. Krone, 2011, The Journal of clinical endocrinology and metabolism.

11 2-Hydroxylase Deficiency Mutations Associated with Nonclassic and Three Mutations Causing Classic Gene : FourCYP 11 B 1 Functional Consequences of Seven Novel Mutations in the Society

M. Quinkler, N. Krone, W. Arlt, 2010 .

Reversibility of retinal flow abnormalities is disease-duration dependent in diabetic rats.

S. Bursell, S. Bursell, A. Clermont, 1998, Diabetes.

Emerging Prospective of Phytomolecules as Antioxidants Against Chronic Diseases

V. Dhir, 2022, ECS Transactions.

Broad phenotypic spectrum of 17[alpha]-hydroxylase deficiency: Functional characterisation of 4 novel mutations in the CYP17A1 gene

T. Cheetham, C. Shackleton, N. Taylor, 2012 .

Prenatal Diagnosis of Congenital Adrenal Hyperplasia Caused by P450 Oxidoreductase Deficiency

O. Abdul-Rahman, R. Harrison, E. Blair, 2013, The Journal of clinical endocrinology and metabolism.

Concomitant Mutations in the P450 Oxidoreductase and Androgen Receptor Genes Presenting with 46,XY Disordered Sex Development and Androgenization at Adrenarche

I. Hughes, C. Shackleton, N. Krone, 2010, The Journal of clinical endocrinology and metabolism.

Pathology and

N. Krone, V. Dhir, Silvia Parajes, 2022 .