Ian T. Rose

David Brewster Road
Edinburgh, SCT EH93FJ, United Kingdom

Last Updated: 09/26/2026

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Found 9 publications

Effect of Bridgehead Methyl Substituents on the Gas Permeability of Tröger's-Base Derived Polymers of Intrinsic Microporosity.

Effect of Bridgehead Methyl Substituents on the Gas Permeability of Tröger's-Base Derived Polymers of Intrinsic Microporosity.

Journal: Membranes

Published: February 27, 2020

Polymer ultrapermeability from the inefficient packing of 2D chains.

Polymer ultrapermeability from the inefficient packing of 2D chains.

Journal: Nature materials

Published: December 09, 2016

Highly Permeable Benzotriptycene-Based Polymer of Intrinsic Microporosity.

Highly Permeable Benzotriptycene-Based Polymer of Intrinsic Microporosity.

Journal: ACS macro letters

Published: September 15, 2015

Characterization of the molecular genetic pathology in patients with 11β-hydroxylase deficiency.

Characterization of the molecular genetic pathology in patients with 11β-hydroxylase deficiency.

Journal: Clinical endocrinology

Published: October 14, 2014

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

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

Journal: The Journal of clinical endocrinology and metabolism

Published: August 14, 2013

Redefining the initiation and maintenance of zebrafish interrenal steroidogenesis by characterizing the key enzyme cyp11a2.

Redefining the initiation and maintenance of zebrafish interrenal steroidogenesis by characterizing the key enzyme cyp11a2.

Journal: Endocrinology

Published: May 15, 2013

Genotype-phenotype correlation in 153 adult patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency: analysis of the United Kingdom Congenital adrenal Hyperplasia Adult Study Executive (CaHASE) cohort.

Genotype-phenotype correlation in 153 adult patients with congenital adrenal hyperplasia due to 21-hydroxylase deficiency: analysis of the United Kingdom Congenital adrenal Hyperplasia Adult Study Executive (CaHASE) cohort.

Journal: The Journal of clinical endocrinology and metabolism

Published: January 23, 2013

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).

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).

Journal: European journal of endocrinology

Published: September 13, 2012

Genotype-phenotype analysis in congenital adrenal hyperplasia due to P450 oxidoreductase deficiency.

Genotype-phenotype analysis in congenital adrenal hyperplasia due to P450 oxidoreductase deficiency.

Journal: The Journal of clinical endocrinology and metabolism

Published: December 14, 2011

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Last Updated: 09/26/2026