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Publications by L A Metherell

Identification and Characterisation of a Novel GHR Defect Disrupting the Polypyrimidine Tract and Resulting in GH Insensitivity

European Journal of Endocrinology

English

Neonatal Presentation of Familial Glucocorticoid Deficiency Resulting From a Novel Splice Mutation in the Melanocortin 2 Receptor Accessory Protein

European Journal of Endocrinology

English

Related publications

A Novel Androgen Receptor Mutation Resulting in Complete Androgen Insensitivity Syndrome and Bilateral Leydig Cell Hyperplasia

Journal of Andrology

2006

English

The Blood-Tendon Barrier: Identification and Characterisation of a Novel Tissue Barrier in Tendon Blood Vessels

2016

English

Pharmacological Characterisation of a New Oral GH Secretagogue, NN703

European Journal of Endocrinology

English

Key Scientific Issues Relevant to the Identification and Characterisation of Endocrine Disrupting Substances—Report of the Endocrine Disrupters Expert Advisory Group

English

Effects of Genetic Polymorphism in Pit1, GH, GHR and KCN3 on Milk Yield and Body Weight of Khuzestan (Iran) Water Buffaloes

Revista Colombiana de Ciencias Pecuarias

English

Drosophila Polypyrimidine-Tract Binding Protein (PTB) Functions Specifically in the Male Germline

English

The Polypyrimidine Tract Binding Protein Is Required for Efficient Picornavirus Gene Expression and Propagation

English

Penetrating Trauma Resulting in Ventricular Septal Defect

World Journal of Cardiovascular Surgery

2014

English

Remodelling of a Polypyrimidine Tract-Binding Protein Complex During Apoptosis Activates Cellular IRESs

Cell Death and Differentiation

Cell Biology

Molecular Biology

2013

English

Amanote Research

Discover open access scientific publications

Search, annotate, share and cite publications

Publications by L A Metherell

Identification and Characterisation of a Novel GHR Defect Disrupting the Polypyrimidine Tract and Resulting in GH Insensitivity

Neonatal Presentation of Familial Glucocorticoid Deficiency Resulting From a Novel Splice Mutation in the Melanocortin 2 Receptor Accessory Protein

Related publications

A Novel Androgen Receptor Mutation Resulting in Complete Androgen Insensitivity Syndrome and Bilateral Leydig Cell Hyperplasia

The Blood-Tendon Barrier: Identification and Characterisation of a Novel Tissue Barrier in Tendon Blood Vessels

Pharmacological Characterisation of a New Oral GH Secretagogue, NN703

Key Scientific Issues Relevant to the Identification and Characterisation of Endocrine Disrupting Substances—Report of the Endocrine Disrupters Expert Advisory Group

Effects of Genetic Polymorphism in Pit1, GH, GHR and KCN3 on Milk Yield and Body Weight of Khuzestan (Iran) Water Buffaloes

Drosophila Polypyrimidine-Tract Binding Protein (PTB) Functions Specifically in the Male Germline

The Polypyrimidine Tract Binding Protein Is Required for Efficient Picornavirus Gene Expression and Propagation

Penetrating Trauma Resulting in Ventricular Septal Defect

Remodelling of a Polypyrimidine Tract-Binding Protein Complex During Apoptosis Activates Cellular IRESs