A. Hunter

发表

Patterns of bromodeoxyuridine incorporation and neuropeptide immunoreactivity during arm regeneration in the starfish Asterias rubens

M. Thorndyke, C. Moss, A. Hunter, 1998 .

Novel Mouse Model of Autosomal Semidominant Adult Hypophosphatasia Has a Splice Site Mutation in the Tissue Nonspecific Alkaline Phosphatase Gene Akp2

S. Rastan, A. Boyde, R. Terkeltaub, 2007, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

Identification of a New Pmp22 Mouse Mutant and Trafficking Analysis of a Pmp22 Allelic Series Suggesting That Protein Aggregates May Be Protective in Pmp22-Associated Peripheral Neuropathy

Steve D. M. Brown, K. Davies, P. Oliver, 2002, Molecular and Cellular Neuroscience.

An ENU-induced mutation in the Ankrd11 gene results in an osteopenia-like phenotype in the mouse mutant Yoda.

Steve D. M. Brown, S. Wells, T. Hough, 2008, Physiological genomics.

Mutation at the Evi1 Locus in Junbo Mice Causes Susceptibility to Otitis Media

Steve D. M. Brown, P. Glenister, F. Mackenzie, 2006, PLoS genetics.

Identification of two new Pmp22 mouse mutants using large-scale mutagenesis and a novel rapid mapping strategy.

S. Rastan, E. Fisher, K. Davies, 2001, Human molecular genetics.

A mutation in the F-box gene, Fbxo11, causes otitis media in the Jeff mouse.

Steve D. M. Brown, M. Cheeseman, Hilda Tateossian, 2006, Human molecular genetics.

The Innovative Medicines Initiative: a pre-competitive initiative to enhance the biomedical science base of Europe to expedite the development of new medicines for patients.

A. Hunter, A Jackie Hunter, 2008, Drug discovery today.

The homeobox gene Emx2 underlies middle ear and inner ear defects in the deaf mouse mutant pardon

Steve D. M. Brown, K. Steel, N. Spurr, 2003, Journal of neurocytology.

Serotonergic involvement in learning and memory.

A. Hunter, 1989, Biochemical Society transactions.

Preparation of chromosomal protein A24 (uH2A) by denaturing gel filtration and preparation of its free nonhistone component ubiquitin by ion-exchange chromatography.

P. Cary, A. Hunter, 1985, Analytical biochemistry.

Novel ENU-induced eye mutations in the mouse: models for human eye disease.

Steve D. M. Brown, S. Cross, I. Jackson, 2002, Human molecular genetics.

The mouse slalom mutant demonstrates a role for Jagged1 in neuroepithelial patterning in the organ of Corti.

S. Rastan, K. Steel, P. Mburu, 2001, Human molecular genetics.

Towards new models of disease and physiology in the neurosciences: the role of induced and naturally occurring mutations.

P. Nolan, A. Hunter, S. Brown, 2000, Human molecular genetics.

Identification of two new Pmp22 mouse mutants using large-scale mutagenesis and a novel rapid mapping strategy

Steve D. M. Brown, S. Rastan, E. Fisher, 2000 .

Three Novel Pigmentation Mutants Generated by Genome-Wide Random ENU Mutagenesis in the Mouse

Steve D. M. Brown, S. Rastan, E. Fisher, 2004, Comparative and functional genomics.

In search of new disease models in the mouse using ENU mutagenesis.

R. Hardisty, P. Nolan, A. Hunter, 2002, Ernst Schering Research Foundation workshop.

Animal and Translational Models of Neurological Disorders: An Industrial Perspective

A. Hunter, 2008 .

A Mutation in Af4 Is Predicted to Cause Cerebellar Ataxia and Cataracts in the Robotic Mouse

Steve D. M. Brown, K. Davies, P. Oliver, 2003, The Journal of Neuroscience.

Probing the function of novel genes in the nervous system: is antisense the answer?

R. Leslie, A. Hunter, I. Gloger, 1995, Trends in Neurosciences.

Identification of a new Pmp22 mouse mutant and trafficking analysis of a Pmp22 allelic series suggesting that protein aggregates may be protective in Pmp22-associated peripheral neuropathy.

Steve D. M. Brown, K. Davies, P. Oliver, 2003, Molecular and cellular neurosciences.