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Publications by A Searle

Phenotype of Autosomal Dominant Cone–rod Dystrophy Due to the R838C Mutation of the GUCY2D Gene Encoding Retinal Guanylate Cyclase-1

Eye
MedicineArtsSensory SystemsOphthalmologyHumanities
2006English

Related publications

Autosomal Dominant Cone-Rod Dystrophy With Negative Electroretinogram.

British Journal of Ophthalmology
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1995English

The Function of Guanylate Cyclase 1 and Guanylate Cyclase 2 in Rod and Cone Photoreceptors

Journal of Biological Chemistry
BiochemistryCell BiologyMolecular Biology
2007English

Phenotypic Diversity in Autosomal-Dominant Cone-Rod Dystrophy Elucidated by Adaptive Optics Retinal Imaging

British Journal of Ophthalmology
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2017English

Disruption of a Retinal Guanylyl Cyclase Gene Leads to Cone-Specific Dystrophy and Paradoxical Rod Behavior

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1999English

A Gly86Arg Mutation in the Calcium-Sensor Protein GCAP1 Alters Regulation of Retinal Guanylyl Cyclase and Causes Dominant Cone-Rod Degeneration

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2019English

Novel CDHR1 Mutation Causing Cone Rod Dystrophy

Acta Ophthalmologica
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2018English

Novel C8ORF37 Mutation Causing Cone Rod Dystrophy

Acta Ophthalmologica
MedicineOphthalmology
2018English

Characterization of Guanylate Cyclase Activity in Single Retinal Rod Outer Segments

Journal of General Physiology
Physiology
1995English

Abnormal Dark Adaptation Kinetics in Autosomal Dominant Sector Retinitis Pigmentosa Due to Rod Opsin Mutation.

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Molecular NeuroscienceOphthalmologySensory SystemsCellular
1992English

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