Jessica C Gardner Selected Research

Cone Dystrophy

1/2012	A novel missense mutation in both OPN1LW and OPN1MW cone opsin genes causes X-linked cone dystrophy (XLCOD5).
7/2010	X-linked cone dystrophy caused by mutation of the red and green cone opsins.

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Jessica C Gardner Research Topics

Disease

3	Blue cone monochromatism 01/2022 - 12/2012
2	Retinal Degeneration 01/2018 - 11/2014
2	Color Vision Defects (Color Blindness) 01/2016 - 07/2010
2	Cone Dystrophy 01/2012 - 07/2010
1	Low Vision (Subnormal Vision) 01/2022
1	Bornholm Eye Disease 01/2016
1	Vision Disorders (Hemeralopia) 12/2013
1	Megalocornea 02/2012
1	Retinitis Pigmentosa (Pigmentary Retinopathy) 07/2010
1	Sclerosteosis 12/2005
1	Osteoporosis 12/2005
1	Osteochondrodysplasias (Spondyloepiphyseal Dysplasia) 06/2002

Drug/Important Bio-Agent (IBA)

3	Cone OpsinsIBA 11/2014 - 07/2010
2	Retinaldehyde (Retinal)IBA 01/2022 - 12/2012
1	diphosphoric acid (pyrophosphoric acid)IBA 01/2018
1	OpsinsIBA 01/2016
1	Nonsense Codon (Nonsense Mutation)IBA 02/2012
1	chordinIBA 02/2012
1	9-cis-retinalIBA 07/2010
1	Rod OpsinsIBA 07/2010
1	Proteins (Proteins, Gene)FDA Link 12/2005
1	Intergenic DNA (Junk DNA)IBA 06/2002

Therapy/Procedure

2	Therapeutics 12/2013 - 12/2005