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Shannon M Conley Selected Research

Retinitis Pigmentosa (Pigmentary Retinopathy)

7/2023Comparative study of PRPH2 D2 loop mutants reveals divergent disease mechanism in rods and cones.
10/2020Retbindin: A riboflavin Binding Protein, Is Critical for Photoreceptor Homeostasis and Survival in Models of Retinal Degeneration.
1/2020Novel molecular mechanisms for Prph2-associated pattern dystrophy.
10/2018Oligomerization of Prph2 and Rom1 is essential for photoreceptor outer segment formation.
1/2017Rom1 converts Y141C-Prph2-associated pattern dystrophy to retinitis pigmentosa.
1/2016The K153Del PRPH2 mutation differentially impacts photoreceptor structure and function.
1/2016RDS Functional Domains and Dysfunction in Disease.
6/2015Genomic DNA nanoparticles rescue rhodopsin-associated retinitis pigmentosa phenotype.
4/2010Gene delivery to mitotic and postmitotic photoreceptors via compacted DNA nanoparticles results in improved phenotype in a mouse model of retinitis pigmentosa.
2/2010Biochemical analysis of phenotypic diversity associated with mutations in codon 244 of the retinal degeneration slow gene.
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Shannon M Conley Research Topics

Disease

29Retinal Degeneration
07/2023 - 01/2009
11Retinitis Pigmentosa (Pigmentary Retinopathy)
07/2023 - 01/2009
8Retinal Diseases
01/2021 - 01/2010
6Macular Degeneration (Age-Related Maculopathy)
07/2023 - 02/2010
4Hypertension (High Blood Pressure)
02/2024 - 01/2019
4Blindness (Hysterical Blindness)
01/2022 - 09/2010
3Cone-Rod Dystrophies
10/2020 - 01/2016
2Hypertrophy
01/2024 - 01/2019
2Cognitive Dysfunction
01/2024 - 01/2019
2Inflammation (Inflammations)
09/2021 - 10/2004
2congenital stationary Night blindness
01/2016 - 06/2015
2Stargardt Disease
01/2016 - 09/2012
2Glaucoma
04/2006 - 02/2004
1Microvascular Rarefaction
01/2024
1Atrophy
01/2022
1Cerebrovascular Disorders (Cerebrovascular Occlusion)
01/2022
1Scotoma (Scintillating Scotoma)
01/2022
1Cochlear Diseases
01/2021
1Phototoxic Dermatitis (Phototoxicity)
01/2020
1Cerebral Hemorrhage
01/2019
1Night Blindness (Nyctalopia)
01/2016
1Hypoxia (Hypoxemia)
01/2016
1Vitelliform Macular Dystrophy
04/2013
1Hyperglycemia
01/2013
1Microaneurysm
01/2013
1Diabetic Retinopathy (Retinopathy, Diabetic)
01/2013
1Enhanced S-Cone Syndrome
01/2013
1Ocular Hypertension (Glaucoma, Suspect)
04/2006
1Starvation
10/2005

Drug/Important Bio-Agent (IBA)

13Proteins (Proteins, Gene)FDA Link
10/2020 - 02/2010
11TetraspaninsIBA
07/2023 - 01/2010
10PeripherinsIBA
10/2020 - 06/2014
7Retinaldehyde (Retinal)IBA
01/2022 - 01/2013
6DNA (Deoxyribonucleic Acid)IBA
01/2018 - 10/2005
4Rhodopsin (Visual Purple)IBA
10/2020 - 06/2015
3Insulin-Like Growth Factor I (IGF-1)IBA
01/2024 - 01/2019
3Glycoproteins (Glycoprotein)IBA
01/2016 - 01/2010
2Angiotensin IIIBA
02/2024 - 01/2019
2riboflavin-binding proteinIBA
10/2020 - 01/2020
2Codon (Codons)IBA
01/2016 - 02/2010
2AntioxidantsIBA
01/2016 - 10/2014
2DisulfidesIBA
12/2010 - 03/2009
2Membrane Proteins (Integral Membrane Proteins)IBA
01/2010 - 03/2009
2SeleniumIBA
04/2006 - 02/2004
1NG-Nitroarginine Methyl Ester (L-NAME)IBA
02/2024
1IGF Type 1 Receptor (IGF 1 Receptor)IBA
01/2024
1Biomarkers (Surrogate Marker)IBA
01/2022
1tyrosine O-sulfateIBA
09/2021
1Flavin-Adenine Dinucleotide (FAD)IBA
10/2020
1Flavin Mononucleotide (FMN)IBA
10/2020
1Riboflavin (Vitamin B2)FDA LinkGeneric
10/2020
1FlavinsIBA
01/2020
1Insulin (Novolin)FDA Link
01/2019
1ElastinIBA
01/2019
1Polyethylene Glycols (Polyethylene Glycol)FDA LinkGeneric
01/2018
1LipidsIBA
01/2018
1PolylysineIBA
01/2018
1Cyclic Nucleotide-Gated Cation ChannelsIBA
03/2016
1Free RadicalsIBA
01/2016
1Catalytic RNA (Ribozymes)IBA
01/2016
1Reactive Oxygen Species (Oxygen Radicals)IBA
01/2016
1SNARE Proteins (SNAREs)IBA
01/2015
1yttria (yttrium oxide)IBA
10/2014
1Retinal Pigments (Pigments, Visual)IBA
06/2014
1Mutant Proteins (Protein, Mutant)IBA
12/2013
1Cysteine (L-Cysteine)FDA Link
12/2010
1OpsinsIBA
04/2010
1Interleukin-10 (Interleukin 10)IBA
10/2004
1Matrix Metalloproteinases (MMPs)IBA
02/2004

Therapy/Procedure

6Therapeutics
01/2022 - 04/2010
1Intravitreal Injections
09/2021