Elvir Becirovic Selected Research

Cone Dystrophy

12/2018

Accessory heterozygous mutations in cone photoreceptor CNGA3 exacerbate CNG channel-associated retinopathy.

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Elvir Becirovic Research Topics

Disease

7	Retinitis Pigmentosa (Pigmentary Retinopathy) 09/2020 - 04/2007
5	Retinal Degeneration 01/2020 - 12/2010
2	Color Vision Defects (Color Blindness) 12/2018 - 01/2018
2	Deafness (Deaf Mutism) 03/2008 - 04/2007
2	Usher Syndromes (Usher Syndrome) 03/2008 - 04/2007
1	Stargardt Disease 10/2023
1	Blindness (Hysterical Blindness) 01/2020
1	Cone Dystrophy 12/2018
1	Channelopathies 03/2018
1	Ciliopathies 01/2018
1	Pain (Aches) 01/2017
1	Bradycardia 12/2013
1	type 1D Usher syndrome 03/2008
1	Autosomal Recessive 12 Deafness 03/2008
1	Autosomal Recessive 31 Deafness 04/2007
1	Sensorineural Hearing Loss 04/2007

Drug/Important Bio-Agent (IBA)

5	Proteins (Proteins, Gene)FDA Link 03/2018 - 04/2007
4	Retinaldehyde (Retinal)IBA 01/2020 - 04/2007
3	Rhodopsin (Visual Purple)IBA 01/2020 - 11/2014
2	Cyclic NucleotidesIBA 12/2018 - 03/2011
2	Hyperpolarization-Activated Cyclic Nucleotide-Gated ChannelsIBA 01/2017 - 12/2013
1	OpsinsIBA 01/2020
1	Ion Channels (Ion Channel)IBA 12/2018
1	pericentrinIBA 01/2018
1	Biomarkers (Surrogate Marker)IBA 01/2018
1	Guanosine Monophosphate (5' Guanylic Acid)IBA 12/2010
1	Messenger RNA (mRNA)IBA 03/2008
1	Protein Isoforms (Isoforms)IBA 04/2007
1	Nonsense Codon (Nonsense Mutation)IBA 04/2007
1	RNA Splice SitesIBA 04/2007

Therapy/Procedure

4	Therapeutics 09/2020 - 01/2018
1	Intravitreal Injections 10/2023
1	Aftercare (After-Treatment) 01/2020