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Matteo Cortese Selected Research

Type IC Usher Syndrome

1/2018Clarin-1 gene transfer rescues auditory synaptopathy in model of Usher syndrome.

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Matteo Cortese Research Topics

Disease

3Usher Syndromes (Usher Syndrome)
01/2018 - 09/2013
2Deafness (Deaf Mutism)
12/2017 - 01/2016
2Blindness (Hysterical Blindness)
12/2017 - 09/2013
1Type IC Usher Syndrome
01/2018
1Nonsyndromic Deafness
12/2017
1Autosomal Recessive 48 Deafness
12/2017
1Hearing Loss (Hearing Impairment)
12/2017
1Autosomal Recessive 30 Deafness
01/2016
1Type Ib Usher Syndrome
09/2013

Drug/Important Bio-Agent (IBA)

2Proteins (Proteins, Gene)FDA Link
01/2018 - 09/2013
1Membrane Proteins (Integral Membrane Proteins)IBA
01/2018
1Nonsense Codon (Nonsense Mutation)IBA
12/2017
1IntegrinsIBA
12/2017
1Carrier Proteins (Binding Protein)IBA
12/2017
1CalciumIBA
12/2017
1Retinaldehyde (Retinal)IBA
12/2017
1Myosins (Myosin)IBA
01/2016
1Myosin VIIaIBA
09/2013
1SpectrinIBA
09/2013

Therapy/Procedure

1Transjugular Intrahepatic Portasystemic Shunt
01/2016