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Duygu Duman Selected Research

Claudins

10/2019A truncating CLDN9 variant is associated with autosomal recessive nonsyndromic hearing loss.

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Duygu Duman Research Topics

Disease

4Hearing Loss (Hearing Impairment)
02/2024 - 05/2010
4Deafness (Deaf Mutism)
10/2019 - 09/2014
2Sensorineural Hearing Loss
01/2019 - 11/2012
1Stroke (Strokes)
01/2022
1Lactic Acidosis
01/2022
1Mitochondrial encephalopathy
01/2022
1Mitochondrial Diseases (Mitochondrial Disease)
01/2022
1Leigh Disease (Leigh's Disease)
01/2022
1MERRF Syndrome (Myoclonic Epilepsy and Ragged Red Fibers)
01/2022
1Nonsyndromic Deafness
01/2022
1Optic Nerve Diseases (Optic Neuropathy)
01/2022
1Branchio-Oto-Renal Syndrome (Branchio Oculo Facial Syndrome)
07/2017
1Pierre Robin syndrome with fetal chondrodysplasia
08/2015
1type 3 Stickler syndrome
08/2015
1Megaepiphyseal dwarfism
08/2015

Drug/Important Bio-Agent (IBA)

5DNA (Deoxyribonucleic Acid)IBA
11/2023 - 01/2016
4Proteins (Proteins, Gene)FDA Link
02/2024 - 05/2010
1Mitochondrial DNA (mtDNA)IBA
01/2022
1Tight Junction ProteinsIBA
10/2019
1ClaudinsIBA
10/2019
1Receptor Tyrosine Kinase-like Orphan ReceptorsIBA
05/2016
1Collagen Type XIIBA
08/2015
1NucleotidesIBA
09/2014
1MorpholinosIBA
11/2012
1Connexin 26IBA
01/2012
1Messenger RNA (mRNA)IBA
05/2010