adenine has been researched along with Hearing Loss in 4 studies
Hearing Loss: A general term for the complete or partial loss of the ability to hear from one or both ears.
| Excerpt | Relevance | Reference |
|---|---|---|
| "MELAS is a multisystem disorder inherited by the mitochondrial DNA with onset typically in childhood." | 1.32 | [Phenotypic variants of A3243G mitochondrial DNA mutation in a Hungarian family]. ( Bene, J; Havasi, V; Herczegfalvi, A; Komlósi, K; Melegh, B; Móser, J; Tihanyi, M, 2004) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (25.00) | 18.2507 |
| 2000's | 2 (50.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bai, Y | 1 |
| Wang, Z | 1 |
| Dai, W | 1 |
| Li, Q | 1 |
| Chen, G | 1 |
| Cong, N | 1 |
| Guan, M | 1 |
| Li, H | 1 |
| Komlósi, K | 1 |
| Bene, J | 1 |
| Havasi, V | 1 |
| Tihanyi, M | 1 |
| Herczegfalvi, A | 1 |
| Móser, J | 1 |
| Melegh, B | 1 |
| Tang, HY | 1 |
| Xia, A | 1 |
| Oghalai, JS | 1 |
| Pereira, FA | 1 |
| Alford, RL | 1 |
| Iwasaki, N | 1 |
| Wasada, T | 1 |
| Takahashi, Y | 1 |
| Babazono, T | 1 |
| Ohgawara, H | 1 |
| Omori, Y | 1 |
4 other studies available for adenine and Hearing Loss
| Article | Year |
|---|---|
A six-generation Chinese family in haplogroup B4C1C exhibits high penetrance of 1555A > G-induced hearing Loss.
Topics: Adenine; Aminoglycosides; Asian People; China; Connexin 26; Connexins; Deafness; DNA Mutational Anal | 2010 |
[Phenotypic variants of A3243G mitochondrial DNA mutation in a Hungarian family].
Topics: Adenine; Child; DNA Mutational Analysis; DNA, Mitochondrial; Female; Genetic Variation; Guanine; Hea | 2004 |
High frequency of the IVS2-2A>G DNA sequence variation in SLC26A5, encoding the cochlear motor protein prestin, precludes its involvement in hereditary hearing loss.
Topics: Adenine; Alleles; Alternative Splicing; Animals; Anion Transport Proteins; Cochlea; DNA, Mitochondri | 2005 |
Insulin sensitivity in patients with NIDDM and the A-to-G mutation at nucleotide 3,243 of the mitochondrial tRNALeu(UUR) gene.
Topics: Adenine; Adult; Blood Glucose; Body Mass Index; C-Peptide; Diabetes Mellitus, Type 2; Family; Female | 1995 |