glycine has been researched along with Hearing Loss, Sensorineural in 5 studies
Hearing Loss, Sensorineural: Hearing loss resulting from damage to the COCHLEA and the sensorineural elements which lie internally beyond the oval and round windows. These elements include the AUDITORY NERVE and its connections in the BRAINSTEM.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Eighty patients with idiopathic sudden sensorineural hearing loss (ISSHL) and 80 healthy subjects were studied." | 1.33 | eNOS gene affects red cell deformability: role of T-786C, G894T, and 4a/4b polymorphisms. ( Abbate, R; Bruschettini, A; Cecchi, E; Fatini, C; Gensini, GF; Leprini, E; Mannini, L; Pagnini, P; Prisco, D; Sticchi, E, 2005) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 4 (80.00) | 29.6817 |
| 2010's | 1 (20.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Li, J | 1 |
| Cheng, J | 1 |
| Lu, Y | 2 |
| Chen, A | 1 |
| Sun, Y | 1 |
| Kang, D | 1 |
| Zhang, X | 1 |
| Dai, P | 1 |
| Han, D | 1 |
| Yuan, H | 1 |
| Street, VA | 1 |
| Kallman, JC | 1 |
| Kiemele, KL | 1 |
| Asamura, K | 1 |
| Abe, S | 1 |
| Fukuoka, H | 1 |
| Nakamura, Y | 1 |
| Usami, S | 1 |
| Fatini, C | 1 |
| Mannini, L | 1 |
| Sticchi, E | 1 |
| Cecchi, E | 1 |
| Bruschettini, A | 1 |
| Leprini, E | 1 |
| Pagnini, P | 1 |
| Gensini, GF | 1 |
| Prisco, D | 1 |
| Abbate, R | 1 |
| Kupka, S | 1 |
| Tóth, T | 1 |
| Wróbel, M | 1 |
| Zeissler, U | 1 |
| Szyfter, W | 1 |
| Szyfter, K | 1 |
| Niedzielska, G | 1 |
| Bal, J | 1 |
| Zenner, HP | 1 |
| Sziklai, I | 1 |
| Blin, N | 1 |
| Pfister, M | 1 |
5 other studies available for glycine and Hearing Loss, Sensorineural
| Article | Year |
|---|---|
Identification of a novel mutation in POU3F4 for prenatal diagnosis in a Chinese family with X-linked nonsyndromic hearing loss.
Topics: Asian People; DNA; Ear, Inner; Female; Genetic Diseases, X-Linked; Glutamic Acid; Glycine; Hearing L | 2010 |
Modifier controls severity of a novel dominant low-frequency MyosinVIIA (MYO7A) auditory mutation.
Topics: Adult; Amino Acid Sequence; Amino Acid Substitution; Chromosome Mapping; Chromosomes, Human, Pair 11 | 2004 |
Mutation analysis of COL9A3, a gene highly expressed in the cochlea, in hearing loss patients.
Topics: Amino Acid Sequence; Aspartic Acid; Base Sequence; Cochlea; Collagen Type IX; DNA Mutational Analysi | 2005 |
eNOS gene affects red cell deformability: role of T-786C, G894T, and 4a/4b polymorphisms.
Topics: Adult; Aged; Aged, 80 and over; Alleles; Erythrocyte Deformability; Erythrocytes; Female; Genotype; | 2005 |
Mutation A1555G in the 12S rRNA gene and its epidemiological importance in German, Hungarian, and Polish patients.
Topics: Adult; Aged; Alanine; Amino Acid Substitution; Child; Child, Preschool; Female; Genetic Predispositi | 2002 |