glycine has been researched along with Cochlear Hearing Loss in 5 studies
| 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 Cochlear Hearing Loss
| 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 |