glycine has been researched along with Deafness in 17 studies
Deafness: A general term for the complete loss of the ability to hear from both ears.
| Excerpt | Relevance | Reference |
|---|---|---|
| "The pharmacologic characteristics of glycine receptors (GlyRs) in the lateral superior olive (LSO) of circling mice, animal model for inherited deafness, were investigated using a GlyR α1 subunit-specific receptor blocker (cyanotriphenylborate [CTB])." | 3.77 | Glycine-induced currents are insensitive to the glycine receptor α1 subunit-specific blocker, cyanotriphenylborate, in older circling mice. ( Ahn, SC; Pradhan, J, 2011) |
| "Alport syndrome is the commonest inherited kidney disease and nearly half the pathogenic variants in the COL4A3-COL4A5 genes that cause Alport syndrome result in Gly substitutions." | 1.72 | Genotype-phenotype correlations for COL4A3-COL4A5 variants resulting in Gly substitutions in Alport syndrome. ( Cerkauskaite, A; Chan, MMY; Deltas, C; Gale, DP; Gibson, JT; Hilbert, P; Huang, M; Lipska-Ziętkiewicz, BS; Rothe, H; Sadeghi-Alavijeh, O; Savige, J; Shenelli Croos Dabrera, M; Shukla, K; Storey, H, 2022) |
| "Stickler syndrome is a dominantly inherited disorder characterized by arthropathy, midline clefting, hearing loss, midfacial hypoplasia, myopia, and retinal detachment." | 1.31 | Variation in the vitreous phenotype of Stickler syndrome can be caused by different amino acid substitutions in the X position of the type II collagen Gly-X-Y triple helix. ( Baguley, DM; Harper, PS; Lane, C; Nicol, M; Richards, AJ; Scott, JD; Snead, MP; Yates, JR, 2000) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 6 (35.29) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 7 (41.18) | 29.6817 |
| 2010's | 3 (17.65) | 24.3611 |
| 2020's | 1 (5.88) | 2.80 |
| Authors | Studies |
|---|---|
| Gibson, JT | 1 |
| Huang, M | 1 |
| Shenelli Croos Dabrera, M | 1 |
| Shukla, K | 1 |
| Rothe, H | 1 |
| Hilbert, P | 1 |
| Deltas, C | 1 |
| Storey, H | 1 |
| Lipska-Ziętkiewicz, BS | 1 |
| Chan, MMY | 1 |
| Sadeghi-Alavijeh, O | 1 |
| Gale, DP | 1 |
| Cerkauskaite, A | 1 |
| Savige, J | 1 |
| Zhang, Y | 1 |
| Hao, H | 1 |
| Argence, M | 1 |
| Vassias, I | 1 |
| Kerhuel, L | 1 |
| Vidal, PP | 1 |
| de Waele, C | 1 |
| Paulshock, BZ | 1 |
| Pradhan, J | 1 |
| Ahn, SC | 1 |
| Couchman, K | 1 |
| Garrett, A | 1 |
| Deardorff, AS | 1 |
| Rattay, F | 1 |
| Resatz, S | 1 |
| Fyffe, R | 1 |
| Walmsley, B | 2 |
| Leão, RN | 2 |
| Oleskevich, S | 1 |
| Sun, H | 1 |
| Bautista, M | 1 |
| Fyffe, RE | 1 |
| Asako, M | 2 |
| Holt, AG | 2 |
| Griffith, RD | 2 |
| Buras, ED | 2 |
| Altschuler, RA | 2 |
| Potashner, SJ | 1 |
| Suneja, SK | 1 |
| Benson, CG | 1 |
| Richards, AJ | 1 |
| Baguley, DM | 1 |
| Yates, JR | 1 |
| Lane, C | 1 |
| Nicol, M | 1 |
| Harper, PS | 1 |
| Scott, JD | 1 |
| Snead, MP | 1 |
| Yamasoba, T | 1 |
| Goto, Yi | 1 |
| Oka, Y | 1 |
| Nishino, I | 1 |
| Tsukuda, K | 1 |
| Nonaka, I | 1 |
| Blehová, B | 1 |
| Păzoutová, N | 1 |
| Hyánek, J | 1 |
| Jirásek, J | 1 |
| Woody, NC | 1 |
| Snyder, CH | 1 |
| Harris, JA | 1 |
| Rosenberg, LE | 1 |
| Durant, JL | 1 |
| Elsas, LJ | 1 |
| Fraser, GR | 1 |
| Friedmann, AI | 1 |
| Patton, VM | 1 |
| Wade, DN | 1 |
| Woolf, LI | 1 |
| Minder, FC | 1 |
| Dubach, UC | 1 |
| Antener, I | 1 |
17 other studies available for glycine and Deafness
| Article | Year |
|---|---|
Genotype-phenotype correlations for COL4A3-COL4A5 variants resulting in Gly substitutions in Alport syndrome.
Topics: Adult; Amino Acid Substitution; Autoantigens; Collagen Type IV; Databases, Genetic; Deafness; Female | 2022 |
Conserved glycine at position 45 of major cochlear connexins constitutes a vital component of the Ca²⁺ sensor for gating of gap junction hemichannels.
Topics: Amino Acid Substitution; Calcium; Calcium Channels; Cell Death; Cell Membrane; Cell Membrane Permeab | 2013 |
Stimulation by cochlear implant in unilaterally deaf rats reverses the decrease of inhibitory transmission in the inferior colliculus.
Topics: Animals; Auditory Pathways; Auditory Perception; Biomarkers; Cochlear Implants; Deafness; Down-Regul | 2008 |
Research and patient care.
Topics: Child; Deafness; Ethics, Research; Glycine; Humans; Imino Acids; Male; Physician-Patient Relations; | 1968 |
Glycine-induced currents are insensitive to the glycine receptor α1 subunit-specific blocker, cyanotriphenylborate, in older circling mice.
Topics: Age Factors; Animals; Borates; Deafness; Disease Models, Animal; GABA Antagonists; Glycine; Homozygo | 2011 |
Lateral superior olive function in congenital deafness.
Topics: Animals; Auditory Pathways; Auditory Perception; Carrier Proteins; Cochlear Nerve; Deafness; Disease | 2011 |
Differences in glycinergic mIPSCs in the auditory brain stem of normal and congenitally deaf neonatal mice.
Topics: Animals; Animals, Newborn; Brain Stem; Deafness; Glycine; Immunohistochemistry; In Vitro Techniques; | 2004 |
Deafness-related decreases in glycine-immunoreactive labeling in the rat cochlear nucleus.
Topics: Animals; Auditory Pathways; Cochlea; Cochlear Nerve; Cochlear Nucleus; Deafness; Denervation; Female | 2005 |
Changes in glycine immunoreactivity in the rat superior olivary complex following deafness.
Topics: Animals; Auditory Pathways; Cell Size; Deafness; Diagnostic Imaging; Female; Glycine; Immunohistoche | 2006 |
Altered glycinergic synaptic activities in guinea pig brain stem auditory nuclei after unilateral cochlear ablation.
Topics: Animals; Auditory Pathways; Brain Stem; Cochlear Nucleus; Deafness; Glycine; Guinea Pigs; Olivary Nu | 2000 |
Variation in the vitreous phenotype of Stickler syndrome can be caused by different amino acid substitutions in the X position of the type II collagen Gly-X-Y triple helix.
Topics: Abnormalities, Multiple; Amino Acid Sequence; Amino Acid Substitution; Base Sequence; Biopolymers; C | 2000 |
Atypical muscle pathology and a survey of cis-mutations in deaf patients harboring a 1555 A-to-G point mutation in the mitochondrial ribosomal RNA gene.
Topics: Adult; Alanine; Anti-Bacterial Agents; Audiology; Cysteine; Cytochrome b Group; Deafness; DNA, Mitoc | 2002 |
Iminoglycinuria in a child in Czechoslovakia.
Topics: Amino Acid Metabolism, Inborn Errors; Cerebrospinal Fluid Proteins; Deafness; Female; Glycine; Human | 1973 |
Hyperprolinemia: clinical and biochemical family study.
Topics: Acute Disease; Amino Acid Metabolism, Inborn Errors; Brain; Bronchopneumonia; Central Nervous System | 1969 |
Familial iminoglycinuria. An inborn error of renal tubular transport.
Topics: Adult; Child; Chromosome Aberrations; Chromosome Disorders; Deafness; Female; Genotype; Glycine; Het | 1968 |
Iminoglycinuria--a "harmless" inborn error of metabolism?
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Amino Acids; Blindness; Consanguinity; Deafness; G | 1968 |
[Hereditary nephropathy and hardness of hearing (with metabolic disorders of amino acids and fats in a family from Switzerland)].
Topics: Adolescent; Adult; Aged; Amino Acid Metabolism, Inborn Errors; Child; Child, Preschool; Deafness; Dw | 1965 |