glutamic acid has been researched along with Eye Abnormalities in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 3 (75.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Bechberger, JF; Kozoriz, MG; Lai, S; Naus, CC; Sáez, JC; Sin, WC; Vega, JL | 1 |
| Attié-Bitach, T; Barbot, C; Bielas, SL; Boltshauser, E; Brancati, F; Castroviejo, IP; Cluckey, A; Doherty, DA; Glass, IA; Gleeson, JG; Hildebrandt, F; Iannicelli, M; Ikegami, K; Johnson, CA; Lee, JE; Lee, JH; Logan, CV; Louie, CM; Marsh, SE; Merriman, B; Nelson, SF; Olvera, J; Rapin, I; Raynes, HR; Schlossman, AM; Schroth, J; Setou, M; Silhavy, JL; Valente, EM; Zaki, MS | 1 |
| Aikawa, T; Amano, K; Fujimaki, T; Ishiguchi, M; Kimata, M; Kishi, N; Kogo, M; Murakami, A | 1 |
| Kutsche, K; Shaw, GM; Wimplinger, I | 1 |
4 other study(ies) available for glutamic acid and Eye Abnormalities
| Article | Year |
|---|---|
Cerebral ischemic injury is enhanced in a model of oculodentodigital dysplasia.
Topics: Animals; Astrocytes; Brain Infarction; Brain Ischemia; Cell Death; Cells, Cultured; Connexin 43; Craniofacial Abnormalities; Disease Models, Animal; Enzyme Inhibitors; Eye Abnormalities; Foot Deformities, Congenital; Gap Junctions; Glutamic Acid; Mice; Mice, Inbred C57BL; Mice, Transgenic; Mutation; Neurons; Serine; Syndactyly; Tooth Abnormalities | 2013 |
CEP41 is mutated in Joubert syndrome and is required for tubulin glutamylation at the cilium.
Topics: Animals; Centrosome; Cerebellar Diseases; Chromosome Mapping; Cilia; Ciliary Motility Disorders; Eye Abnormalities; Female; Genetic Loci; Glutamic Acid; Humans; Male; Mice; Mutation; Peptide Synthases; Polycystic Kidney Diseases; Polymorphism, Single Nucleotide; Protein Processing, Post-Translational; Proteins; Syndrome; Tubulin | 2012 |
Cleft lip in oculodentodigital dysplasia suggests novel roles for connexin43.
Topics: Abnormalities, Multiple; Adenine; Animals; Bone Morphogenetic Protein 4; Child, Preschool; Cleft Lip; Connexin 43; Epithelium; Exons; Eye Abnormalities; Fingers; Galactosyltransferases; Glucosyltransferases; Glutamic Acid; Guanine; Heterozygote; Humans; Infant; Introns; Lip; Lysine; Male; Mice; Models, Animal; Polymorphism, Single Nucleotide; Tooth Abnormalities; Transcription Factor AP-2 | 2012 |
HCCS loss-of-function missense mutation in a female with bilateral microphthalmia and sclerocornea: a novel gene for severe ocular malformations?
Topics: Abnormalities, Multiple; Adenine; Amino Acid Substitution; Animals; CHO Cells; Chromosomes, Human, X; Cohort Studies; Cornea; Cricetinae; Cricetulus; Eye Abnormalities; Female; Glutamic Acid; Guanine; Heterozygote; Humans; Lyases; Lysine; Microphthalmos; Mutation, Missense; Point Mutation; Saccharomyces cerevisiae; Severity of Illness Index; Transfection; X Chromosome Inactivation | 2007 |