glutamic acid has been researched along with Genetic Diseases, X-Chromosome Linked 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 |
---|---|
Bernhardi, E; Brüggemann, N; Capetian, P; Domingo, A; Grütz, K; Klein, C; Naujock, M; Seibler, P; Stanslowsky, N; Wegner, F | 1 |
Brüggemann, N; Capetian, P; Diesta, CC; Domingo, A; Jamora, RD; Klein, C; Lee, LV; Mohr, C; Moll, CK; Moser, A; Münchau, A; Rasche, D; Rosales, R; Tadic, V; Tronnier, VM | 1 |
Chen, A; Cheng, J; Dai, P; Han, D; Kang, D; Li, J; Lu, Y; Sun, Y; Yuan, H; Zhang, X | 1 |
Andrew Futreal, P; Das, P; Edkins, S; Kamath, S; Nayak, R; Ninis, V; Patel, PI; Pemberton, TJ; Stockton, DW; Stratton, MR; Tarpey, P; Wooster, R | 1 |
4 other study(ies) available for glutamic acid and Genetic Diseases, X-Chromosome Linked
Article | Year |
---|---|
Altered glutamate response and calcium dynamics in iPSC-derived striatal neurons from XDP patients.
Topics: Adult; Calcium; Calcium Channels; Corpus Striatum; Dystonic Disorders; Genetic Diseases, X-Linked; Glutamic Acid; Humans; Induced Pluripotent Stem Cells; Male; Middle Aged; Neurons; Receptors, AMPA | 2018 |
Biochemical mechanisms of pallidal deep brain stimulation in X-linked dystonia parkinsonism.
Topics: Adult; Deep Brain Stimulation; Dystonic Disorders; Female; gamma-Aminobutyric Acid; Genetic Diseases, X-Linked; Globus Pallidus; Glutamic Acid; Humans; Male; Microdialysis; Middle Aged; Monitoring, Intraoperative; Neurosurgical Procedures | 2015 |
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 Loss, Sensorineural; Humans; Male; Models, Molecular; Mutation, Missense; Pedigree; POU Domain Factors; Pregnancy; Prenatal Diagnosis; Temporal Bone; Tomography, X-Ray Computed | 2010 |
A novel Gln358Glu mutation in ectodysplasin A associated with X-linked dominant incisor hypodontia.
Topics: Amino Acid Sequence; Amino Acid Substitution; Animals; Anodontia; Base Sequence; Ectodysplasins; Genes, X-Linked; Genetic Diseases, X-Linked; Glutamic Acid; Glycine; Humans; Incisor; Molecular Sequence Data; Mutation; Pedigree; Radiography; Sequence Alignment | 2007 |