glutamic acid has been researched along with Abnormalities, Multiple in 6 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 1 (16.67) | 18.2507 |
2000's | 3 (50.00) | 29.6817 |
2010's | 2 (33.33) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Brathwaite, WA; Casterton, PL; Hlywka, JJ; Nikiforov, AI; Rihner, MO; Sloter, ED | 1 |
Aikawa, T; Amano, K; Fujimaki, T; Ishiguchi, M; Kimata, M; Kishi, N; Kogo, M; Murakami, A | 1 |
Aschauer, HN; Schosser, A | 1 |
Kutsche, K; Shaw, GM; Wimplinger, I | 1 |
Miyoshi, J; Sakane, A; Sasaki, T; Takai, Y | 1 |
Brabec, V; Jarolim, P; Palek, J; Rubin, HL | 1 |
1 review(s) available for glutamic acid and Abnormalities, Multiple
Article | Year |
---|---|
[In search of susceptibility genes for schizophrenia].
Topics: Abnormalities, Multiple; Adult; Animals; Brain; Catechol O-Methyltransferase; Chromosome Aberrations; Chromosomes, Human, Pair 22; Face; Gene Expression; Genetic Linkage; Genetic Predisposition to Disease; Glutamic Acid; Heart Defects, Congenital; Humans; Meta-Analysis as Topic; Mice; Mice, Knockout; Neuregulin-1; Palate, Soft; Proline Oxidase; RGS Proteins; Risk Factors; Schizophrenia; Syndrome | 2004 |
5 other study(ies) available for glutamic acid and Abnormalities, Multiple
Article | Year |
---|---|
A dietary embryo/fetal developmental toxicity study of arruva, an R,R-monatin salt isomer, in Crl:CD(SD) rats.
Topics: Abnormalities, Multiple; Animal Feed; Animals; Body Weight; Diet; Female; Fetal Weight; Glutamic Acid; Indoles; Male; Maternal Exposure; Mice, Inbred ICR; No-Observed-Adverse-Effect Level; Pregnancy; Rats, Sprague-Dawley; Sweetening Agents; Toxicity Tests; Uterus | 2013 |
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 |
Analysis on the emerging role of Rab3 GTPase-activating protein in Warburg Micro and Martsolf syndrome.
Topics: Abnormalities, Multiple; Animals; Calcium; Cricetinae; Glutamic Acid; Humans; Mice; rab3 GTP-Binding Proteins; rab3A GTP-Binding Protein; Synaptosomes; Syndrome | 2008 |
A nonsense mutation 1669Glu-->Ter within the regulatory domain of human erythroid ankyrin leads to a selective deficiency of the major ankyrin isoform (band 2.1) and a phenotype of autosomal dominant hereditary spherocytosis.
Topics: Abnormalities, Multiple; Alleles; Alternative Splicing; Ankyrins; Base Sequence; Erythrocyte Membrane; Erythrocytes, Abnormal; Genes, Dominant; Glutamic Acid; Humans; Infant; Infant, Newborn; Jaundice, Neonatal; Molecular Sequence Data; Mutation; Osmotic Fragility; RNA, Messenger; Spectrin | 1995 |