arginine has been researched along with Abnormalities, Congenital in 6 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (33.33) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 3 (50.00) | 29.6817 |
2010's | 1 (16.67) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Stypułkowska, J; Sutuła, M; Taranta-Janusz, K; Wasilewska, A | 1 |
GROSFELD, JC; MIGHORST, JA; MOOLHUYSEN, TM | 1 |
Aronoff, R; Maricq, AV; Mellem, JE; Seeburg, PH; Sprengel, R | 1 |
Fujimoto, M; Fukami, M; Hasegawa, T; Koitabashi, Y; Ogata, T; Soneda, S | 1 |
Devi, RR; Vijayalakshmi, P | 1 |
Coleman, BW; Grummer, RH; Hoekstra, WG; Reimann, EM; Sunde, ML | 1 |
6 other study(ies) available for arginine and Abnormalities, Congenital
Article | Year |
---|---|
Osteopontin and symmetric dimethylarginine plasma levels in solitary functioning kidney in children.
Topics: Adolescent; Arginine; Biomarkers; Case-Control Studies; Child; Child, Preschool; Congenital Abnormalities; Creatinine; Enzyme-Linked Immunosorbent Assay; Female; Follow-Up Studies; Humans; Infant; Kidney; Kidney Diseases; Kidney Function Tests; Male; Nephrectomy; Osteopontin; Retrospective Studies; ROC Curve | 2012 |
ARGININOSUCCINIC ACIDURIA IN MONILETHRIX.
Topics: Amino Acid Metabolism, Inborn Errors; Amino Acids; Arginine; Argininosuccinic Aciduria; Chromatography; Congenital Abnormalities; Genetics, Medical; Hair; Humans; Intellectual Disability; Monilethrix; Succinates; Urine | 1964 |
Neuronal toxicity in Caenorhabditis elegans from an editing site mutant in glutamate receptor channels.
Topics: Amino Acid Motifs; Amino Acid Sequence; Amino Acid Substitution; Animals; Animals, Genetically Modified; Arginine; Caenorhabditis elegans; Caenorhabditis elegans Proteins; Calcium; Calcium Channels; Calreticulin; Congenital Abnormalities; Endoplasmic Reticulum; Genotype; Glutamine; Ion Transport; Kainic Acid; Mammals; Mice; Molecular Sequence Data; Necrosis; Nerve Degeneration; Neurons; Phenotype; Receptor Cross-Talk; Receptors, AMPA; Receptors, Glutamate; RNA Editing; Sequence Alignment; Sequence Homology, Amino Acid; Structure-Activity Relationship; Synaptic Transmission; Touch; Vesicular Glutamate Transport Proteins | 2004 |
Association of micropenis with Pro185Ala polymorphism of the gene for aryl hydrocarbon receptor repressor involved in dioxin signaling.
Topics: Adolescent; Alanine; Arginine; Basic Helix-Loop-Helix Transcription Factors; Case-Control Studies; Child; Child, Preschool; Congenital Abnormalities; Dioxins; Gene Frequency; Genetic Predisposition to Disease; Humans; Infant; Infant, Newborn; Lysine; Male; Penis; Polymorphism, Genetic; Proline; Receptors, Aryl Hydrocarbon; Repressor Proteins; Signal Transduction | 2005 |
Novel mutations in GJA8 associated with autosomal dominant congenital cataract and microcornea.
Topics: Adult; Arginine; Case-Control Studies; Cataract; Child; Congenital Abnormalities; Connexins; Cornea; Eye Proteins; Genes, Dominant; Glutamic Acid; Glutamine; Humans; India; Middle Aged; Mutation; Mutation, Missense; Myopia; Phenotype; Tyrosine | 2006 |
Antagonistic effect of arginine on zinc metabolism in chicks.
Topics: Animal Nutritional Physiological Phenomena; Animals; Arginine; Body Weight; Bone and Bones; Bone Diseases, Developmental; Caseins; Chickens; Congenital Abnormalities; Deficiency Diseases; Depression, Chemical; Dietary Proteins; Egg White; Feathers; Female; Glycine max; Hindlimb; Histamine; Histidine; Liver; Male; Plant Proteins; Stimulation, Chemical; Tibia; Zinc | 1971 |