arginine has been researched along with Diseases in Twins in 6 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 3 (50.00) | 18.2507 |
| 2000's | 2 (33.33) | 29.6817 |
| 2010's | 1 (16.67) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Banshodani, A; Hattori, M; Kosaki, K; Kozai, K; Moriyama, K; Suda, N; Tanimoto, K | 1 |
| Cao, WH; Guo, XX; Hu, YH; Li, LM; Li, QN; Lv, J; Qin, Y; Zhan, SY | 1 |
| Admiraal, RJ; Brunner, HG; Hendriks, Y; Hoefsloot, LH; Jongmans, MC; Magee, A; van de Laar, I; van der Donk, KP; van Ravenswaaij, CM; Verheij, JB; Walpole, I | 1 |
| Hirano, M; Mori, T; Nagai, Y; Takakura, Y; Tamai, S; Ueno, S | 1 |
| Brennan, SO; George, PM; Janus, ED; Nye, ER; Rall, SC; Wardell, MR; Weisgraber, KH | 1 |
| Jahoda, MG; Kleijer, WJ; Los, FJ; Pijpers, L; Reuss, A; Sachs, ES; Wladimiroff, JW | 1 |
6 other study(ies) available for arginine and Diseases in Twins
| Article | Year |
|---|---|
Correlation between genotype and supernumerary tooth formation in cleidocranial dysplasia.
Topics: Adenine; Adolescent; Adult; Arginine; Child; Cleidocranial Dysplasia; Core Binding Factor Alpha 1 Subunit; Diseases in Twins; DNA Copy Number Variations; Epigenesis, Genetic; Female; Frameshift Mutation; Genetic Heterogeneity; Genetic Variation; Genotype; Glutamine; Humans; Male; Middle Aged; Mutagenesis, Insertional; Mutation; Mutation, Missense; Point Mutation; Proline; Serine; Thymine; Tooth, Supernumerary; Twins, Monozygotic | 2010 |
[A twin study of association of beta3AR Trp64Arg polymorphisms with insulin sensitivity].
Topics: Arginine; Diseases in Twins; Gene Frequency; Genetic Predisposition to Disease; Genotype; Humans; Insulin; Insulin Resistance; Polymorphism, Genetic; Receptors, Adrenergic, beta-3; Tryptophan; Twins, Dizygotic | 2004 |
Familial CHARGE syndrome and the CHD7 gene: a recurrent missense mutation, intrafamilial recurrence and variability.
Topics: Abnormalities, Multiple; Amino Acid Sequence; Amino Acid Substitution; Arginine; Case-Control Studies; Conserved Sequence; Diseases in Twins; DNA Helicases; DNA-Binding Proteins; Female; Genes, Dominant; Genetic Variation; Humans; Male; Molecular Sequence Data; Mosaicism; Mutation, Missense; Pedigree; Sequence Analysis, DNA; Sequence Homology, Amino Acid; Siblings; Syndrome; Twins, Monozygotic | 2008 |
Japanese triplets with cerebrotendinous xanthomatosis are homozygous for a mutant gene coding for the sterol 27-hydroxylase (Arg441Trp).
Topics: Adult; Amino Acid Sequence; Arginine; Base Sequence; Blotting, Northern; Cholestanetriol 26-Monooxygenase; Cytochrome P-450 Enzyme System; Diseases in Twins; DNA Primers; Exons; Female; Genetic Carrier Screening; Homozygote; Humans; Japan; Male; Molecular Sequence Data; Pedigree; Point Mutation; Polymerase Chain Reaction; Polymorphism, Restriction Fragment Length; Restriction Mapping; RNA, Messenger; Steroid Hydroxylases; Triplets; Tryptophan; Xanthomatosis | 1996 |
Apolipoprotein E2-Dunedin (228 Arg replaced by Cys): an apolipoprotein E2 variant with normal receptor-binding activity.
Topics: Amino Acid Sequence; Apolipoprotein E2; Apolipoproteins E; Arginine; Cysteine; Diseases in Twins; Electrophoresis, Gel, Two-Dimensional; Genetic Variation; Heterozygote; Humans; Hyperlipoproteinemia Type III; Hyperlipoproteinemia Type V; Lipoproteins; Male; Middle Aged; Peptide Mapping; Protein Conformation; Receptors, LDL | 1990 |
Transabdominal chorionic villus sampling in a multiple pregnancy at risk of argininosuccinic aciduria: a case report.
Topics: Adult; Arginine; Argininosuccinic Acid; Chorionic Villi Sampling; Diseases in Twins; Female; Humans; Karyotyping; Male; Pregnancy; Pregnancy, Multiple; Prenatal Diagnosis; Risk Factors | 1990 |