proline has been researched along with Diseases in Twins in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (25.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 2 (50.00) | 29.6817 |
| 2010's | 1 (25.00) | 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 |
| ASATOOR, AM; KOPELMAN, H; MILNE, MD | 1 |
| Arlt, W; Draper, N; Hartmann, MF; Stewart, PM; Wudy, SA | 1 |
| Amino, N; Fukui, H; Honda, K; Hosokawa, A; Izumi, Y; Matoba, R; Matsuo, T; Okamoto, S; Takegawa, T; Tatsumi, K; Tun, Z | 1 |
4 other study(ies) available for proline 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 |
HYPERPROLINAEMIA AND HEREDITARY NEPHRITIS.
Topics: 1-Pyrroline-5-Carboxylate Dehydrogenase; Amino Acid Metabolism, Inborn Errors; Blood; Blood Chemical Analysis; Chromatography; Diseases in Twins; Fluids and Secretions; Genetics, Medical; Glycine; Humans; Hydroxyproline; Nephritis, Hereditary; Nephrotic Syndrome; Pathology; Proline; Proline Oxidase; Proteinuria; Urine | 1964 |
A male twin infant with skull deformity and elevated neonatal 17-hydroxyprogesterone: a prismatic case of P450 oxidoreductase deficiency.
Topics: 17-alpha-Hydroxyprogesterone; Abnormalities, Multiple; Alanine; Amino Acid Substitution; Cytosine; Diagnosis, Differential; Diseases in Twins; Ear; Female; Guanine; Humans; Infant, Newborn; Male; Marfan Syndrome; NADPH-Ferrihemoprotein Reductase; Proline; Skull; Steroid Metabolism, Inborn Errors; Steroids | 2004 |
A novel mutation of the KAL1 gene in monozygotic twins with Kallmann syndrome.
Topics: Adult; Base Sequence; Body Height; Body Weight; Cell Adhesion Molecules; Diseases in Twins; Exons; Extracellular Matrix Proteins; Female; Genomic Imprinting; Germ-Line Mutation; Gonadal Steroid Hormones; Humans; Kallmann Syndrome; Male; Nerve Tissue Proteins; Pedigree; Pituitary Hormones; Polymerase Chain Reaction; Proline; Reference Values; Sequence Deletion; Twins, Monozygotic | 2000 |