isomethyleugenol has been researched along with Turner Syndrome in 4 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (25.00) | 18.7374 |
| 1990's | 1 (25.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 1 (25.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Allard, DE; Conley, B; Cook, KD; Davenport, ML; Fry, RC; Magnuson, T; Rager, JE; Shpargel, KB; Starmer, J; Su, MA; Whitfield-Larry, F; Whitmire, JK | 1 |
| Pena, SD; Sturzeneker, R | 1 |
| Dewa, K; Kominami, R; Naito, E; Yamanouchi, H | 1 |
| Calvert, GD | 1 |
4 other study(ies) available for isomethyleugenol and Turner Syndrome
| Article | Year |
|---|---|
T Follicular Helper Cell-Dependent Clearance of a Persistent Virus Infection Requires T Cell Expression of the Histone Demethylase UTX.
Topics: Animals; Antibodies, Viral; Cell Differentiation; Female; Gene Dosage; Gene Expression Regulation; Genetic Predisposition to Disease; Histone Demethylases; Histones; Humans; Immunologic Memory; Interleukin-6 Receptor alpha Subunit; Lymphocyte Cooperation; Lymphocytic Choriomeningitis; Lymphocytic choriomeningitis virus; Methylation; Mice; Models, Immunological; Nuclear Proteins; Otitis Media; Protein Processing, Post-Translational; Receptors, CXCR5; Species Specificity; T-Lymphocyte Subsets; T-Lymphocytes, Helper-Inducer; Transcription, Genetic; Turner Syndrome; Viremia; Virulence; X Chromosome Inactivation | 2015 |
Fetal diagnosis of monosomy X (Turner syndrome) with methylation-specific PCR.
Topics: Female; Humans; Methylation; Polymerase Chain Reaction; Pregnancy; Prenatal Diagnosis; Turner Syndrome | 2003 |
Sex typing of forensic DNA samples using male- and female-specific probes.
Topics: Base Sequence; DNA; DNA Probes; Electrophoresis, Agar Gel; False Positive Reactions; Feasibility Studies; Female; Humans; Male; Methylation; Molecular Sequence Data; Polymerase Chain Reaction; Postmortem Changes; Repetitive Sequences, Nucleic Acid; Sensitivity and Specificity; Sex Determination Analysis; Turner Syndrome; X Chromosome; Y Chromosome | 1994 |
Trimethylaminuria and inherited Noonan's syndrome.
Topics: Abnormalities, Multiple; Adult; Amines; Blood Coagulation Disorders; Cryptorchidism; Dwarfism; Humans; Male; Methylation; Pedigree; Turner Syndrome | 1973 |