tryptophan has been researched along with Disorders of Sex Development in 3 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 1 (33.33) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 1 (33.33) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Devine, SE; Hodes, GE; Lenz, KM; Mahurkar, A; McCarthy, MM; Nugent, BM; Russo, SJ; Shetty, AC; Wright, CL | 1 |
| Argentaro, A; Barroso, I; Clayton, A; Harley, VR; Jans, DA; John, A; Nagai, T; Ogata, T; Preiss, S; Schafer, AJ | 1 |
| Berta, P; Goodfellow, PN; Hawkins, JR; Levilliers, J; Taylor, A; Van der Auwera, B | 1 |
3 other study(ies) available for tryptophan and Disorders of Sex Development
| Article | Year |
|---|---|
Brain feminization requires active repression of masculinization via DNA methylation.
Topics: Animals; Brain; Copulation; CpG Islands; Cytidine; Disorders of Sex Development; DNA (Cytosine-5-)-Methyltransferases; DNA Methylation; DNA Methyltransferase 3A; DNA, Intergenic; Estradiol; Female; Gene Expression Regulation, Developmental; Male; Mice; Microfilament Proteins; Nerve Tissue Proteins; Phthalimides; Preoptic Area; Protein Isoforms; Rats; Rats, Sprague-Dawley; Sex Characteristics; Sex Differentiation; Testosterone; Tryptophan | 2015 |
Compound effects of point mutations causing campomelic dysplasia/autosomal sex reversal upon SOX9 structure, nuclear transport, DNA binding, and transcriptional activation.
Topics: Abnormalities, Multiple; Active Transport, Cell Nucleus; Adult; Amino Acid Sequence; Animals; Bone and Bones; Cell Nucleus; Cells, Cultured; Circular Dichroism; COS Cells; Disorders of Sex Development; DNA; Electrophoresis, Polyacrylamide Gel; Female; Genes, Dominant; Heterozygote; High Mobility Group Proteins; Humans; Immunohistochemistry; Infant, Newborn; Karyopherins; Karyotyping; Kinetics; Molecular Sequence Data; Mutagenesis, Site-Directed; Mutation; Nuclear Proteins; Phenotype; Point Mutation; Polymorphism, Single-Stranded Conformational; Protein Binding; Protein Conformation; Protein Denaturation; Protein Structure, Tertiary; Sequence Analysis, DNA; SOX9 Transcription Factor; Spectrometry, Fluorescence; Structure-Activity Relationship; Temperature; Transcription Factors; Transcriptional Activation; Transfection; Tryptophan | 2001 |
Mutational analysis of SRY: nonsense and missense mutations in XY sex reversal.
Topics: Base Sequence; Codon; Disorders of Sex Development; DNA-Binding Proteins; Female; Genetic Variation; Gonadal Dysgenesis, 46,XY; High Mobility Group Proteins; Humans; Molecular Sequence Data; Mutation; Nuclear Proteins; Oligodeoxyribonucleotides; Polymerase Chain Reaction; Polymorphism, Genetic; Restriction Mapping; Sex Determination Analysis; Sex-Determining Region Y Protein; Transcription Factors; Tryptophan; X Chromosome; Y Chromosome | 1992 |