thymine has been researched along with Deficiency, Mental 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 |
---|---|
Yang, J | 1 |
Horton, JR | 1 |
Li, J | 1 |
Huang, Y | 1 |
Zhang, X | 1 |
Blumenthal, RM | 1 |
Cheng, X | 1 |
Sztriha, L | 1 |
Frossard, P | 1 |
Hofstra, RM | 1 |
Verlind, E | 1 |
Nork, M | 1 |
van Kuilenburg, AB | 1 |
Dobritzsch, D | 1 |
Meinsma, R | 1 |
Haasjes, J | 1 |
Waterham, HR | 1 |
Nowaczyk, MJ | 1 |
Maropoulos, GD | 1 |
Hein, G | 1 |
Kalhoff, H | 1 |
Kirk, JM | 1 |
Baaske, H | 1 |
Aukett, A | 1 |
Duley, JA | 1 |
Ward, KP | 1 |
Lindqvist, Y | 1 |
van Gennip, AH | 1 |
Robbins, JH | 1 |
Kraemer, KH | 1 |
Lutzner, MA | 1 |
Festoff, BW | 1 |
Coon, HG | 1 |
4 other studies available for thymine and Deficiency, Mental
Article | Year |
---|---|
Structural basis for preferential binding of human TCF4 to DNA containing 5-carboxylcytosine.
Topics: Amino Acid Sequence; Arginine; Binding Sites; Cloning, Molecular; Cytosine; DNA; Electrophoretic Mob | 2019 |
Novel missense mutation in the L1 gene in a child with corpus callosum agenesis, retardation, adducted thumbs, spastic paraparesis, and hydrocephalus.
Topics: Agenesis of Corpus Callosum; Child; Guanine; Humans; Hydrocephalus; Intellectual Disability; Leukocy | 2000 |
Novel disease-causing mutations in the dihydropyrimidine dehydrogenase gene interpreted by analysis of the three-dimensional protein structure.
Topics: Age of Onset; Amino Acids; Animals; Cells, Cultured; Child, Preschool; Crystallography, X-Ray; Dihyd | 2002 |
Xeroderma pigmentosum. An inherited diseases with sun sensitivity, multiple cutaneous neoplasms, and abnormal DNA repair.
Topics: Adolescent; Adult; Autoradiography; Carcinoma, Basal Cell; Carcinoma, Squamous Cell; Chemical Phenom | 1974 |