thymine has been researched along with Acute Confusional Senile Dementia in 12 studies
| Excerpt | Relevance | Reference |
|---|---|---|
| "Congenital hydrocephalus (CH) is caused by genetic mutations, but whether factors impacting human genetic mutations are disease-specific remains elusive." | 2.72 | Genes causing congenital hydrocephalus: Their chromosomal characteristics of telomere proximity and DNA compositions. ( Hart, C; McKnight, I; Park, IH; Shim, JW, 2021) |
| "Xanthine levels were increased in the DLB group in the parietal, occipital, and temporal lobes, indicating that peroxynitrite or other deaminating species may be involved." | 1.30 | Oxidative damage to proteins, lipids, and DNA in cortical brain regions from patients with dementia with Lewy bodies. ( Halliwell, B; Ince, PG; Jenner, A; Jenner, P; Lyras, L; Perry, EK; Perry, RH, 1998) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 3 (25.00) | 18.2507 |
| 2000's | 5 (41.67) | 29.6817 |
| 2010's | 2 (16.67) | 24.3611 |
| 2020's | 2 (16.67) | 2.80 |
| Authors | Studies |
|---|---|
| Ozaki, T | 1 |
| Yoshino, Y | 1 |
| Tachibana, A | 1 |
| Shimizu, H | 1 |
| Mori, T | 1 |
| Nakayama, T | 1 |
| Mawatari, K | 1 |
| Numata, S | 1 |
| Iga, JI | 1 |
| Takahashi, A | 1 |
| Ohmori, T | 1 |
| Ueno, SI | 1 |
| McKnight, I | 1 |
| Hart, C | 1 |
| Park, IH | 1 |
| Shim, JW | 1 |
| Wang, G | 1 |
| Zhou, Y | 1 |
| Huang, FJ | 1 |
| Tang, HD | 1 |
| Xu, XH | 1 |
| Liu, JJ | 1 |
| Wang, Y | 1 |
| Deng, YL | 1 |
| Ren, RJ | 1 |
| Xu, W | 1 |
| Ma, JF | 1 |
| Zhang, YN | 1 |
| Zhao, AH | 1 |
| Chen, SD | 1 |
| Jia, W | 1 |
| Lutz, MW | 1 |
| Saul, R | 1 |
| Linnertz, C | 1 |
| Glenn, OC | 1 |
| Roses, AD | 1 |
| Chiba-Falek, O | 1 |
| Ingegni, T | 1 |
| Nocentini, G | 1 |
| Mariani, E | 1 |
| Spazzafumo, L | 1 |
| Polidori, MC | 1 |
| Cherubini, A | 1 |
| Catani, M | 1 |
| Cadini, D | 1 |
| Senin, U | 1 |
| Mecocci, P | 1 |
| Scola, L | 1 |
| Licastro, F | 1 |
| Chiappelli, M | 1 |
| Franceschi, C | 1 |
| Grimaldi, LM | 1 |
| Crivello, A | 1 |
| Colonna-Romano, G | 1 |
| Candore, G | 1 |
| Lio, D | 1 |
| Caruso, C | 1 |
| Wei, X | 1 |
| Chen, X | 1 |
| Fontanilla, C | 1 |
| Zhao, L | 1 |
| Liang, Z | 1 |
| Dodel, R | 1 |
| Hampel, H | 1 |
| Farlow, M | 1 |
| Du, Y | 1 |
| Lyras, L | 1 |
| Perry, RH | 1 |
| Perry, EK | 1 |
| Ince, PG | 1 |
| Jenner, A | 1 |
| Jenner, P | 1 |
| Halliwell, B | 1 |
| Morelli, L | 1 |
| Prat, MI | 1 |
| Levy, E | 1 |
| Mangone, CA | 1 |
| Castaño, EM | 1 |
| Barbieri, S | 1 |
| Hofele, K | 1 |
| Wiederhold, KH | 1 |
| Probst, A | 1 |
| Mistl, C | 1 |
| Danner, S | 1 |
| Kauffmann, S | 1 |
| Sommer, B | 1 |
| Spooren, W | 1 |
| Tolnay, M | 1 |
| Bilbe, G | 1 |
| van der Putten, H | 1 |
| Shibata, N | 1 |
| Ohnuma, T | 1 |
| Takahashi, T | 1 |
| Baba, H | 1 |
| Ishizuka, T | 1 |
| Ohtsuka, M | 1 |
| Ueki, A | 1 |
| Nagao, M | 1 |
| Arai, H | 1 |
| Ghetti, B | 1 |
| Murrell, J | 1 |
| Benson, MD | 1 |
| Farlow, MR | 1 |
2 reviews available for thymine and Acute Confusional Senile Dementia
| Article | Year |
|---|---|
Genes causing congenital hydrocephalus: Their chromosomal characteristics of telomere proximity and DNA compositions.
Topics: Adenine; Alzheimer Disease; Animals; Carrier Proteins; Chromosome Mapping; Chromosomes; Databases, G | 2021 |
Mouse models of alpha-synucleinopathy and Lewy pathology. Alpha-synuclein expression in transgenic mice.
Topics: Adenine; alpha-Synuclein; Alzheimer Disease; Animals; Brain; Disease Models, Animal; Humans; Lewy Bo | 2001 |
10 other studies available for thymine and Acute Confusional Senile Dementia
| Article | Year |
|---|---|
Metabolomic alterations in the blood plasma of older adults with mild cognitive impairment and Alzheimer's disease (from the Nakayama Study).
Topics: Activities of Daily Living; Aged; Alzheimer Disease; Betaine; Biomarkers; Cognitive Dysfunction; Hum | 2022 |
Plasma metabolite profiles of Alzheimer's disease and mild cognitive impairment.
Topics: Aged; Aged, 80 and over; Alzheimer Disease; Arachidonic Acid; Biomarkers; Chromatography, Liquid; Co | 2014 |
A cytosine-thymine (CT)-rich haplotype in intron 4 of SNCA confers risk for Lewy body pathology in Alzheimer's disease and affects SNCA expression.
Topics: Aged; Aged, 80 and over; alpha-Synuclein; Alzheimer Disease; Cytosine; Female; Gene Expression Regul | 2015 |
Cathepsin D polymorphism in Italian elderly subjects with sporadic late-onset Alzheimer's disease.
Topics: Age of Onset; Aged; Alleles; Alzheimer Disease; Apolipoproteins E; Case-Control Studies; Cathepsin D | 2003 |
Allele frequencies of +874T --> A single nucleotide polymorphism at the first intron of IFN-gamma gene in Alzheimer's disease patients.
Topics: Adenine; Age of Onset; Aged; Alzheimer Disease; Base Sequence; DNA Primers; Female; Humans; Interfer | 2003 |
C/T conversion alters interleukin-1A promoter function in a human astrocyte cell line.
Topics: Alzheimer Disease; Astrocytes; Cell Line; Cytosine; Humans; Interleukin-1alpha; Lovastatin; Lucifera | 2007 |
Oxidative damage to proteins, lipids, and DNA in cortical brain regions from patients with dementia with Lewy bodies.
Topics: Adenine; Aged; Aged, 80 and over; Alzheimer Disease; Brain Chemistry; Cerebral Cortex; Cytosine; DNA | 1998 |
Presenilin 1 Met146Leu variant due to an A --> T transversion in an early-onset familial Alzheimer's disease pedigree from Argentina.
Topics: Adenine; Adult; Age of Onset; Alzheimer Disease; Amino Acid Substitution; Argentina; Female; Genetic | 1998 |
The effect of IL4 +33C/T polymorphism on risk of Japanese sporadic Alzheimer's disease.
Topics: Adult; Aged; Aged, 80 and over; Alleles; Alzheimer Disease; Analysis of Variance; Chi-Square Distrib | 2002 |
Spectrum of amyloid beta-protein immunoreactivity in hereditary Alzheimer disease with a guanine to thymine missense change at position 1924 of the APP gene.
Topics: Adult; Alzheimer Disease; Amyloid beta-Peptides; Amyloid beta-Protein Precursor; Brain; Female; Gene | 1992 |