Page last updated: 2024-10-17

cytosine and Frontotemporal Dementia

cytosine has been researched along with Frontotemporal Dementia in 3 studies

Frontotemporal Dementia: The most common clinical form of FRONTOTEMPORAL LOBAR DEGENERATION, this dementia presents with personality and behavioral changes often associated with disinhibition, apathy, and lack of insight.

Research Excerpts

ExcerptRelevanceReference
"Two families with frontotemporal dementia with parkinsonism linked to chromosome 17 (FTDP-17) resulting from the microtubule associated protein tau (MAPT) gene IVS10+16C>T splice site mutation are reported, members of which showed variable clinical phenotypes at presentation."1.35Intrafamilial clinical phenotypic heterogeneity with MAPT gene splice site IVS10+16C>T mutation. ( Larner, AJ, 2009)

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (33.33)29.6817
2010's0 (0.00)24.3611
2020's2 (66.67)2.80

Authors

AuthorsStudies
Potrč, M1
Sebastián, N1
Škarabot, M1
Drevenšek-Olenik, I1
Spindler, L1
Geng, Y1
Liu, C1
Cai, Q1
Luo, Z1
Miao, H1
Shi, X1
Xu, N1
Fung, CP1
Choy, TT1
Yan, B1
Li, N1
Qian, P1
Zhou, B1
Zhu, G1
Larner, AJ1

Other Studies

3 other studies available for cytosine and Frontotemporal Dementia

ArticleYear
Supramolecular Polymorphism of (G
    International journal of molecular sciences, 2021, Apr-26, Volume: 22, Issue:9

    Topics: Amyotrophic Lateral Sclerosis; Circular Dichroism; Cytosine; DNA; DNA Repeat Expansion; Frontotempor

2021
Crystal structure of parallel G-quadruplex formed by the two-repeat ALS- and FTD-related GGGGCC sequence.
    Nucleic acids research, 2021, 06-04, Volume: 49, Issue:10

    Topics: Amyotrophic Lateral Sclerosis; C9orf72 Protein; Circular Dichroism; Cytosine; Dimerization; DNA; DNA

2021
Intrafamilial clinical phenotypic heterogeneity with MAPT gene splice site IVS10+16C>T mutation.
    Journal of the neurological sciences, 2009, Dec-15, Volume: 287, Issue:1-2

    Topics: Atrophy; Base Sequence; Brain; Brain Chemistry; Cytosine; Disease Progression; DNA; DNA Mutational A

2009