Page last updated: 2024-10-17

cytosine and DDPAC

cytosine has been researched along with DDPAC in 3 studies

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 DDPAC

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