dapi has been researched along with Myotonic Dystrophy in 5 studies
DAPI: RN given refers to parent cpd.
Myotonic Dystrophy: Neuromuscular disorder characterized by PROGRESSIVE MUSCULAR ATROPHY; MYOTONIA, and various multisystem atrophies. Mild INTELLECTUAL DISABILITY may also occur. Abnormal TRINUCLEOTIDE REPEAT EXPANSION in the 3' UNTRANSLATED REGIONS of DMPK PROTEIN gene is associated with Myotonic Dystrophy 1. DNA REPEAT EXPANSION of zinc finger protein-9 gene intron is associated with Myotonic Dystrophy 2.
| Excerpt | Relevance | Reference |
|---|---|---|
| "DAPI was positive in 3R/4R (3-repeat/4-repeat) tau deposits in Alzheimer's disease, myotonic dystrophy, and neurodegeneration with brain iron accumulation, and in 4R tau deposits in corticobasal degeneration, but negative in 4R tau deposits in frontotemporal dementia with parkinsonism-17 and progressive supranuclear palsy." | 1.48 | 4',6-Diamidino-2-Phenylindole Distinctly Labels Tau Deposits. ( Kinoshita, E; Li, C; Maruyama, H; Matsubara, T; Matsumoto, M; Shrestha, T; Takahashi, T, 2018) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 3 (60.00) | 29.6817 |
| 2010's | 2 (40.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Huang, TL | 1 |
| Mayence, A | 1 |
| Vanden Eynde, JJ | 1 |
| Li, C | 1 |
| Takahashi, T | 1 |
| Shrestha, T | 1 |
| Kinoshita, E | 1 |
| Matsubara, T | 1 |
| Matsumoto, M | 1 |
| Maruyama, H | 1 |
| Schessl, J | 1 |
| Goemans, NM | 1 |
| Magold, AI | 1 |
| Zou, Y | 1 |
| Hu, Y | 1 |
| Kirschner, J | 1 |
| Sciot, R | 1 |
| Bönnemann, CG | 1 |
| Lucchiari, S | 1 |
| Pagliarani, S | 1 |
| Corti, S | 1 |
| Mancinelli, E | 1 |
| Servida, M | 1 |
| Fruguglietti, E | 1 |
| Sansone, V | 1 |
| Moggio, M | 1 |
| Bresolin, N | 1 |
| Comi, GP | 1 |
| Meola, G | 2 |
| Sallinen, R | 1 |
| Vihola, A | 1 |
| Bachinski, LL | 1 |
| Huoponen, K | 1 |
| Haapasalo, H | 1 |
| Hackman, P | 1 |
| Zhang, S | 1 |
| Sirito, M | 1 |
| Kalimo, H | 1 |
| Horelli-Kuitunen, N | 1 |
| Wessman, M | 1 |
| Krahe, R | 1 |
| Udd, B | 1 |
1 review available for dapi and Myotonic Dystrophy
| Article | Year |
|---|---|
Some non-conventional biomolecular targets for diamidines. A short survey.
Topics: Amidines; Animals; Diabetes Mellitus, Type 2; DNA; Enzymes; Humans; Hypertension; Ion Channels; Myot | 2014 |
4 other studies available for dapi and Myotonic Dystrophy
| Article | Year |
|---|---|
4',6-Diamidino-2-Phenylindole Distinctly Labels Tau Deposits.
Topics: Aged; Aged, 80 and over; Alzheimer Disease; Brain; Fluorescent Dyes; Frontotemporal Dementia; Humans | 2018 |
Predominant fiber atrophy and fiber type disproportion in early ullrich disease.
Topics: Adenosine Triphosphatases; Biopsy; Child, Preschool; Collagen Type VI; Female; Humans; Indoles; Infa | 2008 |
Colocalization of ribonuclear inclusions with muscle blind like-proteins in a family with myotonic dystrophy type 2 associated with a short CCTG expansion.
Topics: Adult; Creatine Kinase; DNA Repeat Expansion; Electromyography; Family Health; Female; Humans; Indol | 2008 |
New methods for molecular diagnosis and demonstration of the (CCTG)n mutation in myotonic dystrophy type 2 (DM2).
Topics: Adult; Aged; Aged, 80 and over; Alleles; Biopsy; DNA Repeat Expansion; Electrophoresis, Capillary; F | 2004 |