| 1 |
28420387 |
Effects of host restriction factors and the HTLV-1 subtype on susceptibility to HTLV-1-associated myelopathy/tropical spastic paraparesis |
Mutation
|
| 2 |
34494950 |
Polymorphisms in HTLV-1 Tax-responsive elements in HTLV-1-associated myelopathy/tropical spastic paraparesis patients are associated with reduced proviral load but not with disease progression |
Mutation
|
| 3 |
23800288 |
Molecular study of HBZ and gp21 human T cell leukemia virus type 1 proteins isolated from different clinical profile infected individuals |
Mutation
|
| 4 |
23510700 |
Molecular characterization of HTLV-1 gp46 glycoprotein from health carriers and HAM/TSP infected individuals |
Mutation
|
| 5 |
27553711 |
Analyses of HTLV-1 sequences suggest interaction between ORF-I mutations and HAM/TSP outcome |
Mutation
|
| 6 |
26472535 |
Deep Sequencing Analysis of Human T Cell Lymphotropic Virus Type 1 Long Terminal Repeat 5' Region from Patients with Tropical Spastic Paraparesis/Human T Cell Lymphotropic Virus Type 1-Associated Myelopathy and Asymptomatic Carriers |
Mutation
|
| 7 |
8011162 |
A spontaneous point mutation in the human T-cell leukemia virus type 1 pX gene leads to expression of a novel doubly spliced pX-mRNA that encodes a 25-kD, amino-terminal deleted rex protein |
Mutation
|
| 8 |
29716616 |
Stability of the HTLV-1 glycoprotein 46 (gp46) gene in an endemic region of the Brazilian Amazon and the presence of a significant mutation (N93D) in symptomatic patients |
Mutation
|
| 9 |
33835501 |
Molecular characterization of HTLV-1 genomic region hbz from patients with different clinical conditions |
Mutation
|
| 10 |
31154802 |
Assessment of Genetic Diversity of HTLV-1 ORF-I Sequences Collected from Patients with Different Clinical Profiles |
Mutation
|
| 11 |
17067264 |
Distribution of human T cell lymphotropic virus type 1 (HTLV-1) subtypes in Brazil: genetic characterization of LTR and tax region |
Mutation
|
| 12 |
39279426 |
Mapping variants in HTLV-1 genome to analyze their impacts on the HAM/TSP development: A systematic review |
Mutation
|