plerixafor has been researched along with alx40 4c in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 2 (50.00) | 18.2507 |
2000's | 2 (50.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Broach, JR; Fujii, N; Haribabu, B; Hiramatu, K; Manfredi, JP; Navenot, JM; Omagari, A; Pei, G; Peiper, SC; Tamamura, H; Zhang, WB | 1 |
Murakami, T; Yamamoto, N | 1 |
Arakaki, R; Fujii, N; Hattori, T; Ibuka, T; Kanbara, K; Nakashima, H; Omagari, A; Otaka, A; Tamamura, H; Xu, Y; Yamamoto, N; Zhang, X | 1 |
Fujii, N; Gotoh, K; Kanamoto, T; Kanbara, K; Mochizuki, K; Nakashima, H; Tamamura, H; Yoshimori, M | 1 |
1 review(s) available for plerixafor and alx40 4c
Article | Year |
---|---|
[Development of anti-HIV drugs targeted to the coreceptors].
Topics: Amino Acid Sequence; Animals; Anti-HIV Agents; Antimicrobial Cationic Peptides; Benzylamines; Chemokine CCL5; Cyclams; Heterocyclic Compounds; HIV-1; Humans; Ligands; Molecular Sequence Data; Oligopeptides; Peptides; Receptors, Chemokine | 1998 |
3 other study(ies) available for plerixafor and alx40 4c
Article | Year |
---|---|
A point mutation that confers constitutive activity to CXCR4 reveals that T140 is an inverse agonist and that AMD3100 and ALX40-4C are weak partial agonists.
Topics: Amino Acid Substitution; Animals; Anti-HIV Agents; Benzylamines; CHO Cells; Cricetinae; Cyclams; Genes, Reporter; Genetic Variation; GTP-Binding Proteins; Heterocyclic Compounds; Humans; Oligopeptides; Open Reading Frames; Point Mutation; Protein Conformation; Receptors, CXCR4; Recombinant Proteins; Saccharomyces cerevisiae; Signal Transduction; Transfection | 2002 |
A low-molecular-weight inhibitor against the chemokine receptor CXCR4: a strong anti-HIV peptide T140.
Topics: Amino Acid Sequence; Anti-HIV Agents; Antimicrobial Cationic Peptides; Benzylamines; Cells, Cultured; Chemokine CXCL12; Chemokines, CXC; Circular Dichroism; Cyclams; DNA-Binding Proteins; Heterocyclic Compounds; HIV-1; Molecular Sequence Data; Oligopeptides; Peptides; Peptides, Cyclic; Receptors, CXCR4; T-Lymphocytes | 1998 |
Increase of R5 HIV-1 infection and CCR5 expression in T cells treated with high concentrations of CXCR4 antagonists and SDF-1.
Topics: Animals; Anti-HIV Agents; Antibodies, Monoclonal; Benzylamines; CD4 Antigens; CD4-Positive T-Lymphocytes; Chemokine CXCL12; Chemokines; Chemokines, CXC; Chlorocebus aethiops; COS Cells; Cyclams; Drug Synergism; Gene Expression Regulation; Heterocyclic Compounds; HIV Long Terminal Repeat; HIV-1; Humans; Methionine; Oligopeptides; Peptide Fragments; Receptors, CCR5; Receptors, CXCR4; Transfection; Tumor Cells, Cultured; Virus Replication; Zidovudine | 2001 |