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T134 peptide

Known as: T134 
 
National Institutes of Health

Papers overview

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2015
2015
In this study, mouth-disintegrating tablets of atenolol and atorvastatin combination were formulated using superdisintegrants to… Expand
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Highly Cited
2005
Highly Cited
2005
Emerging evidence shows that the stromal cell–derived factor 1 (SDF-1)/CXCR4 interaction regulates multiple cell signaling… Expand
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Highly Cited
2001
Highly Cited
2001
The chemokine receptors CXCR4 and CCR5 are used as co-receptors by the T cell-tropic (X4) and macrophage-tropic (R5) HIV-1… Expand
2001
2001
The chemokine receptors CXCR4 and CCR5 are considered to be potential targets for the inhibition of HIV-1 replication. We have… Expand
Highly Cited
2000
Highly Cited
2000
A polyphemusin peptide analogue, T22 ([Tyr(5,12), Lys7]-polyphemusin II), and its shortened potent analogues, T134 (des-[Cys(8,13… Expand
Review
2000
Review
2000
  • E. De Clercq
  • Medicinal research reviews
  • 2000
  • Corpus ID: 41451102
A large variety of natural products have been described as anti‐HIV agents, and for a portion thereof the target of interaction… Expand
Highly Cited
1999
Highly Cited
1999
ABSTRACT T22, an analog of polyphemusin II (18 amino acid residues), was found to block T-tropic human immunodeficiency virus… Expand
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1999
1999
T22 ([Tyr5,12, Lys7]-polyphemusin II) is a strong anti-HIV compound. Six analogs of T22 and two natural forms were synthesized… Expand
Highly Cited
1998
Highly Cited
1998
T22 ([Tyr5,12, Lys7]-polyphemusin II) is an 18-residue peptide amide, which has strong anti-HIV activity. T22 inhibits the T cell… Expand
Highly Cited
1992
Highly Cited
1992
Thymosin beta 4 (T beta 4), a 5-kD peptide which binds G-actin and inhibits its polymerization (Safer, D., M. Elzinga, and V. T… Expand
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