Moses Lee

AzaHx, a novel fluorescent, DNA minor groove and G·C recognition element: Synthesis and DNA binding properties of a p-anisyl-4-aza-benzimidazole-pyrrole-imidazole (azaHx-PI) polyamide.

Shuo Wang, W. Wilson, J. Hartley, 2015, Bioorganic & medicinal chemistry letters.

DNA‐Binding Properties of New Fluorescent AzaHx Amides: Methoxypyridylazabenzimidazolepyrroleimidazole/pyrrole

W. Wilson, J. Hartley, V. Satam, 2018, Chembiochem : a European journal of chemical biology.

Modulation of topoisomerase IIα expression and chemosensitivity through targeted inhibition of NF-Y:DNA binding by a diamino p-anisyl-benzimidazole (Hx) polyamide.

M. Gregory, W. Wilson, D. Hochhauser, 2017, Biochimica et biophysica acta. Gene regulatory mechanisms.

Sequence specific and high affinity recognition of 5'-ACGCGT-3' by rationally designed pyrrole-imidazole H-pin polyamides: thermodynamic and structural studies.

W. Wilson, Binh Nguyen, J. Hartley, 2008, Bioorganic & medicinal chemistry.

Modifying the N-terminus of polyamides: PyImPyIm has improved sequence specificity over f-ImPyIm.

W. Wilson, Binh Nguyen, J. Hartley, 2008, Bioorganic & medicinal chemistry.

Sequence specificity of alkylation for a series of nitrogen mustard-containing analogues of distamycin of increasing binding site size: evidence for increased cytotoxicity with enhanced sequence specificity.

R. Souhami, J. Hartley, M. Lee, 1995, Biochemistry.