Nitin A Patil

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Relaxin family peptides: structure-activity relationship studies (vol 174, pg 950, 2017)

Combination of valproic acid and morpholino splice-switching oligonucleotide produces improved outcomes in spinal muscular atrophy patient-derived fibroblasts

Signal transduction pathways activated by insulin-like peptide 5 at the relaxin family peptide RXFP4 receptor

The actions of relaxin family peptides on signal transduction pathways activated by the relaxin family peptide receptor RXFP4

Total chemical synthesis of an intra-a-chain cystathionine human insulin analogue with enhanced thermal stability

A one-pot chemically cleavable bis-linker tether strategy for the synthesis of heterodimeric peptides

A single-chain derivative of the relaxin hormone is a functionally selective agonist of the G protein-coupled receptor, RXFP1

The complex binding mode of the peptide hormone H2 relaxin to its receptor RXFP1

The C-terminus of the B-chain of human insulin-like peptide 5 is critical for cognate RXFP4 receptor activity

Engineering of a novel simplified human insulin-like peptide 5 agonist

Site of fluorescent label modifies interaction of melittin with live cells and model membranes

Intramolecular acyl transfer in peptide and protein ligation and synthesis

Cellular disulfide bond formation in bioactive peptides and proteins

Minimum active structure of insulin-like peptide 5