Exploring the Trypanosoma brucei Hsp83 Potential as a Target for Structure Guided Drug Design. Read more about Exploring the Trypanosoma brucei Hsp83 Potential as a Target for Structure Guided Drug Design.
Neculai D, Schwake M, Ravichandran M, Zunke F, Collins RF, Peters J, Neculai M, Plumb J, Loppnau P, Pizarro JC, Seitova A, Trimble WS, Saftig P, Grinstein S, Dhe-Paganon S. Read more about Neculai D, Schwake M, Ravichandran M, Zunke F, Collins RF, Peters J, Neculai M, Plumb J, Loppnau P, Pizarro JC, Seitova A, Trimble WS, Saftig P, Grinstein S, Dhe-Paganon S.
Stochastic detection of Pim protein kinases reveals electrostatically enhanced association of a peptide substrate. Read more about Stochastic detection of Pim protein kinases reveals electrostatically enhanced association of a peptide substrate.
Mutant prolactin receptor and familial hyperprolactinemia. Read more about Mutant prolactin receptor and familial hyperprolactinemia.
Medium-throughput production of recombinant human proteins: ligation-independent cloning. Read more about Medium-throughput production of recombinant human proteins: ligation-independent cloning.
Medium-Throughput Production of Recombinant Human Proteins: Protein Production in E. coli. Read more about Medium-Throughput Production of Recombinant Human Proteins: Protein Production in E. coli.
Medium-throughput production of recombinant human proteins: protein production in insect cells. Read more about Medium-throughput production of recombinant human proteins: protein production in insect cells.
Biochemical and Structural Studies of Conserved Maf Proteins Revealed Nucleotide Pyrophosphatases with a Preference for Modified Nucleotides. Read more about Biochemical and Structural Studies of Conserved Maf Proteins Revealed Nucleotide Pyrophosphatases with a Preference for Modified Nucleotides.
Structural determinants for ERK5 (MAPK7) and leucine rich repeat kinase 2 activities of benzo[e]pyrimido-[5,4-b]diazepine-6(11H)-ones. Read more about Structural determinants for ERK5 (MAPK7) and leucine rich repeat kinase 2 activities of benzo[e]pyrimido-[5,4-b]diazepine-6(11H)-ones.
RVX-208, an inhibitor of BET transcriptional regulators with selectivity for the second bromodomain. Read more about RVX-208, an inhibitor of BET transcriptional regulators with selectivity for the second bromodomain.
