E. Kitas

发表

Synergistic Enhancement of Transient Expression by Dioleoyl-Melittin (DOM) and Polyethylenimine (PEI) in Mammalian Cells in Suspensionculture

U. Deuschle, E. Schlaeger, J. Legendre, 1998 .

Transient Transfection in Mammalian Cells

U. Deuschle, E. Schlaeger, J. Legendre, 1998 .

The influence of strongly acidic groups on the protonation of peptides in electrospray MS.

E. Kitas, W. Vetter, M. Svoboda, 1997, Journal of mass spectrometry : JMS.

Binding of oligoarginine to membrane lipids and heparan sulfate: structural and thermodynamic characterization of a cell-penetrating peptide.

J. Seelig, E. Kitas, E. Gonçalves, 2005, Biochemistry.

Purification and characterization of a soluble catalytic fragment of the human transmembrane leukocyte antigen related (LAR) protein tyrosine phosphatase from an Escherichia coli expression system.

C. Walsh, E. Kitas, P. Burn, 1991, Biochemistry.

Isolation and structural elucidation of a novel phosphocysteine intermediate in the LAR protein tyrosine phosphatase enzymatic pathway

C. Walsh, K. Anderson, Hyeongjin Cho, 1992 .

Preparation and use of Nα-fluorenylmethoxycarbonyl-O-dibenzylphosphono-L-tyrosine in continuous flow solid phase peptide synthesis

J. Wade, E. Kitas, R. Johns, 1991 .

Alternative strategies for the Fmoc solid-phase synthesis of O4-phospho-L-tyrosine-containing peptides

A. Trzeciak, E. Kitas, W. Bannwarth, 1991 .

Substrate specificities of catalytic fragments of protein tyrosine phosphatases (HPTPβ, LAR, and CD45) toward phosphotyrosylpeptide substrates and thiophosphotyrosylated peptides as inhibitors

C. Walsh, Hyeongjin Cho, E. Kitas, 1993, Protein science : a publication of the Protein Society.

SEAP expression in transiently transfected mammalian cells grown in serum-free suspension culture

E. Schlaeger, E. Kitas, A. Dorn, 2003, Cytotechnology.

Catalytic domains of the LAR and CD45 protein tyrosine phosphatases from Escherichia coli expression systems: purification and characterization for specificity and mechanism.

C. Walsh, E. Kitas, P. Burn, 1992, Biochemistry.

Purification and characterization of active recombinant human napsin A.

V. Schauer-Vukašinović, E. Kitas, D. Schlatter, 2000, European journal of biochemistry.

riDOM, a cell penetrating peptide. Interaction with phospholipid bilayers.

J. Seelig, E. Kitas, Gabriela Québatte, 2014, Biochimica et biophysica acta.

Structural and thermodynamic aspects of the interaction between heparan sulfate and analogues of melittin.

J. Seelig, E. Kitas, E. Gonçalves, 2006, Biochemistry.

riDOM, a cell-penetrating peptide. Interaction with DNA and heparan sulfate.

J. Seelig, E. Kitas, Gabriela Québatte, 2013, The journal of physical chemistry. B.

Novel orally active, dibenzazepinone-based γ-secretase inhibitors

Guido Galley, Jens-Uwe Peters, J. Peters, 2007 .

Endothelin-converting enzyme-1 inhibition and growth of human glioblastoma cells.

L. Juillerat-Jeanneret, E. Kitas, J. Aebi, 2005, Journal of medicinal chemistry.

Novel oligosaccharide mimetics by solid-phase synthesis

E. Kitas, H. Wessel, G. Müller, 1995 .

Sulfonylureido thiazoles as fructose-1,6-bisphosphatase inhibitors for the treatment of type-2 diabetes.

B. Kuhn, W. Haap, J. Benz, 2010, Bioorganic & medicinal chemistry letters.

Non-radioactive determination of PTH and dabsyl phosphoamino acids by capillary electrophoresis

L. Pinna, E. Kitas, H. Meyer, 1992 .

Labelling of CRF1 and CRF2 receptors using the novel radioligand, [3H]-urocortin

Gavin Kilpatrick, E. Kitas, S. Henriot, 1997, Neuropharmacology.

Phosphorylation of src-phosphopeptides by casein kinases-1 and -2: favourable effect of phosphotyrosine.

L. Pinna, E. Kitas, R. Johns, 1990, Biochemical and biophysical research communications.

Cargo Delivery into the Brain by in vivo identified Transport Peptides

U. Certa, H. Loetscher, P. Freskgård, 2015, Scientific Reports.

Chemical synthesis of O-thiophosphotyrosyl peptides.

E. Kitas, E. Küng, W. Bannwarth, 2009, International journal of peptide and protein research.

Structure-based design of peptidomimetic antagonists of p56lck SH2 domain

I. E. Smith, N. Borkakoti, D. Banner, 2002 .

NMR analysis of regioselectivity in dephosphorylation of a triphosphotyrosyl dodecapeptide autophosphorylation site of the insulin receptor by a catalytic fragment of LAR phosphotyrosine phosphatase

C. Walsh, Hyeongjin Cho, E. Kitas, 1992, Protein science : a publication of the Protein Society.

Synthesis of Multi-O4-phospho-L-tyrosine-Containing Peptides

E. Kitas, W. Bannwarth, 1992 .

The chemical synthesis of O-thiophosphotyrosine peptides

E. Kitas, W. Bannwarth, 1993 .

Potent and Selective BACE-1 Peptide Inhibitors Lower Brain Aβ Levels Mediated by Brain Shuttle Transport

W. Guba, A. Kuglstatter, A. Rufer, 2017, EBioMedicine.

Dioleoylmelittin as a novel serum-insensitive reagent for efficient transfection of mammalian cells.

U. Deuschle, J. Legendre, A. Trzeciak, 1997, Bioconjugate chemistry.

Synthesis of O-phosphotyrosine-containing peptides. 3. Synthesis of H-Pro-Tyr(P)-Val-OH via dimethyl phosphate protection and the use of improved deprotection procedures

E. Kitas, R. Johns, G. Tregear, 1990 .

Protease-triggered siRNA delivery vehicles.

Darren H. Wakefield, D. Lewis, J. Wolff, 2015, Journal of controlled release : official journal of the Controlled Release Society.

Substituted 2-oxo-azepane derivatives are potent, orally active γ-secretase inhibitors

A. Flohr, L. Ozmen, H. Jacobsen, 2008 .

Allosteric FBPase inhibitors gain 10(5) times in potency when simultaneously binding two neighboring AMP sites.

B. Kuhn, J. Benz, C. Joseph, 2008, Bioorganic & medicinal chemistry letters.