E. Kurenova

发表

Focal Adhesion Kinase Suppresses Apoptosis by Binding to the Death Domain of Receptor-Interacting Protein

S. Hanks, Zheng‐gang Liu, W. Cance, 2004, Molecular and Cellular Biology.

Telomere functions. A review.

J. M. Mason, E. Kurenova, 1997, Biochemistry. Biokhimiia.

Inhibition of focal adhesion kinase and src increases detachment and apoptosis in human neuroblastoma cell lines

V. Golubovskaya, W. Cance, E. Beierle, 2009, Molecular carcinogenesis.

Focal Adhesion Kinase Expression in Human Neuroblastoma : Immunohistochemical and Real-time PCRAnalyses

V. Golubovskaya, W. Cance, W. London, 2008 .

Focal Adhesion Kinase Expression in Human Neuroblastoma: Immunohistochemical and Real-time PCR Analyses

V. Golubovskaya, W. Cance, W. London, 2008, Clinical Cancer Research.

N-MYC Regulates Focal Adhesion Kinase Expression in Human Neuroblastoma*

V. Golubovskaya, W. Cance, E. Beierle, 2007, Journal of Biological Chemistry.

Retrotransposons at Drosophila telomeres and terminal chromosome deficiencies

H. Biessmann, J. M. Mason, M. Walter, 1997 .

Control of Telomere Elongation and Telomeric Silencing in Drosophila Melanogaster

H. Biessmann, J. M. Mason, M. Walter, 2004, Genetica.

Vascular endothelial growth factor receptor-3 promotes breast cancer cell proliferation, motility and survival in vitro and tumor formation in vivo

V. Golubovskaya, W. Cance, N. Massoll, 2009, Cell cycle.

Neurofibromin physically interacts with the N‐terminal domain of focal adhesion kinase

V. Golubovskaya, W. Cance, M. Wallace, 2009, Molecular carcinogenesis.

Receptor-Interacting Protein by Binding to the Death Domain of Focal Adhesion Kinase Suppresses Apoptosis

S. Hanks, W. Cance, A. Baldwin, 2004 .

Inhibition of the focal adhesion kinase and vascular endothelial growth factor receptor‐3 interaction leads to decreased survival in human neuroblastoma cell lines

W. Cance, E. Beierle, J. Stewart, 2014, Molecular carcinogenesis.

Vascular endothelial growth factor receptor-3 and focal adhesion kinase bind and suppress apoptosis in breast cancer cells.

V. Golubovskaya, W. Cance, E. Kurenova, 2006, Cancer research.

Inhibiting the interaction of cMET and IGF-1R with FAK effectively reduces growth of pancreatic cancer cells in vitro and in vivo.

A. Magis, S. Sebti, S. Hochwald, 2013, Anti-cancer agents in medicinal chemistry.

Disruption of the protein interaction between FAK and IGF-1R inhibits melanoma tumor growth

S. Sebti, W. Cance, S. Hochwald, 2012, Cell cycle.

Small molecule chloropyramine hydrochloride (C4) targets the binding site of focal adhesion kinase and vascular endothelial growth factor receptor 3 and suppresses breast cancer growth in vivo.

A. Magis, W. Cance, D. Ostrov, 2009, Journal of medicinal chemistry.

TAE226 Inhibits Human Neuroblastoma Cell Survival

V. Golubovskaya, W. Cance, E. Beierle, 2008, Cancer investigation.

Article withdrawal: Disruption of the protein interaction between FAK and IGF-1R inhibits melanoma tumor growth.

S. Sebti, W. Cance, S. Hochwald, 2011, Carcinogenesis.

The 7-amino-acid site in the proline-rich region of the N-terminal domain of p53 is involved in the interaction with FAK and is critical for p53 functioning.

V. Golubovskaya, W. Cance, E. Kurenova, 2008, The Biochemical journal.

Pharmacokinetic analysis of the FAK scaffold inhibitor C4 in dogs

W. Cance, S. Sexton, J. Wilton, 2016, European Journal of Drug Metabolism and Pharmacokinetics.

Directional gene silencing induced by a complex subtelomeric satellite from Drosophila

H. Biessmann, J. M. Mason, L. Champion, 1998, Chromosoma.

Focal Adhesion Kinase with the Interacting Proteins and Signaling in Cancer

V. Golubovskaya, W. Cance, S. Hochwald, 2010 .

The Y chromosome of Drosophila melanogaster contains a distinctive subclass of Het-A-related repeats.

M. Pardue, O. Danilevskaya, E. Kurenova, 1993, Genetics.

[Hoppel-family of mobile elements of Drosophila melanogaster, flanked by short inverted repeats and having preferential localization in the heterochromatin regions of the genome].

M. Pavlova, I. Bass, E. Kurenova, 1990, Genetika.

A repetitive DNA element, associated with telomeric sequences in Drosophila melanogaster, contains open reading frames

D. Petrov, D. Hartl, O. Danilevskaya, 1992, Chromosoma.

A novel strategy to inhibit FAK and IGF‐1R decreases growth of pancreatic cancer xenografts

V. Golubovskaya, W. Cance, S. Hochwald, 2009, Molecular carcinogenesis.

Shb gene knockdown increases the susceptibility of SVR endothelial tumor cells to apoptotic stimuli in vitro and in vivo.

Lily Yang, J. Arbiser, W. Cance, 2008, The Journal of investigative dermatology.

Design, synthesis, and biological evaluation of novel FAK scaffold inhibitors targeting the FAK-VEGFR3 protein-protein interaction.

A. Magis, R. Pandey, W. Cance, 2014, European journal of medicinal chemistry.

The FAK scaffold inhibitor C4 disrupts FAK-VEGFR-3 signaling and inhibits pancreatic cancer growth

W. Bshara, M. Seshadri, W. Cance, 2013, Oncotarget.

Disrupting the Scaffold to Improve Focal Adhesion Kinase–Targeted Cancer Therapeutics

V. Golubovskaya, W. Cance, T. Marlowe, 2013, Science Signaling.

He-T family DNA sequences in the Y chromosome of Drosophila melanogaster share homology with the X-linked Stellate genes

D. Hartl, A. Link, O. Danilevskaya, 1991, Chromosoma.

Telomeres and P-element of Drosophila melanogaster contain sequences that replicate autonomously in Saccharomyces cerevisiae

R. Khesin, B. Leibovitch, O. Danilevskaya, 1984, Molecular and General Genetics MGG.

A FAK scaffold inhibitor disrupts FAK and VEGFR-3 signaling and blocks melanoma growth by targeting both tumor and endothelial cells

W. Bshara, M. Seshadri, U. Sunar, 2014, Cell cycle.

Pharmacokinetic analysis of the FAK scaffold inhibitor C4 in dogs

W. Cance, S. Sexton, J. Wilton, 2016, European Journal of Drug Metabolism and Pharmacokinetics.

FAK and IGF-IR interact to provide survival signals in human pancreatic adenocarcinoma cells.

V. Golubovskaya, W. Cance, S. Hochwald, 2008, Carcinogenesis.

A novel small molecule inhibitor of FAK and IGF-1R protein interactions decreases growth of human esophageal carcinoma.

S. Hochwald, D. Ostrov, D. Ucar, 2011, Anti-cancer agents in medicinal chemistry.

Targeting of the protein interaction site between FAK and IGF-1R.

A. Magis, V. Golubovskaya, W. Cance, 2009, Biochemical and biophysical research communications.

Targeting the C-terminal focal adhesion kinase scaffold in pancreatic cancer.

R. Pandey, W. Cance, Arindam Sen, 2014, Cancer letters.

FAK and IGF-IR interact to provide survival signals in human pancreatic adenocarcinoma cells.

V. Golubovskaya, W. Cance, S. Hochwald, 2008, Carcinogenesis.

TAE226 Inhibits Human Neuroblastoma Cell Survival

V. Golubovskaya, W. Cance, E. Beierle, 2008, Cancer investigation.

Focal Adhesion Kinase Expression in Human Neuroblastoma: Immunohistochemical and Real-time PCR Analyses

V. Golubovskaya, W. Cance, W. London, 2008, Clinical Cancer Research.

Inhibition of FAK and VEGFR‐3 binding decreases tumorigenicity in neuroblastoma

W. Cance, E. Beierle, J. Stewart, 2015, Molecular carcinogenesis.

Crystallization of the focal adhesion kinase targeting (FAT) domain in a primitive orthorhombic space group.

A. Magis, W. Cance, D. Ostrov, 2008, Acta crystallographica. Section F, Structural biology and crystallization communications.