Virginia Espina

Virginia Espina

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Virginia Espina

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Proteomics for cancer drug design.

Expert Rev Proteomics 2019 Aug 4;16(8):647-664. Epub 2019 Aug 4.

Center for Applied Proteomics and Molecular Medicine, George Mason University , Manassas , VA , USA.

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http://dx.doi.org/10.1080/14789450.2019.1650025DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6736641PMC
August 2019

Unlocking bone for proteomic analysis and FISH.

Lab Invest 2019 May 18;99(5):708-721. Epub 2019 Jan 18.

Center for Applied Proteomics and Molecular Medicine, George Mason University, Manassas, VA, USA.

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http://www.nature.com/articles/s41374-018-0168-7
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http://dx.doi.org/10.1038/s41374-018-0168-7DOI Listing
May 2019

Combination Kinase Inhibitor Treatment Suppresses Rift Valley Fever Virus Replication.

Viruses 2018 04 13;10(4). Epub 2018 Apr 13.

National Center for Biodefense and Infectious Diseases, School of Systems Biology, George Mason University, Manassas, VA 20110, USA.

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http://dx.doi.org/10.3390/v10040191DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5923485PMC
April 2018

Dual-Color, Multiplex Analysis of Protein Microarrays for Precision Medicine.

Methods Mol Biol 2017 ;1550:149-170

Center for Applied Proteomics and Molecular Medicine, George Mason University, 10920 George Mason Circle, Life Science Lab Building, MS1A9, Manassas, VA, 20110, USA.

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http://dx.doi.org/10.1007/978-1-4939-6747-6_12DOI Listing
February 2018

One-Step Preservation and Decalcification of Bony Tissue for Molecular Profiling.

Methods Mol Biol 2017 ;1606:85-102

Center for Applied Proteomics and Molecular Medicine, George Mason University, 10920 George Mason Circle, MS1A9, Manassas, VA, 20110, USA.

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http://dx.doi.org/10.1007/978-1-4939-6990-6_6DOI Listing
February 2018

Protein biomarkers for subtyping breast cancer and implications for future research.

Expert Rev Proteomics 2018 02 3;15(2):131-152. Epub 2018 Jan 3.

a Center for Applied Proteomics and Molecular Medicine , George Mason University , Manassas , VA , USA.

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http://dx.doi.org/10.1080/14789450.2018.1421071DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6104835PMC
February 2018

Potential anti-cancer activity of 7-O-pentyl quercetin: Efficient, membrane-targeted kinase inhibition and pro-oxidant effect.

Pharmacol Res 2017 Oct 17;124:9-19. Epub 2017 Jul 17.

CNR Neuroscience Institute, Viale G. Colombo 3, 35121 Padova, Italy; University of Padova, Dept. Biomedical Sciences, Viale G. Colombo 3, 35121 Padova, Italy. Electronic address:

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http://dx.doi.org/10.1016/j.phrs.2017.07.016DOI Listing
October 2017

Chemokine-Releasing Microparticles Improve Bacterial Clearance and Survival of Anthrax Spore-Challenged Mice.

PLoS One 2016 15;11(9):e0163163. Epub 2016 Sep 15.

National Center for Biodefense and Infectious Diseases, Department of Molecular Microbiology, School of Systems Biology, George Mason University, Manassas, VA, 20110, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0163163PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5025034PMC
August 2017

Immune-modulating Activity of Hydrogel Microparticles Contributes to the Host Defense in a Murine Model of Cutaneous Anthrax.

Front Mol Biosci 2017 28;4:62. Epub 2017 Aug 28.

Department of Molecular Microbiology, National Center for Biodefense and Infectious Diseases, School of Systems Biology, George Mason UniversityManassas, VA, United States.

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http://dx.doi.org/10.3389/fmolb.2017.00062DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5581330PMC
August 2017

Rapamycin modulation of p70 S6 kinase signaling inhibits Rift Valley fever virus pathogenesis.

Antiviral Res 2017 07 23;143:162-175. Epub 2017 Apr 23.

National Center for Biodefense and Infectious Diseases, School of Systems Biology, George Mason University, Manassas, VA, 20110, USA. Electronic address:

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http://dx.doi.org/10.1016/j.antiviral.2017.04.011DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5530372PMC
July 2017

Pathology-Driven Comprehensive Proteomic Profiling of the Prostate Cancer Tumor Microenvironment.

Mol Cancer Res 2017 03 5;15(3):281-293. Epub 2017 Jan 5.

UCD Conway Institute of Biomolecular and Biomedical Research, University College Dublin, Dublin, Ireland.

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http://dx.doi.org/10.1158/1541-7786.MCR-16-0358DOI Listing
March 2017

Current state of the art for enhancing urine biomarker discovery.

Expert Rev Proteomics 2016 06;13(6):609-26

a Center for Applied Proteomics and Molecular Medicine , George Mason University , Manassas , VA , USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4978532PMC
http://dx.doi.org/10.1080/14789450.2016.1190651DOI Listing
June 2016

Ductal carcinoma in situ: challenges, opportunities, and uncharted waters.

Am Soc Clin Oncol Educ Book 2012 :40-4

From Duke University, Durham, NC; George Mason University, Manassas, VA.

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http://dx.doi.org/10.14694/EdBook_AM.2012.32.40DOI Listing
April 2016

Reverse-Phase Microarray Analysis Reveals Novel Targets in Lymph Nodes of Bacillus anthracis Spore-Challenged Mice.

PLoS One 2015 19;10(6):e0129860. Epub 2015 Jun 19.

National Center for Biodefense and Infectious Diseases, George Mason University, Manassas, Virginia, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0129860PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4474663PMC
April 2016

Treatment and Long-Term Risks for Patients With a Diagnosis of Ductal Carcinoma In Situ.

JAMA Oncol 2016 Mar;2(3):395

Center for Applied Proteomics and Molecular Medicine, Institute for Advanced Biomedical Research College of Science, George Mason University, Manassas, Virginia.

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http://dx.doi.org/10.1001/jamaoncol.2015.4846DOI Listing
March 2016

PMCA2 regulates HER2 protein kinase localization and signaling and promotes HER2-mediated breast cancer.

Proc Natl Acad Sci U S A 2016 Jan 4;113(3):E282-90. Epub 2016 Jan 4.

Section of Endocrinology and Metabolism, Department of Internal Medicine, Yale University School of Medicine, New Haven, CT 06520;

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http://dx.doi.org/10.1073/pnas.1516138113DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4725473PMC
January 2016

Nitric oxide as a regulator of B. anthracis pathogenicity.

Front Microbiol 2015 2;6:921. Epub 2015 Sep 2.

National Center for Biodefense and Infectious Disease, College of Science, George Mason University, Manassas, VA USA.

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http://dx.doi.org/10.3389/fmicb.2015.00921DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4557104PMC
September 2015

Whole proteome analysis of mouse lymph nodes in cutaneous anthrax.

PLoS One 2014 20;9(10):e110873. Epub 2014 Oct 20.

School of Systems Biology, George Mason University, Manassas, Virginia, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0110873PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4203832PMC
June 2015

Chemokine-Releasing Nanoparticles for Manipulation of Lymph Node Microenvironment.

Nanomaterials (Basel) 2015 Mar;5(1):298-320

National Center for Biodefense and Infectious Diseases, Department of Molecular Microbiology, School of Systems Biology, George Mason University, Manassas, VA 20110, USA.

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http://dx.doi.org/10.3390/nano5010298DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4394634PMC
March 2015

Inhibition of histone deacetylase 4 increases cytotoxicity of docetaxel in gastric cancer cells.

Proteomics Clin Appl 2014 Dec 22;8(11-12):924-31. Epub 2014 Oct 22.

Center for Applied Proteomics and Molecular Medicine, George Mason University, Manassas, VA, USA; Fondazione IOM, Viagrande, Catania, Italy.

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http://dx.doi.org/10.1002/prca.201400058DOI Listing
December 2014

Reverse phase protein arrays: mapping the path towards personalized medicine.

Mol Diagn Ther 2014 Dec;18(6):619-30

Center for Applied Proteomics and Molecular Medicine, George Mason University, 10900 University Blvd, MS1A9, Manassas, VA, 20110, USA.

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http://dx.doi.org/10.1007/s40291-014-0122-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4732707PMC
December 2014

Non-enzymatic, serum-free tissue culture of pre-invasive breast lesions for spontaneous generation of mammospheres.

J Vis Exp 2014 Nov 8(93):e51926. Epub 2014 Nov 8.

Center for Applied Proteomics and Molecular Medicine, George Mason University.

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http://dx.doi.org/10.3791/51926DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4353433PMC
November 2014

Hydrogel nanoparticle harvesting of plasma or urine for detecting low abundance proteins.

J Vis Exp 2014 Aug 7(90):e51789. Epub 2014 Aug 7.

Center for Applied Proteomics and Molecular Medicine, George Mason University;

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http://dx.doi.org/10.3791/51789DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5783330PMC
August 2014

Protein painting reveals solvent-excluded drug targets hidden within native protein-protein interfaces.

Nat Commun 2014 Jul 22;5:4413. Epub 2014 Jul 22.

Center for Applied Proteomics and Molecular Medicine, George Mason University, 10900 University Boulevard, Manassas, Virginia 20110, USA.

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http://dx.doi.org/10.1038/ncomms5413DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4109009PMC
July 2014

Stratification of clear cell renal cell carcinoma by signaling pathway analysis.

Expert Rev Proteomics 2014 Apr 27;11(2):237-49. Epub 2014 Feb 27.

Department of Experimental Oncology and Molecular Medicine, Fondazione IRCCS Istituto Nazionale dei Tumori , Milan , Italy.

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http://dx.doi.org/10.1586/14789450.2014.893193DOI Listing
April 2014

Glioblastoma cell enrichment is critical for analysis of phosphorylated drug targets and proteomic-genomic correlations.

Cancer Res 2014 Feb 17;74(3):818-28. Epub 2013 Dec 17.

Authors' Affiliations: Center for Applied Proteomics and Molecular Medicine, George Mason University, Manassas, Virginia; Departments of Neurosurgery, Henry Ford Hospital, Detroit; and Pathology, Henry Ford Hospital, Detroit, Michigan.

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http://cancerres.aacrjournals.org/cgi/doi/10.1158/0008-5472.
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http://dx.doi.org/10.1158/0008-5472.CAN-13-2172DOI Listing
February 2014

Mapping protein signal pathway interaction in sarcoma bone metastasis: linkage between rank, metalloproteinases turnover and growth factor signaling pathways.

Clin Exp Metastasis 2014 Jan 23;31(1):15-24. Epub 2013 Jul 23.

Laboratory of Experimental Oncology, Rizzoli Orthopedic Institute, Via di Barbiano 1/10, 40136, Bologna, Italy.

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http://dx.doi.org/10.1007/s10585-013-9605-6DOI Listing
January 2014

Retinal pigment epithelium (RPE) exosomes contain signaling phosphoproteins affected by oxidative stress.

Exp Cell Res 2013 Aug 10;319(13):2113-23. Epub 2013 May 10.

CNR Institute of Neuroscience, Viale G. Colombo 3, 35121 Padova, Italy.

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http://dx.doi.org/10.1016/j.yexcr.2013.05.005DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3727419PMC
August 2013

Attacking breast cancer at the preinvasion stage by targeting autophagy.

Womens Health (Lond) 2013 Mar;9(2):157-70

George Mason University, Center for Applied Proteomics & Molecular Medicine, Manassas, VA 20110, USA.

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http://dx.doi.org/10.2217/whe.13.5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3779365PMC
March 2013

Laser capture microdissection for protein and NanoString RNA analysis.

Methods Mol Biol 2013 ;931:213-57

National Cancer Institute-Frederick/SAIC, Frederick, MD, USA.

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http://dx.doi.org/10.1007/978-1-62703-056-4_12DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3766583PMC
February 2013

Improved data normalization methods for reverse phase protein microarray analysis of complex biological samples.

Biotechniques 2012 Sep;0(0):1-7

Laboratory of Experimental Oncology, Istituto Ortopedico Rizzoli, Bologna, Italy; Center for Applied Proteomics and Molecular Medicine, George Mason University, Manassas, VA, USA.

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http://dx.doi.org/10.2144/000113926DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3771668PMC
September 2012

Reduction of preanalytical variability in specimen procurement for molecular profiling.

Methods Mol Biol 2012 ;823:49-57

Center for Applied Proteomics and Molecular Medicine, George Mason University, Manassas, VA, USA.

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http://dx.doi.org/10.1007/978-1-60327-216-2_4DOI Listing
April 2012

Laser capture microdissection: Arcturus(XT) infrared capture and UV cutting methods.

Methods Mol Biol 2012 ;823:157-78

Center for Applied Proteomics and Molecular Medicine, George Mason University, Manassas, VA, USA.

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http://link.springer.com/10.1007/978-1-60327-216-2_11
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http://dx.doi.org/10.1007/978-1-60327-216-2_11DOI Listing
April 2012

Guidelines for the use and interpretation of assays for monitoring autophagy.

Authors:
Daniel J Klionsky Fabio C Abdalla Hagai Abeliovich Robert T Abraham Abraham Acevedo-Arozena Khosrow Adeli Lotta Agholme Maria Agnello Patrizia Agostinis Julio A Aguirre-Ghiso Hyung Jun Ahn Ouardia Ait-Mohamed Slimane Ait-Si-Ali Takahiko Akematsu Shizuo Akira Hesham M Al-Younes Munir A Al-Zeer Matthew L Albert Roger L Albin Javier Alegre-Abarrategui Maria Francesca Aleo Mehrdad Alirezaei Alexandru Almasan Maylin Almonte-Becerril Atsuo Amano Ravi Amaravadi Shoba Amarnath Amal O Amer Nathalie Andrieu-Abadie Vellareddy Anantharam David K Ann Shailendra Anoopkumar-Dukie Hiroshi Aoki Nadezda Apostolova Giuseppe Arancia John P Aris Katsuhiko Asanuma Nana Y O Asare Hisashi Ashida Valerie Askanas David S Askew Patrick Auberger Misuzu Baba Steven K Backues Eric H Baehrecke Ben A Bahr Xue-Yuan Bai Yannick Bailly Robert Baiocchi Giulia Baldini Walter Balduini Andrea Ballabio Bruce A Bamber Edward T W Bampton Gábor Bánhegyi Clinton R Bartholomew Diane C Bassham Robert C Bast Henri Batoko Boon-Huat Bay Isabelle Beau Daniel M Béchet Thomas J Begley Christian Behl Christian Behrends Soumeya Bekri Bryan Bellaire Linda J Bendall Luca Benetti Laura Berliocchi Henri Bernardi Francesca Bernassola Sébastien Besteiro Ingrid Bhatia-Kissova Xiaoning Bi Martine Biard-Piechaczyk Janice S Blum Lawrence H Boise Paolo Bonaldo David L Boone Beat C Bornhauser Karina R Bortoluci Ioannis Bossis Frédéric Bost Jean-Pierre Bourquin Patricia Boya Michaël Boyer-Guittaut Peter V Bozhkov Nathan R Brady Claudio Brancolini Andreas Brech Jay E Brenman Ana Brennand Emery H Bresnick Patrick Brest Dave Bridges Molly L Bristol Paul S Brookes Eric J Brown John H Brumell Nicola Brunetti-Pierri Ulf T Brunk Dennis E Bulman Scott J Bultman Geert Bultynck Lena F Burbulla Wilfried Bursch Jonathan P Butchar Wanda Buzgariu Sergio P Bydlowski Ken Cadwell Monika Cahová Dongsheng Cai Jiyang Cai Qian Cai Bruno Calabretta Javier Calvo-Garrido Nadine Camougrand Michelangelo Campanella Jenny Campos-Salinas Eleonora Candi Lizhi Cao Allan B Caplan Simon R Carding Sandra M Cardoso Jennifer S Carew Cathleen R Carlin Virginie Carmignac Leticia A M Carneiro Serena Carra Rosario A Caruso Giorgio Casari Caty Casas Roberta Castino Eduardo Cebollero Francesco Cecconi Jean Celli Hassan Chaachouay Han-Jung Chae Chee-Yin Chai David C Chan Edmond Y Chan Raymond Chuen-Chung Chang Chi-Ming Che Ching-Chow Chen Guang-Chao Chen Guo-Qiang Chen Min Chen Quan Chen Steve S-L Chen WenLi Chen Xi Chen Xiangmei Chen Xiequn Chen Ye-Guang Chen Yingyu Chen Yongqiang Chen Yu-Jen Chen Zhixiang Chen Alan Cheng Christopher H K Cheng Yan Cheng Heesun Cheong Jae-Ho Cheong Sara Cherry Russ Chess-Williams Zelda H Cheung Eric Chevet Hui-Ling Chiang Roberto Chiarelli Tomoki Chiba Lih-Shen Chin Shih-Hwa Chiou Francis V Chisari Chi Hin Cho Dong-Hyung Cho Augustine M K Choi DooSeok Choi Kyeong Sook Choi Mary E Choi Salem Chouaib Divaker Choubey Vinay Choubey Charleen T Chu Tsung-Hsien Chuang Sheau-Huei Chueh Taehoon Chun Yong-Joon Chwae Mee-Len Chye Roberto Ciarcia Maria R Ciriolo Michael J Clague Robert S B Clark Peter G H Clarke Robert Clarke Patrice Codogno Hilary A Coller María I Colombo Sergio Comincini Maria Condello Fabrizio Condorelli Mark R Cookson Graham H Coombs Isabelle Coppens Ramon Corbalan Pascale Cossart Paola Costelli Safia Costes Ana Coto-Montes Eduardo Couve Fraser P Coxon James M Cregg José L Crespo Marianne J Cronjé Ana Maria Cuervo Joseph J Cullen Mark J Czaja Marcello D'Amelio Arlette Darfeuille-Michaud Lester M Davids Faith E Davies Massimo De Felici John F de Groot Cornelis A M de Haan Luisa De Martino Angelo De Milito Vincenzo De Tata Jayanta Debnath Alexei Degterev Benjamin Dehay Lea M D Delbridge Francesca Demarchi Yi Zhen Deng Jörn Dengjel Paul Dent Donna Denton Vojo Deretic Shyamal D Desai Rodney J Devenish Mario Di Gioacchino Gilbert Di Paolo Chiara Di Pietro Guillermo Díaz-Araya Inés Díaz-Laviada Maria T Diaz-Meco Javier Diaz-Nido Ivan Dikic Savithramma P Dinesh-Kumar Wen-Xing Ding Clark W Distelhorst Abhinav Diwan Mojgan Djavaheri-Mergny Svetlana Dokudovskaya Zheng Dong Frank C Dorsey Victor Dosenko James J Dowling Stephen Doxsey Marlène Dreux Mark E Drew Qiuhong Duan Michel A Duchosal Karen Duff Isabelle Dugail Madeleine Durbeej Michael Duszenko Charles L Edelstein Aimee L Edinger Gustavo Egea Ludwig Eichinger N Tony Eissa Suhendan Ekmekcioglu Wafik S El-Deiry Zvulun Elazar Mohamed Elgendy Lisa M Ellerby Kai Er Eng Anna-Mart Engelbrecht Simone Engelender Jekaterina Erenpreisa Ricardo Escalante Audrey Esclatine Eeva-Liisa Eskelinen Lucile Espert Virginia Espina Huizhou Fan Jia Fan Qi-Wen Fan Zhen Fan Shengyun Fang Yongqi Fang Manolis Fanto Alessandro Fanzani Thomas Farkas Jean-Claude Farré Mathias Faure Marcus Fechheimer Carl G Feng Jian Feng Qili Feng Youji Feng László Fésüs Ralph Feuer Maria E Figueiredo-Pereira Gian Maria Fimia Diane C Fingar Steven Finkbeiner Toren Finkel Kim D Finley Filomena Fiorito Edward A Fisher Paul B Fisher Marc Flajolet Maria L Florez-McClure Salvatore Florio Edward A Fon Francesco Fornai Franco Fortunato Rati Fotedar Daniel H Fowler Howard S Fox Rodrigo Franco Lisa B Frankel Marc Fransen José M Fuentes Juan Fueyo Jun Fujii Kozo Fujisaki Eriko Fujita Mitsunori Fukuda Ruth H Furukawa Matthias Gaestel Philippe Gailly Malgorzata Gajewska Brigitte Galliot Vincent Galy Subramaniam Ganesh Barry Ganetzky Ian G Ganley Fen-Biao Gao George F Gao Jinming Gao Lorena Garcia Guillermo Garcia-Manero Mikel Garcia-Marcos Marjan Garmyn Andrei L Gartel Evelina Gatti Mathias Gautel Thomas R Gawriluk Matthew E Gegg Jiefei Geng Marc Germain Jason E Gestwicki David A Gewirtz Saeid Ghavami Pradipta Ghosh Anna M Giammarioli Alexandra N Giatromanolaki Spencer B Gibson Robert W Gilkerson Michael L Ginger Henry N Ginsberg Jakub Golab Michael S Goligorsky Pierre Golstein Candelaria Gomez-Manzano Ebru Goncu Céline Gongora Claudio D Gonzalez Ramon Gonzalez Cristina González-Estévez Rosa Ana González-Polo Elena Gonzalez-Rey Nikolai V Gorbunov Sharon Gorski Sandro Goruppi Roberta A Gottlieb Devrim Gozuacik Giovanna Elvira Granato Gary D Grant Kim N Green Aleš Gregorc Frédéric Gros Charles Grose Thomas W Grunt Philippe Gual Jun-Lin Guan Kun-Liang Guan Sylvie M Guichard Anna S Gukovskaya Ilya Gukovsky Jan Gunst Asa B Gustafsson Andrew J Halayko Amber N Hale Sandra K Halonen Maho Hamasaki Feng Han Ting Han Michael K Hancock Malene Hansen Hisashi Harada Masaru Harada Stefan E Hardt J Wade Harper Adrian L Harris James Harris Steven D Harris Makoto Hashimoto Jeffrey A Haspel Shin-ichiro Hayashi Lori A Hazelhurst Congcong He You-Wen He Marie-Joseé Hébert Kim A Heidenreich Miep H Helfrich Gudmundur V Helgason Elizabeth P Henske Brian Herman Paul K Herman Claudio Hetz Sabine Hilfiker Joseph A Hill Lynne J Hocking Paul Hofman Thomas G Hofmann Jörg Höhfeld Tessa L Holyoake Ming-Huang Hong David A Hood Gökhan S Hotamisligil Ewout J Houwerzijl Maria Høyer-Hansen Bingren Hu Chien-An A Hu Hong-Ming Hu Ya Hua Canhua Huang Ju Huang Shengbing Huang Wei-Pang Huang Tobias B Huber Won-Ki Huh Tai-Ho Hung Ted R Hupp Gang Min Hur James B Hurley Sabah N A Hussain Patrick J Hussey Jung Jin Hwang Seungmin Hwang Atsuhiro Ichihara Shirin Ilkhanizadeh Ken Inoki Takeshi Into Valentina Iovane Juan L Iovanna Nancy Y Ip Yoshitaka Isaka Hiroyuki Ishida Ciro Isidoro Ken-ichi Isobe Akiko Iwasaki Marta Izquierdo Yotaro Izumi Panu M Jaakkola Marja Jäättelä George R Jackson William T Jackson Bassam Janji Marina Jendrach Ju-Hong Jeon Eui-Bae Jeung Hong Jiang Hongchi Jiang Jean X Jiang Ming Jiang Qing Jiang Xuejun Jiang Xuejun Jiang Alberto Jiménez Meiyan Jin Shengkan Jin Cheol O Joe Terje Johansen Daniel E Johnson Gail V W Johnson Nicola L Jones Bertrand Joseph Suresh K Joseph Annie M Joubert Gábor Juhász Lucienne Juillerat-Jeanneret Chang Hwa Jung Yong-Keun Jung Kai Kaarniranta Allen Kaasik Tomohiro Kabuta Motoni Kadowaki Katarina Kagedal Yoshiaki Kamada Vitaliy O Kaminskyy Harm H Kampinga Hiromitsu Kanamori Chanhee Kang Khong Bee Kang Kwang Il Kang Rui Kang Yoon-A Kang Tomotake Kanki Thirumala-Devi Kanneganti Haruo Kanno Anumantha G Kanthasamy Arthi Kanthasamy Vassiliki Karantza Gur P Kaushal Susmita Kaushik Yoshinori Kawazoe Po-Yuan Ke John H Kehrl Ameeta Kelekar Claus Kerkhoff David H Kessel Hany Khalil Jan A K W Kiel Amy A Kiger Akio Kihara Deok Ryong Kim Do-Hyung Kim Dong-Hou Kim Eun-Kyoung Kim Hyung-Ryong Kim Jae-Sung Kim Jeong Hun Kim Jin Cheon Kim John K Kim Peter K Kim Seong Who Kim Yong-Sun Kim Yonghyun Kim Adi Kimchi Alec C Kimmelman Jason S King Timothy J Kinsella Vladimir Kirkin Lorrie A Kirshenbaum Katsuhiko Kitamoto Kaio Kitazato Ludger Klein Walter T Klimecki Jochen Klucken Erwin Knecht Ben C B Ko Jan C Koch Hiroshi Koga Jae-Young Koh Young Ho Koh Masato Koike Masaaki Komatsu Eiki Kominami Hee Jeong Kong Wei-Jia Kong Viktor I Korolchuk Yaichiro Kotake Michael I Koukourakis Juan B Kouri Flores Attila L Kovács Claudine Kraft Dimitri Krainc Helmut Krämer Carole Kretz-Remy Anna M Krichevsky Guido Kroemer Rejko Krüger Oleg Krut Nicholas T Ktistakis Chia-Yi Kuan Roza Kucharczyk Ashok Kumar Raj Kumar Sharad Kumar Mondira Kundu Hsing-Jien Kung Tino Kurz Ho Jeong Kwon Albert R La Spada Frank Lafont Trond Lamark Jacques Landry Jon D Lane Pierre Lapaquette Jocelyn F Laporte Lajos László Sergio Lavandero Josée N Lavoie Robert Layfield Pedro A Lazo Weidong Le Laurent Le Cam Daniel J Ledbetter Alvin J X Lee Byung-Wan Lee Gyun Min Lee Jongdae Lee Ju-Hyun Lee Michael Lee Myung-Shik Lee Sug Hyung Lee Christiaan Leeuwenburgh Patrick Legembre Renaud Legouis Michael Lehmann Huan-Yao Lei Qun-Ying Lei David A Leib José Leiro John J Lemasters Antoinette Lemoine Maciej S Lesniak Dina Lev Victor V Levenson Beth Levine Efrat Levy Faqiang Li Jun-Lin Li Lian Li Sheng Li Weijie Li Xue-Jun Li Yan-bo Li Yi-Ping Li Chengyu Liang Qiangrong Liang Yung-Feng Liao Pawel P Liberski Andrew Lieberman Hyunjung J Lim Kah-Leong Lim Kyu Lim Chiou-Feng Lin Fu-Cheng Lin Jian Lin Jiandie D Lin Kui Lin Wan-Wan Lin Weei-Chin Lin Yi-Ling Lin Rafael Linden Paul Lingor Jennifer Lippincott-Schwartz Michael P Lisanti Paloma B Liton Bo Liu Chun-Feng Liu Kaiyu Liu Leyuan Liu Qiong A Liu Wei Liu Young-Chau Liu Yule Liu Richard A Lockshin Chun-Nam Lok Sagar Lonial Benjamin Loos Gabriel Lopez-Berestein Carlos López-Otín Laura Lossi Michael T Lotze Peter Lőw Binfeng Lu Bingwei Lu Bo Lu Zhen Lu Frédéric Luciano Nicholas W Lukacs Anders H Lund Melinda A Lynch-Day Yong Ma Fernando Macian Jeff P MacKeigan Kay F Macleod Frank Madeo Luigi Maiuri Maria Chiara Maiuri Davide Malagoli May Christine V Malicdan Walter Malorni Na Man Eva-Maria Mandelkow Stéphen Manon Irena Manov Kai Mao Xiang Mao Zixu Mao Philippe Marambaud Daniela Marazziti Yves L Marcel Katie Marchbank Piero Marchetti Stefan J Marciniak Mateus Marcondes Mohsen Mardi Gabriella Marfe Guillermo Mariño Maria Markaki Mark R Marten Seamus J Martin Camille Martinand-Mari Wim Martinet Marta Martinez-Vicente Matilde Masini Paola Matarrese Saburo Matsuo Raffaele Matteoni Andreas Mayer Nathalie M Mazure David J McConkey Melanie J McConnell Catherine McDermott Christine McDonald Gerald M McInerney Sharon L McKenna BethAnn McLaughlin Pamela J McLean Christopher R McMaster G Angus McQuibban Alfred J Meijer Miriam H Meisler Alicia Meléndez Thomas J Melia Gerry Melino Maria A Mena Javier A Menendez Rubem F S Menna-Barreto Manoj B Menon Fiona M Menzies Carol A Mercer Adalberto Merighi Diane E Merry Stefania Meschini Christian G Meyer Thomas F Meyer Chao-Yu Miao Jun-Ying Miao Paul A M Michels Carine Michiels Dalibor Mijaljica Ana Milojkovic Saverio Minucci Clelia Miracco Cindy K Miranti Ioannis Mitroulis Keisuke Miyazawa Noboru Mizushima Baharia Mograbi Simin Mohseni Xavier Molero Bertrand Mollereau Faustino Mollinedo Takashi Momoi Iryna Monastyrska Martha M Monick Mervyn J Monteiro Michael N Moore Rodrigo Mora Kevin Moreau Paula I Moreira Yuji Moriyasu Jorge Moscat Serge Mostowy Jeremy C Mottram Tomasz Motyl Charbel E-H Moussa Sylke Müller Sylviane Muller Karl Münger Christian Münz Leon O Murphy Maureen E Murphy Antonio Musarò Indira Mysorekar Eiichiro Nagata Kazuhiro Nagata Aimable Nahimana Usha Nair Toshiyuki Nakagawa Kiichi Nakahira Hiroyasu Nakano Hitoshi Nakatogawa Meera Nanjundan Naweed I Naqvi Derek P Narendra Masashi Narita Miguel Navarro Steffan T Nawrocki Taras Y Nazarko Andriy Nemchenko Mihai G Netea Thomas P Neufeld Paul A Ney Ioannis P Nezis Huu Phuc Nguyen Daotai Nie Ichizo Nishino Corey Nislow Ralph A Nixon Takeshi Noda Angelika A Noegel Anna Nogalska Satoru Noguchi Lucia Notterpek Ivana Novak Tomoyoshi Nozaki Nobuyuki Nukina Thorsten Nürnberger Beat Nyfeler Keisuke Obara Terry D Oberley Salvatore Oddo Michinaga Ogawa Toya Ohashi Koji Okamoto Nancy L Oleinick F Javier Oliver Laura J Olsen Stefan Olsson Onya Opota Timothy F Osborne Gary K Ostrander Kinya Otsu Jing-hsiung James Ou Mireille Ouimet Michael Overholtzer Bulent Ozpolat Paolo Paganetti Ugo Pagnini Nicolas Pallet Glen E Palmer Camilla Palumbo Tianhong Pan Theocharis Panaretakis Udai Bhan Pandey Zuzana Papackova Issidora Papassideri Irmgard Paris Junsoo Park Ohkmae K Park Jan B Parys Katherine R Parzych Susann Patschan Cam Patterson Sophie Pattingre John M Pawelek Jianxin Peng David H Perlmutter Ida Perrotta George Perry Shazib Pervaiz Matthias Peter Godefridus J Peters Morten Petersen Goran Petrovski James M Phang Mauro Piacentini Philippe Pierre Valérie Pierrefite-Carle Gérard Pierron Ronit Pinkas-Kramarski Antonio Piras Natik Piri Leonidas C Platanias Stefanie Pöggeler Marc Poirot Angelo Poletti Christian Poüs Mercedes Pozuelo-Rubio Mette Prætorius-Ibba Anil Prasad Mark Prescott Muriel Priault Nathalie Produit-Zengaffinen Ann Progulske-Fox Tassula Proikas-Cezanne Serge Przedborski Karin Przyklenk Rosa Puertollano Julien Puyal Shu-Bing Qian Liang Qin Zheng-Hong Qin Susan E Quaggin Nina Raben Hannah Rabinowich Simon W Rabkin Irfan Rahman Abdelhaq Rami Georg Ramm Glenn Randall Felix Randow V Ashutosh Rao Jeffrey C Rathmell Brinda Ravikumar Swapan K Ray Bruce H Reed John C Reed Fulvio Reggiori Anne Régnier-Vigouroux Andreas S Reichert John J Reiners Russel J Reiter Jun Ren José L Revuelta Christopher J Rhodes Konstantinos Ritis Elizete Rizzo Jeffrey Robbins Michel Roberge Hernan Roca Maria C Roccheri Stephane Rocchi H Peter Rodemann Santiago Rodríguez de Córdoba Bärbel Rohrer Igor B Roninson Kirill Rosen Magdalena M Rost-Roszkowska Mustapha Rouis Kasper M A Rouschop Francesca Rovetta Brian P Rubin David C Rubinsztein Klaus Ruckdeschel Edmund B Rucker Assaf Rudich Emil Rudolf Nelson Ruiz-Opazo Rossella Russo Tor Erik Rusten Kevin M Ryan Stefan W Ryter David M Sabatini Junichi Sadoshima Tapas Saha Tatsuya Saitoh Hiroshi Sakagami Yasuyoshi Sakai Ghasem Hoseini Salekdeh Paolo Salomoni Paul M Salvaterra Guy Salvesen Rosa Salvioli Anthony M J Sanchez José A Sánchez-Alcázar Ricardo Sánchez-Prieto Marco Sandri Uma Sankar Poonam Sansanwal Laura Santambrogio Shweta Saran Sovan Sarkar Minnie Sarwal Chihiro Sasakawa Ausra Sasnauskiene Miklós Sass Ken Sato Miyuki Sato Anthony H V Schapira Michael Scharl Hermann M Schätzl Wiep Scheper Stefano Schiaffino Claudio Schneider Marion E Schneider Regine Schneider-Stock Patricia V Schoenlein Daniel F Schorderet Christoph Schüller Gary K Schwartz Luca Scorrano Linda Sealy Per O Seglen Juan Segura-Aguilar Iban Seiliez Oleksandr Seleverstov Christian Sell Jong Bok Seo Duska Separovic Vijayasaradhi Setaluri Takao Setoguchi Carmine Settembre John J Shacka Mala Shanmugam Irving M Shapiro Eitan Shaulian Reuben J Shaw James H Shelhamer Han-Ming Shen Wei-Chiang Shen Zu-Hang Sheng Yang Shi Kenichi Shibuya Yoshihiro Shidoji Jeng-Jer Shieh Chwen-Ming Shih Yohta Shimada Shigeomi Shimizu Takahiro Shintani Orian S Shirihai Gordon C Shore Andriy A Sibirny Stan B Sidhu Beata Sikorska Elaine C M Silva-Zacarin Alison Simmons Anna Katharina Simon Hans-Uwe Simon Cristiano Simone Anne Simonsen David A Sinclair Rajat Singh Debasish Sinha Frank A Sinicrope Agnieszka Sirko Parco M Siu Efthimios Sivridis Vojtech Skop Vladimir P Skulachev Ruth S Slack Soraya S Smaili Duncan R Smith Maria S Soengas Thierry Soldati Xueqin Song Anil K Sood Tuck Wah Soong Federica Sotgia Stephen A Spector Claudia D Spies Wolfdieter Springer Srinivasa M Srinivasula Leonidas Stefanis Joan S Steffan Ruediger Stendel Harald Stenmark Anastasis Stephanou Stephan T Stern Cinthya Sternberg Björn Stork Peter Strålfors Carlos S Subauste Xinbing Sui David Sulzer Jiaren Sun Shi-Yong Sun Zhi-Jun Sun Joseph J Y Sung Kuninori Suzuki Toshihiko Suzuki Michele S Swanson Charles Swanton Sean T Sweeney Lai-King Sy Gyorgy Szabadkai Ira Tabas Heinrich Taegtmeyer Marco Tafani Krisztina Takács-Vellai Yoshitaka Takano Kaoru Takegawa Genzou Takemura Fumihiko Takeshita Nicholas J Talbot Kevin S W Tan Keiji Tanaka Kozo Tanaka Daolin Tang Dingzhong Tang Isei Tanida Bakhos A Tannous Nektarios Tavernarakis Graham S Taylor Gregory A Taylor J Paul Taylor Lance S Terada Alexei Terman Gianluca Tettamanti Karin Thevissen Craig B Thompson Andrew Thorburn Michael Thumm FengFeng Tian Yuan Tian Glauco Tocchini-Valentini Aviva M Tolkovsky Yasuhiko Tomino Lars Tönges Sharon A Tooze Cathy Tournier John Tower Roberto Towns Vladimir Trajkovic Leonardo H Travassos Ting-Fen Tsai Mario P Tschan Takeshi Tsubata Allan Tsung Boris Turk Lorianne S Turner Suresh C Tyagi Yasuo Uchiyama Takashi Ueno Midori Umekawa Rika Umemiya-Shirafuji Vivek K Unni Maria I Vaccaro Enza Maria Valente Greet Van den Berghe Ida J van der Klei Wouter van Doorn Linda F van Dyk Marjolein van Egmond Leo A van Grunsven Peter Vandenabeele Wim P Vandenberghe Ilse Vanhorebeek Eva C Vaquero Guillermo Velasco Tibor Vellai Jose Miguel Vicencio Richard D Vierstra Miquel Vila Cécile Vindis Giampietro Viola Maria Teresa Viscomi Olga V Voitsekhovskaja Clarissa von Haefen Marcela Votruba Keiji Wada Richard Wade-Martins Cheryl L Walker Craig M Walsh Jochen Walter Xiang-Bo Wan Aimin Wang Chenguang Wang Dawei Wang Fan Wang Fen Wang Guanghui Wang Haichao Wang Hong-Gang Wang Horng-Dar Wang Jin Wang Ke Wang Mei Wang Richard C Wang Xinglong Wang Xuejun Wang Ying-Jan Wang Yipeng Wang Zhen Wang Zhigang Charles Wang Zhinong Wang Derick G Wansink Diane M Ward Hirotaka Watada Sarah L Waters Paul Webster Lixin Wei Conrad C Weihl William A Weiss Scott M Welford Long-Ping Wen Caroline A Whitehouse J Lindsay Whitton Alexander J Whitworth Tom Wileman John W Wiley Simon Wilkinson Dieter Willbold Roger L Williams Peter R Williamson Bradly G Wouters Chenghan Wu Dao-Cheng Wu William K K Wu Andreas Wyttenbach Ramnik J Xavier Zhijun Xi Pu Xia Gengfu Xiao Zhiping Xie Zhonglin Xie Da-zhi Xu Jianzhen Xu Liang Xu Xiaolei Xu Ai Yamamoto Akitsugu Yamamoto Shunhei Yamashina Michiaki Yamashita Xianghua Yan Mitsuhiro Yanagida Dun-Sheng Yang Elizabeth Yang Jin-Ming Yang Shi Yu Yang Wannian Yang Wei Yuan Yang Zhifen Yang Meng-Chao Yao Tso-Pang Yao Behzad Yeganeh Wei-Lien Yen Jia-jing Yin Xiao-Ming Yin Ook-Joon Yoo Gyesoon Yoon Seung-Yong Yoon Tomohiro Yorimitsu Yuko Yoshikawa Tamotsu Yoshimori Kohki Yoshimoto Ho Jin You Richard J Youle Anas Younes Li Yu Long Yu Seong-Woon Yu Wai Haung Yu Zhi-Min Yuan Zhenyu Yue Cheol-Heui Yun Michisuke Yuzaki Olga Zabirnyk Elaine Silva-Zacarin David Zacks Eldad Zacksenhaus Nadia Zaffaroni Zahra Zakeri Herbert J Zeh Scott O Zeitlin Hong Zhang Hui-Ling Zhang Jianhua Zhang Jing-Pu Zhang Lin Zhang Long Zhang Ming-Yong Zhang Xu Dong Zhang Mantong Zhao Yi-Fang Zhao Ying Zhao Zhizhuang J Zhao Xiaoxiang Zheng Boris Zhivotovsky Qing Zhong Cong-Zhao Zhou Changlian Zhu Wei-Guo Zhu Xiao-Feng Zhu Xiongwei Zhu Yuangang Zhu Teresa Zoladek Wei-Xing Zong Antonio Zorzano Jürgen Zschocke Brian Zuckerbraun

Autophagy 2012 Apr;8(4):445-544

Life Sciences Institute, University of Michigan, Ann Arbor, MI, USA.

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http://dx.doi.org/10.4161/auto.19496DOI Listing
April 2012

Phosphoprotein stability in clinical tissue and its relevance for reverse phase protein microarray technology.

Methods Mol Biol 2011 ;785:23-43

Center for Applied Proteomics and Molecular Medicine, George Mason University, Manassas, VA, USA.

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http://dx.doi.org/10.1007/978-1-61779-286-1_3DOI Listing
January 2012

Reverse phase protein microarrays: fluorometric and colorimetric detection.

Methods Mol Biol 2011 ;723:275-301

George Mason University, Center for Applied Proteomics and Molecular Medicine, Manassas, VA, USA.

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http://dx.doi.org/10.1007/978-1-61779-043-0_18DOI Listing
June 2011

The use of hydrogel microparticles to sequester and concentrate bacterial antigens in a urine test for Lyme disease.

Biomaterials 2011 Feb 28;32(4):1157-66. Epub 2010 Oct 28.

Center for Applied Proteomics and Molecular Medicine, George Mason University, 10900 University Boulevard, Manassas, VA 20110, USA.

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February 2011

What is the malignant nature of human ductal carcinoma in situ?

Nat Rev Cancer 2011 01 2;11(1):68-75. Epub 2010 Dec 2.

George Mason University, Center for Applied Proteomics and Molecular Medicine, Manassas, Virginia 20110, USA.

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January 2011

Breast cancer stem cells: a new target for therapy.

Oncology (Williston Park) 2011 Jan;25(1):25-8, 30

Department of Hematology, Oncology and Molecular Medicine, Istituto Superiore di Sanità, Rome, Italy.

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January 2011

Reverse phase protein microarrays advance to use in clinical trials.

Mol Oncol 2010 Dec 16;4(6):461-81. Epub 2010 Oct 16.

George Mason University, Center for Applied Proteomics and Molecular Medicine, Manassas, VA 20110, USA.

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December 2010

Tumorigenic and metastatic activity of human thyroid cancer stem cells.

Cancer Res 2010 Nov 19;70(21):8874-85. Epub 2010 Oct 19.

Department of Surgical and Oncological Sciences, Cellular and Molecular Pathophysiology Laboratory, University of Palermo, Palermo, Italy.

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http://dx.doi.org/10.1158/0008-5472.CAN-10-1994DOI Listing
November 2010

Tissue is alive: New technologies are needed to address the problems of protein biomarker pre-analytical variability.

Proteomics Clin Appl 2009 Aug;3(8):874-882

George Mason University, Center for Applied Proteomics and Molecular Medicine, Manassas, VA, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2944287PMC
August 2009

Anthrax infection inhibits the AKT signaling involved in the E-cadherin-mediated adhesion of lung epithelial cells.

FEMS Immunol Med Microbiol 2009 Jul 8;56(2):129-42. Epub 2009 Apr 8.

National Center for Biodefense and Infectious Diseases, George Mason University, Manassas, VA 20110, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2734923PMC
July 2009

Reverse-phase protein microarrays for theranostics and patient tailored therapy.

Methods Mol Biol 2009 ;520:89-105

Center for Applied Proteomics and Molecular Medicine, George Mason University, Manassas, VA, USA.

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May 2009

Application of laser microdissection and reverse-phase protein microarrays to the molecular profiling of cancer signal pathway networks in the tissue microenvironment.

Clin Lab Med 2009 Mar;29(1):1-13

Department of Molecular and Microbiology, Center for Applied Proteomics and Molecular Medicine, George Mason University, 10900 University Boulevard, Manassas, VA 20110, USA.

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http://dx.doi.org/10.1016/j.cll.2009.03.001DOI Listing
March 2009

Molecular network analysis using reverse phase protein microarrays for patient tailored therapy.

Adv Exp Med Biol 2008 ;610:177-86

University of Tübingen, Faculty of Medicine, Department of Obstetrics and Gynecology, Tübingen, Germany.

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http://dx.doi.org/10.1007/978-0-387-73898-7_13DOI Listing
July 2008

Automated laser capture microdissection for tissue proteomics.

Methods Mol Biol 2008 ;441:71-90

Center for Cancer Research, Laboratory of Pathology, National Cancer Institute, Bethesda, MD, USA.

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http://dx.doi.org/10.1007/978-1-60327-047-2_5DOI Listing
May 2008

Reverse phase protein microarrays for theranostics and patient-tailored therapy.

Methods Mol Biol 2008 ;441:113-28

Laboratory of Pathology, National Cancer Institute, Center for Cancer Research, Bethesda, MD, USA.

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May 2008

Multiplexed cell signaling analysis of human breast cancer applications for personalized therapy.

J Proteome Res 2008 Apr 8;7(4):1508-17. Epub 2008 Feb 8.

Center for Applied Proteomics and Molecular Medicine, George Mason University, Manassas, Virginia 20110, USA.

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April 2008

Development of reverse phase protein microarrays for clinical applications and patient-tailored therapy.

Cancer Genomics Proteomics 2007 May-Jun;4(3):157-64

University of Tubingen, Faculty of Medicine, Department of Obstetrics and Gynecology, Calwer Str. 7, 72076 Tubingen, Germany, and Department of Surgery, Inova Fairfax Hospital Cancer Center, Falls Church, VA, USA.

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November 2007

Laser-capture microdissection.

Nat Protoc 2006 ;1(2):586-603

Center for Applied Proteomics and Molecular Medicine, George Mason University, 10900 University Blvd. MS 4E3, Manassas, Virginia, USA.

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http://dx.doi.org/10.1038/nprot.2006.85DOI Listing
September 2007

Reverse-phase protein microarrays: application to biomarker discovery and translational medicine.

Expert Rev Mol Diagn 2007 Sep;7(5):625-33

George Mason University, Center for Applied Proteomics and Molecular Medicine, Manassas, VA 20110, USA.

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http://dx.doi.org/10.1586/14737159.7.5.625DOI Listing
September 2007

Laser capture microdissection technology.

Expert Rev Mol Diagn 2007 Sep;7(5):647-57

Center for Applied Proteomics & Molecular Medicine, George Mason University, Manassas, VA 20110, USA.

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http://dx.doi.org/10.1586/14737159.7.5.647DOI Listing
September 2007

Phosphoprotein pathway mapping: Akt/mammalian target of rapamycin activation is negatively associated with childhood rhabdomyosarcoma survival.

Cancer Res 2007 Apr;67(7):3431-40

Food and Drug Administration, Center for Biologics Evaluation and Research, Office of Cellular and Gene Therapy, National Cancer Institute, NIH, Bethesda, Maryland, USA.

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http://dx.doi.org/10.1158/0008-5472.CAN-06-1344DOI Listing
April 2007

Physicochemically modified silicon as a substrate for protein microarrays.

Biomaterials 2007 Jan 20;28(3):550-8. Epub 2006 Sep 20.

Comprehensive Cancer Center, The Ohio State University, 473 W 12th Ave, #326 Columbus, OH 43210, USA.

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http://dx.doi.org/10.1016/j.biomaterials.2006.08.051DOI Listing
January 2007

Laser capture microdissection.

Methods Mol Biol 2006 ;319:213-29

Center for Applied Proteomics and Molecular Medicine, George Mason University, Manassas, VA, USA.

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August 2006

Role of proteomics in personalized medicine.

Per Med 2006 Aug;3(3):223-226

George Mason University, Center for Applied Proteomics and Molecular Medicine, Manassas, VA 20110, USA.

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http://dx.doi.org/10.2217/17410541.3.3.223DOI Listing
August 2006

Proteomic analysis of malignant ovarian cancer effusions as a tool for biologic and prognostic profiling.

Clin Cancer Res 2006 Feb;12(3 Pt 1):791-9

Molecular Signaling Section, Laboratory of Pathology, National Cancer Institute, Bethesda Maryland 20892, USA

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February 2006

Manual exfoliation of fresh tissue obviates the need for frozen sections for molecular profiling.

Cancer 2005 Dec;105(6):483-91

Department of Pathology, University at Buffalo, State University of New York, Buffalo, New York 14203, USA.

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http://dx.doi.org/10.1002/cncr.21347DOI Listing
December 2005

[Development of the protein microarray technique and usefulness in individualized molecular tumor therapy]].

Authors:
Virginia Espina

Onkologie 2005 Oct 3;28 Suppl 4:40-2. Epub 2005 Oct 3.

Center for Applied Proteomics and Molecular Medicine, George Mason University, Manassas, VA, USA.

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http://dx.doi.org/10.1159/000088828DOI Listing
October 2005

Pegylated, steptavidin-conjugated quantum dots are effective detection elements for reverse-phase protein microarrays.

Bioconjug Chem 2005 May-Jun;16(3):559-66

FDA-NCI Clinical Proteomics Program, Laboratory of Pathology, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.

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http://dx.doi.org/10.1021/bc0497113DOI Listing
September 2005

A transforming growth factor-beta receptor-interacting protein frequently mutated in human ovarian cancer.

Cancer Res 2005 Aug;65(15):6526-33

Department of Pharmacology and Health Evaluation Sciences, Pennsylvania State University College of Medicine, Hershey, Pennsylvania 17033, USA.

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http://dx.doi.org/10.1158/0008-5472.CAN-04-4385DOI Listing
August 2005

Proteomic analysis of apoptotic pathways reveals prognostic factors in follicular lymphoma.

Clin Cancer Res 2005 Aug;11(16):5847-55

National Cancer Institute--Food and Drug Administration Clinical Proteomics Program, Laboratory of Pathology, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1158/1078-0432.CCR-05-0637DOI Listing
August 2005

Mapping molecular networks using proteomics: a vision for patient-tailored combination therapy.

J Clin Oncol 2005 May;23(15):3614-21

US Food and Drug Administration-National Cancer Institute Clinical Proteomics Program, Office of Cellular and Gene Therapy, Center for Biologics Evaluation and Research, FDA, Bethesda, MD, USA.

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http://dx.doi.org/10.1200/JCO.2005.02.509DOI Listing
May 2005

CSF proteome: a protein repository for potential biomarker identification.

Expert Rev Proteomics 2005 Jan;2(1):57-70

Laboratory of Pathology, Center for Cancer Research, National Cancer Institute, National Institutes of Health, 9000 Rockville Pike, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1586/14789450.2.1.57DOI Listing
January 2005