Payne Lab: Publications: Difference between revisions

From OpenWetWare
Jump to navigationJump to search
Line 17: Line 17:


==Publications==
==Publications==
8. "Endo-Lysosomal Vesicles Positive for Rab7 and LAMP1 Are Terminal Vesicles for the Transport of Dextran," W.H. Humphries IV, C.J. Szymanski, C.K. Payne, PLoS ONE 6, e26626. doi:10.1371/journal.pone.0026626.  [http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0026626 Link]
8. "Endo-lysosomal vesicles positive for Rab7 and LAMP1 are terminal vesicles for the transport of dextran," W.H. Humphries IV, C.J. Szymanski, C.K. Payne, PLoS ONE 6, e26626. doi:10.1371/journal.pone.0026626.  [http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0026626 Link]


7. "Single particle tracking as a method to resolve differences in highly colocalized proteins," C.J. Szymanski, W.H. Humphries IV, C.K. Payne, Analyst, 136, 3527-3533 (2011).
7. "Single particle tracking as a method to resolve differences in highly colocalized proteins," C.J. Szymanski, W.H. Humphries IV, C.K. Payne, Analyst, 136, 3527-3533 (2011).

Revision as of 08:55, 4 January 2012

Research        People        Publications        Funding        News        Seminars        Positions Available        Outreach        Contact       



Publications

8. "Endo-lysosomal vesicles positive for Rab7 and LAMP1 are terminal vesicles for the transport of dextran," W.H. Humphries IV, C.J. Szymanski, C.K. Payne, PLoS ONE 6, e26626. doi:10.1371/journal.pone.0026626. Link

7. "Single particle tracking as a method to resolve differences in highly colocalized proteins," C.J. Szymanski, W.H. Humphries IV, C.K. Payne, Analyst, 136, 3527-3533 (2011).

6. "Cellular binding of nanoparticles in the presence of serum proteins," G.W. Doorley and C.K. Payne, Chem. Commun., 47, 466-468 (2011). PDF

5. "Intracellular degradation of low-density lipoprotein probed with two-color fluorescence microscopy," W.H. Humphries IV, N.C. Fay, C.K. Payne, Integr. Biol., 2, 536 - 544 (2010). PDF

4. "Imaging intracellular quantum dots: Fluorescence microscopy and transmission electron microscopy," C.J. Szymanski, H. Yi, J.L. Liu, E.R. Wright, C.K. Payne, Nanobiotechnology Protocols, in press (2010).

3. "Pyrenebutyrate leads to cellular binding, not intracellular delivery, of polyarginine quantum dots," A.E. Jablonski, T. Kawakami, A.Y. Ting, C.K. Payne, J. Phys. Chem. Lett., 1, 1312–1315 (2010). PDF

x. "Pyrenebutyrate-Mediated Delivery of Quantum Dots across the Plasma Membrane of Living Cells," A.E. Jablonski, W.H. Humphries, C.K. Payne, J. Phys. Chem. B, 113 (2), 405-408 (2009), pmid:19099434, withdrawn. The conclusions drawn from the data in this manuscript were incorrect. A full discussion can be found in, "Pyrenebutyrate Leads to Cellular Binding, Not Intracellular Delivery, of Polyarginine Quantum Dots," A.E. Jablonski, T. Kawakami, A.Y. Ting, C.K. Payne, J. Phys. Chem. Lett., 1, 1312–1315 (2010).

2. "Imaging gene delivery with fluorescence microscopy," C.K. Payne, Nanomedicine, 2, 847-860 (2007). pmid:18095850.

1. "Cellular binding, motion, and internalization of synthetic gene delivery polymers," G.T. Hess, W.H. Humphries IV, N.C. Fay, and C.K. Payne, Biochim. Biophys. Acta, Mol. Cell Res., 1773, 1583-1588 (2007). pmid:17888530. PDF

C.K. Payne publications prior to Georgia Tech