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Items: 1 to 20 of 226

1.
2.

Why do the abundances of ions generated by MALDI look thermally determined?

Bae YJ, Choe JC, Moon JH, Kim MS.

J Am Soc Mass Spectrom. 2013 Nov;24(11):1807-15. doi: 10.1007/s13361-013-0717-7. Epub 2013 Aug 29.

PMID:
23990058
3.

Degree of ionization in MALDI of peptides: thermal explanation for the gas-phase ion formation.

Bae YJ, Shin YS, Moon JH, Kim MS.

J Am Soc Mass Spectrom. 2012 Aug;23(8):1326-35. doi: 10.1007/s13361-012-0406-y. Epub 2012 Jun 1.

PMID:
22653466
4.
5.

A density functional theory (DFT) study on gas-phase proton transfer reactions of derivatized and underivatized peptide ions generated by matrix-assisted laser desorption ionization.

Brancia FL, Stener M, Magistrato A.

J Am Soc Mass Spectrom. 2009 Jul;20(7):1327-33. doi: 10.1016/j.jasms.2009.03.008. Epub 2009 Mar 20.

6.

Efficient methods to generate reproducible mass spectra in matrix-assisted laser desorption ionization of peptides.

Ahn SH, Park KM, Bae YJ, Kim MS.

J Am Soc Mass Spectrom. 2013 Jun;24(6):868-76. doi: 10.1007/s13361-013-0612-2. Epub 2013 Apr 18.

PMID:
23595259
7.

Expansion cooling in the matrix plume is under-recognized in MALDI mass spectrometry.

Bae YJ, Moon JH, Kim MS.

J Am Soc Mass Spectrom. 2011 Jun;22(6):1070-8. doi: 10.1007/s13361-011-0115-y. Epub 2011 Apr 9.

PMID:
21953048
8.

Reproducibility of temperature-selected mass spectra in matrix-assisted laser desorption ionization of peptides.

Bae YJ, Park KM, Kim MS.

Anal Chem. 2012 Aug 21;84(16):7107-11. doi: 10.1021/ac3014077. Epub 2012 Jul 30.

PMID:
22845786
9.

Using fluorescence dyes as a tool for analyzing the MALDI process.

Jaskolla TW, Karas M.

J Am Soc Mass Spectrom. 2008 Aug;19(8):1054-61. doi: 10.1016/j.jasms.2008.04.032. Epub 2008 May 3.

10.

Compelling evidence for Lucky Survivor and gas phase protonation: the unified MALDI analyte protonation mechanism.

Jaskolla TW, Karas M.

J Am Soc Mass Spectrom. 2011 Jun;22(6):976-88. doi: 10.1007/s13361-011-0093-0. Epub 2011 Mar 8.

PMID:
21953039
12.
13.

CHCA-modified Au nanoparticles for laser desorption ionization mass spectrometric analysis of peptides.

Duan J, Linman MJ, Chen CY, Cheng QJ.

J Am Soc Mass Spectrom. 2009 Aug;20(8):1530-9. doi: 10.1016/j.jasms.2009.04.009. Epub 2009 Apr 18.

14.

Alkylated dihydroxybenzoic acid as a MALDI matrix additive for hydrophobic peptide analysis.

Fukuyama Y, Tanimura R, Maeda K, Watanabe M, Kawabata S, Iwamoto S, Izumi S, Tanaka K.

Anal Chem. 2012 May 1;84(9):4237-43. doi: 10.1021/ac300540r. Epub 2012 Apr 16. Erratum in: Anal Chem. 2014 May 20;86(10):5187.

PMID:
22506777
15.

Ion yields for some salts in MALDI: mechanism for the gas-phase ion formation from preformed ions.

Moon JH, Shin YS, Bae YJ, Kim MS.

J Am Soc Mass Spectrom. 2012 Jan;23(1):162-70. doi: 10.1007/s13361-011-0278-6. Epub 2011 Nov 3.

PMID:
22048904
16.
17.

In-source decay and fragmentation characteristics of peptides using 5-aminosalicylic acid as a matrix in matrix-assisted laser desorption/ionization mass spectrometry.

Sakakura M, Takayama M.

J Am Soc Mass Spectrom. 2010 Jun;21(6):979-88. doi: 10.1016/j.jasms.2010.01.018. Epub 2010 Jan 28.

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20.

High-reactivity matrices increase the sensitivity of matrix enhanced secondary ion mass spectrometry.

Svara FN, Kiss A, Jaskolla TW, Karas M, Heeren RM.

Anal Chem. 2011 Nov 1;83(21):8308-13. doi: 10.1021/ac202222h. Epub 2011 Oct 7.

PMID:
21939214
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