The DOI matches its Crossref record; 8 of the 8 references it cites were found in a registry or an index.
LIPID MAPS online tools for lipid research
Open accessAbstract
The LIPID MAPS consortium has developed a number of online tools for performing tasks such as drawing lipid structures and predicting possible structures from mass spectrometry (MS) data. A simple online interface has been developed to enable an end-user to rapidly generate a variety of lipid chemical structures, along with corresponding systematic names and ontological information. The structure-drawing tools are available for six categories of lipids: (i) fatty acyls, (ii) glycerolipids, (iii) glycerophospholipids, (iv) cardiolipins, (v) sphingolipids and (vi) sterols. Within each category, the structure-drawing tools support the specification of various parameters such as chain lengths at a specific sn position, head groups, double bond positions and stereochemistry to generate a specific lipid structure. The structure-drawing tools have also been integrated with a second set of online tools which predict possible lipid structures from precursor-ion and product-ion MS experimental data. The MS prediction tools are available for three categories of lipids: (i) mono/di/triacylglycerols, (ii) glycerophospholipids and (iii) cardiolipins. The LIPID MAPS online tools are publicly available at www.lipidmaps.org/tools/.
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Weininger, D. (1988) · Journal of Chemical Information and Computer Sciences · doi:10.1021/ci00057a005 · Cited by 7,436
Specification of Molecular Chirality
Cahn, R. S., Ingold, C., & Prelog, V. (1966) · Angewandte Chemie International Edition in English · doi:10.1002/anie.196603851 · Cited by 1,877
A comprehensive classification system for lipids
Fahy, E., Subramaniam, S., Brown, H. A., Glass, C. K., Merrill, A. H., Murphy, R. C., Raetz, C. R. H., Russell, D. W., Seyama, Y., Shaw, W., et al. (2005) · Journal of Lipid Research · doi:10.1194/jlr.e400004-jlr200 · Cited by 1,699
Self-citationLMSD: LIPID MAPS structure database
Sud, M., Fahy, E., Cotter, D., Brown, A., Dennis, E. A., Glass, C. K., Merrill, A. H., Murphy, R. C., Raetz, C. R. H., Russell, D. W., et al. (2007) · Nucleic Acids Research · doi:10.1093/nar/gkl838 · Cited by 1,375
Self-citationBasic Principles of the CIP‐System and Proposals for a Revision
Prelog, V., & Helmchen, G. (1982) · Angewandte Chemie International Edition in English · doi:10.1002/anie.198205671 · Cited by 592
Analysis of Nonvolatile Lipids by Mass Spectrometry
Murphy, R. C., Fiedler, J., & Hevko, J. (2001) · Chemical Reviews · doi:10.1021/cr9900883 · Cited by 304
Caffrey, M., & Hogan, J. (1992) · Chemistry and Physics of Lipids · doi:10.1016/0009-3084(92)90002-7 · Cited by 137
Watanabe, K., Yasugi, E., & Oshima, M. (2000) · Trends in Glycoscience and Glycotechnology · doi:10.4052/tigg.12.175 · Cited by 72
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Self-citationGenetics meets metabolomics: a genome-wide association study of metabolite profiles in human serum
Gieger, C., Geistlinger, L., Altmaier, E., Hrabé de Angelis, M., Kronenberg, F., Meitinger, T., Mewes, H.-W., Wichmann, H.-E., Weinberger, K. M., Adamski, J., et al. (2008) · PLoS Genetics · doi:10.1371/journal.pgen.1000282 · Cited by 737
Transmission-mode MALDI-2 mass spectrometry imaging of cells and tissues at subcellular resolution
Niehaus, M., Soltwisch, J., Belov, M. E., & Dreisewerd, K. (2019) · Nature Methods · doi:10.1038/s41592-019-0536-2 · Cited by 429
Koelmel, J. P., Kroeger, N. M., Ulmer, C. Z., Bowden, J. A., Patterson, R. E., Cochran, J. A., Beecher, C. W. W., Garrett, T. J., & Yost, R. A. (2017) · BMC Bioinformatics · doi:10.1186/s12859-017-1744-3 · Cited by 346
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Metadata
- Authors
- Fahy, E., Sud, M., Cotter, D., & Subramaniam, S.
- Venue
- Nucleic Acids Research
- Publisher
- Oxford University Press (OUP)
- Published
- 2007-05-08
- Volume
- 35
- Issue
- Web Server
- Pages
- W606-W612
- ISSN
- 0305-1048 (ISSN-L)
- 1362-4962
- OpenAlex
- W2009453329
- Cited by
- 911
- References
- 8
- FWCI
- 4.67
- Type
- journal article
- Language
- en
- Open access
- gold
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