Bibliographies thématiques / Fucose

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Littérature scientifique sur le sujet « Fucose »

Auteur : Grafiati
Publié le 4 juin 2021
Mis à jour le 4 mai 2024

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Articles de revues sur le sujet "Fucose"

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Becerra, Jimmy E., María J. Yebra, and Vicente Monedero. "An l-Fucose Operon in the Probiotic Lactobacillus rhamnosus GG Is Involved in Adaptation to Gastrointestinal Conditions." Applied and Environmental Microbiology 81, no. 11 (March 27, 2015): 3880–88. http://dx.doi.org/10.1128/aem.00260-15.

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ABSTRACTl-Fucose is a sugar present in human secretions as part of human milk oligosaccharides, mucins, and other glycoconjugates in the intestinal epithelium. The genome of the probioticLactobacillus rhamnosusGG (LGG) carries a gene cluster encoding a putativel-fucose permease (fucP),l-fucose catabolic pathway (fucI,fucK,fucU, andfucA), and a transcriptional regulator (fucR). The metabolism ofl-fucose in LGG results in 1,2-propanediol production, and theirfucIandfucPmutants displayed a severe and mild growth defect onl-fucose, respectively. Transcriptional analysis revealed that thefucgenes a
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Liu, Xixi, Zhexian Zhang, Hui Mao, Pin Wang, Zhichuang Zuo, Li Gao, Xiang Shi, Ronghua Yin, Na Gao, and Jinhua Zhao. "Characterization of the Hydrolysis Kinetics of Fucosylated Glycosaminoglycan in Mild Acid and Structures of the Resulting Oligosaccharides." Marine Drugs 18, no. 6 (May 29, 2020): 286. http://dx.doi.org/10.3390/md18060286.

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Mild acid hydrolysis is a common method for the structure analysis of fucosylated glycosaminoglycan (FG). In this work, the effects of acid hydrolysis on the structure of FG from S. variegatus (SvFG) and the reaction characteristic were systemically studied. The degree of defucosylation (DF) and molecular weights (Mw) of partial fucosylated glycosaminoglycans (pFs) were monitored by 1H NMR and size-exclusion chromatography, respectively. The kinetic plots of DF, degree of desulfation (DS) from fucose branches, and degree of hydrolysis (DH) of the backbone are exponentially increased with time,
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Pérez-Escalante, Emmanuel, Luis Guillermo González-Olivares, Araceli Castañeda-Ovando, Alma Elizabeth Cruz-Guerrero, John F. Trant, Wendolyne López-Orozco, Luis Humberto Mendoza-Huizar та Sergio Alatorre-Santamaría. "An In Silico Approach to Enzymatic Synthesis of Fucooligosaccharides Using α-l-Fucosidase from Thermotoga maritima". Chemistry Proceedings 3, № 1 (14 листопада 2020): 10. http://dx.doi.org/10.3390/ecsoc-24-08303.

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Fucooligosaccharides comprise the primary group of human milk oligosaccharides. Due to their beneficial properties, a series of synthetic methods have been proposed to obtain them. Enzymatic methods show great promise, and α-l-fucosidase from Thermotoga maritima has emerged as a powerful catalyst for their production. Nonetheless, the enzyme’s limited substrate scope has delayed its wider application. The present work aims to compare the relative reactivity of fucose, pNP-fucose, and ethyl-fucose, while also exploring the molecular interactions of these fucosyl-donors with the enzyme through a
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Ojeda, Kristylea J., Jodie M. Box, and K. Dale Noel. "Genetic Basis for Rhizobium etli CE3 O-Antigen O-Methylated Residues That Vary According to Growth Conditions." Journal of Bacteriology 192, no. 3 (November 30, 2009): 679–90. http://dx.doi.org/10.1128/jb.01154-09.

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ABSTRACT The Rhizobium etli CE3 O antigen is a fixed-length heteropolymer with O methylation being the predominant type of sugar modification. There are two O-methylated residues that occur, on average, once per complete O antigen: a multiply O-methylated terminal fucose and 2-O methylation of a fucose residue within a repeating unit. The amount of the methylated terminal fucose decreases and the amount of 2-O-methylfucose increases when bacteria are grown in the presence of the host plant, Phaseolus vulgaris, or its seed exudates. Insertion mutagenesis was used to identify open reading frames
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Nuñez, Samantha, Maria Barra, and Daniel Garrido. "Developing a Fluorescent Inducible System for Free Fucose Quantification in Escherichia coli." Biosensors 13, no. 3 (March 15, 2023): 388. http://dx.doi.org/10.3390/bios13030388.

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L-Fucose is a monosaccharide abundant in mammalian glycoconjugates. In humans, fucose can be found in human milk oligosaccharides (HMOs), mucins, and glycoproteins in the intestinal epithelium. The bacterial consumption of fucose and fucosylated HMOs is critical in the gut microbiome assembly of infants, dominated by Bifidobacterium. Fucose metabolism is important for the production of short-chain fatty acids and is involved in cross-feeding microbial interactions. Methods for assessing fucose concentrations in complex media are lacking. Here we designed and developed a molecular quantificatio
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Chan, Pan F., Karen M. O'Dwyer, Leslie M. Palmer, Jennifer D. Ambrad, Karen A. Ingraham, Chi So, Michael A. Lonetto, et al. "Characterization of a Novel Fucose-Regulated Promoter (PfcsK) Suitable for Gene Essentiality and Antibacterial Mode-of-Action Studies in Streptococcus pneumoniae." Journal of Bacteriology 185, no. 6 (March 15, 2003): 2051–58. http://dx.doi.org/10.1128/jb.185.6.2051-2058.2003.

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ABSTRACT The promoter of the Streptococcus pneumoniae putative fuculose kinase gene (fcsK), the first gene of a novel fucose utilization operon, is induced by fucose and repressed by glucose or sucrose. When the streptococcal polypeptide deformylase (PDF) gene (def1, encoding PDF) was placed under the control of P fcsK , fucose-dependent growth of the S. pneumoniae (P fcsK ::def1) strain was observed, confirming the essential nature of PDF in this organism. The mode of antibacterial action of actinonin, a known PDF inhibitor, was also confirmed with this strain. The endogenous fuculose kinase
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Robles-Gómez, Laura, Paula Sáez-Espinosa, Eliana Marina López-Viloria, Andrea López-Botella, Jon Aizpurua, and María José Gómez-Torres. "Quantification and Topographical Distribution of Terminal and Linked Fucose Residues in Human Spermatozoa by Using Field Emission Scanning Electron Microscopy (FE-SEM)." International Journal of Molecular Sciences 22, no. 21 (November 4, 2021): 11947. http://dx.doi.org/10.3390/ijms222111947.

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The modification of sperm glycocalyx is an essential process during sperm capacitation. The presence and redistribution of terminal and linked fucose have been described during in vitro capacitation in humans. However, the influence of the capacitation time on the quantification and localization of terminal and linked fucose is still unknown. In this study, the quantitative and qualitative changes in fucosyl residues during different in vitro capacitation times (1 and 4 h), are simultaneously characterized by using Aleuria aurantia (AAA) lectin–gold labelling and high-resolution field emission
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Tollefsen, S. E., and J. L. Rosenblum. "Role of terminal fucose residues in clearance of human glycosylated alpha-amylase." American Journal of Physiology-Gastrointestinal and Liver Physiology 255, no. 3 (September 1, 1988): G374—G381. http://dx.doi.org/10.1152/ajpgi.1988.255.3.g374.

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Human glycosylated alpha-amylase contains a single biantennary N-linked oligosaccharide that terminates with the structure Fuc alpha 1,3(Gal beta 1,4)GlcNAc. To examine the role of terminal fucose in the clearance of alpha-amylase, we used lectin affinity chromatography to isolate an alpha-amylase fraction that contains two terminal fucoses (one in each branch of the oligosaccharide) and a fraction from which both terminal fucoses have been enzymatically removed. In the rat, the rate of clearance of the radioiodinated fraction with terminal fucoses is rapid (t1/2 = 12 min) and is slowed by man
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Kim, In Jung, and Kyoung Heon Kim. "Thermophilic l-fucose isomerase from Thermanaeromonas toyohensis for l-fucose synthesis from l-fuculose." Process Biochemistry 96 (September 2020): 131–37. http://dx.doi.org/10.1016/j.procbio.2020.05.017.

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Ropartz, David, Lery Marion, Mathieu Fanuel, Jasna Nikolic, Murielle Jam, Robert Larocque, Elizabeth Ficko-Blean, Gurvan Michel, and Helene Rogniaux. "In-depth structural characterization of oligosaccharides released by GH107 endofucanase MfFcnA reveals enzyme subsite specificity and sulfated fucan substructural features." Glycobiology 32, no. 4 (December 4, 2021): 276–88. http://dx.doi.org/10.1093/glycob/cwab125.

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Abstract The extracellular matrix of brown algae represents an abundant source of fucose-containing sulfated polysaccharides (FCSPs). FCSPs include sulfated fucans, essentially composed of fucose, and highly heterogeneous fucoidans, comprising various monosaccharides. Despite a range of potentially valuable biological activities, the structures of FCSPs are only partially characterized and enzymatic tools leading to their deconstruction are rare. Previously, the enzyme MfFcnA was isolated from the marine bacterium Mariniflexile fucanivorans and biochemically characterized as an endo-α-1 → 4-l-
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Thèses sur le sujet "Fucose"

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Smelt, Kathryn Helena. "Synthesis of L-fucose analogues." Thesis, University of Oxford, 1997. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.362080.

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Yuan, Kun. "Effects of defucosylation on human breast cancer cells." Thesis, Birmingham, Ala. : University of Alabama at Birmingham, 2007. https://www.mhsl.uab.edu/dt/2010r/yuan.pdf.

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McCabe, N. R. "Training and fucose metabolism in chick brain." Thesis, Open University, 1985. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.355645.

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Doknic, D. "SYNTHESIS OF FUCOSE-BASED LIGANDS FOR DC-SIGN." Doctoral thesis, Università degli Studi di Milano, 2012. http://hdl.handle.net/2434/203241.

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DC-SIGN is a C-type lectin that is expressed in dendritic cells and that is involved in a number of infection processes such as HIV or Ebola. Within the scope of this work a library of monovalent, fucose-based ligands was synthesised to block DC-SIGN. The structures originate from three scaffolds containing 2-aminocyclohexane carboxylic acid in different configurations. The compounds were tested by means of SPR competition assays and were found to be similar to the natural ligand Lewis X in terms of affinity for DC-SIGN. On the one hand, the most potent ligand, and on the other hand, the most
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Sanz, Sender Silvia. "Synthesis and biological function of fucose in Plasmodium falciparum." Doctoral thesis, Universitat de Barcelona, 2017. http://hdl.handle.net/10803/587108.

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Malaria is a parasitic disease caused by Plasmodium parasites and it is transmitted by female Anopheles mosquito. P. falciparum has a complex life cycle that includes important stages in two different hosts: a mosquito and a human. The transmission between the human and the mosquito host also involves the transition between asexual and sexual forms of the parasites. Glycobiology includes the study of carbohydrate metabolism and glycoconjugate (glycoprotein and glycolipid) structures. Protozoan parasites synthesize different glycoconjugates for protection and to respond to changes in the envir
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Bandini, Giulia. "Studies on fucosylation in Trypanosoma brucei." Thesis, University of Dundee, 2011. https://discovery.dundee.ac.uk/en/studentTheses/c74554c1-f4d3-4bb3-aa31-899fcf507e11.

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The biosynthesis of GDP-Fucose, the activated donor for fucose, has been recently shown to be essential in the parasite Trypanosoma brucei. Fucose is a common sugar modification on eukaryotic glycan structures, but it has not been well described in trypanosomatids. To elucidate the role of fucose in T. brucei we searched for putative fucosyltransferases in this parasite. A single putative T. brucei fucosyltransferase (TbFT) was identified and recombinantly expressed in Escherichia coli. The protein was active and structural characterization of its reaction product identified it as a GDP-Fuc: ß
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Muiry, Jennifer Anne Ross. "The bacterial transport systems for L-rhamnose and L-fucose." Thesis, University of Cambridge, 1989. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.315190.

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Yao, David C. "Roles of O-fucose Molecules in Notch Signaling and Hematopoiesis." Case Western Reserve University School of Graduate Studies / OhioLINK, 2011. http://rave.ohiolink.edu/etdc/view?acc_num=case1311379342.

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Weidner, Stefan. "Enzymatische Synthese von GDP-[beta]-L-Fucose [GDP-beta-L-Fucose] ausgehend von D-Mannose Klonierung, Expression und Charakterisierung von Enzymen aus nicht-pathogenen Enterobacteriaceae /." [S.l. : s.n.], 2003. http://deposit.ddb.de/cgi-bin/dokserv?idn=972659331.

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Staib, Lena [Verfasser], Thilo M. [Akademischer Betreuer] [Gutachter] Fuchs, and Hannelore [Gutachter] Daniel. "Investigation of propanediol and fucose degradation by Salmonella Typhimurium / Lena Staib ; Gutachter: Hannelore Daniel, Thilo M. Fuchs ; Betreuer: Thilo M. Fuchs." München : Universitätsbibliothek der TU München, 2016. http://d-nb.info/1121206808/34.

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Livres sur le sujet "Fucose"

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Černoušková, Dagmar. Orbis pictus Bohuslava Fuchse: Orbis pictus von Bohuslav Fuchs = Orbis pictus de Bohuslav Fuchs = Orbis pictus of Bohuslav Fuchs. Brno: Muzeum města Brna, 2012.

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Pinelli, Dominique. U Fucone. La Tour d'Aigues: Editions de l'Aube, 1998.

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Luder, Gustav. Schlaue fuchse, stolze hahne: Fabelhaftes - kurzprosa. Hannover: Moorburg, 1986.

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Arbeitman, Yoël L., ed. Fucus. Amsterdam: John Benjamins Publishing Company, 1988. http://dx.doi.org/10.1075/cilt.58.

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Riedel, Michael S. Fuchs. London: Koenig Books, 2017.

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Heidenreich, Gert. Fuchse Jagen: Epilog auf das Jahr 1968. Munich: Piper, 1987.

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Kubinszky, Mihály. Bohuslav Fuchs. Budapest: Akadémiai Kiadó, 1985.

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Fuchs, Eckehard. Eckehard Fuchs. Edited by Schmidt Johannes 1969- and Roedel Anke. Dresden: Ed. Azur, 2009.

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Mihály, Kubinszky. Bohuslav Fuchs. Berlin: Henschelverlag Kunst und Gesellschaft, 1986.

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Goethe, Johann Wolfgang von. Reineke Fuchs. Köln: Anaconda, 2010.

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Chapitres de livres sur le sujet "Fucose"

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Schomburg, Dietmar, and Dörte Stephan. "Fucose-1-phosphate guanylyltransferase." In Enzyme Handbook, 625–27. Berlin, Heidelberg: Springer Berlin Heidelberg, 1997. http://dx.doi.org/10.1007/978-3-642-59025-2_111.

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Renkonen, Risto. "Fucose-1-Phosphate Guanylyltransferase (FPGT)." In Handbook of Glycosyltransferases and Related Genes, 1631–35. Tokyo: Springer Japan, 2014. http://dx.doi.org/10.1007/978-4-431-54240-7_112.

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Bakker, Hans, Angel Ashikov, Francoise H. Routier, and Rita Gerardy-Schahn. "GDP-Fucose Transporter 1 (SLC35C1)." In Handbook of Glycosyltransferases and Related Genes, 1403–11. Tokyo: Springer Japan, 2014. http://dx.doi.org/10.1007/978-4-431-54240-7_38.

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Matsumoto, Kenjiroo, Akira Ishio, and Kenji Matsuno. "O-Fucose Glycan in Drosophila Notch Signaling." In Glycoscience: Biology and Medicine, 1–7. Tokyo: Springer Japan, 2014. http://dx.doi.org/10.1007/978-4-431-54836-2_163-1.

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Matsumoto, Kenjiroo, Akira Ishio, and Kenji Matsuno. "O-Fucose Glycan in Drosophila Notch Signaling." In Glycoscience: Biology and Medicine, 841–47. Tokyo: Springer Japan, 2014. http://dx.doi.org/10.1007/978-4-431-54841-6_163.

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Ogorek, Christiane, Ingo Jordan, Volker Sandig, and Hans Henning von Horsten. "Fucose-Targeted Glycoengineering of Pharmaceutical Cell Lines." In Antibody Engineering, 507–17. Totowa, NJ: Humana Press, 2012. http://dx.doi.org/10.1007/978-1-61779-974-7_29.

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Kannagi, Reiji. "Fucosyltransferase 6. GDP-Fucose Lactosamine α3-Fucosyltransferase (FUT6)." In Handbook of Glycosyltransferases and Related Genes, 559–71. Tokyo: Springer Japan, 2014. http://dx.doi.org/10.1007/978-4-431-54240-7_80.

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Kannagi, Reiji. "Fucosyltransferase 5. GDP-Fucose Lactosamine α3/4-Fucosyltransferase (FUT5)." In Handbook of Glycosyltransferases and Related Genes, 549–58. Tokyo: Springer Japan, 2014. http://dx.doi.org/10.1007/978-4-431-54240-7_79.

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Ihara, Hideyuki, Hiroki Tsukamoto, Jianguo Gu, Eiji Miyoshi, Naoyuki Taniguchi, and Yoshitaka Ikeda. "Fucosyltransferase 8. GDP-Fucose N-Glycan Core α6-Fucosyltransferase (FUT8)." In Handbook of Glycosyltransferases and Related Genes, 581–96. Tokyo: Springer Japan, 2014. http://dx.doi.org/10.1007/978-4-431-54240-7_59.

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Kudo, Takashi, and Hisashi Narimatsu. "Fucosyltransferase 4. GDP-Fucose Lactosamine α1,3-Fucosyltransferase. Myeloid Specific (FUT4)." In Handbook of Glycosyltransferases and Related Genes, 541–47. Tokyo: Springer Japan, 2014. http://dx.doi.org/10.1007/978-4-431-54240-7_95.

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Actes de conférences sur le sujet "Fucose"

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Al-Samarra, Esraa Ali Abdul Karim, and Rafah Razooq Hameed Al-Samarrai. "Evaluation of the correlation between D-dimer and total L-fucose, fucose binding protein and fucose binding lipids in type 2 diabetes patients infected with COVID-19." In International Conference of Chemistry and Petrochemical Techniques (ICCPT). AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0095332.

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Arzhanova, E. L. "L-FUCOSE EFFECT ON DISRUPTIONS IN MITOCHONDRIAL FUNCTION AND METABOLISM OF PERITONEAL MACROPHAGES OF MUC2–/–MICE." In X Международная конференция молодых ученых: биоинформатиков, биотехнологов, биофизиков, вирусологов и молекулярных биологов — 2023. Novosibirsk State University, 2023. http://dx.doi.org/10.25205/978-5-4437-1526-1-289.

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L-fucose is a monosaccharide present in various glycolipids and glycoproteins and may participate in signaling processes of both epithelial and immune cells, in particular macrophages. We studied the metabolic and functional differences of peritoneal macrophages derived from a model of IBD and control mice before and after L-fucose treatment in vitro.
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Singh, Sudhir, Kuntal Pal, Elliot Ensink, Jessica Yadav, Doron Kletter, Marshall Bern, Anand Mehta, Karsten Melcher, and Brian B. Haab. "Abstract B31: Development of fucose based pancreatic cancer biomarkers using modified lectins." In Abstracts: AACR Special Conference on Pancreatic Cancer: Innovations in Research and Treatment; May 18-21, 2014; New Orleans, LA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7445.panca2014-b31.

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Braster, Rens, Remco Visser, Gestur Vidarsson, and Marjolein van Egmond. "Abstract A02: The art of omission: Low fucose antibodies enhance tumor cell clearance in vivo." In Abstracts: AACR Special Conference: Tumor Immunology and Immunotherapy: A New Chapter; December 1-4, 2014; Orlando, FL. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/2326-6074.tumimm14-a02.

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Kato, Junji, Rishu Takimoto, Takahiro Osuga, Michihiro Ono, Masahiro Hirakawa, Makoto Yoshida, Yasushi Sato, and Fumito Tamura. "Abstract 4463: Targeting SN38 delivery to gastrointestinal cancer cells using a fucose-bound nanoparticle approach." In Proceedings: AACR Annual Meeting 2014; April 5-9, 2014; San Diego, CA. American Association for Cancer Research, 2014. http://dx.doi.org/10.1158/1538-7445.am2014-4463.

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Listinsky, JJ, GP Siegal, and CM Listinsky. "P5-07-04: Is a-L-Fucose Overexpressed on Cells of Aggressive Human Breast Cancers?" In Abstracts: Thirty-Fourth Annual CTRC‐AACR San Antonio Breast Cancer Symposium‐‐ Dec 6‐10, 2011; San Antonio, TX. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/0008-5472.sabcs11-p5-07-04.

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Kerr, Sheena C., Stephen D. Carrington, Michaela Wimmerova, Iwona Bucior, Joanne N. Engel, and John V. Fahy. "Inhibiting Fucose Binding Lectins As An Anti-Adhesion And Anti-Infection Strategy For Pseudomonas Airway Infections." In American Thoracic Society 2012 International Conference, May 18-23, 2012 • San Francisco, California. American Thoracic Society, 2012. http://dx.doi.org/10.1164/ajrccm-conference.2012.185.1_meetingabstracts.a2468.

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Yang, Yurui, Hongbin Lan, Huawei Zhu, and Yiran Zhu. "The Investigation of P7 Peptide Delivery Targeting Cdc24 in Ras-driven Pancreatic Cancer by L-fucose-bound Liposome." In The International Conference on Biomedical Engineering and Bioinformatics. SCITEPRESS - Science and Technology Publications, 2022. http://dx.doi.org/10.5220/0011251700003443.

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Ibrahim, Waleed Satar, and Rafah Razooq Hameed Al-Samarrai. "Evaluation the correlation between serum fucose and lipid profile in sera of patients with dyslipidemia in Samarra city." In 1ST SAMARRA INTERNATIONAL CONFERENCE FOR PURE AND APPLIED SCIENCES (SICPS2021): SICPS2021. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0121797.

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Listinsky, JJ, GP Siegal, and CM Listinsky. "P2-18-06: Conventional Trastuzumab Is an Antagonist of Natural Killer Cells: Making the Case for Fucose-Depleted Trastuzumab." In Abstracts: Thirty-Fourth Annual CTRC‐AACR San Antonio Breast Cancer Symposium‐‐ Dec 6‐10, 2011; San Antonio, TX. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/0008-5472.sabcs11-p2-18-06.

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Rapports d'organisations sur le sujet "Fucose"

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Spiegel, Yitzhak, Michael McClure, Itzhak Kahane, and B. M. Zuckerman. Characterization of the Phytophagous Nematode Surface Coat to Provide New Strategies for Biocontrol. United States Department of Agriculture, November 1995. http://dx.doi.org/10.32747/1995.7613015.bard.

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Chemical composition and biological role of the surface coat (SC) of the root-knot nematodes, Meloidogyne spp. are described. SC proteins of M. incognita race 3 infective juveniles (J2) were characterized by electrophoresis and western blotting of extracts from radioiodine and biotin-labelled nematodes. J2 labelled with radioiodine and biotin released 125I and biotin-labelled molecules into water after 20 hours incubation, indicating that SC proteins may be loosely attached to the nematode. Antiserum to the principal protein reacted with the surface of live J2 and with surface proteins previou
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Meade, Roger, and Linda Meade. Klaus Fuchs: The Second Confession. Office of Scientific and Technical Information (OSTI), October 2014. http://dx.doi.org/10.2172/1159562.

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Shay, H. Report on Simulations of the Royle-Sentoku-Fuchs Experiment. Office of Scientific and Technical Information (OSTI), February 2013. http://dx.doi.org/10.2172/1069000.

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Hamilton, T., T. Brown, A. Marchetti, R. Martinelli, and S. Kehl. Determination of Plutonium Activity Concentrations and 240Pu/239Pu Atom Ratios in Brown Algae (Fucus distichus) Collected from Amchitka Island, Alaska. Office of Scientific and Technical Information (OSTI), May 2005. http://dx.doi.org/10.2172/15016341.

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Edwards, Susan L., Marcus E. Berzofsky, and Paul P. Biemer. Addressing Nonresponse for Categorical Data Items Using Full Information Maximum Likelihood with Latent GOLD 5.0. RTI Press, September 2018. http://dx.doi.org/10.3768/rtipress.2018.mr.0038.1809.

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Full information maximum likelihood (FIML) is an important approach to compensating for nonresponse in data analysis. Unfortunately, only a few software packages implement FIML and even fewer have the capability to compensate for missing not at random (MNAR) nonresponse. One of these packages is Statistical Innovations’ Latent GOLD; however, the user documentation for Latent GOLD provides no mention of this capability. The purpose of this paper is to provide guidance for fitting MNAR FIML models for categorical data items using the Latent GOLD 5.0 software. By way of comparison, we also provid
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Robinson, Dale. The distribution and morphology of Fucus distichus in an estuarine environment and the effect of selected ions on the uptake of inorganic carbon and nitrate. Portland State University Library, January 2000. http://dx.doi.org/10.15760/etd.3316.

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