"Microbodies" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Electron-dense cytoplasmic particles bounded by a single membrane, such as PEROXISOMES; GLYOXYSOMES; and glycosomes.
Descriptor ID |
D008830
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MeSH Number(s) |
A11.284.430.214.190.500.585 A11.284.430.214.190.875.190.190.755
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Concept/Terms |
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Below are MeSH descriptors whose meaning is more general than "Microbodies".
Below are MeSH descriptors whose meaning is more specific than "Microbodies".
This graph shows the total number of publications written about "Microbodies" by people in this website by year, and whether "Microbodies" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
Year | Major Topic | Minor Topic | Total |
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1996 | 1 | 1 | 2 |
1997 | 0 | 1 | 1 |
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Below are the most recent publications written about "Microbodies" by people in Profiles.
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Obourn JD, Frame SR, Bell RH, Longnecker DS, Elliott GS, Cook JC. Mechanisms for the pancreatic oncogenic effects of the peroxisome proliferator Wyeth-14,643. Toxicol Appl Pharmacol. 1997 Aug; 145(2):425-36.
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Fukuda S, Shimozawa N, Suzuki Y, Zhang Z, Tomatsu S, Tsukamoto T, Hashiguchi N, Osumi T, Masuno M, Imaizumi K, Kuroki Y, Fujiki Y, Orii T, Kondo N. Human peroxisome assembly factor-2 (PAF-2): a gene responsible for group C peroxisome biogenesis disorder in humans. Am J Hum Genet. 1996 Dec; 59(6):1210-20.
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Shimozawa N, Suzuki Y, Tomatsu S, Tsukamoto T, Osumi T, Fujiki Y, Kamijo K, Hashimoto T, Kondo N, Orii T. Correction by gene expression of biochemical abnormalities in fibroblasts from Zellweger patients. Pediatr Res. 1996 May; 39(5):812-5.
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Suzuki Y, Shimozawa N, Yajima S, Tomatsu S, Kondo N, Nakada Y, Akaboshi S, Lai M, Tanabe Y, Hashimoto T, et al. Novel subtype of peroxisomal acyl-CoA oxidase deficiency and bifunctional enzyme deficiency with detectable enzyme protein: identification by means of complementation analysis. Am J Hum Genet. 1994 Jan; 54(1):36-43.
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Singh N, Zoeller RA, Tykocinski ML, Lazarow PB, Tartakoff AM. Addition of lipid substituents of mammalian protein glycosylphosphoinositol anchors. Mol Cell Biol. 1994 Jan; 14(1):21-31.
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Suzuki Y, Shimozawa N, Kawabata I, Yajima S, Inoue K, Uchida Y, Izai K, Tomatsu S, Kondo N, Orii T. Prenatal diagnosis of peroxisomal disorders. Biochemical and immunocytochemical studies on peroxisomes in human amniocytes. Brain Dev. 1994 Jan-Feb; 16(1):27-31.
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Paul DA, Goldsmith LS, Miles DK, Moser AB, Spiro AJ, Grover WD. Neonatal adrenoleukodystrophy presenting as infantile progressive spinal muscular atrophy. Pediatr Neurol. 1993 Nov-Dec; 9(6):496-7.
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Laposata M, Minda M, Capriotti AM, Hartman EJ, Furth EE, Iozzo RV. Reversible phenotypic modulation induced by deprivation of exogenous essential fatty acids. Lab Invest. 1988 Dec; 59(6):838-47.
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Rodrigues MM, Fine BS, Laibson PR, Zimmerman LE. Disorders of the corneal epithelium. A clinicopathologic study of dot, geographic, and fingerprint patterns. Arch Ophthalmol. 1974 Dec; 92(6):475-82.
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Solter D, Biczysko W, Pienkowski M, Koprowski H. Ultrastructure of mouse egg cylinders developed in vitro. Anat Rec. 1974 Oct; 180(2):263-79.