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Cited by 503

The DOI matches its Crossref record; 114 of the 114 references it cites were found in a registry or an index.

Lysosome‐related organelles

Dell'Angelica, Esteban C., Mullins, Chris, Caplan, Steve, Bonifacino, Juan S.·2000·The FASEB Journal

Abstract

Lysosomes are membrane‐bound cytoplasmic organelles involved in intracellular protein degradation. They contain an assortment of soluble acid‐dependent hydrolases and a set of highly glycosylated integral membrane proteins. Most of the properties of lysosomes are shared with a group of cell type‐specific compartments referred to as ‘lysosome‐related organelles’, which include melanosomes, lytic granules, MHC class II compartments, platelet‐dense granules, basophil granules, azurophil granules, and Drosophila pigment granules. In addition to lysosomal proteins, these organelles contain cell type‐specific components that are responsible for their specialized functions. Abnormalities in both lysosomes and lysosome‐related organelles have been observed in human genetic diseases such as the Chediak‐Higashi and Hermansky‐Pudlak syndromes, further demonstrating the close relationship between these organelles. Identification of genes mutated in these human diseases, as well as in mouse and Drosophila pigmentation mutants, is beginning to shed light on the molecular machinery involved in the biogenesis of lysosomes and lysosome‐related organelles.—Dell'Angelica, E. C., Mullins, C., Caplan, S., Bonifacino, J. S. Lysosome‐related organelles. FASEB J. 14, 1265–1278 (2000)

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Show all 114 references

Research works printed but not linked: 15

  1. 10.1007/s109-1998-8099-y · doi:10.1007/s109-1998-8099-y
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  4. Bonifacino J. S., 1989, Internal ization and recycling to serotonin‐containing granules of the 80K integral membrane protein exposed on the surface of secreting rat basophilic leukaemia cells, J. Cell Sci., 92, 701, 10.1242/jcs.92.4.701 · doi:10.1242/jcs.92.4.701
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  7. Rendu F., 1983, Evidence that abnormal platelet functions in human Chediak‐Higashi syndrome are the result of a lack of dense bodies, Am. J. Pathol., 111, 307
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  10. Pastural E., 1999, Griscelli disease maps to chromosome 15q and is associated with mutations in the Myosin‐Va gene (Correction), Nat Genet, 23, 373, 10.1038/15565 · doi:10.1038/15565
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  14. Masson D., 1990, Interaction of chondroitin sulfate with perforin and granzymes of cytolytic T‐cells is dependent on pH, Biochemistry, 25, 11229, 10.1021/bi00503a011 · doi:10.1021/bi00503a011
  15. Copier J., 1996, Targeting signal and subcellular compartments involved in the intracellular trafficking of HLA‐DMB, J. Immunol., 157, 1017, 10.4049/jimmunol.157.3.1017 · doi:10.4049/jimmunol.157.3.1017

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Metadata

Authors
Dell'Angelica, E. C., Mullins, C., Caplan, S., & Bonifacino, J. S.
Venue
The FASEB Journal
Publisher
Wiley
Published
2000-07
Volume
14
Issue
10
Pages
1265-1278
ISSN
  • 0892-6638 (ISSN-L)
  • 1530-6860
OpenAlex
W1939081758
Cited by
503
References
114
FWCI
10.71
Type
journal article
Language
en
Open access
closed
Funders
  • National Research Council
  • Human Frontier Science Program

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CoChat. (2026). Citation check: Lysosome‐related organelles. https://app.cochat.ai/papers/10.1096/fasebj.14.10.1265
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Dell'Angelica, E. C., Mullins, C., Caplan, S., & Bonifacino, J. S. (2000). Lysosome‐related organelles. The FASEB Journal. https://doi.org/10.1096/fasebj.14.10.1265

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

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