Regulation of intracellular ceramide content in B16 melanoma cells. Biological implications of ceramide glycosylation (Q74620451)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10085144%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

title

Regulation of intracellular ceramide content in B16 melanoma cells. Biological implications of ceramide glycosylation (English)

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12 November 2019

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H Komori

1

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12 November 2019

S Ichikawa

series ordinal

2

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12 November 2019

Y Hirabayashi

series ordinal

3

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12 November 2019

M Ito

series ordinal

4

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12 November 2019

language of work or name

English

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publication date

1 March 1999

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Journal of Biological Chemistry

12 November 2019

published in

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12 November 2019

volume

274

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12 November 2019

issue

13

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12 November 2019

page(s)

8981-8987

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Glycosphingolipids in cellular interaction, differentiation, and oncogenesis

12 November 2019

cites work

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Animal glycosphingolipids as membrane attachment sites for bacteria

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GM3-enriched Microdomain Involved in Cell Adhesion and Signal Transduction through Carbohydrate-Carbohydrate Interaction in Mouse Melanoma B16 Cells

21 January 2018

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Functions of ceramide in coordinating cellular responses to stress

21 January 2018

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TNF receptor death domain-associated proteins TRADD and FADD signal activation of acid sphingomyelinase

21 January 2018

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Ceramide synthase mediates daunorubicin-induced apoptosis: An alternative mechanism for generating death signals

21 January 2018

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Specific hydrolysis of intact erythrocyte cell-surface glycosphingolipids by endoglycoceramidase. Lack of modulation of erythrocyte glucose transporter by endogenous glycosphingolipids

21 January 2018

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The hydrolysis of cell surface glycosphingolipids by endoglycoceramidase reduces epidermal growth factor receptor phosphorylation in A431 cells

21 January 2018

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Homeostasis of cell-surface glycosphingolipid content in B16 melanoma cells. Evidence revealed by an endoglycoceramidase

21 January 2018

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A mouse B16 melanoma mutant deficient in glycolipids

21 January 2018

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Conversion of short‐chain ceramides to short‐chain ceramide GM3 in B16 melanoma cells

21 January 2018

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Clear differences in ceramide metabolism between glycosphingolipids and sphingomyelin in a human promyelocytic leukemia cell line HL‐60 stimulated by a differentiation inducer

21 January 2018

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Coomassie brilliant blue staining of lipids on thin-layer plates

21 January 2018

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Cytokine response modifier A (CrmA) inhibits ceramide formation in response to tumor necrosis factor (TNF)-alpha: CrmA and Bcl-2 target distinct components in the apoptotic pathway

21 January 2018

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Expression cloning of a cDNA for human ceramide glucosyltransferase that catalyzes the first glycosylation step of glycosphingolipid synthesis

21 January 2018

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The phosphorylcholine acceptor in the phosphatidylcholine: ceramide cholinephosphotransferase reaction is the enzyme a transferase or a hydrolase?

21 January 2018

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Complete removal of sphingolipids from the plasma membrane disrupts cell to substratum adhesion of mouse melanoma cells

21 January 2018

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Expression of neutral sphingomyelinase identifies a distinct pool of sphingomyelin involved in apoptosis.

21 January 2018

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Suppression of ceramide-mediated programmed cell death by sphingosine-1-phosphate

21 January 2018

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Sphingomyelin synthase, a potential regulator of intracellular levels of ceramide and diacylglycerol during SV40 transformation. Does sphingomyelin synthase account for the putative phosphatidylcholine-specific phospholipase C?

21 January 2018

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Decreased synthesis of glycosphingolipids in cells lacking vimentin intermediate filaments.

21 January 2018

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Glucosylceramide is synthesized at the cytosolic surface of various Golgi subfractions

21 January 2018

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Dihydroceramide biology. Structure-specific metabolism and intracellular localization

21 January 2018

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Ceramide transport from endoplasmic reticulum to Golgi apparatus is not vesicle-mediated

21 January 2018

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Accumulation of glucosylceramides in multidrug-resistant cancer cells

21 January 2018

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Agents that reverse multidrug resistance, tamoxifen, verapamil, and cyclosporin A, block glycosphingolipid metabolism by inhibiting ceramide glycosylation in human cancer cells

21 January 2018

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21 January 2018

Identifiers

DOI

10.1074/JBC.274.13.8981

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10085144%20AND%20SRC:MED&resulttype=core&format=json

12 November 2019

1 reference