Mammalian cell mutants of membrane phospholipid biogenesis (Q36914504)

17 August 2017

title

Mammalian cell mutants of membrane phospholipid biogenesis (English)

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17 August 2017

Nishjima M

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17 August 2017

Kuge O

series ordinal

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17 August 2017

Hanada K

series ordinal

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17 August 2017

publication date

1 August 1997

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17 August 2017

published in

Trends in Cell Biology

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17 August 2017

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17 August 2017

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17 August 2017

page(s)

324-329

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17 August 2017

cites work

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Activation of glycosylasparaginase. Formation of active N-terminal threonine by intramolecular autoproteolysis.

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Stimulation of CTP:phosphocholine cytidylyltransferase by free cholesterol loading of macrophages involves signaling through protein dephosphorylation

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Abortive infection with Sindbis virus of a Chinese hamster ovary cell mutant defective in phosphatidylserine and phosphatidylethanolamine biosynthesis

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Phospholipid binding by a synaptic vesicle protein homologous to the regulatory region of protein kinase C

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7 January 2021

Immunochemical identification of the pssA gene product as phosphatidylserine synthase I of Chinese hamster ovary cells

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7 January 2021

Post-translational processing of the phosphatidylserine decarboxylase gene product in Chinese hamster ovary cells

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7 January 2021

Restoration by a 35K membrane protein of peroxisome assembly in a peroxisome-deficient mammalian cell mutant

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Both sphingolipids and cholesterol participate in the detergent insolubility of alkaline phosphatase, a glycosylphosphatidylinositol-anchored protein, in mammalian membranes.

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A Chinese hamster ovary cell mutant defective in the non-endocytic uptake of fluorescent analogs of phosphatidylserine: isolation using a cytosol acidification protocol

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Homozygous disruption of the murine mdr2 P-glycoprotein gene leads to a complete absence of phospholipid from bile and to liver disease

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Identifiers

DOI

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17 August 2017

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