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Assessment of the expression of candidate human plasma membrane phospholipid scramblase in Scott syndrome cells.

Thrombosis and haemostasis - 1 Feb 1999

Janel N, Leroy C, Laude I, Toti F, Fressinaud E, Meyer D, Freyssinet J M, Kerbiriou-Nabias D

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Biological Transport
Blood Coagulation Disorders
Cell Membrane
Genes, Recessive
Membrane Lipids
Phosphatidylserines
Phospholipid Transfer Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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PMID: 10064019

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Assessment of the expression of candidate human plasma membrane phospholipid scramblase in Scott syndrome cells.PMID 10064019Read ↗

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Platelet membrane phospholipid asymmetry: from the characterization of a scramblase activity to the identification of an essential protein mutated in Scott syndrome.Semantic proximity Read ↗

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Molecular insights into human phosphatidylserine synthase 1 reveal its inhibition promotes LDL uptakeSemantic proximity Read ↗

The C-terminal transmembrane domain of human phospholipid scramblase 1 is essential for the protein flip-flop activity and Ca²⁺-binding.Semantic proximity Read ↗

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SPG5 siblings with different phenotypes showing reduction of 27-hydroxycholesterol after simvastatin-ezetimibe treatment.Semantic proximity Read ↗

Scott syndrome, characterized by impaired transmembrane migration of procoagulant phosphatidylserine and hemorrhagic complications, is an inherited disorderSemantic proximity Read ↗

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