Exclusion of ABCA-1 as a candidate gene for canine Scott syndrome

[11] Impaired platelet activation in familial high density lipoprotein deficiency (Tangier disease) [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (32) : 34032 - 34037

[12] Transport of lipids from Golgi to plasma membrane is defective in Tangier disease patients and Abc1-deficient mice [J]. NATURE GENETICS, 2000, 24 (02) : 192 - 196

[13] COMPUTER-SIMULATION METHODS IN HUMAN LINKAGE ANALYSIS [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (11) : 4175 - 4178

[14] Molecular defects in the ABCA1 pathway affect platelet function [J]. PATHOPHYSIOLOGY OF HAEMOSTASIS AND THROMBOSIS, 2006, 35 (1-2) : 166 - 174

[15] Sims PJ, 2001, THROMB HAEMOSTASIS, V86, P266

[16] Scott syndrome, characterized by impaired transmembrane migration of procoagulant phosphatidylserine and hemorrhagic complications, is an inherited disorder [J]. BLOOD, 1996, 87 (04) : 1409 - 1415

[17] ISOLATED DEFICIENCY OF PLATELET PROCOAGULANT ACTIVITY [J]. AMERICAN JOURNAL OF MEDICINE, 1979, 67 (02) : 206 - 213

[18] ABCA1, from pathology to membrane function [J]. PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 2007, 453 (05): : 569 - 579

[19] Surface exposure of phosphatidylserine in pathological cells [J]. CELLULAR AND MOLECULAR LIFE SCIENCES, 2005, 62 (09) : 971 - 988

[11] Impaired platelet activation in familial high density lipoprotein deficiency (Tangier disease) [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2004, 279 (32) : 34032 - 34037

[12] Transport of lipids from Golgi to plasma membrane is defective in Tangier disease patients and Abc1-deficient mice [J]. NATURE GENETICS, 2000, 24 (02) : 192 - 196

[13] COMPUTER-SIMULATION METHODS IN HUMAN LINKAGE ANALYSIS [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (11) : 4175 - 4178

[14] Molecular defects in the ABCA1 pathway affect platelet function [J]. PATHOPHYSIOLOGY OF HAEMOSTASIS AND THROMBOSIS, 2006, 35 (1-2) : 166 - 174

[15] Sims PJ, 2001, THROMB HAEMOSTASIS, V86, P266

[16] Scott syndrome, characterized by impaired transmembrane migration of procoagulant phosphatidylserine and hemorrhagic complications, is an inherited disorder [J]. BLOOD, 1996, 87 (04) : 1409 - 1415

[17] ISOLATED DEFICIENCY OF PLATELET PROCOAGULANT ACTIVITY [J]. AMERICAN JOURNAL OF MEDICINE, 1979, 67 (02) : 206 - 213

[18] ABCA1, from pathology to membrane function [J]. PFLUGERS ARCHIV-EUROPEAN JOURNAL OF PHYSIOLOGY, 2007, 453 (05): : 569 - 579

[19] Surface exposure of phosphatidylserine in pathological cells [J]. CELLULAR AND MOLECULAR LIFE SCIENCES, 2005, 62 (09) : 971 - 988