Exclusion of ABCA-1 as a candidate gene for canine Scott syndrome
Open Access
- 18 August 2008
- journal article
- Published by Wiley in Journal of Thrombosis and Haemostasis
- Vol. 6 (9) , 1608-1610
- https://doi.org/10.1111/j.1538-7836.2008.03068.x
Abstract
No abstract availableThis publication has 19 references indexed in Scilit:
- Calcium-Diacylglycerol Guanine Nucleotide Exchange Factor I gene mutations associated with loss of function in canine plateletsTranslational Research, 2007
- Molecular Defects in the ABCA1 Pathway Affect Platelet FunctionPathophysiology of Haemostasis and Thrombosis, 2006
- Flow Cytometric Measurement of Platelet-Leukocyte Aggregates: A Possible Target to Monitor Platelet Function?Seminars in Thrombosis and Hemostasis, 2005
- A novel missense mutation in ABCA1 results in altered protein trafficking and reduced phosphatidylserine translocation in a patient with Scott syndromeBlood, 2005
- Surface exposure of phosphatidylserine in pathological cellsCellular and Molecular Life Sciences, 2005
- Impaired Platelet Activation in Familial High Density Lipoprotein Deficiency (Tangier Disease)Published by Elsevier ,2004
- Chromosome-specific microsatellite multiplex sets for linkage studies in the domestic dogGenomics, 2004
- The ABCA1 Transporter Modulates Late Endocytic TraffickingJournal of Biological Chemistry, 2004
- Transport of lipids from Golgi to plasma membrane is defective in Tangier disease patients and Abc1-deficient miceNature Genetics, 2000
- Isolated deficiency of platelet procoagulant activityThe American Journal of Medicine, 1979