Literature DB >> 18844827

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

M B Brooks, J L Catalfamo, K Etter, A Brisbin, C D Bustamante.   

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Year:  2008        PMID： 18844827      PMCID： PMC2766810          DOI： 10.1111/j.1538-7836.2008.03068.x

Source DB:  PubMed          Journal:  J Thromb Haemost        ISSN： 1538-7836            Impact factor:   5.824


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  19 in total

1.  Transport of lipids from golgi to plasma membrane is defective in tangier disease patients and Abc1-deficient mice.

Authors:  E Orsó; C Broccardo; W E Kaminski; A Böttcher; G Liebisch; W Drobnik; A Götz; O Chambenoit; W Diederich; T Langmann; T Spruss; M F Luciani; G Rothe; K J Lackner; G Chimini; G Schmitz
Journal:  Nat Genet       Date:  2000-02       Impact factor: 38.330

2.  Flow cytometric measurement of platelet-leukocyte aggregates: a possible target to monitor platelet function?

Authors:  Ute Klinkhardt; Sebastian Harder
Journal:  Semin Thromb Hemost       Date:  2005       Impact factor: 4.180

Review 3.  Molecular defects in the ABCA1 pathway affect platelet function.

Authors:  Gerd Schmitz; Christian M Schambeck
Journal:  Pathophysiol Haemost Thromb       Date:  2006

4.  Chromosome-specific microsatellite multiplex sets for linkage studies in the domestic dog.

Authors:  Leigh Anne Clark; Kate L Tsai; Jörg M Steiner; David A Williams; Trina Guerra; Elaine A Ostrander; Francis Galibert; Keith E Murphy
Journal:  Genomics       Date:  2004-09       Impact factor: 5.736

5.  Isolated deficiency of platelet procoagulant activity.

Authors:  H J Weiss; W J Vicic; B A Lages; J Rogers
Journal:  Am J Med       Date:  1979-08       Impact factor: 4.965

6.  Computer-simulation methods in human linkage analysis.

Authors:  J Ott
Journal:  Proc Natl Acad Sci U S A       Date:  1989-06       Impact factor: 11.205

7.  Rapid detection of hereditary and acquired platelet storage pool deficiency by flow cytometry.

Authors:  N Gordon; J Thom; C Cole; R Baker
Journal:  Br J Haematol       Date:  1995-01       Impact factor: 6.998

8.  The ABCA1 transporter modulates late endocytic trafficking: insights from the correction of the genetic defect in Tangier disease.

Authors:  Edward B Neufeld; John A Stonik; Stephen J Demosky; Catherine L Knapper; Christian A Combs; Adele Cooney; Marcella Comly; Nancy Dwyer; Joan Blanchette-Mackie; Alan T Remaley; Silvia Santamarina-Fojo; H Bryan Brewer
Journal:  J Biol Chem       Date:  2004-01-27       Impact factor: 5.157

9.  Scott syndrome, characterized by impaired transmembrane migration of procoagulant phosphatidylserine and hemorrhagic complications, is an inherited disorder.

Authors:  F Toti; N Satta; E Fressinaud; D Meyer; J M Freyssinet
Journal:  Blood       Date:  1996-02-15       Impact factor: 22.113

10.  Impaired platelet activation in familial high density lipoprotein deficiency (Tangier disease).

Authors:  Jerzy-Roch Nofer; Grazyna Herminghaus; Martin Brodde; Eberhard Morgenstern; Stephan Rust; Thomas Engel; Udo Seedorf; Gerd Assmann; Horst Bluethmann; Beate E Kehrel
Journal:  J Biol Chem       Date:  2004-05-25       Impact factor: 5.157
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