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A polymorphism in thrombospondin-1 associated with familial premature coronary heart disease causes a local change in conformation of the Ca2+-binding repeats.
J Biol Chem. 2003 Mar 14;278(11):8929-34. doi: 10.1074/jbc.m211185200.
J Biol Chem. 2003.
PMID: 12643280
Free article.
Interactions among the three structural motifs of the C-terminal region of human thrombospondin-2.
Misenheimer TM, Hannah BL, Annis DS, Mosher DF.
Misenheimer TM, et al. Among authors: hannah bl.
Biochemistry. 2003 May 6;42(17):5125-32. doi: 10.1021/bi026983p.
Biochemistry. 2003.
PMID: 12718556
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A polymorphism in thrombospondin-1 associated with familial premature coronary artery disease alters Ca2+ binding.
Hannah BL, Misenheimer TM, Pranghofer MM, Mosher DF.
Hannah BL, et al.
J Biol Chem. 2004 Dec 10;279(50):51915-22. doi: 10.1074/jbc.M409632200. Epub 2004 Sep 28.
J Biol Chem. 2004.
PMID: 15456750
Free article.
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Structure of the calcium-rich signature domain of human thrombospondin-2.
Carlson CB, Bernstein DA, Annis DS, Misenheimer TM, Hannah BL, Mosher DF, Keck JL.
Carlson CB, et al. Among authors: hannah bl.
Nat Struct Mol Biol. 2005 Oct;12(10):910-4. doi: 10.1038/nsmb997. Epub 2005 Sep 25.
Nat Struct Mol Biol. 2005.
PMID: 16186819
Free PMC article.
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