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12篇 您的检索式:作者名="Kushner JD"
    题名 作者 年代 出处 被引量
1Cardiac magnetic resonance imaging of myocardial contrast uptake and blood flow in patients affected with idiopathic or familial dilated cardiomyopathy 显示文摘Jerosch-Herold M Sheridan DC Kushner JD 2008Am J Physiol Heart Circ Physiol2008,295,3:1
2Lamin A/C mutationanalysis in a cohort of 324 unrelated patients with idiopathic orfamilial dilated cardiomyopathy 显示文摘Parks SB Kushner JD Nauman D 2008Am Heart J2008,156,:1
3Biosynthesis of heme in mammals显示文摘Ajioka RS Phillips JD Kushner JP 2006Biochim Biophys Acta2006,1763,7:1
4Cardiac magnetic resonance imaging of myocardial contrast uptake and blood flow in patients affected with id- iopathic or familial dilated cardiomyopathy显示文摘Jerosch-Herold M Sheridan DC Kushner JD 2008Am J Physiol Heart Circ Physi- o12008,295,3:1
5The nuclear hormone receptor gene superfamily显示文摘Ribeiro RC Kushner PJ Baxter JD 1995Annu Rev Med1995,46,:1
6Car- diac magnetic resonance imaging of myocardial contrast uptake and blood flow in patients affected with idiopathic or familial dilated cardiomyopathy 显示文摘Jeroseh-Herold M Sheridan DC Kushner JD 2008Am J Physiol Heart Circ Physiol2008,295,3:1
7Lamin A/C mutation analysis in a cohort of 324 unrelated patients with idiopathic or familial dilated cardiomyopathy显示文摘Parks SB Kushner JD Nauman D 2008Am Heart J2008,156,1:1
8Hormone - dependent coacfivator binding to a hydrophobie deft on nuclear receptors显示文摘Feng W Ribeiro RC Wanger RL Nguyen H Apriletti JW Fletterick RJ Baxter JD Kushner PJ West BL 1998 1998Science1998,280,5370:1
9Coding sequence mutations identified in MYH7,TNNT2,SCN5A,CSRP3,LBD3,and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy显示文摘Hershberger RE Parks SB Kushner JD 0,,:1
10Characterization and crystallization of human uroporphyrinogen decarboxylase 显示文摘Phillips JD Whithy FG Kushner JP 1997Protein Sci1997,6,6:1
11Structural Basis for Tetrapyrrole Coordination by Uroporphyrinogen Decarboxylase显示文摘PHILLPS JD WHITBY F G KUSHNER J P 2003EMBO J2003,22,:1
12Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy显示文摘Hershberger RE Parks SB Kushner JD 2008Clin Transl Sci2008,1,1:1
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