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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

107 related items for PubMed ID: 17596203

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  • 2. Identification of a novel PROS1 c.1113T-->GG frameshift mutation in a family with mixed type I/type III protein S deficiency.
    ten Kate MK, Mulder R, Platteel M, Brouwer JL, van der Steege G, van der Meer J.
    Haematologica; 2006 Aug; 91(8):1151-2. PubMed ID: 16885060
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  • 7. p53-dependent repression of the human MCL-1 gene encoding an anti-apoptotic member of the BCL-2 family: the role of Sp1 and of basic transcription factor binding sites in the MCL-1 promoter.
    Pietrzak M, Puzianowska-Kuznicka M.
    Biol Chem; 2008 Apr; 389(4):383-93. PubMed ID: 18208354
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  • 8. First case of sporadic protein S deficiency due to a novel candidate mutation, Ala 484-->Pro, in the protein S active gene (PROS1).
    Borgel D, Jude B, Aiach M, Gandrille S.
    Thromb Haemost; 1996 Jun; 75(6):883-6. PubMed ID: 8822580
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  • 9. Influence of PROS1 gene mutations affecting protein S amino-acid 275 on plasma free protein S measurement.
    Alhenc Gelas M, Juin F, de Raucourt E, Gandrille S, Borgel D, Aiach M.
    Thromb Haemost; 2007 Apr; 97(4):678-80. PubMed ID: 17393035
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  • 12. Synergistic activation of the human adrenomedullin gene promoter by Sp1 and AP-2alpha.
    Zhang Y, Li Y, Shibahara S, Takahashi K.
    Peptides; 2008 Mar; 29(3):465-72. PubMed ID: 17719138
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  • 18. First case of protein S deficiency due to a translocation t(3;21)(q11.2;q22).
    Hurtado B, Nadal M, Margarit E, Sánchez A, Abasolo N, García N, Doménech P, Sala N.
    Thromb Haemost; 2009 May; 101(5):977-9. PubMed ID: 19404554
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  • 20. Heterozygous missense protein S mutation in a young boy with incomplete tetraplegia.
    Mauz-Koerholz C, Müller T, Kunze C, Schneppenheim R, Bernstaedt M, Koerholz D.
    Klin Padiatr; 2009 May; 221(3):180. PubMed ID: 19437370
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