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Journal Abstract Search
66 related items for PubMed ID: 10823288
21. Confirmation of inherited protein S deficiency by PROS1 mutational screening: Identification of three novel PROS1 mutations and haplotype analysis of p.Q279X recurrence. Hurtado B, Abasolo N, Domènech-Santasusana P, Fuentes-Prior P, García de Frutos P, Sala N. Thromb Haemost; 2008 Oct; 100(4):721-4. PubMed ID: 18841302 [No Abstract] [Full Text] [Related]
22. The effects of C161-->T polymorphisms in exon 6 of peroxisome proliferator-activated receptor-gamma gene on bone mineral metabolism and serum osteoprotegerin levels in healthy middle-aged women. Rhee EJ, Oh KW, Lee WY, Kim SY, Oh ES, Baek KH, Kang MI, Kim SW. Am J Obstet Gynecol; 2005 Apr; 192(4):1087-93. PubMed ID: 15846185 [Abstract] [Full Text] [Related]
23. An Sp1 binding site mutation of the PROS1 promoter in a patient with protein S deficiency. Sanda N, Fujimori Y, Kashiwagi T, Takagi A, Murate T, Mizutani E, Matsushita T, Naoe T, Kojima T. Br J Haematol; 2007 Sep; 138(5):663-5. PubMed ID: 17596203 [No Abstract] [Full Text] [Related]
24. The prevalence of, and molecular defects underlying, inherited protein S deficiency in the general population. Beauchamp NJ, Dykes AC, Parikh N, Campbell Tait R, Daly ME. Br J Haematol; 2004 Jun; 125(5):647-54. PubMed ID: 15147381 [Abstract] [Full Text] [Related]
32. A novel G-to-A mutation in the intron-N of the protein S gene leading to abnormal RNA splicing in a patient with protein S deficiency. D'Andrea G, Di Perna P, Brancaccio V, Faioni EM, Castaman G, Cibelli G, Di Minno G, Margaglione M, Protein S Italian Team. Haematologica; 2003 Apr; 88(4):459-64. PubMed ID: 12681974 [Abstract] [Full Text] [Related]
37. Protein S-K196E mutation as a genetic risk factor for deep vein thrombosis in Japanese patients. Kimura R, Honda S, Kawasaki T, Tsuji H, Madoiwa S, Sakata Y, Kojima T, Murata M, Nishigami K, Chiku M, Hayashi T, Kokubo Y, Okayama A, Tomoike H, Ikeda Y, Miyata T. Blood; 2006 Feb 15; 107(4):1737-8. PubMed ID: 16461766 [No Abstract] [Full Text] [Related]