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153 related items for PubMed ID: 9126659
1. A G+1 to C mutation in a donor splice site of intron 2 in the apolipoprotein (apo) C-II gene in a patient with apo C-II deficiency. A possible interaction between apo C-II deficiency and apo E4 in a severely hypertriglyceridemic patient. Okubo M, Hasegawa Y, Aoyama Y, Murase T. Atherosclerosis; 1997 Apr; 130(1-2):153-60. PubMed ID: 9126659 [Abstract] [Full Text] [Related]
2. Donor splice site mutation in the apolipoprotein (Apo) C-II gene (Apo C-IIHamburg) of a patient with Apo C-II deficiency. Fojo SS, Beisiegel U, Beil U, Higuchi K, Bojanovski M, Gregg RE, Greten H, Brewer HB. J Clin Invest; 1988 Nov; 82(5):1489-94. PubMed ID: 3263393 [Abstract] [Full Text] [Related]
3. A thymidine to cytosine substitution for codon 26 of exon 3 of apolipoprotein C-II gene in a patient with apolipoprotein C-II deficiency. Kuniyoshi A, Okamoto Y, Tamagawa T, Matsuyama Y, Fuku H. Intern Med; 1999 Feb; 38(2):140-4. PubMed ID: 10225669 [Abstract] [Full Text] [Related]
4. Apolipoprotein C-II deficiency syndrome due to apo C-IIHamburg: clinical and biochemical features and HphI restriction enzyme polymorphism. Beil FU, Fojo SS, Brewer HB, Greten H, Beisiegel U. Eur J Clin Invest; 1992 Feb; 22(2):88-95. PubMed ID: 1349286 [Abstract] [Full Text] [Related]
15. Apolipoprotein and lipoprotein concentrations in familial apolipoprotein C-II deficiency. Breckenridge WC, Alaupovic P, Cox DW, Little JA. Atherosclerosis; 1982 Aug; 44(2):223-35. PubMed ID: 7138621 [Abstract] [Full Text] [Related]
16. Interaction between variant apolipoproteins C-II and E that affects plasma lipoprotein concentrations. Hegele RA, Breckenridge WC, Cox DW, Maguire GF, Little JA, Connelly PW. Arterioscler Thromb; 1991 Aug; 11(5):1303-9. PubMed ID: 1911716 [Abstract] [Full Text] [Related]
17. Apoprotein C-III deficiency markedly stimulates triglyceride secretion in vivo: comparison with apoprotein E. Hirano T, Takahashi T, Saito S, Tajima H, Ebara T, Adachi M. Am J Physiol Endocrinol Metab; 2001 Oct; 281(4):E665-9. PubMed ID: 11551841 [Abstract] [Full Text] [Related]
18. Apo C-II deficiency type Bari. Capurso A, Resta F, Turturro F, Colacicco AM, Crecchio C, Pepe G. Eur J Epidemiol; 1992 May; 8 Suppl 1():64-70. PubMed ID: 1354624 [Abstract] [Full Text] [Related]
19. Association of apolipoprotein E gene polymorphism with ischemic stroke involving large-vessel disease and its relation to serum lipid levels. Saidi S, Slamia LB, Ammou SB, Mahjoub T, Almawi WY. J Stroke Cerebrovasc Dis; 2007 May; 16(4):160-6. PubMed ID: 17689412 [Abstract] [Full Text] [Related]
20. A deletion mutation in the ApoC-II gene (ApoC-II Nijmegen) of a patient with a deficiency of apolipoprotein C-II. Fojo SS, Stalenhoef AF, Marr K, Gregg RE, Ross RS, Brewer HB. J Biol Chem; 1988 Dec 05; 263(34):17913-6. PubMed ID: 3192518 [Abstract] [Full Text] [Related] Page: [Next] [New Search]