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Results: 7

Cited In for PubMed (Select 2828430)

1.

Interactions between α-tocopherol, polyunsaturated fatty acids, and lipoxygenases during embryogenesis.

Lebold KM, Traber MG.

Free Radic Biol Med. 2014 Jan;66:13-9. doi: 10.1016/j.freeradbiomed.2013.07.039. Epub 2013 Aug 3. Review.

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 Jr.

J Clin Invest. 1988 Nov;82(5):1489-94.

3.

Genetic evidence from two families that the apolipoprotein B gene is not involved in abetalipoproteinemia.

Talmud PJ, Lloyd JK, Muller DP, Collins DR, Scott J, Humphries S.

J Clin Invest. 1988 Nov;82(5):1803-6.

4.

Inference of a molecular defect of apolipoprotein B in hypobetalipoproteinemia by linkage analysis in a large kindred.

Leppert M, Breslow JL, Wu L, Hasstedt S, O'Connell P, Lathrop M, Williams RR, White R, Lalouel JM.

J Clin Invest. 1988 Sep;82(3):847-51.

5.

Truncated variants of apolipoprotein B cause hypobetalipoproteinaemia.

Collins DR, Knott TJ, Pease RJ, Powell LM, Wallis SC, Robertson S, Pullinger CR, Milne RW, Marcel YL, Humphries SE, et al.

Nucleic Acids Res. 1988 Sep 12;16(17):8361-75.

7.

Liver fibrosis in a patient with familial homozygous hypobetalipoproteinaemia: possible role of vitamin supplementation.

Scoazec JY, Bouma ME, Roche JF, Blache D, Verthier N, Feldmann G, Gay G.

Gut. 1992 Mar;33(3):414-7.

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