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2. 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. PubMed ID: 2903181 [Abstract] [Full Text] [Related]
6. Apolipoprotein B gene variants are involved in the determination of blood glucose and lipid levels in patients with non-insulin dependent diabetes mellitus. Duman BS, Oztürk M, Yilmazer S, Cağatay P, Hatemi H. Cell Biochem Funct; 2006 Nov; 24(3):261-7. PubMed ID: 16634094 [Abstract] [Full Text] [Related]
7. [Abetalipoproteinemia in a Polish family]. Kaciński M, Grzenda-Adamek Z, Miezyński W, Kaczmarski F, Miszczuk-Jamska B. Pediatr Pol; 1989 Nov; 64(8-9):551-8. PubMed ID: 2642215 [No Abstract] [Full Text] [Related]
13. [Effects of apolipoprotein A1 and B gene polymorphism on avascular necrosis of the femoral head in Chinese population]. Wang XY, Niu XH, Chen WH, Lin N, Song JN, Chen B, Jin H. Zhongguo Gu Shang; 2008 Feb; 21(2):99-102. PubMed ID: 19105467 [Abstract] [Full Text] [Related]
14. Using genetically engineered mice to understand apolipoprotein-B deficiency syndromes in humans. Raabe M, Kim E, Véniant M, Nielsen LB, Young SG. Proc Assoc Am Physicians; 1998 Feb; 110(6):521-30. PubMed ID: 9824535 [Abstract] [Full Text] [Related]
15. Abetalipoproteinemia is caused by defects of the gene encoding the 97 kDa subunit of a microsomal triglyceride transfer protein. Shoulders CC, Brett DJ, Bayliss JD, Narcisi TM, Jarmuz A, Grantham TT, Leoni PR, Bhattacharya S, Pease RJ, Cullen PM. Hum Mol Genet; 1993 Dec; 2(12):2109-16. PubMed ID: 8111381 [Abstract] [Full Text] [Related]
16. Abetalipoproteinemia in Israel: evidence for a founder mutation in the Ashkenazi Jewish population and a contiguous gene deletion in an Arab patient. Benayoun L, Granot E, Rizel L, Allon-Shalev S, Behar DM, Ben-Yosef T. Mol Genet Metab; 2007 Apr; 90(4):453-7. PubMed ID: 17275380 [Abstract] [Full Text] [Related]
17. Molecular genetic analysis of two functional candidate genes in the autosomal recessive retinitis pigmentosa, RP25, locus. Abd El-Aziz MM, El-Ashry MF, Barragan I, Marcos I, Borrego S, Antiñolo G, Bhattacharya SS. Curr Eye Res; 2005 Dec; 30(12):1081-7. PubMed ID: 16354621 [Abstract] [Full Text] [Related]
18. Clinical features and molecular genetics of two Tunisian families with abetalipoproteinemia. Hammer MB, El Euch-Fayache G, Nehdi H, Feki M, Maamouri-Hicheri W, Hentati F, Amouri R. J Clin Neurosci; 2014 Feb; 21(2):311-5. PubMed ID: 24139731 [Abstract] [Full Text] [Related]
19. Allele frequency distributions of Apo B VNTR locus in Cukurova, Turkey. Yalin E, Attila G, Yalin S, Aksoy K. Cell Biochem Funct; 2007 Feb; 25(6):665-8. PubMed ID: 16981218 [Abstract] [Full Text] [Related]