| 1 | ADRB3, APOA1
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| β3-Adrenergic receptor regulates hepatic apolipoprotein A-I gene expression.
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| Cao X, Li Y.
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| J Clin Lipidol 11(5):1168-1176. doi: 10.1016/j.jacl.2017.07.007. Epub 2017 Jul 27.
2017
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| 2 | APOA1, APOM
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| Increased mRNA levels of apolipoprotein M and apolipoprotein AI in the placental tissues with fetal macrosomia.
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| Yu Y, Luo GH, Zhang J, Jiang H, Wei J, Shi YP, Zhang XY, Xu N.
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| Arch Gynecol Obstet 291(2):299-303. doi: 10.1007/s00404-014-3441-z. Epub 2014 Sep 7.
2015
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| 3 | ABCA1, APOA1
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| ABCA1 and nascent HDL biogenesis.
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| Wang S, Smith JD.
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| Biofactors 40(6):547-54. doi: 10.1002/biof.1187. Epub 2014 Oct 30. Review.
2014
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| 4 | APOA1, APOA2, APOB, APOC1, APOC2, APOC3, APOE, CLU
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| Apolipoprotein localization in isolated drusen and retinal apolipoprotein gene expression.
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| Li CM, Clark ME, Chimento MF, Curcio CA.
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| Invest Ophthalmol Vis Sci 47(7):3119-28. 2006
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| 5 | APOA1, APOA4, APOA5, APOC3, HLP5
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| Linkage and association between distinct variants of the APOA1/C3/A4/A5 gene cluster and familial combined hyperlipidemia.
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| Eichenbaum-Voline S, Olivier M, Jones EL, Naoumova RP, Jones B, Gau B, Patel HN, Seed M, Betteridge DJ, Galton DJ, Rubin EM, Scott J, Shoulders CC, Pennacchio LA.
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| Arterioscler Thromb Vasc Biol 24(1):167-74. Epub 2003 Oct 09. 2004
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| 6 | APOA1
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| A novel apoA-I mutation (L178P) leads to endothelial dysfunction, increased arterial wall thickness, and premature coronary artery disease.
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| Hovingh GK, Brownlie A, Bisoendial RJ, Dube MP, Levels JH, Petersen W, Dullaart RP, Stroes ES, Zwinderman AH, de Groot E, Hayden MR, Kuivenhoven JA, Kastelein JJ.
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| J Am Coll Cardiol 44(7):1429-35. 2004
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| 7 | APOA1, HDLD2
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| Recurrent mutations of the apolipoprotein A-I gene in three kindreds with severe HDL deficiency.
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| Pisciotta L, Miccoli R, Cantafora A, Calabresi L, Tarugi P, Alessandrini P, Bittolo Bon G, Franceschini G, Cortese C, Calandra S, Bertolini S.
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| Atherosclerosis 167(2):335-45. 2003
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| 8 | APOA1, NNHA
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| Hereditary systemic amyloidosis with renal involvement.
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| Hawkins PN.
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| J Nephrol 16(3):443-8. Review.
2003
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| 9 | APOA1, NNHA
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| Misdiagnosis of hereditary amyloidosis as AL (primary) amyloidosis.
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| Lachmann HJ, Booth DR, Booth SE, Bybee A, Gilbertson JA, Gillmore JD, Pepys MB, Hawkins PN.
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| N Engl J Med 346(23):1786-91. 2002
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| 10 | APOA1, LAMP2, MEAX, NNHA
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| The new apolipoprotein A-I variant leu(174) --> Ser causes hereditary cardiac amyloidosis, and the amyloid fibrils are constituted by the 93-residue N-terminal polypeptide.
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| Obici L, Bellotti V, Mangione P, Stoppini M, Arbustini E, Verga L, Zorzoli I, Anesi E, Zanotti G, Campana C, Viganò M, Merlini G.
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| Am J Pathol 155(3):695-702. 1999
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| 11 | APOA1, CCLD
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| A novel homozygous missense mutation in the apo A-I gene with apo A-I deficiency.
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| Huang W, Sasaki J, Matsunaga A, Nanimatsu H, Moriyama K, Han H, Kugi M, Koga T, Yamaguchi K, Arakawa K.
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| Arterioscler Thromb Vasc Biol 18(3):389-96.
1998
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| 12 | APOA1, NNHA
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| Hereditary hepatic and systemic amyloidosis caused by a new deletion/insertion mutation in the apolipoprotein AI gene.
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| Booth DR, Tan SY, Booth SE, Tennent GA, Hutchinson WL, Hsuan JJ, Totty NF, Truong O, Soutar AK, Hawkins PN, Bruguera M, Caballería J, Solé M, Campistol JM, Pepys MB.
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| J Clin Invest 97(12):2714-21. 1996
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