Similar articles for PMID: 1901417

Year	Number of Results
1978	1
1983	3
1984	7
1985	6
1986	12
1987	5
1988	6
1989	14
1990	23
1991	19
1992	8
1993	8
1994	12
1995	7
1996	3
1997	2
1998	1
2000	2
2001	3
2002	2
2003	3
2004	2
2005	3
2006	1
2007	1
2008	1
2009	1
2013	1
2015	2
2024	0

1

Apolipoprotein A-I deficiency due to a codon 84 nonsense mutation of the apolipoprotein A-I gene.

Matsunaga T, Hiasa Y, Yanagi H, Maeda T, Hattori N, Yamakawa K, Yamanouchi Y, Tanaka I, Obara T, Hamaguchi H. Matsunaga T, et al. Proc Natl Acad Sci U S A. 1991 Apr 1;88(7):2793-7. doi: 10.1073/pnas.88.7.2793. Proc Natl Acad Sci U S A. 1991. PMID: 1901417 Free PMC article.

2

Apolipoprotein A-I Q[-2]X causing isolated apolipoprotein A-I deficiency in a family with analphalipoproteinemia.

Ng DS, Leiter LA, Vezina C, Connelly PW, Hegele RA. Ng DS, et al. J Clin Invest. 1994 Jan;93(1):223-9. doi: 10.1172/JCI116949. J Clin Invest. 1994. PMID: 8282791 Free PMC article.

3

A new case of apoA-I deficiency showing codon 8 nonsense mutation of the apoA-I gene without evidence of coronary heart disease.

Takata K, Saku K, Ohta T, Takata M, Bai H, Jimi S, Liu R, Sato H, Kajiyama G, Arakawa K. Takata K, et al. Arterioscler Thromb Vasc Biol. 1995 Nov;15(11):1866-74. doi: 10.1161/01.atv.15.11.1866. Arterioscler Thromb Vasc Biol. 1995. PMID: 7583566

4

A mutation in the human apolipoprotein A-I gene. Dominant effect on the level and characteristics of plasma high density lipoproteins.

Deeb SS, Cheung MC, Peng RL, Wolf AC, Stern R, Albers JJ, Knopp RH. Deeb SS, et al. J Biol Chem. 1991 Jul 25;266(21):13654-60. J Biol Chem. 1991. PMID: 1906882 Free article.

5

Familial apolipoprotein A-I, C-III, and A-IV deficiency and premature atherosclerosis due to deletion of a gene complex on chromosome 11.

Ordovas JM, Cassidy DK, Civeira F, Bisgaier CL, Schaefer EJ. Ordovas JM, et al. J Biol Chem. 1989 Oct 5;264(28):16339-42. J Biol Chem. 1989. PMID: 2506176 Free article.

6

A polymorphism affecting apolipoprotein A-II translational efficiency determines high density lipoprotein size and composition.

Doolittle MH, LeBoeuf RC, Warden CH, Bee LM, Lusis AJ. Doolittle MH, et al. J Biol Chem. 1990 Sep 25;265(27):16380-8. J Biol Chem. 1990. PMID: 2118905 Free article.

7

The baboon gene for apolipoprotein A-I: characterization of a cDNA clone and identification of DNA polymorphisms for genetic studies of cholesterol metabolism.

Hixson JE, Borenstein S, Cox LA, Rainwater DL, VandeBerg JL. Hixson JE, et al. Gene. 1988 Dec 30;74(2):483-90. doi: 10.1016/0378-1119(88)90181-3. Gene. 1988. PMID: 2907746

8

High density lipoprotein deficiency with xanthomas. A defect in reverse cholesterol transport caused by a point mutation in the apolipoprotein A-I gene.

Lackner KJ, Dieplinger H, Nowicka G, Schmitz G. Lackner KJ, et al. J Clin Invest. 1993 Nov;92(5):2262-73. doi: 10.1172/JCI116830. J Clin Invest. 1993. PMID: 7693760 Free PMC article.

9

Familial apolipoprotein A-I and C-III deficiency, variant II.

Schaefer EJ, Ordovas JM, Law SW, Ghiselli G, Kashyap ML, Srivastava LS, Heaton WH, Albers JJ, Connor WE, Lindgren FT, et al. Schaefer EJ, et al. J Lipid Res. 1985 Sep;26(9):1089-101. J Lipid Res. 1985. PMID: 3934306 Free article.

10

Marked high density lipoprotein deficiency due to apolipoprotein A-I Tomioka (codon 138 deletion).

Wada M, Iso T, Asztalos BF, Takama N, Nakajima T, Seta Y, Kaneko K, Taniguchi Y, Kobayashi H, Nakajima K, Schaefer EJ, Kurabayashi M. Wada M, et al. Atherosclerosis. 2009 Nov;207(1):157-61. doi: 10.1016/j.atherosclerosis.2009.04.018. Epub 2009 Apr 24. Atherosclerosis. 2009. PMID: 19473658

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