Citations for
1PLA2G7
Identification of a domain that mediates association of platelet-activating factor acetylhydrolase with high density lipoprotein.
Gardner AA, Reichert EC, Topham MK, Stafforini DM.
J Biol Chem 283(25):17099-106. Epub 2008 Apr 22. 2008
2PLA2G7
Comprehensive genetic analysis of the platelet activating factor acetylhydrolase (PLA2G7) gene and cardiovascular disease in case-control and family datasets.
Sutton BS, Crosslin DR, Shah SH, Nelson SC, Bassil A, Hale AB, Haynes C, Goldschmidt-Clermont PJ, Vance JM, Seo D, Kraus WE, Gregory SG, Hauser ER.
Hum Mol Genet 17(9):1318-28. Epub 2008 Jan 18. 2008
3PTAFR, PLA2G7
Platelet-activating factor-acetylhydrolase and PAF-receptor gene haplotypes in relation to future cardiovascular event in patients with coronary artery disease.
Ninio E, Tregouet D, Carrier JL, Stengel D, Bickel C, Perret C, Rupprecht HJ, Cambien F, Blankenberg S, Tiret L.
Hum Mol Genet 13(13):1341-51. Epub 2004 Apr 28. 2004
4PLA2G7
Functional impairment of two novel mutations detected in lipoprotein-associated phospholipase A2 (Lp-PLA2) deficiency patients.
Ishihara M, Iwasaki T, Nagano M, Ishii J, Takano M, Kujiraoka T, Tsuji M, Hattori H, Emi M.
J Hum Genet 49(6):302-7. Epub 2004 May 18. 2004
5PLA2G7
Molecular characterization of the constitutive expression of the plasma platelet-activating factor acetylhydrolase gene in macrophages.
Wu X, McIntyre TM, Zimmerman GA, Prescott SM, Stafforini DM.
Biochem J 375(Pt 2):351-63. 2003
6PLA2G7
The Ile198Thr and Ala379Val variants of plasmatic PAF-acetylhydrolase impair catalytical activities and are associated with atopy and asthma.
Kruse S, Mao XQ, Heinzmann A, Blattmann S, Roberts MH, Braun S, Gao PS, Forster J, Kuehr J, Hopkin JM, Shirakawa T, Deichmann KA.
Am J Hum Genet 66(5):1522-30. 2000
7LIS1, PAFAH1B1, PLA2G7
LIS1 is a microtubule-associated phosphoprotein.
Sapir T, Cahana A, Seger R, Nekhai S, Reiner O.
Eur J Biochem 265(1):181-8 1999
8PLA2G7
Plasma platelet-activating factor acetylhydrolase deficiency in Japanese patients with asthma.
Satoh N, Asano K, Naoki K, Fukunaga K, Iwata M, Kanazawa M, Yamaguchi K.
Am J Respir Crit Care Med 159(3):974-9. 1999
9PLA2G7
Deficiency of platelet-activating factor acetylhydrolase is a severity factor for asthma.
Stafforini DM, Numao T, Tsodikov A, Vaitkus D, Fukuda T, Watanabe N, Fueki N, McIntyre TM, Zimmerman GA, Makino S, Prescott SM.
J Clin Invest 103(7):989-97. 1999
10LIS1, PAFAH1B1, PLA2G7
Graded reduction of Pafah1b1 (Lis1) activity results in neuronal migration defects and early embryonic lethality.
Hirotsune, S.; Fleck, M. W.; Gambello, M. J.; Bix, G. J.; Chen, A.; Clark, G. D.; Ledbetter, D. H.; McBain, C. J.; Wynshaw-Boris, A
Nat Genet 19 : 333-339. 1998
11LIS1, MDS, PLA2G7
Alteration of the LIS1 gene in Japanese patients with isolated lissencephaly sequence of Miller-Dieker syndrome.
Sakamoto M, et al.
Hum Genet 103 : 586-589. 1998
12DCX, PLA2G7
LIS1 and XLIS (DCX) mutations cause most classical lissencephaly, but different patterns of malformation.
Pilz DT, et al.
Hum Mol Genet 7 : 2029-2037. 1998
13PLA2G7
Association of a G994-->T missense mutation in the plasma platelet-activating factor acetylhydrolase gene with genetic susceptibility to nonfamilial dilated cardiomyopathy in Japanese.
Ichihara S, Yamada Y, Yokota M.
Circulation 98(18):1881-5. 1998
14PLA2G7
Identification of the G994--> T missense in exon 9 of the plasma platelet-activating factor acetylhydrolase gene as an independent risk factor for coronary artery disease in Japanese men.
Yamada Y, Ichihara S, Fujimura T, Yokota M.
Metabolism 47(2):177-81. 1998
15LIS1, MDS, PLA2G7
Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndrome.
Lo Nigro C, et al.
Hum Mol Genet 6 : 157-164. 1997
16LIS1, MDS, PLA2G7, YWHAE
A revision of the lissencephaly and Miller-Dieker syndrome critical regions in chromosome 17p13.3.
Chong SS, et al.
Hum Mol Genet 6 : 147-155. 1997
17PLA2G7
A mutation in plasma platelet-activating factor acetylhydrolase (Val279-->Phe) is a genetic risk factor for stroke.
Hiramoto M, et al.
Stroke 28(12):2417-20 1997
18PLA2G7
Loss of activity of plasma platelet-activating factor acetylhydrolase due to a novel Gln281-->Arg mutation.
Yamada Y, Yokota M.
Biochem Biophys Res Commun 236(3):772-5. 1997
19PLA2G7
Genetics reveals importance of platelet activating factor in asthma and possibly other inflammatory states.
Nadel JA.
J Clin Invest 97 : 2689-2690. 1996
20PLA2G7
Platelet-activating factor acetylhydrolase deficiency. A missense mutation near the active site of an anti-inflammatory phospholipase.
Stafforini DM, et al.
J Clin Invest 97 : 2784-2791. 1996
21PLA2G7
Purification, properties, sequencing, and cloning of a lipoprotein-associated, serine-dependent phospholipase involved in the oxidative modification of low-density lipoproteins.
Tew DG, et al.
Arterioscler Thromb Vasc Biol 16(4):591-9 1996
22PLA2G7
Anti-inflammatory properties of a platelet-activating factor acetylhydrolase.
Tjoelker LW, et al.
Nature 374(6522):549-53 1995
23LIS1, MDS, PLA2G7
Miller-Dieker lissencephaly gene encodes a subunit of brain platelet-activating factor acetylhydrolase.
Hattori M, et al.
Nature 370 : 216-218. 1994