| 1 | AGPAT1, AGPAT2, AGPAT3, AGPAT4, AGPAT5, AGPAT6, AGPAT9, LPCAT4
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| Membrane topology of human AGPAT3 (LPAAT3).
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| Schmidt JA, Yvone GM, Brown WJ.
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| Biochem Biophys Res Commun 397(4):661-7. Epub 2010 Jun 9. 2010
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| 2 | AGPAT1, AGPAT2
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| A role for 1-acylglycerol-3-phosphate-O-acyltransferase-1 in myoblast differentiation.
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| Subauste AR, Elliott B, Das AK, Burant CF.
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| Differentiation 80(2-3):140-6. Epub 2010 Jun 19.PMID: 20561744 2010
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| 3 | AGPAT2, BSCL1, BSCL2, BSCL3, CAV1
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| Novel subtype of congenital generalized lipodystrophy associated with muscular weakness and cervical spine instability.
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| Simha V, Agarwal AK, Aronin PA, Iannaccone ST, Garg A.
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| Am J Med Genet A 146A(18):2318-26.
2008
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| 4 | AGPAT1, AGPAT2, AGPAT3
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| Activation of cytosolic phospholipase A2 and fatty acid transacylase is essential but not sufficient for thrombin-induced smooth muscle cell proliferation.
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| Gluck N, Schwob O, Krimsky M, Yedgar S.
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| Am J Physiol Cell Physiol 294(6):C1597-603. Epub 2008 Apr 2.PMID: 18385289 2008
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| 5 | AGPAT1, AGPAT2, AGPAT3, AGPAT4, AGPAT5, AGPAT6
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| Cloning and characterization of murine 1-acyl-sn-glycerol 3-phosphate acyltransferases and their regulation by PPARalpha in murine heart.
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| Lu B, Jiang YJ, Zhou Y, Xu FY, Hatch GM, Choy PC.
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| Biochem J 385(Pt 2):469-77. 2005
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| 6 | BSCL1, BSCL2, AGPAT2
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| Phenotypic heterogeneity in biochemical parameters correlates with mutations in AGPAT2 or Seipin genes among Berardinelli-Seip congenital lipodystrophy patients.
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| Gomes KB, Pardini VC, Ferreira AC, Fernandes AP.
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| J Inherit Metab Dis 28(6):1123-31. 2005
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| 7 | AGPAT1, AGPAT2, AGPAT3
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| Expression and regulation of 1-acyl-sn-glycerol- 3-phosphate acyltransferases in the epidermis.
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| Lu B, Jiang YJ, Man MQ, Brown B, Elias PM, Feingold KR.
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| J Lipid Res 46(11):2448-57. Epub 2005 Sep 8.PMID: 16150824 2005
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| 8 | BSCL1, BSCL2, AGPAT2
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| Mutations in the seipin and AGPAT2 genes clustering in consanguineous families with Berardinelli-Seip congenital lipodystrophy from two separate geographical regions of Brazil.
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| Gomes KB, Fernandes AP, Ferreira AC, Pardini H, Garg A, Magre J, Pardini VC.
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| J Clin Endocrinol Metab 89(1):357-61. 2004
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| 9 | BSCL2, BSCL1, AGPAT2
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| Mutations in Gng3lg and AGPAT2 in Berardinelli-Seip congenital lipodystrophy and Brunzell syndrome: phenotype variability suggests important modifier effects.
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| Fu M, Kazlauskaite R, Baracho Mde F, Santos MG, Brandao-Neto J, Villares S, Celi FS, Wajchenberg BL, Shuldiner AR.
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| J Clin Endocrinol Metab 89(6):2916-22. 2004
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| 10 | AGPAT2, BSCL1
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| Prevalence of mutations in AGPAT2 among human lipodystrophies.
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| Magre J, Delepine M, Van Maldergem L, Robert JJ, Maassen JA, Meier M, Panz VR, Kim CA, Tubiana-Rufi N, Czernichow P, Seemanova E, Buchanan CR, Lacombe D, Vigouroux C, Lascols O, Kahn CR, Capeau J, Lathrop M.
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| Diabetes 52(6):1573-8. 2003
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| 11 | AGPAT2, BSCL1
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| AGPAT2 is mutated in congenital generalized lipodystrophy linked to chromosome 9q34.
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| Agarwal AK, Arioglu E, De Almeida S, Akkoc N, Taylor SI, Bowcock AM, Barnes RI, Garg A.
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| Nat Genet 31(1):21-3. 2002
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| 12 | AGPAT2
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| Human lysophosphatidic acid acyltransferase. cDNA cloning, expression, and localization to chromosome 9q34.3.
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| Eberhardt C, Gray PW, Tjoelker LW.
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| J Biol Chem 272(32):20299-305. 1997
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| 13 | AGPAT1, AGPAT2
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| Cloning and expression of two human lysophosphatidic acid acyltransferase cDNAs that enhance cytokine-induced signaling responses in cells.
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| West J, et al.
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| DNA Cell Biol 16 : 691-701. 1997
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