Molecular species of lecithin in familial lecithin cholesterol acyltransferase lcat deficiency
Subbaiah, P.V.; Pritchard, P.H.; Bagdade, J.D.
Arteriosclerosis 8(5): 582A
1988
ISSN/ISBN: 0276-5047 Accession: 028736712
Full Text Article emailed within 1 workday: $29.90
Related References
Guerin, M.; Dachet, C.; Goulinet, S.; Chevet, D.; Dolphin, P.J.; Chapman, M.J.; Rouis, M. 1997: Familial lecithin:cholesterol acyltransferase deficiency: molecular analysis of a compound heterozygote: LCAT (Arg147 --> Trp) and LCAT (Tyr171 --> Stop) Atherosclerosis 131(1): 85-95Banerji, B.; Subbaiah, P.V.; Bagdade, J.D.; Gregg, R.E. 1988: Molecular species of lecithin in abetalipoproteinemia abl influence of lecithin cholesterol acyltransferase lcat and lysolecithin acyltransferase lat FASEB Journal 2(5): Abstract 4320
Bujo, H.; Kusunoki, J.; Ogasawara, M.; Yamamoto, T.; Ohta, Y.; Shimada, T.; Saito, Y.; Yoshida, S. 1991: Molecular defect in familial lecithin:cholesterol acyltransferase (LCAT) deficiency: a single nucleotide insertion in LCAT gene causes a complete deficient type of the disease Biochemical and Biophysical Research Communications 181(3): 933-940
Funke, H.; Von Eckardstein, A.; Pritchard, P.H.; Hayden, M.R.; Albers, J.J.; Jacotot, B.; Gerdes, U.; Assmann, G. 1990: Identification of several molecular defects responsible for familial lecithin cholesterol acyltransferase lcat deficiency Circulation 82(4 Suppl 3): III426
Bujo, H.; Saito, Y. 1995: Lecithin: cholesterol acyltransferase (LCAT)--the genetic analysis of familial LCAT deficiency and fish eye disease Nihon Rinsho. Japanese Journal of Clinical Medicine 53(5): 1260-1266
Godin, D.V.; Frohlich, J. 1981: Erythrocyte alterations in praseodymium-induced lecithin:cholesterol acyltransferase (LCAT) deficiency in the rat: comparison with familial LCAT deficiency in man Research Communications in Chemical Pathology and Pharmacology 31(3): 555-566
Bender, B.U.; Quaschning, T.; Neumann, H.P.H.; Schmidt, D.; Kraemer-Guth, A. 2007: A novel frameshift mutation of the lecithin:cholesterol acyltransferase (LCAT) gene associated with renal failure in familial LCAT deficiency Clinical Chemistry and Laboratory Medicine 45(4): 483-486
Park, C.W.; Lim, M.-H.; Youn, D.-Y.; Jung, S.E.; Chung, S.; Ahn, Y.S.; Chang, Y.S.; Lee, J.-H. 2009: Two novel frame shift mutations in lecithin:cholesterol acyltransferase (LCAT) gene associated with a familial LCAT deficiency phenotype Atherosclerosis 206(2): 346-348
Idzior-Waluś, B.; Sieradzki, J.; Kostner, G.; Małecki, M.T.; Klupa, T.; Wesołowska, T.; Rostworowski, W.; Hartwich, J.; Waluś, M.łg.; Kieć, A.D.ńs.; Naruszewicz, M. 2006: Familial lecithin-cholesterol acyltransferase deficiency: biochemical characteristics and molecular analysis of a new LCAT mutation in a Polish family Atherosclerosis 185(2): 413-420
Takata, K.; Kajiyama, G.; Horiuchi, I.; Watanabe, T.; Tokumo, H.; Hirata, Y. 1989: A new case of familial lecithin: cholesterol acyltransferase (LCAT) deficiency--paradoxical findings regarding LCAT mass and activity in 23 members of a family Japanese Journal of Medicine 28(6): 765-771
Gjone, E. 1982: Familial lecithin cholesterol acyltransferase (LCAT) deficiency Birth Defects Original Article Series 18(6): 423-431
Takahashi, S. 2007: Familial lecithin-cholesterol acyltransferase (LCAT) deficiency Nihon Rinsho. Japanese Journal of Clinical Medicine 65(Suppl 7): 614-617
Dorval, I.; Jezequel, P.; Dubourg, C.; Chauvel, B.; Le Pogamp, P.; Le Gall, J.Y. 1994: Identification of the homozygous missense mutation in the lecithin:cholesterol-acyltransferase (LCAT) gene, causing LCAT familial deficiency in two French patients Atherosclerosis 105(2): 251-252
Frohlich, J.; Hon, K.; McLeod, R. 1982: Detection of heterozygotes for familial lecithin: cholesterol acyltransferase (LCAT) deficiency American Journal of Human Genetics 34(1): 65-72
Teisberg, P.; Gjone, E. 1981: Genetic heterogeneity in familial lecithin:cholesterol acyltransferase (LCAT) deficiency Acta Medica Scandinavica 210(1-2): 1-2
Althaf, M.M.; Almana, H.; Abdelfadiel, A.; Amer, S.M.; Al-Hussain, T.O. 2015: Familial lecithin-cholesterol acyltransferase (LCAT) deficiency; a differential of proteinuria Journal of Nephropathology 4(1): 25-28
Moriyama, K.; Sasaki, J.; Arakawa, F.; Takami, N.; Maeda, E.; Matsunaga, A.; Takada, Y.; Midorikawa, K.; Yanase, T.; Yoshino, G. 1995: Two novel point mutations in the lecithin:cholesterol acyltransferase (LCAT) gene resulting in LCAT deficiency: LCAT (G873 deletion) and LCAT (Gly344-->Ser) Journal of Lipid Research 36(11): 2329-2343
Klein, H.G.; Lohse, P.; Duverger, N.; Albers, J.J.; Rader, D.J.; Zech, L.A.; Santamarina-Fojo, S.; Brewer, H.B. 1993: Two different allelic mutations in the lecithin:cholesterol acyltransferase (LCAT) gene resulting in classic LCAT deficiency: LCAT (tyr83-->stop) and LCAT (tyr156-->asn) Journal of Lipid Research 34(1): 49-58
Hosooka, T.; Yaso, S.; Maeda, E.; Kasuga, M. 1999: Familial lecithin : Cholesterol acyltransferase (LCAT) deficiency with impaired glucose tolerance Journal of the Japan Diabetes Society 42(2): 157-161
Sakuma, M.; Akanuma, Y.; Kodama, T.; Yamada, N.; Murata, S.; Murase, T.; Itakura, H.; Kosaka, K. 1982: Familial plasma lecithin: cholesterol acyltransferase deficiency. a new family with partial LCAT activity Acta Medica Scandinavica 212(4): 225-232