-
1
-
-
0027987314
-
Genetic heterogeneity of apolipoprotein E and its influence on plasma lipid and lipoprotein levels
-
DE KNIJFF P, VAN DEN MAAGDENBERG AMJM, FRANTS RR, HAVEKES LM: Genetic heterogeneity of apolipoprotein E and its influence on plasma lipid and lipoprotein levels. Hum Mutat 4: 178-194, 1994.
-
(1994)
Hum Mutat
, vol.4
, pp. 178-194
-
-
De Knijff, P.1
Van Den Maagdenberg, A.M.J.M.2
Frants, R.R.3
Havekes, L.M.4
-
2
-
-
0030068756
-
Apolipoprotein E2 (Arg136→Cys), a variant of apolipoprotein E associated with late-onset dominance of type III hyperlipoproteinaemia
-
FEUSSNER G, ALBANESE M, MANN WA, VALENCIA A, SCHUSTER H: Apolipoprotein E2 (Arg136→Cys), a variant of apolipoprotein E associated with late-onset dominance of type III hyperlipoproteinaemia. Eur J Clin Invest 26: 13-23, 1996.
-
(1996)
Eur J Clin Invest
, vol.26
, pp. 13-23
-
-
Feussner, G.1
Albanese, M.2
Mann, W.A.3
Valencia, A.4
Schuster, H.5
-
3
-
-
0031969628
-
Molecular basis of type III hyperlipoproteinemia in Germany
-
FEUSSNER G, FEUSSNER V, HOFFMAN MM, LOHRMANN J, WIELAND H, MARZ W: Molecular basis of type III hyperlipoproteinemia in Germany. Hum Mutat 11: 417-423, 1998.
-
(1998)
Hum Mutat
, vol.11
, pp. 417-423
-
-
Feussner, G.1
Feussner, V.2
Hoffman, M.M.3
Lohrmann, J.4
Wieland, H.5
Marz, W.6
-
4
-
-
0025257612
-
Restriction isotyping of human apolipoprotein E by gene amplification and cleavage with HhaI
-
HIXSON JE, VERNIER DT: Restriction isotyping of human apolipoprotein E by gene amplification and cleavage with HhaI. J Lipid Res 1: 545-548, 1990.
-
(1990)
J Lipid Res
, vol.1
, pp. 545-548
-
-
Hixson, J.E.1
Vernier, D.T.2
-
5
-
-
0034046051
-
Apolipoproteins and atherosclerosis. Apolipoprotein E and apolipoprotein (a) as candidate genes of premature development of atherosclerosis
-
HOŘEJŠÍ B, ČEŠKA R: Apolipoproteins and atherosclerosis. Apolipoprotein E and apolipoprotein (a) as candidate genes of premature development of atherosclerosis. Physiol Res 49 (Suppl 1): S63-S69, 2000.
-
(2000)
Physiol Res
, vol.49
, Issue.SUPPL. 1
-
-
Hořejší, B.1
Češka, R.2
-
6
-
-
0033840486
-
Variable expression of hypercholesterolemia in apolipoprotein E 2*(Arg136→Cys) heterozygotes
-
HUBÁČEK JA, PIŤHA J, STÁVEK P, SCHMITZ G, POLEDNE R: Variable expression of hypercholesterolemia in apolipoprotein E 2*(Arg136→Cys) heterozygotes. Physiol Res 49: 307-314, 2000.
-
(2000)
Physiol Res
, vol.49
, pp. 307-314
-
-
Hubáček, J.A.1
Piťha, J.2
Stávek, P.3
Schmitz, G.4
Poledne, R.5
-
7
-
-
0036194248
-
Rare variant of apolipoprotein E 2*(Arg136→Cys) in a subject with normal lipid values
-
HUBÁČEK JA, PIŤHA J, ŠKODOVÁ Z, POLEDNE R: Rare variant of apolipoprotein E 2*(Arg136→Cys) in a subject with normal lipid values. Physiol Res 51: 107-108, 2002.
-
(2002)
Physiol Res
, vol.51
, pp. 107-108
-
-
Hubáček, J.A.1
Piťha, J.2
Škodová, Z.3
Poledne, R.4
-
8
-
-
0031594336
-
Apolipoprotein E2 (Arg136→Cys) mutation in the receptor binding domain of apoE is not associated with dominant type III hyperlipoproteinemia
-
MÄRZ W, HOFFMAN MM, SCHARNAGL H, FISHER E, CHEN M, NAUCK M, FEUSSNER G, WIELAND H: Apolipoprotein E2 (Arg136→Cys) mutation in the receptor binding domain of apoE is not associated with dominant type III hyperlipoproteinemia. J Lipid Res 39: 658-669, 1998.
-
(1998)
J Lipid Res
, vol.39
, pp. 658-669
-
-
März, W.1
Hoffman, M.M.2
Scharnagl, H.3
Fisher, E.4
Chen, M.5
Nauck, M.6
Feussner, G.7
Wieland, H.8
-
9
-
-
0026718601
-
The role of apolipoprotein E genetic variants in lipoprotein disorders
-
RALL SC Jr., MAHLEY RW: The role of apolipoprotein E genetic variants in lipoprotein disorders. J Intern Med 231: 653-659, 1992.
-
(1992)
J Intern Med
, vol.231
, pp. 653-659
-
-
Rall S.C., Jr.1
Mahley, R.W.2
-
10
-
-
0023117993
-
Apolipoprotein E polymorphism in health and disease
-
UTERMANN G. Apolipoprotein E polymorphism in health and disease. Am Heart J 113: 443-440, 1987.
-
(1987)
Am Heart J
, vol.113
, pp. 443-440
-
-
Utermann, G.1
-
11
-
-
0028325469
-
Detection of a new apolipoprotein E mutation in type III hyperlipidaemia using deoxyribonucleic acid restriction isotyping
-
WALDEN CC, HUFF MW, LEITER LA, CONNELY PW, HEGELE RA: Detection of a new apolipoprotein E mutation in type III hyperlipidaemia using deoxyribonucleic acid restriction isotyping. J Clin Endocrinol Metab 78: 699-704, 1994.
-
(1994)
J Clin Endocrinol Metab
, vol.78
, pp. 699-704
-
-
Walden, C.C.1
Huff, M.W.2
Leiter, L.A.3
Connely, P.W.4
Hegele, R.A.5
|