-
1
-
-
0032893470
-
Review of risk factors for cardiovascular diseases
-
Wu, L. L.: Review of risk factors for cardiovascular diseases. Ann. Clin. Lab. Sci., 1999, 29, s. 127-133.
-
(1999)
Ann. Clin. Lab. Sci.
, vol.29
, pp. 127-133
-
-
Wu, L.L.1
-
2
-
-
0026704002
-
Familial hypercholesterolaemia and LDL receptor mutations
-
Soutar, A. K.: Familial hypercholesterolaemia and LDL receptor mutations. J. Intern. Med., 1992, 231, s. 633-641.
-
(1992)
J. Intern. Med.
, vol.231
, pp. 633-641
-
-
Soutar, A.K.1
-
3
-
-
0028939476
-
Rare and common mutations in hyperlipidemia and atherosclerosis. With special reference to familial defective apolipoprotein B-100
-
Tybjaerg-Hansen, A.: Rare and common mutations in hyperlipidemia and atherosclerosis. With special reference to familial defective apolipoprotein B-100. Scand. J. Clin. Lab. Invest., 1995, 220 (Suppl.), s. 57-76.
-
(1995)
Scand. J. Clin. Lab. Invest.
, vol.220
, Issue.SUPPL.
, pp. 57-76
-
-
Tybjaerg-Hansen, A.1
-
4
-
-
0032813809
-
The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease
-
Bodzioch, M., Orso, E., Klucken, J. et al.: The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease. Nat. Genet., 1999, 22, s. 347-351.
-
(1999)
Nat. Genet.
, vol.22
, pp. 347-351
-
-
Bodzioch, M.1
Orso, E.2
Klucken, J.3
-
5
-
-
17744390348
-
Accumulation of dietary cholesterol in sitosterolemia caused by mutations in adjacent ABC transporters
-
Berge, K. E., Tian, H., Graf, G. A. et al.: Accumulation of dietary cholesterol in sitosterolemia caused by mutations in adjacent ABC transporters. Science, 2000, 290, s. 1771-1775.
-
(2000)
Science
, vol.290
, pp. 1771-1775
-
-
Berge, K.E.1
Tian, H.2
Graf, G.A.3
-
6
-
-
0035491250
-
Mutation in ATP-cassette binding proteins G5 (ABCG5) and G8 (ABCG8) causing sitosterolemia
-
Hubáček, J. A., Berge, K. E., Cohen, J. C., Hobbs, H. H.: Mutation in ATP-cassette binding proteins G5 (ABCG5) and G8 (ABCG8) causing sitosterolemia. Hum. Mutat., 2001, 18, s. 359-360.
-
(2001)
Hum. Mutat.
, vol.18
, pp. 359-360
-
-
Hubáček, J.A.1
Berge, K.E.2
Cohen, J.C.3
Hobbs, H.H.4
-
7
-
-
0035906961
-
Autosomal recessive hypercholesterolemia caused by mutations in a putative LDL receptor adaptor protein
-
Garcia, C. K., Wilund, K., Arca, M. et al.: Autosomal recessive hypercholesterolemia caused by mutations in a putative LDL receptor adaptor protein. Science, 2001, 292, s. 1394-1398.
-
(2001)
Science
, vol.292
, pp. 1394-1398
-
-
Garcia, C.K.1
Wilund, K.2
Arca, M.3
-
8
-
-
0022339844
-
Localization of genes encoding apolipoproteins CI, CII, and E to the p 13 - Cen region of human chromosome 19
-
Scott, J., Knott, T. J., Shaw, D. J., Brook, J. D.: Localization of genes encoding apolipoproteins CI, CII, and E to the p 13 - cen region of human chromosome 19. Hum. Genet., 1985, 71, s. 144-146.
-
(1985)
Hum. Genet.
, vol.71
, pp. 144-146
-
-
Scott, J.1
Knott, T.J.2
Shaw, D.J.3
Brook, J.D.4
-
9
-
-
0033015655
-
Role of apoCs in lipoprotein metabolism. Functional differences between apoC1, apoC2 and apoC3
-
Jong, M. C., Hofker, M. H., Havekes, L. M.: Role of apoCs in lipoprotein metabolism. Functional differences between apoC1, apoC2 and apoC3. Arterioscler. Thromb. Vasc. Biol., 1999, 19, s. 472-484.
-
(1999)
Arterioscler. Thromb. Vasc. Biol.
, vol.19
, pp. 472-484
-
-
Jong, M.C.1
Hofker, M.H.2
Havekes, L.M.3
-
10
-
-
0023664061
-
Human apolipoprotein CI (apo CI) gene locus: Dra I dimorphic site
-
Frossard, P. M., Coleman, R. T., Malloz, M. J. et al.: Human apolipoprotein CI (apo CI) gene locus: Dra I dimorphic site. Nucleic Acids Res., 1987, 15, s. 1884.
-
(1987)
Nucleic Acids Res.
, vol.15
, pp. 1884
-
-
Frossard, P.M.1
Coleman, R.T.2
Malloz, M.J.3
-
11
-
-
18244426336
-
Human apolipoprotein C1 (apo CI) gene locus: Bgl I dimorphic site
-
Frossard, P. M., Lim, D. V., Coleman, R. T. et al.: Human apolipoprotein C1 (apo CI) gene locus: Bgl I dimorphic site. Nucleic Acids Res., 1987, 15, s. 1344.
-
(1987)
Nucleic Acids Res.
, vol.15
, pp. 1344
-
-
Frossard, P.M.1
Lim, D.V.2
Coleman, R.T.3
-
12
-
-
0023123110
-
A common restriction fragment lenght polymorphism of the human apolipoprotein E gene and its relationship to type III hyperlipidemia
-
Klasen, E. C., Talmud, P. J., Havekes, L. et al.: A common restriction fragment lenght polymorphism of the human apolipoprotein E gene and its relationship to type III hyperlipidemia. Hum. Genet., 1987, 75, s. 244-247.
-
(1987)
Hum. Genet.
, vol.75
, pp. 244-247
-
-
Klasen, E.C.1
Talmud, P.J.2
Havekes, L.3
-
13
-
-
0023885544
-
Exact localization of the familial dysbeta lipoproteinemia associated Hpa I restriction site in the promoter region of the apo CI gene
-
Smit, H., Kooij-Meijs, E., Woudt, L. P. et al.: Exact localization of the familial dysbeta lipoproteinemia associated Hpa I restriction site in the promoter region of the apo CI gene. Bioch. Bioph. Res. Com., 1988, 152, s. 1282-1288.
-
(1988)
Bioch. Bioph. Res. Com.
, vol.152
, pp. 1282-1288
-
-
Smit, H.1
Kooij-Meijs, E.2
Woudt, L.P.3
-
14
-
-
0032941603
-
A common Hpa I RFLP of apolipoprotein C-I increases gene transcription and exhibits an ethnically distinct pattern of linkage disequilibrium with the alleles of apolipoprotein E
-
Xu, Y., Berglund, L., Ramakrishnan, R. et al.: A common Hpa I RFLP of apolipoprotein C-I increases gene transcription and exhibits an ethnically distinct pattern of linkage disequilibrium with the alleles of apolipoprotein E. J. Lipid Res., 1999, 40, s. 50-58.
-
(1999)
J. Lipid Res.
, vol.40
, pp. 50-58
-
-
Xu, Y.1
Berglund, L.2
Ramakrishnan, R.3
-
15
-
-
0031979670
-
Apolipoprotein E a jeho role v lipidovém metabolismu, kardiovaskulárních onemocněních a Alzheimerově chorobě
-
Hubáček, J. A., Poledne, R.: Apolipoprotein E a jeho role v lipidovém metabolismu, kardiovaskulárních onemocněních a Alzheimerově chorobě. Prakt. Lék., 1998, 78, s. 105-108.
-
(1998)
Prakt. Lék.
, vol.78
, pp. 105-108
-
-
Hubáček, J.A.1
Poledne, R.2
-
16
-
-
12444269979
-
Apolipoprotein E and apolipoprotein CI polymorphisms in the Czech population. Almost complete linkage disequilibrium of the less frequent alleles of both polymorphisms
-
Hubáček, J. A., Pitha, J., Adámková, V. et al.: Apolipoprotein E and apolipoprotein CI polymorphisms in the Czech population. Almost complete linkage disequilibrium of the less frequent alleles of both polymorphisms. Physiol. Res., 2003, 52, s. 195-200.
-
(2003)
Physiol. Res.
, vol.52
, pp. 195-200
-
-
Hubáček, J.A.1
Pitha, J.2
Adámková, V.3
-
17
-
-
0025757252
-
Cholesterolaemia in school-age children and hypercholesterolaemia aggregation in the family
-
Pistulková, H., Poledne, R., Kaucká, J. et al.: Cholesterolaemia in school-age children and hypercholesterolaemia aggregation in the family. Cor Vasa, 1991, 33, s. 139-149.
-
(1991)
Cor Vasa
, vol.33
, pp. 139-149
-
-
Pistulková, H.1
Poledne, R.2
Kaucká, J.3
-
18
-
-
0024284028
-
A simple salting out procedure for extraction DNA from human nucleated cells
-
Miller, S. A., Dykes, D. D., Polesky, H. F.: A simple salting out procedure for extraction DNA from human nucleated cells. Nucleic Acid Res., 1988, 16, s. 1215.
-
(1988)
Nucleic Acid Res.
, vol.16
, pp. 1215
-
-
Miller, S.A.1
Dykes, D.D.2
Polesky, H.F.3
-
19
-
-
0025705431
-
Human apo CI Hpa I restriction site polymorphism revealed by the polymerase chain reaction
-
Nillesen, W. M., Smeets, H. J. M., van Oost, B. A.: Human apo CI Hpa I restriction site polymorphism revealed by the polymerase chain reaction. Nucleic Acid Res., 1990, 11, s. 3428.
-
(1990)
Nucleic Acid Res.
, vol.11
, pp. 3428
-
-
Nillesen, W.M.1
Smeets, H.J.M.2
Van Oost, B.A.3
-
20
-
-
0023860891
-
Apolipoprotein E and atherosclerosis
-
Davignon, J., Gregg, R. E., Sing, Ch. F.: Apolipoprotein E and atherosclerosis. Atherosclerosis, 1988, 8, s. 1-21.
-
(1988)
Atherosclerosis
, vol.8
, pp. 1-21
-
-
Davignon, J.1
Gregg, R.E.2
Sing, Ch.F.3
-
21
-
-
0035812707
-
An apolipoprotein influencing triglycerides in humans and mice revealed by comparative sequencing
-
Pennacchio, L. A., Olivier, M., Hubáček, J. A. et al.: An apolipoprotein influencing triglycerides in humans and mice revealed by comparative sequencing. Science, 2001, 294, s. 169-173.
-
(2001)
Science
, vol.294
, pp. 169-173
-
-
Pennacchio, L.A.1
Olivier, M.2
Hubáček, J.A.3
-
22
-
-
1842864853
-
Two independent apolipoprotein AV haplotypes influence human plasma triglyceride levels
-
Pennacchio, L. A., Olivier, M., Hubáček, J. A. et al.: Two independent apolipoprotein AV haplotypes influence human plasma triglyceride levels. Hum. Mol. Genet., 2002, 11, s. 3031-3038.
-
(2002)
Hum. Mol. Genet.
, vol.11
, pp. 3031-3038
-
-
Pennacchio, L.A.1
Olivier, M.2
Hubáček, J.A.3
-
23
-
-
0028087813
-
Genetic markers in hypercholesterolemic and normocholesterolemic Czech children
-
Poledne, R., Hubáček, J., Píša, Z. et al.: Genetic markers in hypercholesterolemic and normocholesterolemic Czech children. Clin. Genet., 1994, 46, s. 88-91.
-
(1994)
Clin. Genet.
, vol.46
, pp. 88-91
-
-
Poledne, R.1
Hubáček, J.2
Píša, Z.3
-
24
-
-
0032797545
-
(TTA)n repeat polymorphism in the HMG-CoA reductase gene and cholesterolemia
-
Hubáček, J. A., Pistulková, H., Valenta, Z., Poledne, R.: (TTA)n repeat polymorphism in the HMG-CoA reductase gene and cholesterolemia. VASA, 1999, 28, s. 169-171.
-
(1999)
VASA
, vol.28
, pp. 169-171
-
-
Hubáček, J.A.1
Pistulková, H.2
Valenta, Z.3
Poledne, R.4
-
25
-
-
0032827320
-
Variability gene effect of apo All polymorphism in high-cholesterolemic children
-
Hubáček, J. A., Pistulková, H., Š kodová, Z. et al.: Variability gene effect of apo All polymorphism in high-cholesterolemic children. Med. Sci. Monit., 1999, 5, s. 605-608.
-
(1999)
Med. Sci. Monit.
, vol.5
, pp. 605-608
-
-
Hubáček, J.A.1
Pistulková, H.2
Škodová, Z.3
-
26
-
-
0035866254
-
Polymorfismy v genech pro cholesterol ester transferový protein, apolipoprotein CIII a lipoproteinovou lipázu u dětí s nízkou a s vysokou hladinou cholesterolu
-
Hubáček, J. A., Pistulková, H., Š kodová, Z. et al.: Polymorfismy v genech pro cholesterol ester transferový protein, apolipoprotein CIII a lipoproteinovou lipázu u dětí s nízkou a s vysokou hladinou cholesterolu. Čas. Lék. čes., 2001, 140, s. 79-81.
-
(2001)
Čas. Lék. Čes.
, vol.140
, pp. 79-81
-
-
Hubáček, J.A.1
Pistulková, H.2
Škodová, Z.3
-
27
-
-
17544394569
-
Polymorfizmus v regulační části genu pro cholesterol 7α hydroxylázu u dětí s vysokou a nízkou hladinou cholesterolu
-
Hubáček, J. A., Pistulková, H., Š kodová, Z. et al.: Polymorfizmus v regulační části genu pro cholesterol 7α hydroxylázu u dětí s vysokou a nízkou hladinou cholesterolu. Čas. Lék. čes., 2003, 142, s. 423-426.
-
(2003)
Čas. Lék. Čes.
, vol.142
, pp. 423-426
-
-
Hubáček, J.A.1
Pistulková, H.2
Škodová, Z.3
-
28
-
-
0034937543
-
Association between apolipoprotein B promotor haplotypes and cholesterol status
-
Hubáček, J. A., Pistulková, H., Š kodová, Z. et al.: Association between apolipoprotein B promotor haplotypes and cholesterol status. Ann. Clin. Biochem., 2001, 38, s. 399-400.
-
(2001)
Ann. Clin. Biochem.
, vol.38
, pp. 399-400
-
-
Hubáček, J.A.1
Pistulková, H.2
Škodová, Z.3
-
29
-
-
0031816201
-
Lack of association of the Xbal polymorphism in the apolipoprotein B gene and cholesterolemia in childhood
-
Hubáček, J.A., Pistulková, H., Škodová , Z. et al.: Lack of association of the Xbal polymorphism in the apolipoprotein B gene and cholesterolemia in childhood. Physiol. Res., 1998, 46, s. 89-93.
-
(1998)
Physiol. Res.
, vol.46
, pp. 89-93
-
-
Hubáček, J.A.1
Pistulková, H.2
Škodová, Z.3
|