These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
54 related articles for article (PubMed ID: 11590998)
1. Absence of the R3531C mutation in the apoB gene in Czech hypercholesterolaemic patients. Vrablík M; Ceska R; Horínek A; Wichterle D Nutr Metab Cardiovasc Dis; 2001 Jun; 11(3):212-4. PubMed ID: 11590998 [No Abstract] [Full Text] [Related]
2. Identification of the haplotype associated with the APOB-3500 mutation in a French hypercholesterolemic subject: further support for a unique European ancestral mutation. Loux N; Saint-Jore B; Collod G; Benlian P; Cambou JP; Denat M; Junien C; Boileau C Hum Mutat; 1993; 2(2):145-7. PubMed ID: 8318993 [No Abstract] [Full Text] [Related]
3. Update of the molecular basis of familial hypercholesterolemia in The Netherlands. Fouchier SW; Kastelein JJ; Defesche JC Hum Mutat; 2005 Dec; 26(6):550-6. PubMed ID: 16250003 [TBL] [Abstract][Full Text] [Related]
4. High frequency of the ApoB-100 R3500Q mutation in Bulgarian hypercholesterolaemic subjects. Horvath A; Savov A; Kirov S; Karshelova E; Paskaleva I; Goudev A; Ganev V J Med Genet; 2001 Aug; 38(8):536-40. PubMed ID: 11494965 [No Abstract] [Full Text] [Related]
5. Association of mutations in the apolipoprotein B gene with hypercholesterolemia and the risk of ischemic heart disease. Schaefer JR; Herzum M; Maisch B N Engl J Med; 1998 Nov; 339(22):1641-2. PubMed ID: 9867530 [No Abstract] [Full Text] [Related]
6. Association of mutations in the apolipoprotein B gene with hypercholesterolemia and the risk of ischemic heart disease. Gaffney D; Pullinger C; Kane J N Engl J Med; 1998 Nov; 339(22):1640-1; author reply 1641-2. PubMed ID: 9867529 [No Abstract] [Full Text] [Related]
7. Molecular characterization of familial hypercholesterolemia in German and Greek patients. Dedoussis GV; Genschel J; Bochow B; Pitsavos C; Skoumas J; Prassa M; Lkhagvasuren S; Toutouzas P; Vogt A; Kassner U; Thomas HP; Schmidt H Hum Mutat; 2004 Mar; 23(3):285-6. PubMed ID: 14974088 [TBL] [Abstract][Full Text] [Related]
8. Familial defective apolipoprotein B-100 in a group of hypercholesterolaemic patients in Poland. Identification of a new mutation Thr3492Ile in the apolipoprotein B gene. Bednarska-Makaruk M; Bisko M; Pulawska MF; Hoffman-Zacharska D; Rodo M; Roszczynko M; Solik-Tomassi A; Broda G; Polakowska M; Pytlak A; Wehr H Eur J Hum Genet; 2001 Nov; 9(11):836-42. PubMed ID: 11781700 [TBL] [Abstract][Full Text] [Related]
9. High-resolution melting analysis for detection of familial ligand-defective apolipoprotein B-100 mutations. Liyanage KE; Hooper AJ; Defesche JC; Burnett JR; van Bockxmeer FM Ann Clin Biochem; 2008 Mar; 45(Pt 2):170-6. PubMed ID: 18325181 [TBL] [Abstract][Full Text] [Related]
10. Familial hypercholesterolemia in St-Petersburg: the known and novel mutations found in the low density lipoprotein receptor gene in Russia. Zakharova FM; Damgaard D; Mandelshtam MY; Golubkov VI; Nissen PH; Nilsen GG; Stenderup A; Lipovetsky BM; Konstantinov VO; Denisenko AD; Vasilyev VB; Faergeman O BMC Med Genet; 2005 Feb; 6():6. PubMed ID: 15701167 [TBL] [Abstract][Full Text] [Related]
11. [Screening for the new variant of defective receptor-binding apolipoprotein B-100]. Li Y; Feng J; Li W Zhonghua Yi Xue Za Zhi; 2001 Dec; 81(23):1434-5. PubMed ID: 11930615 [TBL] [Abstract][Full Text] [Related]
18. Familial defective apolipoprotein B-100: a mutation emerged in the mesolithic ancestors of Celtic peoples? Miserez AR; Muller PY Atherosclerosis; 2000 Feb; 148(2):433-6. PubMed ID: 10657582 [No Abstract] [Full Text] [Related]
19. The use of gene probes to investigate the etiology of hyperlipidaemia and arterial diseases. Humphries SE Acta Cardiol Suppl; 1988; 29():85-95. PubMed ID: 2898851 [No Abstract] [Full Text] [Related]
20. Molecular genetic analysis of 1053 Danish individuals with clinical signs of familial hypercholesterolemia. Brusgaard K; Jordan P; Hansen H; Hansen AB; Hørder M Clin Genet; 2006 Mar; 69(3):277-83. PubMed ID: 16542394 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]