Kontula K - Search Results

1

Screening for a prevalent LDL receptor mutation in patients with severe hypercholesterolaemia.

Savolainen MJ, Korhonen T, Aalto-Setälä K, Kontula K, Kesäniemi YA. Savolainen MJ, et al. Among authors: kontula k. Hum Genet. 1991 Jun;87(2):125-8. doi: 10.1007/BF00204166. Hum Genet. 1991. PMID: 2066099

2

Genetic polymorphism of the apolipoprotein B gene locus influences serum LDL cholesterol level in familial hypercholesterolemia.

Aalto-Setälä K, Gylling H, Helve E, Kovanen P, Miettinen TA, Turtola H, Kontula K. Aalto-Setälä K, et al. Among authors: kontula k. Hum Genet. 1989 Jul;82(4):305-7. doi: 10.1007/BF00273986. Hum Genet. 1989. PMID: 2567693

3

Effect of apolipoprotein E polymorphism and XbaI polymorphism of apolipoprotein B on response to lovastatin treatment in familial and non-familial hypercholesterolaemia.

Ojala JP, Helve E, Ehnholm C, Aalto-Setälä K, Kontula KK, Tikkanen MJ. Ojala JP, et al. Among authors: kontula kk. J Intern Med. 1991 Nov;230(5):397-405. doi: 10.1111/j.1365-2796.1991.tb00464.x. J Intern Med. 1991. PMID: 1940775 Clinical Trial.

4

The gene encoding human low-molecular weight insulin-like growth-factor binding protein (IGF-BP25): regional localization to 7p12-p13 and description of a DNA polymorphism.

Alitalo T, Kontula K, Koistinen R, Aalto-Setälä K, Julkunen M, Jänne OA, Seppälä M, de la Chapelle A. Alitalo T, et al. Among authors: kontula k. Hum Genet. 1989 Nov;83(4):335-8. doi: 10.1007/BF00291377. Hum Genet. 1989. PMID: 2478445

5

Finnish type of low density lipoprotein receptor gene mutation (FH-Helsinki) deletes exons encoding the carboxy-terminal part of the receptor and creates an internalization-defective phenotype.

Aalto-Setälä K, Helve E, Kovanen PT, Kontula K. Aalto-Setälä K, et al. Among authors: kontula k. J Clin Invest. 1989 Aug;84(2):499-505. doi: 10.1172/JCI114192. J Clin Invest. 1989. PMID: 2760198 Free PMC article.

6

Identification of a deletion in the LDL receptor gene. A Finnish type of mutation.

Aalto-Setälä K, Gylling H, Miettinen T, Kontula K. Aalto-Setälä K, et al. Among authors: kontula k. FEBS Lett. 1988 Mar 28;230(1-2):31-4. doi: 10.1016/0014-5793(88)80635-5. FEBS Lett. 1988. PMID: 2895023 Free article.

7

XbaI and c/g polymorphisms of the apolipoprotein B gene locus are associated with serum cholesterol and LDL-cholesterol levels in Finland.

Aalto-Setälä K, Tikkanen MJ, Taskinen MR, Nieminen M, Holmberg P, Kontula K. Aalto-Setälä K, et al. Among authors: kontula k. Atherosclerosis. 1988 Nov;74(1-2):47-54. doi: 10.1016/0021-9150(88)90190-6. Atherosclerosis. 1988. PMID: 2905601

8

Variability gene effects of DNA polymorphisms at the apo B, apo A I/C III and apo E loci on serum lipids: the Cardiovascular Risk in Young Finns Study.

Porkka KV, Taimela S, Kontula K, Lehtimäki T, Aalto-Setälä K, Akerblom HK, Viikari JS. Porkka KV, et al. Among authors: kontula k. Clin Genet. 1994 Mar;45(3):113-21. doi: 10.1111/j.1399-0004.1994.tb04007.x. Clin Genet. 1994. PMID: 7913004

9

Familial hypercholesterolaemia in Finland: common, rare and mild mutations of the LDL receptor and their clinical consequences. Finnish FH-group.

Vuorio AF, Aalto-Setälä K, Koivisto UM, Turtola H, Nissen H, Kovanen PT, Miettinen TA, Gylling H, Oksanen H, Kontula K; Finnish FH-group. Vuorio AF, et al. Among authors: kontula k. Ann Med. 2001 Sep;33(6):410-21. doi: 10.3109/07853890108995954. Ann Med. 2001. PMID: 11585102 Free article.

10

The familial hypercholesterolemia (FH)-North Karelia mutation of the low density lipoprotein receptor gene deletes seven nucleotides of exon 6 and is a common cause of FH in Finland.

Koivisto UM, Turtola H, Aalto-Setälä K, Top B, Frants RR, Kovanen PT, Syvänen AC, Kontula K. Koivisto UM, et al. Among authors: kontula k. J Clin Invest. 1992 Jul;90(1):219-28. doi: 10.1172/JCI115839. J Clin Invest. 1992. PMID: 1634609 Free PMC article.

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