Leren TP - Search Results

1

Identification and characterization of two novel mutations in the LPL gene causing type I hyperlipoproteinemia.

Pingitore P, Lepore SM, Pirazzi C, Mancina RM, Motta BM, Valenti L, Berge KE, Retterstøl K, Leren TP, Wiklund O, Romeo S. Pingitore P, et al. Among authors: leren tp. J Clin Lipidol. 2016 Jul-Aug;10(4):816-823. doi: 10.1016/j.jacl.2016.02.015. Epub 2016 Mar 10. J Clin Lipidol. 2016. PMID: 27578112 Free article.

2

A new polymorphism in exon 11 of the LDL receptor gene in healthy people and in familial hypercholesterolemia subjects.

Leren TP, Solberg K, Røsby O, Rødningen OK, Tonstad S, Ose L, Berg K. Leren TP, et al. Clin Genet. 1992 Nov;42(5):224-8. doi: 10.1111/j.1399-0004.1992.tb03245.x. Clin Genet. 1992. PMID: 1486698

3

Two novel point mutations in the EGF precursor homology domain of the LDL receptor gene causing familial hypercholesterolemia.

Leren TP, Solberg K, Rødningen OK, Tonstad S, Ose L. Leren TP, et al. Hum Genet. 1995 Aug;96(2):241-2. doi: 10.1007/BF00207391. Hum Genet. 1995. PMID: 7635482

4

Screening for known mutations in the LDL receptor gene causing familial hypercholesterolemia.

Leren TP, Sundvold H, Rødningen OK, Tonstad S, Solberg K, Ose L, Berg K. Leren TP, et al. Hum Genet. 1995 Jun;95(6):671-6. doi: 10.1007/BF00209485. Hum Genet. 1995. PMID: 7789953

5

Two novel missense mutations in the LDL receptor gene causing familial hypercholesterolemia.

Gundersen KE, Solberg K, Rødningen OK, Tonstad S, Ose L, Berg K, Leren TP. Gundersen KE, et al. Among authors: leren tp. Clin Genet. 1996 Feb;49(2):85-7. doi: 10.1111/j.1399-0004.1996.tb04333.x. Clin Genet. 1996. PMID: 8740918

6

Identification of deletions and duplications in the low density lipoprotein receptor gene by MLPA.

Holla Ø, Teie C, Berge KE, Leren TP. Holla Ø, et al. Among authors: leren tp. Clin Chim Acta. 2005 Jun;356(1-2):164-71. doi: 10.1016/j.cccn.2005.01.028. Epub 2005 Mar 16. Clin Chim Acta. 2005. PMID: 15936313

7

[Cardiac ion channel disorders--diagnosis and treatment].

Haugaa KH, Berge KE, Früh A, Anfinsen OG, Arnestad M, Hallerud M, Gjesdal K, Leren TP, Amlie JP. Haugaa KH, et al. Among authors: leren tp. Tidsskr Nor Laegeforen. 2005 Oct 20;125(20):2778-81. Tidsskr Nor Laegeforen. 2005. PMID: 16244679 Free article. Review. Norwegian.

8

[DNA-based diagnostics of long QT syndrome].

Berge KE, Haugaa KH, Anfinsen OG, Früh A, Hallerud M, Jonsrud C, Øyen N, Gjesdal K, Amlie JP, Leren TP. Berge KE, et al. Among authors: leren tp. Tidsskr Nor Laegeforen. 2005 Oct 20;125(20):2783-6. Tidsskr Nor Laegeforen. 2005. PMID: 16244680 Free article. Norwegian.

9

Missense mutations in the PCSK9 gene are associated with hypocholesterolemia and possibly increased response to statin therapy.

Berge KE, Ose L, Leren TP. Berge KE, et al. Among authors: leren tp. Arterioscler Thromb Vasc Biol. 2006 May;26(5):1094-100. doi: 10.1161/01.ATV.0000204337.81286.1c. Epub 2006 Jan 19. Arterioscler Thromb Vasc Biol. 2006. PMID: 16424354

10

Effect of mutations in the PCSK9 gene on the cell surface LDL receptors.

Cameron J, Holla ØL, Ranheim T, Kulseth MA, Berge KE, Leren TP. Cameron J, et al. Among authors: leren tp. Hum Mol Genet. 2006 May 1;15(9):1551-8. doi: 10.1093/hmg/ddl077. Epub 2006 Mar 28. Hum Mol Genet. 2006. PMID: 16571601

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