Gregersen N - Search Results

1

Identification of a novel mutation in exon 13 of the LDL receptor gene causing familial hypercholesterolemia in two Spanish families.

Cenarro A, Jensen HK, Casao E, Civeira F, Gonzàlez-Bonillo J, Pocoví M, Gregersen N. Cenarro A, et al. Among authors: gregersen n. Biochim Biophys Acta. 1996 May 24;1316(1):1-4. doi: 10.1016/0925-4439(96)00006-3. Biochim Biophys Acta. 1996. PMID: 8634338 Free article.

2

The Trp23-Stop and Trp66-Gly mutations in the LDL receptor gene: common causes of familial hypercholesterolemia in Denmark.

Jensen HK, Jensen LG, Hansen PS, Faergeman O, Gregersen N. Jensen HK, et al. Among authors: gregersen n. Atherosclerosis. 1996 Feb;120(1-2):57-65. doi: 10.1016/0021-9150(95)05680-7. Atherosclerosis. 1996. PMID: 8645371

3

High sensitivity of the single-strand conformation polymorphism method for detecting sequence variations in the low-density lipoprotein receptor gene validated by DNA sequencing.

Jensen HK, Jensen LG, Hansen PS, Faergeman O, Gregersen N. Jensen HK, et al. Among authors: gregersen n. Clin Chem. 1996 Aug;42(8 Pt 1):1140-6. Clin Chem. 1996. PMID: 8697568

4

An Iranian-Armenian LDLR frameshift mutation causing familial hypercholesterolemia.

Jensen HK, Jensen LG, Hansen PS, Faergeman O, Gregersen N. Jensen HK, et al. Among authors: gregersen n. Clin Genet. 1996 Feb;49(2):88-90. doi: 10.1111/j.1399-0004.1996.tb04334.x. Clin Genet. 1996. PMID: 8740919

5

Two novel mutations in the LDL receptor gene: common causes of familial hypercholesterolemia in a Spanish population.

Cenarro A, Jensen HK, Civeira F, Casao E, Ferrando J, González-Bonillo J, Pocoví M, Gregersen N. Cenarro A, et al. Among authors: gregersen n. Clin Genet. 1996 Apr;49(4):180-5. doi: 10.1111/j.1399-0004.1996.tb03283.x. Clin Genet. 1996. PMID: 8828982

6

Two mutations in the same low-density lipoprotein receptor allele act in synergy to reduce receptor function in heterozygous familial hypercholesterolemia.

Jensen HK, Jensen TG, Faergeman O, Jensen LG, Andresen BS, Corydon MJ, Andreasen PH, Hansen PS, Heath F, Bolund L, Gregersen N. Jensen HK, et al. Among authors: gregersen n. Hum Mutat. 1997;9(5):437-44. doi: 10.1002/(SICI)1098-1004(1997)9:5<437::AID-HUMU10>3.0.CO;2-3. Hum Mutat. 1997. PMID: 9143924

7

Identification of recurrent and novel mutations in the LDL receptor gene in Spanish patients with familial hypercholesterolemia. Mutations in brief no. 135. Online.

Cenarro A, Jensen HK, Casao E, Civeira F, González-Bonillo J, Rodríguez-Rey JC, Gregersen N, Pocoví M. Cenarro A, et al. Among authors: gregersen n. Hum Mutat. 1998;11(5):413. doi: 10.1002/(SICI)1098-1004(1998)11:5<413::AID-HUMU16>3.0.CO;2-I. Hum Mutat. 1998. PMID: 10206683

8

No genetic linkage or molecular evidence for involvement of the PCSK9, ARH or CYP7A1 genes in the Familial Hypercholesterolemia phenotype in a sample of Danish families without pathogenic mutations in the LDL receptor and apoB genes.

Damgaard D, Jensen JM, Larsen ML, Soerensen VR, Jensen HK, Gregersen N, Jensen LG, Faergeman O. Damgaard D, et al. Among authors: gregersen n. Atherosclerosis. 2004 Dec;177(2):415-22. doi: 10.1016/j.atherosclerosis.2004.07.028. Atherosclerosis. 2004. PMID: 15530918

9

Complexity of molecular genetics of dyslipidemia in a family highly susceptible to ischemic heart disease.

Jensen HK, Hansen PS, Jensen LG, Kristensen MJ, Klausen IC, Kjeldsen M, Lemming L, Bolund L, Gregersen N, Faergeman O. Jensen HK, et al. Among authors: gregersen n. Clin Genet. 1995 Jul;48(1):23-8. doi: 10.1111/j.1399-0004.1995.tb04049.x. Clin Genet. 1995. PMID: 7586640

10

An alanine29-serine variant in exon 2 of the low density lipoprotein receptor gene: no association with hypercholesterolemia.

Jensen HK, Jensen LG, Hansen PS, Petersen LS, Gerdes LU, Bolund L, Faergeman O, Gregersen N. Jensen HK, et al. Among authors: gregersen n. Clin Genet. 1994 Aug;46(2):214-5. doi: 10.1111/j.1399-0004.1994.tb04228.x. Clin Genet. 1994. PMID: 7820934 No abstract available.

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