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Items: 1 to 50 of 85

1.

Single-strand conformation polymorphism analysis using capillary electrophoresis.

Larsen LA, Christiansen M, Vuust J, Andersen PS.

Curr Protoc Hum Genet. 2003 May;Chapter 7:Unit 7.12. doi: 10.1002/0471142905.hg0712s36.

PMID:
18428343
2.

Whole genome amplification on DNA from filter paper blood spot samples: an evaluation of selected systems.

Sørensen KM, Jespersgaard C, Vuust J, Hougaard D, Nørgaard-Pedersen B, Andersen PS.

Genet Test. 2007 Spring;11(1):65-71.

PMID:
17394394
3.

[Screening for fragile X syndrome. International experiences].

Vuust J, Larsen LA, Grønskov K, Nørgaard-Pedersen B, Brøndum-Nielsen K.

Ugeskr Laeger. 2006 Oct 23;168(43):3704-9. Review. Danish.

PMID:
17069733
4.

Optimization of capillary array electrophoresis single-strand conformation polymorphism analysis for routine molecular diagnostics.

Jespersgaard C, Larsen LA, Baba S, Kukita Y, Tahira T, Christiansen M, Vuust J, Hayashi K, Andersen PS.

Electrophoresis. 2006 Oct;27(19):3816-22.

PMID:
16941449
5.

P53 mutations in tissue from Danish ovarian cancer patients: from the Danish "MALOVA" ovarian cancer study.

Høgdall EV, Kjaer SK, Blaakaer J, Christensen L, Glud E, Vuust J, Høgdall CK.

Gynecol Oncol. 2006 Jan;100(1):76-82. Epub 2005 Sep 23.

PMID:
16183105
6.

Adverse reactions to injectable soft tissue permanent fillers.

Christensen L, Breiting V, Janssen M, Vuust J, Hogdall E.

Aesthetic Plast Surg. 2005 Jan-Feb;29(1):34-48. Epub 2005 Mar 11. Review.

PMID:
15759096
7.

One third of Danish hypertrophic cardiomyopathy patients with MYH7 mutations have mutations [corrected] in MYH7 rod region.

Hougs L, Havndrup O, Bundgaard H, Køber L, Vuust J, Larsen LA, Christiansen M, Andersen PS.

Eur J Hum Genet. 2005 Feb;13(2):161-5. Erratum in: Eur J Hum Genet. 2005 May;13(5):694.

8.

Identification and molecular characterization of the gene encoding coli surface antigen 20 of enterotoxigenic Escherichia coli.

Valvatne H, Steinsland H, Grewal HM, Mølbak K, Vuust J, Sommerfelt H.

FEMS Microbiol Lett. 2004 Oct 1;239(1):131-8.

9.

Genetic and phenotypic characterization of mutations in myosin-binding protein C (MYBPC3) in 81 families with familial hypertrophic cardiomyopathy: total or partial haploinsufficiency.

Andersen PS, Havndrup O, Bundgaard H, Larsen LA, Vuust J, Pedersen AK, Kjeldsen K, Christiansen M.

Eur J Hum Genet. 2004 Aug;12(8):673-7.

10.

Evaluation of a polymorphism in intron 2 of the p53 gene in ovarian cancer patients. From the Danish "Malova" Ovarian Cancer Study.

Høgdall EV, Kjaer SK, Glud E, Christensen L, Blaakaer J, Vuust J, Bock JE, Norgaard-Pedersen B, Hogdall CK.

Anticancer Res. 2003 Jul-Aug;23(4):3397-404.

PMID:
12926080
11.

K-ras alterations in Danish ovarian tumour patients. From the Danish "Malova" Ovarian Cancer study.

Høgdall EV, Høgdall CK, Blaakaer J, Christensen L, Bock JE, Vuust J, Glud E, Kjaer SK; Danish "Malova" Ovarian Cancer Study.

Gynecol Oncol. 2003 Apr;89(1):31-6.

PMID:
12694651
12.

Capillary electrophoresis-based single strand DNA conformation analysis in high-throughput mutation screening.

Andersen PS, Jespersgaard C, Vuust J, Christiansen M, Larsen LA.

Hum Mutat. 2003 May;21(5):455-65. Review.

PMID:
12673787
13.

Outcome of clinical versus genetic family screening in hypertrophic cardiomyopathy with focus on cardiac beta-myosin gene mutations.

Havndrup O, Bundgaard H, Andersen PS, Allan Larsen L, Vuust J, Kjeldsen K, Christiansen M.

Cardiovasc Res. 2003 Feb;57(2):347-57.

PMID:
12566107
14.

High-throughput single strand conformation polymorphism mutation detection by automated capillary array electrophoresis: validation of the method.

Andersen PS, Jespersgaard C, Vuust J, Christiansen M, Larsen LA.

Hum Mutat. 2003 Feb;21(2):116-22.

PMID:
12552558
15.

Distribution of p53 codon 72 polymorphisms in ovarian tumour patients and their prognostic significance in ovarian cancer patients.

Høgdall EV, Høgdall CK, Christensen L, Glud E, Blaakaer J, Bock JE, Vuust J, Nørgaard-Pedersen B, Kjaer SK.

Anticancer Res. 2002 May-Jun;22(3):1859-64.

PMID:
12168882
16.

Myosin light chain mutations in familial hypertrophic cardiomyopathy: phenotypic presentation and frequency in Danish and South African populations.

Andersen PS, Havndrup O, Bundgaard H, Moolman-Smook JC, Larsen LA, Mogensen J, Brink PA, Børglum AD, Corfield VA, Kjeldsen K, Vuust J, Christiansen M.

J Med Genet. 2001 Dec;38(12):E43. No abstract available.

17.

Novel feto-specific mRNA species suitable for identification of fetal cells from the maternal circulation.

Boye K, Hougaard DM, Ebbesen P, Vuust J, Christiansen M.

Prenat Diagn. 2001 Oct;21(10):806-12.

PMID:
11746119
18.

Recent developments in high-throughput mutation screening.

Larsen LA, Christiansen M, Vuust J, Andersen PS.

Pharmacogenomics. 2001 Nov;2(4):387-99. Review.

PMID:
11722288
19.

Automated mutation screening using dideoxy fingerprinting and capillary array electrophoresis.

Larsen LA, Johnson M, Brown C, Christiansen M, Frank-Hansen R, Vuust J, Andersen PS.

Hum Mutat. 2001 Nov;18(5):451-7.

PMID:
11668638
20.

Analysis of FMR1 (CGG)(n) alleles and DXS548-FRAXAC1 haplotypes in three European circumpolar populations: traces of genetic relationship with Asia.

Larsen LA, Vuust J, Nystad M, Evseeva I, Van Ghelue M, Tranebjaerg L.

Eur J Hum Genet. 2001 Sep;9(9):724-7.

21.

Screening for mutations and polymorphisms in the genes KCNH2 and KCNE2 encoding the cardiac HERG/MiRP1 ion channel: implications for acquired and congenital long Q-T syndrome.

Larsen LA, Andersen PS, Kanters J, Svendsen IH, Jacobsen JR, Vuust J, Wettrell G, Tranebjaerg L, Bathen J, Christiansen M.

Clin Chem. 2001 Aug;47(8):1390-5.

22.

The Val606Met mutation in the cardiac beta-myosin heavy chain gene in patients with familial hypertrophic cardiomyopathy is associated with a high risk of sudden death at young age.

Havndrup O, Bundgaard H, Andersen PS, Larsen LA, Vuust J, Kjeldsen K, Christiansen M.

Am J Cardiol. 2001 Jun 1;87(11):1315-7. No abstract available.

PMID:
11377367
23.

A novel missense mutation, Leu390Val, in the cardiac beta-myosin heavy chain associated with pronounced septal hypertrophy in two families with hypertrophic cardiomyopathy.

Havndrup O, Bundgaard H, Andersen PS, Larsen LA, Vuust J, Kjeldsen K, Christiansen M.

Scand Cardiovasc J. 2000 Dec;34(6):558-63.

PMID:
11214007
24.

Conservation and heterogeneity of the glutamate-rich protein (GLURP) among field isolates and laboratory lines of Plasmodium falciparum.

de Stricker K, Vuust J, Jepsen S, Oeuvray C, Theisen M.

Mol Biochem Parasitol. 2000 Nov;111(1):123-30.

PMID:
11087922
25.

High throughput mutation screening by automated capillary electrophoresis.

Larsen LA, Christiansen M, Vuust J, Andersen PS.

Comb Chem High Throughput Screen. 2000 Oct;3(5):393-409. Review.

PMID:
11032956
27.

Haplotype and AGG-interspersion analysis of FMR1 (CGG)(n) alleles in the Danish population: implications for multiple mutational pathways towards fragile X alleles.

Larsen LA, Armstrong JS, Grønskov K, Hjalgrim H, Macpherson JN, Brøndum-Nielsen K, Hasholt L, Nørgaard-Pedersen B, Vuust J.

Am J Med Genet. 2000 Jul 17;93(2):99-106.

PMID:
10869110
28.

Long QT syndrome with a high mortality rate caused by a novel G572R missense mutation in KCNH2.

Larsen LA, Svendsen IH, Jensen AM, Kanters JK, Andersen PS, Møller M, Sørensen SA, Sandøe E, Jacobsen JR, Vuust J, Christiansen M.

Clin Genet. 2000 Feb;57(2):125-30.

PMID:
10735633
29.

Simple preparation method of PCR fragments for automated DNA sequencing.

Høgdall E, Boye K, Vuust J.

J Cell Biochem. 1999 Jun 15;73(4):433-6.

PMID:
10733337
30.

Analysis of FMR1 (CGG)n alleles and FRAXA microsatellite haplotypes in the population of Greenland: implications for the population of the New World from Asia.

Larsen LA, Armstrong JS, Grønskov K, Hjalgrim H, Brøndum-Nielsen K, Hasholt L, Nørgaard-Pedersen B, Vuust J.

Eur J Hum Genet. 1999 Oct-Nov;7(7):771-7.

31.

Adult-onset familial hypertrophic cardiomyopathy caused by a novel mutation, R694C, in the MYH7 gene.

Andersen PS, Havndrup O, Bundgaard H, Larsen LA, Vuust J, Kjeldsen K, Christiansen M.

Clin Genet. 1999 Sep;56(3):244-6. No abstract available.

PMID:
10563488
32.
33.

Recessive Romano-Ward syndrome associated with compound heterozygosity for two mutations in the KVLQT1 gene.

Larsen LA, Fosdal I, Andersen PS, Kanters JK, Vuust J, Wettrell G, Christiansen M.

Eur J Hum Genet. 1999 Sep;7(6):724-8.

34.

Familial hypertrophic cardiomyopathy associated with a novel missense mutation affecting the ATP-binding region of the cardiac beta-myosin heavy chain.

Bundgaard H, Havndrup O, Andersen PS, Larsen LA, Brandt NJ, Vuust J, Kjeldsen K, Christiansen M.

J Mol Cell Cardiol. 1999 Apr;31(4):745-50.

PMID:
10329202
36.

A single strand conformation polymorphism/heteroduplex (SSCP/HD) method for detection of mutations in 15 exons of the KVLQT1 gene, associated with long QT syndrome.

Larsen LA, Andersen PS, Kanters JK, Jacobsen JR, Vuust J, Christiansen M.

Clin Chim Acta. 1999 Feb;280(1-2):113-25.

PMID:
10090529
37.

Mutation Detection by Cleavase in Combination With Capillary Electrophoresis Analysis: Application to Mutations Causing Hypertrophic Cardiomyopathy and Long-QT Syndrome.

Andersen PS, Larsen LA, Kanters Jr Jr, Havndrup O, Bundgaard H, Brandt NJ, Vuust J, Christiansen M.

Mol Diagn. 1998 Jun;3(2):105-111.

PMID:
10029661
38.

Polyamine-stimulated binding of diamine oxidase to DNA.

Bruun L, Hłgdall EV, Vuust J, Houen G.

Acta Chem Scand. 1998 Jul;52(7):921-9.

PMID:
9661267
39.

Novel donor splice site mutation in the KVLQT1 gene is associated with long QT syndrome.

Kanters JK, Larsen LA, Orholm M, Agner E, Andersen PS, Vuust J, Christiansen M.

J Cardiovasc Electrophysiol. 1998 Jun;9(6):620-4.

PMID:
9654228
40.

Structure and tissue-specific expression of genes encoding bovine copper amine oxidases.

Høgdall EV, Houen G, Borre M, Bundgaard JR, Larsson LI, Vuust J.

Eur J Biochem. 1998 Jan 15;251(1-2):320-8.

41.

The glutamate-rich protein (GLURP) of Plasmodium falciparum is a target for antibody-dependent monocyte-mediated inhibition of parasite growth in vitro.

Theisen M, Soe S, Oeuvray C, Thomas AW, Vuust J, Danielsen S, Jepsen S, Druilhe P.

Infect Immun. 1998 Jan;66(1):11-7.

42.

High-throughput analysis of fragile X (CGG)n alleles in the normal and premutation range by PCR amplification and automated capillary electrophoresis.

Larsen LA, Grønskov K, Nørgaard-Pedersen B, Brøndum-Nielsen K, Hasholt L, Vuust J.

Hum Genet. 1997 Oct;100(5-6):564-8.

PMID:
9341871
43.

New consensus features for tyrosine O-sulfation determined by mutational analysis.

Bundgaard JR, Vuust J, Rehfeld JF.

J Biol Chem. 1997 Aug 29;272(35):21700-5.

44.

Quantitative detection of male DNA by polymerase chain reaction using a single primer set: application to sex determination and counting of rare fetal cells.

Larsen LA, Christiansen M, Norgaard-Pedersen B, Vuust J.

Anal Biochem. 1996 Aug 15;240(1):148-50. No abstract available.

PMID:
8811895
46.

An efficient cellular system for mutational analysis of prohormone processing.

Bundgaard JR, Cowland JB, Vuust J, Rehfeld JF.

DNA Cell Biol. 1996 Feb;15(2):147-57.

PMID:
8634142
47.

Tyrosine O-sulfation promotes proteolytic processing of progastrin.

Bundgaard JR, Vuust J, Rehfeld JF.

EMBO J. 1995 Jul 3;14(13):3073-9.

48.

erm genes in erythromycin-resistant Staphylococcus aureus and coagulase-negative staphylococci.

Westh H, Hougaard DM, Vuust J, Rosdahl VT.

APMIS. 1995 Mar;103(3):225-32.

PMID:
7755979
49.

Development of a PCR-based technique for detection of Helicobacter pylori.

Thoreson AC, Borre MB, Andersen LP, Elsborg L, Holck S, Conway P, Henrichsen J, Vuust J, Krogfelt KA.

FEMS Immunol Med Microbiol. 1995 Feb;10(3-4):325-33.

PMID:
7773250
50.

Prevalence of erm gene classes in erythromycin-resistant Staphylococcus aureus strains isolated between 1959 and 1988.

Westh H, Hougaard DM, Vuust J, Rosdahl VT.

Antimicrob Agents Chemother. 1995 Feb;39(2):369-73.

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