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

Clinical chemistry (Baltimore, Md.), 2001-08, Vol.47 (8), p.1390-1395

2001

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

Journal of medical genetics, 2001-12, Vol.38 (12), p.e43-43

2001

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Adverse reactions to injectable soft tissue permanent fillers

Aesthetic plastic surgery, 2005-01, Vol.29 (1), p.34-48

2005

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Polymerase chain reaction for detection of Mycoplasma genitalium in clinical samples

Journal of Clinical Microbiology, 1991-01, Vol.29 (1), p.46-50

1991

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Tyrosine O‐sulfation promotes proteolytic processing of progastrin

The EMBO journal, 1995-07, Vol.14 (13), p.3073-3079

1995

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Antigenicity and immunogenicity of recombinant glutamate-rich protein of Plasmodium falciparum expressed in Escherichia coli

Clinical and Diagnostic Laboratory Immunology, 1995-01, Vol.2 (1), p.30

1995

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

Antimicrobial Agents and Chemotherapy, 1995-02, Vol.39 (2), p.369-373

1995

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Polymorphism in ospC gene of Borrelia burgdorferi and immunoreactivity of OspC protein: implications for taxonomy and for use of OspC protein as a diagnostic antigen

Journal of Clinical Microbiology, 1993-10, Vol.31 (10), p.2570-2576

1993

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Recent developments in high-throughput mutation screening

Pharmacogenomics, 2001-11, Vol.2 (4), p.387-399

2001

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Recombinant Toxoplasma gondii surface antigen 1 (P30) expressed in Escherichia coli is recognized by human Toxoplasma-specific immunoglobulin M (IgM) and IgG antibodies

Clinical and Diagnostic Laboratory Immunology, 1996-05, Vol.3 (3), p.355

1996

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

Human mutation, 2003-05, Vol.21 (5), p.455-465

2003

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High throughput mutation screening by automated capillary electrophoresis

Combinatorial chemistry & high throughput screening, 2000-10, Vol.3 (5), p.393

2000

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

Human mutation, 2003-02, Vol.21 (2), p.116-122

2003

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The human ubiquitin multigene family: some genes contain multiple directly repeated ubiquitin coding sequences

The EMBO journal, 1985-03, Vol.4 (3), p.755-759

1985

Volltextzugriff (PDF)

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

European journal of human genetics : EJHG, 2004-08, Vol.12 (8), p.673-677

2004

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Molecular Cloning of Human Gastrin cDNA: Evidence for Evolution of Gastrin by Gene Duplication

Proceedings of the National Academy of Sciences - PNAS, 1983-01, Vol.80 (10), p.2866-2869

1983

Volltextzugriff (PDF)

Immunogenicity of the Plasmodium falciparum glutamate-rich protein expressed by vaccinia virus

Infection and Immunity, 1994-08, Vol.62 (8), p.3270-3275

1994

Volltextzugriff (PDF)

One third of Danish hypertrophic cardiomyopathy patients have mutations in MYH7 rod region

European journal of human genetics : EJHG, 2005-02, Vol.13 (2), p.161-165

2005

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New Consensus Features for Tyrosine O-Sulfation Determined by Mutational Analysis

The Journal of biological chemistry, 1997-08, Vol.272 (35), p.21700-21705

1997

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Comparison of in vitro culture and polymerase chain reaction for detection of Borrelia burgdorferi in tissue from experimentally infected animals

Journal of Clinical Microbiology, 1991-04, Vol.29 (4), p.731-737

1991

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

Clinical genetics, 1999-09, Vol.56 (3), p.244-246

1999

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High-throughput single-strand conformation polymorphism analysis by automated capillary electrophoresis: Robust multiplex analysis and pattern-based identification of allelic variants

Human mutation, 1999, Vol.13 (4), p.318-327

1999

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

APMIS : acta pathologica, microbiologica et immunologica Scandinavica, 1995-01, Vol.103 (1-6), p.225-232

1995

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A novel missense mutation, Leu390val, in the cardiac β-myosin heavy chain associated with pronounced septal hypertrophy in two families with hypertrophic cardiomyopathy

Scandinavian cardiovascular journal : SCJ, 2000-12, Vol.34 (6), p.558-563

2000

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

Genetic testing, 2007-04, Vol.11 (1), p.65

2007

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

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

Adverse reactions to injectable soft tissue permanent fillers

Polymerase chain reaction for detection of Mycoplasma genitalium in clinical samples

Tyrosine O‐sulfation promotes proteolytic processing of progastrin

Antigenicity and immunogenicity of recombinant glutamate-rich protein of Plasmodium falciparum expressed in Escherichia coli

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

Polymorphism in ospC gene of Borrelia burgdorferi and immunoreactivity of OspC protein: implications for taxonomy and for use of OspC protein as a diagnostic antigen

Recent developments in high-throughput mutation screening

Recombinant Toxoplasma gondii surface antigen 1 (P30) expressed in Escherichia coli is recognized by human Toxoplasma-specific immunoglobulin M (IgM) and IgG antibodies

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

High throughput mutation screening by automated capillary electrophoresis

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

The human ubiquitin multigene family: some genes contain multiple directly repeated ubiquitin coding sequences

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

Molecular Cloning of Human Gastrin cDNA: Evidence for Evolution of Gastrin by Gene Duplication

Immunogenicity of the Plasmodium falciparum glutamate-rich protein expressed by vaccinia virus

One third of Danish hypertrophic cardiomyopathy patients have mutations in MYH7 rod region

New Consensus Features for Tyrosine O-Sulfation Determined by Mutational Analysis

Comparison of in vitro culture and polymerase chain reaction for detection of Borrelia burgdorferi in tissue from experimentally infected animals

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

High-throughput single-strand conformation polymorphism analysis by automated capillary electrophoresis: Robust multiplex analysis and pattern-based identification of allelic variants

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

A novel missense mutation, Leu390val, in the cardiac β-myosin heavy chain associated with pronounced septal hypertrophy in two families with hypertrophic cardiomyopathy

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

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