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Rare mtDNA haplogroups and genetic differences in rich and poor Danish Iron-Age villages

American journal of physical anthropology, 2008-02, Vol.135 (2), p.206-215

2008

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Simultaneous Detection of ACP1 and GC Genotypes Using PCR/SSCP

Annals of human genetics, 2003-01, Vol.67 (1), p.81-85

2003

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Rapid, Simple Alkaline Extraction of Human Genomic DNA from Whole Blood, Buccal Epithelial Cells, Semen and Forensic Stains for PCR

BioTechniques, 1998-10, Vol.25 (4), p.588-592

1998

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Human red cell acid phosphatase (ACP1). The amino acid sequence of the two isozymes Bf and Bs encoded by the ACP1B allele

The Journal of biological chemistry, 1991-11, Vol.266 (31), p.20619-20625

1991

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Rapid and simple determination of hereditary haemochromatosis mutations by multiplex PCR–SSCP: detection of a new polymorphic mutation

Annals of human genetics, 1999-05, Vol.63 (3), p.193-197

1999

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Surprising stability of DNA in stains at extreme humidity and temperature

International Congress series, 2004-04, Vol.1261, p.616-618

2004

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Human Red Cell Galactose-1-Phosphate Uridylyltransferase (EC 2.7.7.12)

Human heredity, 2008-08, Vol.30 (1), p.27-32

2008

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Immunochemical characterization of human red cell acid phosphatase isozymes

Biochemical genetics, 1987-12, Vol.25 (11-12), p.901-918

DISSING, J

1987

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Exon Structure at the Human ACP1 Locus Supports Alternative Splicing Model for f-Isozyme and s-Isozyme Generation

Biochemical and biophysical research communications, 1993-10, Vol.196 (1), p.440-446

1993

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Human 18 kDa phosphotyrosine protein phosphatase (ACP1) polymorphism: studies of rare variants provide evidence that substitutions within or near alternatively spliced exons affect splicing result

Annals of human genetics, 2000-03, Vol.64 (2), p.107-116

2000

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The last Viking King: A royal maternity case solved by ancient DNA analysis

Forensic science international, 2007-02, Vol.166 (1), p.21-27

2007

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mtDNA analysis of human remains from an early Danish Christian cemetery

American journal of physical anthropology, 2005-10, Vol.128 (2), p.424-429

2005

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Evolutionary aspects of the gene for the classical enzyme polymorphism, ACP1

International Congress series, 2003, Vol.1239, p.733-736

2003

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HFE mutations and hemochromatosis in Danish patients admitted for HFE genotyping

Scandinavian journal of clinical and laboratory investigation, 2002, Vol.62 (7), p.527-535

2002

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Hydatidiform mole: genetic origin in polyploid conceptuses

Human genetics, 1987-05, Vol.76 (1), p.11-19

1987

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Demonstration of Enolase Activity Connected to the Brain‐Specific Protein 14‐3‐2

Scandinavian journal of immunology, 1975-07, Vol.4 (s2), p.31-36

1975

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ADENOSINE-DEAMINASE DEFICIENCY AND COMBINED IMMUNODEFICIENCY SYNDROME

The Lancet (British edition), 1972-01, Vol.300 (7790), p.1316-1316

1972

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Human red cell acid phosphatase (ACP1): evidence for differences in the primary structure of the two isozymes encoded by the ACP1B allele

Biochemical genetics, 1987-12, Vol.25 (11-12), p.919-927

1987

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Human red cell esterase D polymorphism in Denmark, its use in paternity cases and the description of a new phenotype

Human heredity, 1984-01, Vol.34 (3), p.148-155

1984

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Human 18 kDa phosphotyrosine protein phosphatase (ACP1) polymorphism: studies of rare variants provide evidence that substitutions within or near alternatively spliced exons affect splicing result

Annals of human genetics, 2000-03, Vol.64, p.107-116

2000

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Association between the C3F gene and atherosclerotic vascular diseases

Human heredity, 1975-01, Vol.25 (4), p.279-283

1975

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The effect of VAM on growth and uptake of nutrients in lucerne

Agriculture, Ecosystems & Environment [AGRIC. ECOSYST. ENVIRON.]. Vol. 29, no. 1-4. 1990, 1990, Vol.29 (1), p.99-102

1990

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Human red cell galactose-1-phosphate uridylyltransferase (EC 2.7.7.12). Electrophoretically determined polymorphism in Denmark and its use in paternity cases

Human heredity, 1980, Vol.30 (1), p.27

1980

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C3 polymorphism in relation to age

Human heredity, 1975-01, Vol.25 (4), p.284-295

1975

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Delirium tremens: Some clinico‐chemical features A STUDY OF ALANINE‐AMINOTRANSFERASE, ALCALINE PHOSPHATASE, PROTHROMBINE AND ENOLASE

Acta psychiatrica Scandinavica, 1980-12, Vol.62 (5), p.503-510

1980

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Rare mtDNA haplogroups and genetic differences in rich and poor Danish Iron-Age villages

Simultaneous Detection of ACP1 and GC Genotypes Using PCR/SSCP

Rapid, Simple Alkaline Extraction of Human Genomic DNA from Whole Blood, Buccal Epithelial Cells, Semen and Forensic Stains for PCR

Human red cell acid phosphatase (ACP1). The amino acid sequence of the two isozymes Bf and Bs encoded by the ACP1B allele

Rapid and simple determination of hereditary haemochromatosis mutations by multiplex PCR–SSCP: detection of a new polymorphic mutation

Surprising stability of DNA in stains at extreme humidity and temperature

Human Red Cell Galactose-1-Phosphate Uridylyltransferase (EC 2.7.7.12)

Immunochemical characterization of human red cell acid phosphatase isozymes

Exon Structure at the Human ACP1 Locus Supports Alternative Splicing Model for f-Isozyme and s-Isozyme Generation

Human 18 kDa phosphotyrosine protein phosphatase (ACP1) polymorphism: studies of rare variants provide evidence that substitutions within or near alternatively spliced exons affect splicing result

The last Viking King: A royal maternity case solved by ancient DNA analysis

mtDNA analysis of human remains from an early Danish Christian cemetery

Evolutionary aspects of the gene for the classical enzyme polymorphism, ACP1

HFE mutations and hemochromatosis in Danish patients admitted for HFE genotyping

Hydatidiform mole: genetic origin in polyploid conceptuses

Demonstration of Enolase Activity Connected to the Brain‐Specific Protein 14‐3‐2

ADENOSINE-DEAMINASE DEFICIENCY AND COMBINED IMMUNODEFICIENCY SYNDROME

Human red cell acid phosphatase (ACP1): evidence for differences in the primary structure of the two isozymes encoded by the ACP1B allele

Human red cell esterase D polymorphism in Denmark, its use in paternity cases and the description of a new phenotype

Human 18 kDa phosphotyrosine protein phosphatase (ACP1) polymorphism: studies of rare variants provide evidence that substitutions within or near alternatively spliced exons affect splicing result

Association between the C3F gene and atherosclerotic vascular diseases

The effect of VAM on growth and uptake of nutrients in lucerne

Human red cell galactose-1-phosphate uridylyltransferase (EC 2.7.7.12). Electrophoretically determined polymorphism in Denmark and its use in paternity cases

C3 polymorphism in relation to age

Delirium tremens: Some clinico‐chemical features A STUDY OF ALANINE‐AMINOTRANSFERASE, ALCALINE PHOSPHATASE, PROTHROMBINE AND ENOLASE

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