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Rare apolipoprotein E variant cosegregating with a unique APOE-C1-C2 haplotype in a normolipidemic family

Human heredity, 1988, Vol.38 (5), p.277

1988

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The Flaccid Lung Syndrome and α1-Protease Inhibitor Deficiency

Chest, 1988-04, Vol.93 (4), p.831-835

1988

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PI (alpha 1-Antitrypsin) subtypes: frequency of PIM4 in several populations

Human genetics, 1982-12, Vol.62 (2), p.139-141

1982

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Alpha-1-antitrypsin phenotypes and serum concentrations in duodenal ulcer patients in The Netherlands

Digestion, 1988, Vol.39 (1), p.20

1988

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A Pro----Leu substitution in codon 369 of the alpha-1-antitrypsin deficiency variant PI MHeerlen

Human genetics, 1989-02, Vol.81 (3), p.264-268

1989

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alpha 1-antitrypsin phenotype and gene distribution in Southern Italy

Human heredity, 1981, Vol.31 (3), p.180

Klasen, E C

1981

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Development of a screening system for detection of somatic mutations. I. Enzyme immunoassay for detection of antibodies against specific hemoglobin determinants

Journal of immunological methods, 1982-10, Vol.54 (2), p.241-250

1982

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Development of a screening system for detection of somatic mutations. II. The use of peptides and insoluble protein fragments in a non-competitive solid-phase enzyme immunoassay

Journal of immunological methods, 1983-05, Vol.59 (3), p.281-287

1983

Volltextzugriff (PDF)

Use of N-(7-dimethylamino-4-methylcoumarinyl)maleinimide for the detection of cysteine-containing peptides in peptide maps

Analytical biochemistry, 1982-04, Vol.121 (2), p.230-233

Klasen, Eduard C.

1982

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Apolipoprotein E polymorphism in the Netherlands and its effect on plasma lipid and apolipoprotein levels

Human genetics, 1988-11, Vol.80 (3), p.287-292

1988

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Phenotype and gene distribution of alpha-1-antitrypsin in a North Italian population

Human heredity, 1978-01, Vol.28 (6), p.474

1978

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Exclusion of the dysplastic nevus syndrome (DNS) locus from the short arm of chromosome 1 by linkage studies in dutch families

Genomics (San Diego, Calif.), 1989-07, Vol.5 (1), p.61-64

1989

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Bifunctionality and polarized infidelity at the hisB locus of Aspergillus nidulans

Molecular & general genetics, 1984-01, Vol.193 (2), p.332-339

1984

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Alpha 1-antitrypsin serum concentration and phenotypes in ulcerative colitis

Digestion, 1984, Vol.29 (2), p.124

1984

Volltextzugriff (PDF)

Use of bispecific hybrid antibodies for the development of a homogeneous enzyme immunoassay

Journal of immunological methods, 1989-09, Vol.123 (1), p.131-140

1989

Volltextzugriff (PDF)

Use of bispecific hybrid antibodies for the development of a homogeneous enzyme immunoassay

Journal of immunological methods, 1989, Vol.123 (2), p.131-140

1989

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Apolipoprotein gene cluster on chromosome 19: definite localization of the APOC2 gene and the polymorphic HpaI site associated with type III hyperlipoproteinemia

Human genetics, 1988, Vol.78 (1), p.90-93

1988

Volltextzugriff (PDF)

A Pro→Leu substitution in codon 369 of the alpha-1-antitrypsin drficiency variant PI MHeerlen

Human genetics, 1989, Vol.81 (3), p.264-268

1989

Volltextzugriff (PDF)

The ?1 antitrypsin variant PIWFINNEYTOWN in a family of Caucasian origin

Human genetics, 1985-02, Vol.69 (2), p.190-191

1985

Volltextzugriff (PDF)

The alpha 1 antitrypsin variant PI WFINNEYTOWN in a family of Caucasian origin

Human genetics, 1985, Vol.69 (2), p.190-191

1985

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The α1 antitrypsin variant PI#7B-ÙWFINNEYTOWN in a family of Caucasian origin

Human genetics, 1985, Vol.69 (2), p.190-191

1985

Volltextzugriff (PDF)

Meningeal dissemination in primary CNS lymphoma: prospective evaluation of 282 patients

Neurology, 2008-09, Vol.71 (14), p.1102

2008

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Population genetics of ?1-Antitrypsin in the Netherlands: Description of a new electrophoretic variant

Human genetics, 1977, Vol.37 (3), p.303-313

1977

Volltextzugriff (PDF)

The physics of ultraperipheral collisions at the LHC

Physics reports, 2008-03, Vol.458 (1), p.1-171

2008

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A minimal model for two-component dark matter

The journal of high energy physics, 2014-09, Vol.2014 (9), p.1, Article 108

2014

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Rare apolipoprotein E variant cosegregating with a unique APOE-C1-C2 haplotype in a normolipidemic family

The Flaccid Lung Syndrome and α1-Protease Inhibitor Deficiency

PI (alpha 1-Antitrypsin) subtypes: frequency of PIM4 in several populations

Alpha-1-antitrypsin phenotypes and serum concentrations in duodenal ulcer patients in The Netherlands

A Pro----Leu substitution in codon 369 of the alpha-1-antitrypsin deficiency variant PI MHeerlen

alpha 1-antitrypsin phenotype and gene distribution in Southern Italy

Development of a screening system for detection of somatic mutations. I. Enzyme immunoassay for detection of antibodies against specific hemoglobin determinants

Development of a screening system for detection of somatic mutations. II. The use of peptides and insoluble protein fragments in a non-competitive solid-phase enzyme immunoassay

Use of N-(7-dimethylamino-4-methylcoumarinyl)maleinimide for the detection of cysteine-containing peptides in peptide maps

Apolipoprotein E polymorphism in the Netherlands and its effect on plasma lipid and apolipoprotein levels

Phenotype and gene distribution of alpha-1-antitrypsin in a North Italian population

Exclusion of the dysplastic nevus syndrome (DNS) locus from the short arm of chromosome 1 by linkage studies in dutch families

Bifunctionality and polarized infidelity at the hisB locus of Aspergillus nidulans

Alpha 1-antitrypsin serum concentration and phenotypes in ulcerative colitis

Use of bispecific hybrid antibodies for the development of a homogeneous enzyme immunoassay

Use of bispecific hybrid antibodies for the development of a homogeneous enzyme immunoassay

Apolipoprotein gene cluster on chromosome 19: definite localization of the APOC2 gene and the polymorphic HpaI site associated with type III hyperlipoproteinemia

A Pro→Leu substitution in codon 369 of the alpha-1-antitrypsin drficiency variant PI MHeerlen

The ?1 antitrypsin variant PIWFINNEYTOWN in a family of Caucasian origin

The alpha 1 antitrypsin variant PI WFINNEYTOWN in a family of Caucasian origin

The α1 antitrypsin variant PI#7B-ÙWFINNEYTOWN in a family of Caucasian origin

Meningeal dissemination in primary CNS lymphoma: prospective evaluation of 282 patients

Population genetics of ?1-Antitrypsin in the Netherlands: Description of a new electrophoretic variant

The physics of ultraperipheral collisions at the LHC

A minimal model for two-component dark matter

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