N. Gregersen

发表

Improved RNase protection assay for quantifying LDL-receptor mRNA; estimation of analytical imprecision and biological variance in peripheral blood mononuclear cells.

L. K. Larsen, H. Nissen, L. Jensen, 1995, Clinical chemistry.

Acyl-CoA-binding protein/diazepam-binding inhibitor gene and pseudogenes. A typical housekeeping gene family.

K. Kristiansen, S. Mandrup, R. Hummel, 1992, Journal of molecular biology.

Fatty Acyl-CoA dehydrogenase deficiency: Enzyme measurement and studies on alternative metabolism

N. Gregersen, 1984, Journal of Inherited Metabolic Disease.

Decreased expression of the mitochondrial matrix proteases Lon and ClpP in cells from a patient with hereditary spastic paraplegia (SPG13)

A. Durr, A. Dürr, P. Bross, 2008, Neuroscience.

Myopathy in very-long-chain acyl-CoA dehydrogenase deficiency: clinical and biochemical differences with the fatal cardiac phenotype

B. Andresen, B. Poorthuis, H. Scholte, 1999, Neuromuscular Disorders.

Structure of the rat gene encoding the multifunctional acyl-CoA-binding protein: conservation of intron 1 sequences in rodents and man. Addendum.

K. Kristiansen, S. Mandrup, J. Nøhr, 1996, Gene.

A polymerase chain reaction-based method for the semiquantitative study of interleukin-8 mRNA in human basophil leukocytes.

J. Justesen, K. Paludan, N. Rüdiger, 1995, Scandinavian journal of clinical and laboratory investigation.

An Iranian‐Armenian LDLR frameshift mutation causing familial hypercholesterolemia

O. Faergeman, N. Gregersen, P. Hansen, 1996, Clinical genetics.

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

O. Faergeman, N. Gregersen, P. Hansen, 1996, Clinical chemistry.

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

O. Faergeman, N. Gregersen, P. Hansen, 1994, Atherosclerosis.