A. Thompson

发表

Expression and characterization of human beta-secretase candidates metalloendopeptidase MP78 and cathepsin D in beta APP-overexpressing cells.

P. Malherbe, A. Thompson, G. Huber, 1997, Brain research. Molecular brain research.

Somatic gene transfer in the development of an animal model for primary hyperparathyroidism.

R. Mulligan, A. Rosenberg, H. Kronenberg, 1992, Endocrinology.

cDNA cloning of a novel secreted isoform of the human receptor for advanced glycation end products and characterization of cells co-expressing cell-surface scavenger receptors and Swedish mutant amyloid precursor protein.

P. Malherbe, C. Diener, J. Richards, 1999, Brain research. Molecular brain research.

Genetic Polymorphism of CYP2C19 Gene in the Stanislas Cohort. A link with Inflammation

G. Siest, S. Visvikis-Siest, D. Foernzler, 2008, Annals of human genetics.

X-linked immunodeficiency with hyperimmunoglobulinemia M appears to be linked to the DXS42 restriction fragment length polymorphism locus

L. Sandkuyl, E. Mensink, R. Schuurman, 1987, Human Genetics.

Heterogeneity in the map distance between X-linked agammaglobulinemia and a map of nine RFLP loci

J. Ott, E. Mensink, R. Schuurman, 1986, Human Genetics.

Mapping of a gene for X-linked agammaglobulinemia and evidence for genetic heterogeneity

L. Sandkuyl, E. Mensink, R. Schuurman, 1986, Human Genetics.

Genetic heterogeneity in X‐linked agammaglobulinemia complicates carrier detection and prenatal diagnosis

L. Sandkuyl, E. Mensink, R. Schuurman, 1987, Clinical genetics.

Full-length chicken parathyroid hormone. Biosynthesis in Escherichia coli and analysis of biologic activity.

S. K. Lim, H. Kronenberg, T. Gardella, 1991, The Journal of biological chemistry.

Nontruncating APC germ-line mutations and mismatch repair deficiency play a minor role in APC mutation-negative polyposis.

G. Marra, K. Heinimann, D. Foernzler, 2001, Cancer research.

Nontruncating APC Germline Mutations and Mismatch Repair Deficiency Play a Minor Role in APC Mutation-negative Polyposis 1

G. Marra, K. Heinimann, D. Foernzler, 2001 .

cDNA Cloning and Molecular Characterization of Human Brain Metalloprotease MP100

H. Hauri, P. Malherbe, R. Hochstrasser, 1999 .

Lack of association between the SOST gene and bone mineral density in perimenopausal women: analysis of five polymorphisms.

K. Lindpaintner, D. Reid, M. Ebeling, 2002, Bone.

Evidence for male X chromosomal mosaicism in X-linked agammaglobulinemia

E. Mensink, R. Hendriks, R. Schuurman, 1989, Human Genetics.

Interaction between CYP1A1 T3801C and AHR G1661A polymorphisms according to smoking status on blood pressure in the Stanislas cohort

G. Siest, S. Visvikis-Siest, D. Foernzler, 2006, Journal of hypertension.

Pharmacogenetic analysis of adverse drug effect reveals genetic variant for susceptibility to liver toxicity

J. Ott, J. Hoh, K. Lindpaintner, 2002, The Pharmacogenomics Journal.

A semi‐automated system for analysis and storage of SNPs

M. Ott, D. Foernzler, A. Thompson, 2001, Human mutation.