P. Eurlings

发表

Identification of differentially expressed genes in subcutaneous adipose tissue from subjects with familial combined hyperlipidemia.

C. V. D. van der Kallen, P. Eurlings, J. Geurts, 2002, Journal of lipid research.

Genetic dissection of familial combined hyperlipidemia.

C. V. D. van der Kallen, M. V. van Greevenbroek, P. Eurlings, 2001, Molecular genetics and metabolism.

Identification of the PPARA locus on chromosome 22q13.3 as a modifier gene in familial combined hyperlipidemia.

C. V. D. van der Kallen, P. Eurlings, J. Geurts, 2002, Molecular genetics and metabolism.

Human KCNQ1 S140G mutation is associated with atrioventricular blocks.

Luying Peng, Li Li, P. Eurlings, 2007, Heart rhythm.

Variants in the PPARγ gene affect fatty acid and glycerol metabolism in familial combined hyperlipidemia

P. Eurlings, T. D. Bruin, C. Kallen, 2003 .

Atherosclerotic plaque rupture: local or systemic process?

M. Daemen, E. Lutgens, P. Eurlings, 2003, Arteriosclerosis, thrombosis, and vascular biology.

Mapping a novel locus for familial atrial fibrillation on chromosome 10p11-q21.

P. Volders, Li Li, P. Eurlings, 2007, Heart rhythm.

A Kir2.1 gain-of-function mutation underlies familial atrial fibrillation.

Yusong He, Li Li, Yi Liu, 2005, Biochemical and biophysical research communications.

Atherosclerotic Plaque Rupture

M. Daemen, E. Lutgens, P. Eurlings, 2003 .

Nonfatal Plaque Rupture , Intraplaque Hemorrhage , and Plaque Growth

M. Daemen, E. Lutgens, P. Eurlings, 2003 .

The FASEB Journal express article 10.1096/fj.04-2403fje. Published online October 11, 2005. Up-regulation of CD36/FAT in preadipocytes in familial combined hyperlipidemia

C. Evelo, P. Eurlings, J. Glatz, 2022 .

Variants in the PPARgamma gene affect fatty acid and glycerol metabolism in familial combined hyperlipidemia.

C. V. D. van der Kallen, P. Eurlings, T. D. de Bruin, 2003, Molecular genetics and metabolism.