Geurts JM - Search Results

1

Identification of TNFRSF1B as a novel modifier gene in familial combined hyperlipidemia.

Geurts JM, Janssen RG, van Greevenbroek MM, van der Kallen CJ, Cantor RM, Bu X, Aouizerat BE, Allayee H, Rotter JI, de Bruin TW. Geurts JM, et al. Hum Mol Genet. 2000 Sep 1;9(14):2067-74. doi: 10.1093/hmg/9.14.2067. Hum Mol Genet. 2000. PMID: 10958645

2

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

Eurlings PM, Van Der Kallen CJ, Geurts JM, Kouwenberg P, Boeckx WD, De Bruin TW. Eurlings PM, et al. Among authors: geurts jm. J Lipid Res. 2002 Jun;43(6):930-5. J Lipid Res. 2002. PMID: 12032168 Free article.

3

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

Eurlings PM, van der Kallen CJ, Geurts JM, Flavell DM, de Bruin TW. Eurlings PM, et al. Among authors: geurts jm. Mol Genet Metab. 2002 Dec;77(4):274-81. doi: 10.1016/s1096-7192(02)00174-9. Mol Genet Metab. 2002. PMID: 12468272

4

Soluble receptors for tumor necrosis factor-alpha (TNF-R p55 and TNF-R p75) in familial combined hyperlipidemia.

van Greevenbroek MM, van der Kallen CJ, Geurts JM, Janssen RG, Buurman WA, de Bruin TW. van Greevenbroek MM, et al. Among authors: geurts jm. Atherosclerosis. 2000 Nov;153(1):1-8. doi: 10.1016/s0021-9150(00)00375-0. Atherosclerosis. 2000. PMID: 11058695

5

Genome scan for adiposity in Dutch dyslipidemic families reveals novel quantitative trait loci for leptin, body mass index and soluble tumor necrosis factor receptor superfamily 1A.

van der Kallen CJ, Cantor RM, van Greevenbroek MM, Geurts JM, Bouwman FG, Aouizerat BE, Allayee H, Buurman WA, Lusis AJ, Rotter JI, de Bruin TW. van der Kallen CJ, et al. Among authors: geurts jm. Int J Obes Relat Metab Disord. 2000 Nov;24(11):1381-91. doi: 10.1038/sj.ijo.0801412. Int J Obes Relat Metab Disord. 2000. PMID: 11126332

6

Genetic dissection of familial combined hyperlipidemia.

Eurlings PM, van der Kallen CJ, Geurts JM, van Greevenbroek MM, de Bruin TW. Eurlings PM, et al. Among authors: geurts jm. Mol Genet Metab. 2001 Sep-Oct;74(1-2):98-104. doi: 10.1006/mgme.2001.3232. Mol Genet Metab. 2001. PMID: 11592807 Review.

7

Association between the alpha-adducin Gly460Trp polymorphism and systolic blood pressure in familial combined hyperlipidemia.

Beeks E, Janssen RG, Kroon AA, Keulen ET, Geurts JM, de Leeuw PW, de Bruin TW. Beeks E, et al. Among authors: geurts jm. Am J Hypertens. 2001 Dec;14(12):1185-90. doi: 10.1016/s0895-7061(01)02216-6. Am J Hypertens. 2001. PMID: 11775124

8

Toward positional cloning of the curly tail gene.

Brouns MR, Peeters MC, Geurts JM, Merckx DM, Engelen JJ, Hekking JW, Terwindt-Rouwenhorst EA, Oosterbaan ME, Geraedts JP, van Straaten HW. Brouns MR, et al. Among authors: geurts jm. Birth Defects Res A Clin Mol Teratol. 2005 Mar;73(3):154-61. doi: 10.1002/bdra.20109. Birth Defects Res A Clin Mol Teratol. 2005. PMID: 15678492

9

Molecular characterization of a complex chromosomal rearrangement in a pleomorphic salivary gland adenoma involving the 3'-UTR of HMGIC.

Geurts JM, Schoenmakers EF, Van de Ven WJ. Geurts JM, et al. Cancer Genet Cytogenet. 1997 Jun;95(2):198-205. doi: 10.1016/s0165-4608(96)00411-6. Cancer Genet Cytogenet. 1997. PMID: 9169041

10

Identification, molecular cloning, and characterization of the chromosome 12 breakpoint cluster region of uterine leiomyomas.

Schoenmakers EF, Mols R, Wanschura S, Kools PF, Geurts JM, Bartnitzke S, Bullerdiek J, van den Berghe H, Van de Ven WJ. Schoenmakers EF, et al. Among authors: geurts jm. Genes Chromosomes Cancer. 1994 Oct;11(2):106-18. doi: 10.1002/gcc.2870110207. Genes Chromosomes Cancer. 1994. PMID: 7529547

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