Testers L - Search Results

1

Park7, a novel locus for autosomal recessive early-onset parkinsonism, on chromosome 1p36.

van Duijn CM, Dekker MC, Bonifati V, Galjaard RJ, Houwing-Duistermaat JJ, Snijders PJ, Testers L, Breedveld GJ, Horstink M, Sandkuijl LA, van Swieten JC, Oostra BA, Heutink P. van Duijn CM, et al. Among authors: testers l. Am J Hum Genet. 2001 Sep;69(3):629-34. doi: 10.1086/322996. Epub 2001 Jul 2. Am J Hum Genet. 2001. PMID: 11462174 Free PMC article.

2

Evidence for novel loci for late-onset Parkinson's disease in a genetic isolate from the Netherlands.

Bertoli-Avella AM, Dekker MC, Aulchenko YS, Houwing-Duistermaat JJ, Simons E, Testers L, Pardo LM, Rademaker TA, Snijders PJ, van Swieten JC, Bonifati V, Heutink P, van Duijn CM, Oostra BA. Bertoli-Avella AM, et al. Among authors: testers l. Hum Genet. 2006 Mar;119(1-2):51-60. doi: 10.1007/s00439-005-0108-7. Epub 2005 Dec 14. Hum Genet. 2006. PMID: 16369765

3

The gene for triphalangeal thumb maps to the subtelomeric region of chromosome 7q.

Heutink P, Zguricas J, van Oosterhout L, Breedveld GJ, Testers L, Sandkuijl LA, Snijders PJ, Weissenbach J, Lindhout D, Hovius SE, et al. Heutink P, et al. Among authors: testers l. Nat Genet. 1994 Mar;6(3):287-92. doi: 10.1038/ng0394-287. Nat Genet. 1994. PMID: 8012392

4

The primary erythermalgia-susceptibility gene is located on chromosome 2q31-32.

Drenth JP, Finley WH, Breedveld GJ, Testers L, Michiels JJ, Guillet G, Taieb A, Kirby RL, Heutink P. Drenth JP, et al. Among authors: testers l. Am J Hum Genet. 2001 May;68(5):1277-82. doi: 10.1086/320107. Epub 2001 Mar 20. Am J Hum Genet. 2001. PMID: 11283792 Free PMC article.

5

A genome-wide search for linkage-disequilibrium with type 1 diabetes in a recent genetically isolated population from the Netherlands.

Vaessen N, Heutink P, Houwing-Duistermaat JJ, Snijders PJ, Rademaker T, Testers L, Batstra MR, Sandkuijl LA, van Duijn CM, Oostra BA. Vaessen N, et al. Among authors: testers l. Diabetes. 2002 Mar;51(3):856-9. doi: 10.2337/diabetes.51.3.856. Diabetes. 2002. PMID: 11872691 Free article.

6

Autosomal dominant central areolar choroidal dystrophy caused by a mutation in codon 142 in the peripherin/RDS gene.

Hoyng CB, Heutink P, Testers L, Pinckers A, Deutman AF, Oostra BA. Hoyng CB, et al. Among authors: testers l. Am J Ophthalmol. 1996 Jun;121(6):623-9. doi: 10.1016/s0002-9394(14)70627-0. Am J Ophthalmol. 1996. PMID: 8644804 Free article.

7

A polymorphism in the gene for IGF-I: functional properties and risk for type 2 diabetes and myocardial infarction.

Vaessen N, Heutink P, Janssen JA, Witteman JC, Testers L, Hofman A, Lamberts SW, Oostra BA, Pols HA, van Duijn CM. Vaessen N, et al. Among authors: testers l. Diabetes. 2001 Mar;50(3):637-42. doi: 10.2337/diabetes.50.3.637. Diabetes. 2001. PMID: 11246885 Free article.

8

Myocardial capillaries: increase in number by splitting of existing vessels.

van Groningen JP, Wenink AC, Testers LH. van Groningen JP, et al. Among authors: testers lh. Anat Embryol (Berl). 1991;184(1):65-70. doi: 10.1007/BF01744262. Anat Embryol (Berl). 1991. PMID: 1928745

9

Taking Affective Learning in Digital Education One Step Further: Trainees' Affective Characteristics Predicting Multicontextual Pre-training Transfer Intention.

Testers L, Gegenfurtner A, Brand-Gruwel S. Testers L, et al. Front Psychol. 2020 Sep 17;11:2189. doi: 10.3389/fpsyg.2020.02189. eCollection 2020. Front Psychol. 2020. PMID: 33041888 Free PMC article.

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