Luijendijk MW - Search Results

1

Disturbed CXCR4/CXCL12 axis in paediatric precursor B-cell acute lymphoblastic leukaemia.

van den Berk LC, van der Veer A, Willemse ME, Theeuwes MJ, Luijendijk MW, Tong WH, van der Sluis IM, Pieters R, den Boer ML. van den Berk LC, et al. Among authors: luijendijk mw. Br J Haematol. 2014 Jul;166(2):240-9. doi: 10.1111/bjh.12883. Epub 2014 Apr 4. Br J Haematol. 2014. PMID: 24697337 Free article.

2

PKCζ and PKMζ are overexpressed in TCF3-rearranged paediatric acute lymphoblastic leukaemia and are associated with increased thiopurine sensitivity.

Hartsink-Segers SA, Beaudoin JJ, Luijendijk MW, Exalto C, Pieters R, Den Boer ML. Hartsink-Segers SA, et al. Among authors: luijendijk mw. Leukemia. 2015 Feb;29(2):304-11. doi: 10.1038/leu.2014.210. Epub 2014 Jul 3. Leukemia. 2015. PMID: 24990612 Free PMC article.

3

Aurora kinases in childhood acute leukemia: the promise of aurora B as therapeutic target.

Hartsink-Segers SA, Zwaan CM, Exalto C, Luijendijk MW, Calvert VS, Petricoin EF, Evans WE, Reinhardt D, de Haas V, Hedtjärn M, Hansen BR, Koch T, Caron HN, Pieters R, Den Boer ML. Hartsink-Segers SA, et al. Among authors: luijendijk mw. Leukemia. 2013 Mar;27(3):560-8. doi: 10.1038/leu.2012.256. Epub 2012 Sep 3. Leukemia. 2013. PMID: 22940834 Free PMC article.

4

Cloning, characterization, and mRNA expression analysis of novel human fetal cochlear cDNAs.

Luijendijk MW, van de Pol TJ, van Duijnhoven G, den Hollander AI, ten Caat J, van Limpt V, Brunner HG, Kremer H, Cremers FP. Luijendijk MW, et al. Genomics. 2003 Oct;82(4):480-90. doi: 10.1016/s0888-7543(03)00150-2. Genomics. 2003. PMID: 13679028

5

Identification and molecular modelling of a mutation in the motor head domain of myosin VIIA in a family with autosomal dominant hearing impairment (DFNA11).

Luijendijk MW, Van Wijk E, Bischoff AM, Krieger E, Huygen PL, Pennings RJ, Brunner HG, Cremers CW, Cremers FP, Kremer H. Luijendijk MW, et al. Hum Genet. 2004 Jul;115(2):149-56. doi: 10.1007/s00439-004-1137-3. Epub 2004 Jun 2. Hum Genet. 2004. PMID: 15221449

6

A novel mutation identified in the DFNA5 gene in a Dutch family: a clinical and genetic evaluation.

Bischoff AM, Luijendijk MW, Huygen PL, van Duijnhoven G, De Leenheer EM, Oudesluijs GG, Van Laer L, Cremers FP, Cremers CW, Kremer H. Bischoff AM, et al. Among authors: luijendijk mw. Audiol Neurootol. 2004 Jan-Feb;9(1):34-46. doi: 10.1159/000074185. Audiol Neurootol. 2004. PMID: 14676472

7

Cochleovestibular and ocular features in a Dutch DFNA11 family.

Bischoff AM, Pennings RJ, Huygen PL, Luijendijk MW, van Wijk E, Cruysberg JR, Kremer H, Cremers CW. Bischoff AM, et al. Among authors: luijendijk mw. Otol Neurotol. 2006 Apr;27(3):323-31. doi: 10.1097/00129492-200604000-00006. Otol Neurotol. 2006. PMID: 16639269

8

Cross-sectional analysis of hearing threshold in relation to age in a large family with cochleovestibular impairment thoroughly genotyped for DFNA9/COCH.

Bom SJ, Kemperman MH, Huygen PL, Luijendijk MW, Cremers CW. Bom SJ, et al. Among authors: luijendijk mw. Ann Otol Rhinol Laryngol. 2003 Mar;112(3):280-6. doi: 10.1177/000348940311200316. Ann Otol Rhinol Laryngol. 2003. PMID: 12656423

9

Mutations in the VLGR1 gene implicate G-protein signaling in the pathogenesis of Usher syndrome type II.

Weston MD, Luijendijk MW, Humphrey KD, Möller C, Kimberling WJ. Weston MD, et al. Among authors: luijendijk mw. Am J Hum Genet. 2004 Feb;74(2):357-66. doi: 10.1086/381685. Epub 2004 Jan 20. Am J Hum Genet. 2004. PMID: 14740321 Free PMC article.

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