de Boer M - Search Results

1

Nonallelic homologous recombination of the FCGR2/3 locus results in copy number variation and novel chimeric FCGR2 genes with aberrant functional expression.

Nagelkerke SQ, Tacke CE, Breunis WB, Geissler J, Sins JW, Appelhof B, van den Berg TK, de Boer M, Kuijpers TW. Nagelkerke SQ, et al. Among authors: de boer m. Genes Immun. 2015 Sep;16(6):422-9. doi: 10.1038/gene.2015.25. Epub 2015 Jul 2. Genes Immun. 2015. PMID: 26133275

2

Novel insights in the genomic organization and hotspots of recombination in the human KIR locus through analysis of intergenic regions.

Vendelbosch S, de Boer M, van Leeuwen K, Pourfarzad F, Geissler J, van den Berg TK, Kuijpers TW. Vendelbosch S, et al. Among authors: de boer m. Genes Immun. 2015 Mar;16(2):103-11. doi: 10.1038/gene.2014.68. Epub 2014 Dec 11. Genes Immun. 2015. PMID: 25503311

3

KIR3DL1 and KIR3DL2 gene copy number variation in axial spondyloarthritis.

Vendelbosch S, de Boer M, van der Heijde D, van den Berg TK, van Gaalen FA, Kuijpers TW. Vendelbosch S, et al. Among authors: de boer m. Tissue Antigens. 2015 Jun;85(6):497-8. doi: 10.1111/tan.12563. Tissue Antigens. 2015. PMID: 25940819 No abstract available.

4

Study on the protective effect of the KIR3DL1 gene in ankylosing spondylitis.

Vendelbosch S, Heslinga SC, John M, van Leeuwen K, Geissler J, de Boer M, Tanck MW, van den Berg TK, Crusius JB, van der Horst-Bruinsma IE, Kuijpers TW. Vendelbosch S, et al. Among authors: de boer m. Arthritis Rheumatol. 2015 Nov;67(11):2957-65. doi: 10.1002/art.39288. Arthritis Rheumatol. 2015. PMID: 26238044

5

Point mutations in the promoter region of the CYBB gene leading to mild chronic granulomatous disease.

Weening RS, De Boer M, Kuijpers TW, Neefjes VM, Hack WW, Roos D. Weening RS, et al. Among authors: de boer m. Clin Exp Immunol. 2000 Dec;122(3):410-7. doi: 10.1046/j.1365-2249.2000.01405.x. Clin Exp Immunol. 2000. PMID: 11122248 Free PMC article.

6

Leukocyte adhesion deficiency type 1 (LAD-1)/variant. A novel immunodeficiency syndrome characterized by dysfunctional beta2 integrins.

Kuijpers TW, Van Lier RA, Hamann D, de Boer M, Thung LY, Weening RS, Verhoeven AJ, Roos D. Kuijpers TW, et al. Among authors: de boer m. J Clin Invest. 1997 Oct 1;100(7):1725-33. doi: 10.1172/JCI119697. J Clin Invest. 1997. PMID: 9312170 Free PMC article.

7

A novel syndrome of severe neutrophil dysfunction: unresponsiveness confined to chemotaxin-induced functions.

Roos D, Kuijpers TW, Mascart-Lemone F, Koenderman L, de Boer M, van Zwieten R, Verhoeven AJ. Roos D, et al. Among authors: de boer m. Blood. 1993 May 15;81(10):2735-43. Blood. 1993. PMID: 8098232 Free article.

8

Molecular diagnosis of chronic granulomatous disease.

Roos D, de Boer M. Roos D, et al. Among authors: de boer m. Clin Exp Immunol. 2014 Feb;175(2):139-49. doi: 10.1111/cei.12202. Clin Exp Immunol. 2014. PMID: 24016250 Free PMC article. Review.

9

Complex medical history of a patient with a compound heterozygous mutation in C1QC.

Lubbers R, Beaart-van de Voorde LJJ, van Leeuwen K, de Boer M, Gelderman KA, van den Berg MJ, Ketel AG, Simon A, de Ree J, Huizinga TWJ, Steup-Beekman GM, Trouw LA. Lubbers R, et al. Among authors: de boer m, de ree j. Lupus. 2019 Sep;28(10):1255-1260. doi: 10.1177/0961203319865029. Epub 2019 Jul 29. Lupus. 2019. PMID: 31357913 Free PMC article.

10

Gene-scan method for the recognition of carriers and patients with p47(phox)-deficient autosomal recessive chronic granulomatous disease.

Dekker J, de Boer M, Roos D. Dekker J, et al. Among authors: de boer m. Exp Hematol. 2001 Nov;29(11):1319-25. doi: 10.1016/s0301-472x(01)00731-7. Exp Hematol. 2001. PMID: 11698128 Free article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

1,721 results

Search Page