Hendriks RW - Search Results

1

Mapping of the X linked form of hyper IgM syndrome (HIGM1).

Padayachee M, Levinsky RJ, Kinnon C, Finn A, McKeown C, Feighery C, Notarangelo LD, Hendriks RW, Read AP, Malcolm S. Padayachee M, et al. Among authors: hendriks rw. J Med Genet. 1993 Mar;30(3):202-5. doi: 10.1136/jmg.30.3.202. J Med Genet. 1993. PMID: 8097258 Free PMC article.

2

Screening for mutations causing X-linked severe combined immunodeficiency in the IL-2R gamma chain gene by single-strand conformation polymorphism analysis.

Clark PA, Lester T, Genet S, Jones AM, Hendriks R, Levinsky RJ, Kinnon C. Clark PA, et al. Hum Genet. 1995 Oct;96(4):427-32. doi: 10.1007/BF00191801. Hum Genet. 1995. PMID: 7557965

3

The X-linked immunodeficiency defect in the mouse is corrected by expression of human Bruton's tyrosine kinase from a yeast artificial chromosome transgene.

Maas A, Dingjan GM, Savelkoul HF, Kinnon C, Grosveld F, Hendriks RW. Maas A, et al. Among authors: hendriks rw. Eur J Immunol. 1997 Sep;27(9):2180-7. doi: 10.1002/eji.1830270910. Eur J Immunol. 1997. PMID: 9341757

4

BTKbase: a database of XLA-causing mutations. International Study Group.

Vihinen M, Cooper MD, de Saint Basile G, Fischer A, Good RA, Hendriks RW, Kinnon C, Kwan SP, Litman GW, Notarangelo LD, et al. Vihinen M, et al. Among authors: hendriks rw. Immunol Today. 1995 Oct;16(10):460-5. doi: 10.1016/0167-5699(95)80027-1. Immunol Today. 1995. PMID: 7576047 Review. No abstract available.

5

B-cell antigen receptor stimulation activates the human Bruton's tyrosine kinase, which is deficient in X-linked agammaglobulinemia.

de Weers M, Brouns GS, Hinshelwood S, Kinnon C, Schuurman RK, Hendriks RW, Borst J. de Weers M, et al. Among authors: hendriks rw. J Biol Chem. 1994 Sep 30;269(39):23857-60. J Biol Chem. 1994. PMID: 7929028 Free article.

6

Evidence for male X chromosomal mosaicism in X-linked agammaglobulinemia.

Hendriks RW, Mensink EJ, Kraakman ME, Thompson A, Schuurman RK. Hendriks RW, et al. Hum Genet. 1989 Oct;83(3):267-70. doi: 10.1007/BF00285169. Hum Genet. 1989. PMID: 2571563

7

X chromosome inactivation patterns in haematopoietic cells of female carriers of X-linked severe combined immunodeficiency determined by methylation analysis at the hypervariable DXS255 locus.

Hendriks RW, Kraakman ME, Schuurman RK. Hendriks RW, et al. Clin Genet. 1992 Sep;42(3):114-21. doi: 10.1111/j.1399-0004.1992.tb03221.x. Clin Genet. 1992. PMID: 1395081

8

Polyclonal hyper-immunoglobulin G1(A1) syndrome. Evidence for a dominant immunoglobulin production regulator within the human immunoglobulin heavy chain gene complex.

Hendriks RW, Sandkuyl LA, Kraakman ME, de Lange GG, Schuurman RK. Hendriks RW, et al. Hum Genet. 1989 May;82(2):194-6. doi: 10.1007/BF00284057. Hum Genet. 1989. PMID: 2498199

9

Identification of a CD40L gene mutation and genetic counselling in a family with immunodeficiency with hyperimmunoglobulinemia M.

Kraakman ME, de Weers M, Español T, Schuurman RK, Hendriks RW. Kraakman ME, et al. Among authors: hendriks rw. Clin Genet. 1995 Jul;48(1):46-8. doi: 10.1111/j.1399-0004.1995.tb04053.x. Clin Genet. 1995. PMID: 7586644

10

Absence of the XIST gene from late-replicating isodicentric X chromosomes in leukaemia.

Rack KA, Chelly J, Gibbons RJ, Rider S, Benjamin D, Lafreniére RG, Oscier D, Hendriks RW, Craig IW, Willard HF, et al. Rack KA, et al. Among authors: hendriks rw. Hum Mol Genet. 1994 Jul;3(7):1053-9. doi: 10.1093/hmg/3.7.1053. Hum Mol Genet. 1994. PMID: 7981672

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