de Klein A - Search Results

1

[Molecular genetic studies in alpha-thalassemia].

de Korte D, Cuypers HT, de Klein A, Winkel I, Vuil H, Roos D. de Korte D, et al. Among authors: de klein a. Ned Tijdschr Geneeskd. 1992 May 2;136(18):872-5. Ned Tijdschr Geneeskd. 1992. PMID: 1350329 Dutch.

2

Chronic granulomatous disease: mutations in cytochrome b558.

Roos D, De Boer M, De Klein A, Bolscher BG, Weening RS. Roos D, et al. Among authors: de boer m, de klein a. Immunodeficiency. 1993;4(1-4):289-301. Immunodeficiency. 1993. PMID: 8167720 Review. No abstract available.

3

Point mutations in the beta-subunit of cytochrome b558 leading to X-linked chronic granulomatous disease.

Bolscher BG, de Boer M, de Klein A, Weening RS, Roos D. Bolscher BG, et al. Among authors: de boer m, de klein a. Blood. 1991 Jun 1;77(11):2482-7. Blood. 1991. PMID: 1710153 Free article.

4

Effect of interferon-gamma, in vitro and in vivo, on mRNA levels of phagocyte oxidase components.

Weening RS, de Klein A, de Boer M, Roos D. Weening RS, et al. Among authors: de boer m, de klein a. J Leukoc Biol. 1996 Dec;60(6):716-20. doi: 10.1002/jlb.60.6.716. J Leukoc Biol. 1996. PMID: 8975873 Clinical Trial.

5

Cytochrome b558-negative, autosomal recessive chronic granulomatous disease: two new mutations in the cytochrome b558 light chain of the NADPH oxidase (p22-phox).

de Boer M, de Klein A, Hossle JP, Seger R, Corbeel L, Weening RS, Roos D. de Boer M, et al. Among authors: de klein a. Am J Hum Genet. 1992 Nov;51(5):1127-35. Am J Hum Genet. 1992. PMID: 1415254 Free PMC article.

6

Disturbed interaction of p21-rac with mutated p67-phox causes chronic granulomatous disease.

Leusen JH, de Klein A, Hilarius PM, Ahlin A, Palmblad J, Smith CI, Diekmann D, Hall A, Verhoeven AJ, Roos D. Leusen JH, et al. Among authors: de klein a. J Exp Med. 1996 Oct 1;184(4):1243-9. doi: 10.1084/jem.184.4.1243. J Exp Med. 1996. PMID: 8879195 Free PMC article.

7

[Oncogenes, tumor suppression genes and medical genetics of cancer].

Bootsma AH, Cornelisse CJ, de Klein A. Bootsma AH, et al. Among authors: de klein a. Ned Tijdschr Geneeskd. 1992 May 23;136(21):1009-13. Ned Tijdschr Geneeskd. 1992. PMID: 1318508 Review. Dutch. No abstract available.

8

Cytogenetic and molecular analysis in Philadelphia negative CML.

van der Plas DC, Hermans AB, Soekarman D, Smit EM, de Klein A, Smadja N, Alimena G, Goudsmit R, Grosveld G, Hagemeijer A. van der Plas DC, et al. Among authors: de klein a. Blood. 1989 Mar;73(4):1038-44. Blood. 1989. PMID: 2920204 Free article.

9

Absence of both subunits of cytochrome b558 in the UM384 cell line relative to the inability to generate superoxide anions.

Champelovier P, Laporte F, Verhoeven AJ, Hilarius P, de Klein A, Revol C, Seigneurin D, Kolodie L. Champelovier P, et al. Among authors: de klein a. Exp Hematol. 1993 Jul;21(7):885-92. Exp Hematol. 1993. PMID: 8391470

10

A G-->A transition creates a branch point sequence and activation of a cryptic exon, resulting in the hereditary disorder neurofibromatosis 2.

De Klein A, Riegman PH, Bijlsma EK, Heldoorn A, Muijtjens M, den Bakker MA, Avezaat CJ, Zwarthoff EC. De Klein A, et al. Hum Mol Genet. 1998 Mar;7(3):393-8. doi: 10.1093/hmg/7.3.393. Hum Mol Genet. 1998. PMID: 9466995 Free article.

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